Decadal-scale Dynamics of Water, Carbon and Nitrogen in a California Chaparral Ecosystem: DAYCENT Modeling Results

The Mediterranean climate, with its characteristic of dry summers and wet winters, influences the hydrologic and microbial processes that control carbon (C) and nitrogen (N) biogeochemical processes in chaparral ecosystems. These biogeochemical processes in turn determine N cycling under chronic N deposition. In order to examine connections between climate and N dynamics, we quantified decadal-scale water, C and N states and fluxes at annual, monthly and daily time steps for a California chaparral ecosystem in the Sierra Nevada using the DAYCENT model. The daily output simulations of net mineralization, stream flow and stream nitrate (NO₃⁻) export were developed for DAYCENT in order to simulate the N dynamics most appropriate for the abrupt rewetting events characteristic of Mediterranean chaparral ecosystems. Overall, the magnitude of annual modeled net N mineralization, soil and plant biomass C and N, nitrate export and gaseous N emission agreed with those of observations. Gaseous N emission was a major N loss pathway in chaparral ecosystems, in which nitric oxide (NO) is the dominant species. The modeled C and N fluxes of net primary production (NPP), N uptake and N mineralization, NO₃⁻ export and gaseous N emission showed both high inter-annual and intra-annual variability. Our simulations also showed dramatic fire effects on NPP, N uptake, N mineralization and gaseous N emission for three years of postfire. The decease in simulated soil organic C and N storages was not dramatic, but lasted a longer time. For the seasonal pattern, the predicted C and N fluxes were greatest during December to March, and lowest in the summer. The model predictions suggested that an increase in the N deposition rate would increase N losses through gaseous N emission and stream N export in the chaparral ecosystems of the Sierra Nevada due to changes in N saturation status. The model predictions could not capture stream NO₃⁻ export during most rewetting events suggesting that a dry-rewetting mechanism representing the increase in N mineralization following soil wetting needs to be incorporated into biogeochemical models of semi-arid ecosystems.     

The saturation of N cycling in Central Plains streams: <Superscript>15</Superscript>N experiments across a broad gradient of nitrate concentrations

We conducted ¹⁵NO₃⁻ stable isotope tracer releases in nine streams with varied intensities and types of human impacts in the upstream watershed to measure nitrate (NO₃⁻) cycling dynamics. Mean ambient NO₃⁻ concentrations of the streams ranged from 0.9 to 21,000 μg l⁻¹ NO₃⁻–N. Major N-transforming processes, including uptake, nitrification, and denitrification, all increased approximately two to three orders of magnitude along the same gradient. Despite increases in transformation rates, the efficiency with which stream biota utilized available NO₃⁻-decreased along the gradient of increasing NO₃⁻. Observed functional relationships of biological N transformations (uptake and nitrification) with NO₃⁻ concentration did not support a 1st order model and did not show signs of Michaelis–Menten type saturation. The empirical relationship was best described by a Efficiency Loss model, in which log-transformed rates (uptake and nitrification) increase with log-transformed nitrate concentration with a slope less than one. Denitrification increased linearly across the gradient of NO₃⁻ concentrations, but only accounted for ∼1% of total NO₃⁻ uptake. On average, 20% of stream water NO₃⁻ was lost to denitrification per km, but the percentage removed in most streams was <5% km⁻¹. Although the rate of cycling was greater in streams with larger NO₃⁻ concentrations, the relative proportion of NO₃⁻ retained per unit length of stream decreased as NO₃⁻ concentration increased. Due to the rapid rate of NO₃⁻ turnover, these streams have a great potential for short-term retention of N from the landscape, but the ability to remove N through denitrification is highly variable.     

Minimal response in watershed nitrate export to severe soil frost raises questions about nutrient dynamics in the Hubbard Brook experimental forest

Experimental and theoretical work emphasize the role of plant nutrient uptake in regulating ecosystem nutrient losses and predict that forest succession, ecosystem disturbance, and continued inputs of atmospheric nitrogen (N) will increase watershed N export. In ecosystems where snowpack insulates soils, soil-frost disturbances resulting from low or absent snowpack are thought to increase watershed N export and may become more common under climate-change scenarios. This study monitored watershed N export from the Hubbard Brook Experimental Forest (HBEF) in response to a widespread, severe soil-frost event in the winter of 2006. We predicted that nitrate (NO₃ ⁻) export following the disturbance would be high compared to low background streamwater NO₃ ⁻ export in recent years. However, post-disturbance annual NO₃ ⁻ export was the lowest on record from both reference (undisturbed) and treated experimental harvest or CaSiO₃ addition watersheds. These results are consistent with other studies finding greater than expected forest NO₃ ⁻ retention throughout the northeastern US and suggest that changes over the last five decades have reduced impacts of frost events on watershed NO₃ ⁻ export. While it is difficult to parse out causes from a complicated array of potential factors, based on long-term records and watershed-scale experiments conducted at the HBEF, we propose that reduced N losses in response to frost are due to a combination of factors including the long-term legacies of land use, process-level alterations in N pathways, climate-driven hydrologic changes, and depletion of base cations and/or reduced soil pH due to cumulative effects of acid deposition.     

Site-dependent N uptake from N-form mixtures by arctic plants,soil microbes and ectomycorrhizal fungi

Soil microbes constitute an important control on nitrogen (N) turnover and retention in arctic ecosystems where N availability is the main constraint on primary production. Ectomycorrhizal (ECM) symbioses may facilitate plant competition for the specific N pools available in various arctic ecosystems. We report here our study on the N uptake patterns of coexisting plants and microbes at two tundra sites with contrasting dominance of the circumpolar ECM shrub Betula nana. We added equimolar mixtures of glycine-N, NH₄⁺–N and NO₃⁻–N, with one N form labelled with ¹⁵N at a time, and in the case of glycine, also labelled with ¹³C, either directly to the soil or to ECM fungal ingrowth bags. After 2 days, the vegetation contained 5.6, 7.7 and 9.1% (heath tundra) and 7.1, 14.3 and 12.5% (shrub tundra) of the glycine-, NH₄⁺- and NO₃⁻–¹⁵N, respectively, recovered in the plant–soil system, and the major part of ¹⁵N in the soil was immobilized by microbes (chloroform fumigation-extraction). In the subsequent 24 days, microbial N turnover transferred about half of the immobilized ¹⁵N to the non-extractable soil organic N pool, demonstrating that soil microbes played a major role in N turnover and retention in both tundra types. The ECM mycelial communities at the two tundras differed in N-form preferences, with a higher contribution of glycine to total N uptake at the heath tundra; however, the ECM mycelial communities at both sites strongly discriminated against NO₃⁻. Betula nana did not directly reflect ECM mycelial N uptake, and we conclude that N uptake by ECM plants is modulated by the N uptake patterns of both fungal and plant components of the symbiosis and by competitive interactions in the soil. Our field study furthermore showed that intact free amino acids are potentially important N sources for arctic ECM fungi and plants as well as for soil microorganisms. Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Whole-system Estimates of Nitrification and Nitrate Uptake in Streams of the Hubbard Brook Experimental Forest

Although they drain remarkably similar forest types, streams of the Hubbard Brook Experimental Forest (HBEF) vary widely in their NO₃ ⁻ concentrations during the growing season. This variation may be caused by differences in the terrestrial systems they drain (for example, varying forest age or composition, hydrology, soil organic matter content, and so on) and/or by differences between the streams themselves (for example, contrasting geomorphology, biotic nitrogen [N] demand, rates of instream nitrogen transformations). We examined interstream variation in N processing by measuring NH₄ ⁺ and NO₃ ⁻ uptake and estimating nitrification rates for 13 stream reaches in the HBEF during the summers of 1998 and 1999. We modeled nitrification rates using a best-fit model of the downstream change in NO₃ ⁻ concentrations following short-term NH₄ ⁺ enrichments. Among the surveyed streams, the fraction of NH₄ ⁺ uptake that was subsequently nitrified varied, and this variation was positively correlated with ambient streamwater NO₃ ⁻ concentrations. We examined whether this variation in instream nitrification rates contributed significantly to the observed variation in NO₃ ⁻ concentrations across streams. In some cases, instream nitrification provided a substantial portion of instream NO₃ ⁻ demand. However, because there was also substantial instream NO₃ ⁻ uptake, the net effect of instream processing was to reduce rather than supplement the total amount of NO₃ ⁻ exported from a watershed. Thus, instream rates of nitrification in conjunction with instream NO₃ ⁻ uptake were too low to account for the wide range of streamwater NO₃ ⁻. The relationship between streamwater NO₃ ⁻ concentration and rates of instream nitrification may instead be due to a shift in the competitive balance between heterotrophic N uptake and nitrification when external inputs of NO₃ ⁻ are relatively high. Received 11 October 2000; accepted 14 December 2001.     

The effects of gap disturbance on nitrogen cycling and retention in late-successional northern hardwood–hemlock forests

Late-successional forests in the upper Great Lakes region are susceptible to nitrogen (N) saturation and subsequent nitrate (NO₃⁻) leaching loss. Endemic wind disturbances (i.e., treefall gaps) alter tree uptake and soil N dynamics; and, gaps are particular susceptible to NO₃⁻ leaching loss. Inorganic N was measured throughout two snow-free periods in throughfall, forest floor leachates, and mineral soil leachates in gaps (300–2,000 m², 6–9 years old), gap-edges, and closed forest plots in late-successional northern hardwood, hemlock, and northern hardwood–hemlock stands. Differences in forest water inorganic N among gaps, edges, and closed forest plots were consistent across these cover types: NO₃⁻ inputs in throughfall were significantly greater in undisturbed forest plots compared with gaps and edges; forest floor leachate NO₃⁻ was significantly greater in gaps compared to edges and closed forest plots; and soil leachate NO₃⁻ was significantly greater in gaps compared to the closed forest. Significant differences in forest water ammonium and pH were not detected. Compared to suspected N-saturated forests with high soil NO₃⁻ leaching, undisturbed forest plots in these late-successional forests are not losing NO₃⁻ (net annual gain of 2.8 kg ha⁻¹) and are likely not N-saturated. Net annual NO₃⁻ losses were observed in gaps (1.3 kg ha⁻¹) and gap-edges (0.2 kg ha⁻¹), but we suspect these N leaching losses are a result of decreased plant uptake and increased soil N mineralization associated with disturbance, and not N-saturation.     

Distribution of nitrogen-15 tracers applied to the canopy of a mature spruce-hemlock stand,Howland, Maine,USA

In N-limited ecosystems, fertilization by N deposition may enhance plant growth and thus impact C sequestration. In many N deposition–C sequestration experiments, N is added directly to the soil, bypassing canopy processes and potentially favoring N immobilization by the soil. To understand the impact of enhanced N deposition on a low fertility unmanaged forest and better emulate natural N deposition processes, we added 18 kg N ha⁻¹ year⁻¹ as dissolved NH₄NO₃ directly to the canopy of 21 ha of spruce-hemlock forest. In two 0.3-ha subplots, the added N was isotopically labeled as ¹⁵NH₄ ⁺ or ¹⁵NO₃ ⁻ (1% final enrichment). Among ecosystem pools, we recovered 38 and 67% of the ¹⁵N added as ¹⁵NH₄ ⁺ and ¹⁵NO₃ ⁻, respectively. Of ¹⁵N recoverable in plant biomass, only 3–6% was recovered in live foliage and bole wood. Tree twigs, branches, and bark constituted the most important plant sinks for both NO₃ ⁻ and NH₄ ⁺, together accounting for 25–50% of ¹⁵N recovery for these ions, respectively. Forest floor and soil ¹⁵N retention was small compared to previous studies; the litter layer and well-humified O horizon were important sinks for NH₄ ⁺ (9%) and NO₃ ⁻ (7%). Retention by canopy elements (surfaces of branches and boles) provided a substantial sink for N that may have been through physico-chemical processes rather than by N assimilation as indicated by poor recoveries in wood tissues. Canopy retention of precipitation-borne N added in this particular manner may thus not become plant-available N for several years. Despite a large canopy N retention potential in this forest, C sequestration into new wood growth as a result of the N addition was only ~16 g C m⁻² year⁻¹ or about 10% above the current net annual C sequestration for this site.     

Effects of forest management on soil N cycling in beech forests stocking on calcareous soils

The effects of forest management (thinning) on gross and net N conversion, the balance of inorganic N production and consumption, inorganic N concentrations and on soil microbial biomass in the Ah layer were studied in situ during eight intensive field measuring campaigns in the years 2002–2004 at three beech (Fagus sylvatica L.) forest sites. At all sites adjacent thinning plots (“T”) and untreated control plots (“C”) were established. Since the sites are characterized either by cool-moist microclimate (NE site and NW site) or by warm-dry microclimate (SW site) and thinning took place in the year 1999 at the NE and SW sites and in the year 2003 at the NW site the experimental design allowed to evaluate (1) short-term effects (years 1–2) of thinning at the NW site and (2) medium-term effects (years 4–6) of thinning under different microclimate at the SW and NE site. Microbial biomass N was consistently higher at the thinning plots of all sites during most of the field campaigns and was overall significantly higher at the SWT and NWT plots as compared to the corresponding untreated control plots. The size of the microbial biomass N pool was found to correlate positively with both gross ammonification and gross nitrification as well as with extractable soil NO₃⁻ concentrations. At the SW site neither gross ammonification, gross nitrification, gross ammonium (NH₄⁺) immobilization and gross nitrate (NO₃⁻) immobilization nor net ammonification, net nitrification and extractable NH₄⁺ and NO₃⁻ contents were significantly different between control and thinning plot. At the NET plot lower gross ammonification and gross NH₄⁺ immobilization in conjunction with constant nitrification rates coincided with higher net nitrification and significantly higher extractable NO₃⁻ concentrations. Thus, the medium-term effects of thinning varied with different microclimate. The most striking thinning effects were found at the newly thinned NW site, where gross ammonification and gross NH₄⁺ immobilization were dramatically higher immediately after thinning. However, they subsequently tended to decrease in favor of gross nitrification, which was significantly higher at the NWT plot as compared to␣the␣NWC plot during all field campaigns after␣thinning except for April 2004. This increase␣in␣gross nitrification at the NWT plot (1.73 mg N kg⁻¹ sdw day⁻¹ versus 0.48 mg N kg⁻¹ sdw day⁻¹ at the NWC plot) coincided with significantly higher extractable NO₃⁻ concentrations (4.59 mg N kg⁻¹ sdw at the NWT plot versus 0.96 mg N kg⁻¹ sdw at the NWC plot). Pronounced differences in relative N retention (the ratio of gross NH₄⁺ immobilization + gross NO₃⁻ immobilization to gross ammonification + gross nitrification) were found across the six research plots investigated and could be positively correlated to the soil C/N ratio (R = 0.94; p = 0.005). In sum, the results obtained in this study show that (1) thinning can lead to a shift in the balance of microbial inorganic N production and consumption causing a clear decrease in the N retention capacity in the monitored forest soils especially in the first two years after thinning, (2)␣the resistance of the investigated forest ecosystems to disturbances of N cycling by thinning may vary with different soil C contents and C/N ratios, e. g. caused by differences in microclimate, (3) thinning effects tend to decline with the growth of understorey vegetation in the years 4–6 after thinning.     

Correlations between nitrate and sulfate in the soil solution of disturbed forest ecosystems

Based on data from three German forest ecosystems severely disturbed by windthrow events, correlation patterns between NO₃ ⁻ and SO₄ ²⁻ dynamics in the soil solution are described. Each of the correlation types was related to site-specific SO₄ ²⁻ retention processes. The relative importance of SO₄ ²⁻ adsorption/desorption and precipitation/dissolution was found to be different for the studied soils depending on their contents of SO₄ ²⁻ -adsorbing sesquioxides and of A1 hydroxy sulfate minerals. Enhanced NO₃ ⁻ concentrations in the soil solution resulting from excess nitrification promoted either SO₄ ²⁻ adsorption or the dissolution of Al hydroxy sulfates. Both processes result in different ecological consequences: Whereas the former reaction reduces anion concentration peaks in the soil solution, the latter increases them. Thus, a prediction of cation export from soil ecosystems subjected to excess nitrification has to regard site-specific interrelationships between NO₃ ⁻ and SO₄ ²⁻. As a third type of conelation the independence of NO₃ ⁻ and SO₄ ²⁻ concentrations in the soil solution is presented. This type is suggested to be typical for soils with low SO₄ ²⁻. adsorption capacity and absence of A1 hydroxy sulfates.     

A Stable Isotope Tracer Study of the Influences of Adjacent Land Use and Riparian Condition on Fates of Nitrate in Streams

The influence of land use on potential fates of nitrate (NO₃ ⁻) in stream ecosystems, ranging from denitrification to storage in organic matter, has not been documented extensively. Here, we describe the Pacific Northwest component of Lotic Intersite Nitrogen eXperiment, phase II (LINX II) to examine how land-use setting influences fates of NO₃ ⁻ in streams. We used 24 h releases of a stable isotope tracer (¹⁵NO₃-N) in nine streams flowing through forest, agricultural, and urban land uses to quantify NO₃ ⁻ uptake processes. NO₃ ⁻ uptake lengths varied two orders of magnitude (24–4247 m), with uptake rates (6.5–158.1 mg NO₃-N m⁻² day⁻¹) and uptake velocities (0.1–2.3 mm min⁻¹) falling within the ranges measured in other LINX II regions. Denitrification removed 0–7% of added tracer from our streams. In forest streams, 60.4 to 77.0% of the isotope tracer was exported downstream as NO₃ ⁻, with 8.0 to 14.8% stored in wood biofilms, epilithon, fine benthic organic matter, and bryophytes. Agricultural and urban streams with streamside forest buffers displayed hydrologic export and organic matter storage of tracer similar to those measured in forest streams. In agricultural and urban streams with a partial or no riparian buffer, less than 1 to 75% of the tracer was exported downstream; much of the remainder was taken up and stored in autotrophic organic matter components with short N turnover times. Our findings suggest restoration and maintenance of riparian forests can help re-establish the natural range of NO₃ ⁻ uptake processes in human-altered streams.     

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.     

Unusual seasonal patterns and inferred processes of nitrogen retention in forested headwaters of the Upper Susquehanna River

Atmospheric deposition contributes a large fraction of the annual nitrogen (N) input to the basin of the Susquehanna River, a river that provides two-thirds of the annual N load to the Chesapeake Bay. Yet, there are few measurements of the retention of atmospheric N in the Upper Susquehanna’s forested headwaters. We characterized the amount, form (nitrate, ammonium, and dissolved organic nitrogen), isotopic composition (δ¹⁵N- and δ¹⁸O-nitrate), and seasonality of stream N over 2 years for 7–13 catchments. We expected high rates of N retention and seasonal nitrate patterns typical of other seasonally snow-covered catchments: dormant season maxima and growing season minima. Coarse estimates of N export indicated high rates of inorganic N retention (>95%), yet streams had unexpected seasonal nitrate patterns, with summer peaks (14–96 μmol L⁻¹), October crashes (<1 μmol L⁻¹), and modest rebounds during the dormant season (<1–20 μmol L⁻¹). Stream δ¹⁸O-nitrate values indicated microbial nitrification as the primary source of stream nitrate, although snowmelt or other atmospheric source contributed up to 47% of stream nitrate in some March samples. The autumn nitrate crash coincided with leaffall, likely due to in-stream heterotrophic uptake of N. Hypothesized sources of the summer nitrate peaks include: delayed release of nitrate previously flushed to groundwater, weathering of geologic N, and summer increases in net nitrate production. Measurements of shale δ¹⁵N and soil-, well-, and streamwater nitrate within one catchment point toward a summer increase in soil net nitrification as the driver of this pattern. Rather than seasonal plant demand, processes governing the seasonal production, retention, and transport of nitrate in soils may drive nitrate seasonality in this and many other systems.     

Microbial Cycling of C and N in Northern Hardwood Forests Receiving Chronic Atmospheric NO 3 − Deposition

Sugar maple (Acer saccharum Marsh.)-dominated northern hardwood forests in the upper Lakes States region appear to be particularly sensitive to chronic atmospheric NO₃⁻ deposition. Experimental NO₃⁻ deposition (3 g NO₃⁻ N m⁻² y⁻¹) has significantly reduced soil respiration and increased the export of DOC/DON and NO₃⁻ across the region. Here, we evaluate the possibility that diminished microbial activity in mineral soil was responsible for these ecosystem-level responses to NO₃⁻ deposition. To test this alternative, we measured microbial biomass, respiration, and N transformations in the mineral soil of four northern hardwood stands that have received 9 years of experimental NO₃⁻ deposition. Microbial biomass, microbial respiration, and daily rates of gross and net N transformations were not changed by NO₃⁻ deposition. We also observed no effect of NO₃⁻ deposition on annual rates of net N mineralization. However, NO₃⁻ deposition significantly increased (27%) annual net nitrification, a response that resulted from rapid microbial NO₃⁻ assimilation, the subsequent turnover of NH₄⁺, and increased substrate availability for this process. Nonetheless, greater rates of net nitrification were insufficient to produce the 10-fold observed increase in NO₃⁻ export, suggesting that much of the exported NO₃⁻ resulted directly from the NO₃⁻ deposition treatment. Results suggest that declines in soil respiration and increases in DOC/DON export cannot be attributed to NO₃⁻-induced physiological changes in mineral soil microbial activity. Given the lack of response we have observed in mineral soil, our results point to the potential importance of microbial communities in forest floor, including both saprotrophs and mycorrhizae, in mediating ecosystem-level responses to chronic NO₃⁻ deposition in Lake States northern hardwood forests.     

Soil-mixing effects on inorganic nitrogen production and consumption in forest and shrubland soils

Soils that are physically disturbed are often reported to show net nitrification and NO₃⁻ loss. To investigate the response of soil N cycling rates to soil mixing, we assayed gross rates of mineralization, nitrification, NH₄⁺ consumption, and NO₃⁻ consumption in a suite of soils from eleven woody plant communities in Oregon, New Mexico, and Utah. Results suggest that the common response of net NO₃⁻ flux from disturbed soils is not a straightforward response of increased gross nitrification, but instead may be due to the balance of several factors. While mineralization and NH₄⁺ assimilation were higher in mixed than intact cores, NO₃⁻ consumption declined. Mean net nitrification was 0.12 mg N kg⁻¹ d⁻¹ in disturbed cores, which was significantly higher than in intact cores (−0.19 mg N kg⁻¹ d⁻¹). However, higher net nitrification rates in disturbed soils were due to the suppression of NO₃⁻ consumption, rather than an increase in nitrification. Our results suggest that at least in the short term, disturbance may significantly increase NO₃⁻ flux at the ecosystem level, and that N cycling rates measured in core studies employing mixed soils may not be representative of rates in undisturbed soils.     

Evaluation of denitrification in an urban stream receiving wastewater effluent

Urban streams often contain elevated concentrations of nitrogen (N) which can be amplified in systems receiving effluent from wastewater treatment plants (WWTP). In this study, we evaluated the importance of denitrification in a stream draining urban Greensboro, NC, USA, using two approaches: (1) natural abundance of ¹⁵N–NO₃⁻ in conjunction with background NO₃⁻–N concentrations along a 7 km transect downstream of a WWTP; and (2) C₂H₂ block experiments at three sites and at three habitat types within each site. Overall lack of a longitudinal pattern of δ¹⁵N–NO₃⁻ and NO₃⁻–N, combined with high concentrations of NO₃⁻–N suggested that other factors were controlling NO₃⁻–N flux in the study transect. However, denitrification did appear to be significant along one portion of the transect. C₂H₂ block experiments showed that denitrification rates were much higher downstream of the WWTP compared to upstream, and showed that denitrification rates were highest in erosional and depositional areas downstream of the WWTP and in erosional areas upstream of the plant. Thus, the combination of the two methods for evaluating denitrification provided more insight into the spatial dynamics of denitrification activity than either approach alone. Denitrification appeared to be a significant sink for NO₃⁻–N upstream of the WWTP, but not downstream. Approximately 46% of the total NO₃⁻–N load was removed via denitrification in the upstream, urban section of the stream, while only 2.3% of NO₃⁻–N was lost downstream of the plant. This result suggests that controlling NO₃⁻–N loading from the plant could result in considerable improvement of downstream water quality.     

Indicators for nitrogen status and leaching in subtropical forest ecosystems,South China

The deposition of nitrogen (N) is high in subtropical forest in South China and it is expected to increase further in the coming decades. To assess effects of increasing deposition on N cycling, we investigated the current N status of two selected 40–45-year-old masson pine-dominated Chinese subtropical forest stands at Tieshanping (TSP, near Chongqing City) and Caijiatang (CJT in Shaoshan, Hunan province), and explored the applicability of several indicators for N status and leaching, suggested for temperate and boreal forest ecosystems. Current atmospheric N deposition to the systems is from 25 to 49 kg ha⁻¹ year⁻¹. The concentration of total N in the upper 15 cm of the soil is from as low as 0.05% in the B₂ horizon to as high as 0.53% in the O/A horizon. The concentration of organic carbon (C) varies from 0.74 (B₂) to 9.54% (O/A). Pools of N in the upper 15 cm of the soils range from 1460 to 2290 kg N ha⁻¹, where 25–55% of the N pool is in the O/A horizon (upper 3 cm of the soil). Due to a lack of a well-developed continuous O horizon (forest floor), the C/N ratio of this layer cannot be used as an indicator for the N status, as is commonly done in temperate and boreal forests. The net N mineralization rate (mg N g⁻¹ C year⁻¹) in individual horizons correlates significantly with the C/N ratio, which is from as high as 18.2 in the O/A horizon to as low as 11.2 in the B₂ horizon. The N₂O emission flux from soil is significantly correlated with the KCl extractable NH₄⁺–N in the O/A horizon and with the net nitrification in the upper 15 cm of the soil. However, the spatial and temporal variation of the N₂O emission rate is high and rates are small and often difficult to detect in the field. The soil flux density of mineral N, defined as the sum of the throughfall N input rate and the rate of in situ net N mineralization in the upper 15 cm of the soil, i.e., the combination of deposition input and the N status of the system, explains the NO₃⁻ leaching potential at 30 cm soil depth best. The seasonality of stream water N concentration at TSP and CJT is climatic and hydrologically controlled, with highest values commonly occurring in the wet growing season and lowest in the dry dormant season. This is different from temperate forest ecosystems, where N saturation is indicated by elevated NO₃⁻ leaching in stream water during summer.     

Dual isotope analyses indicate efficient processing of atmospheric nitrate by forested watersheds in the northeastern U.S.

Nitrogen from atmospheric deposition serves as the dominant source of new nitrogen to forested ecosystems in the northeastern U.S. By combining isotopic data obtained using the denitrifier method, with chemical and hydrologic measurements we determined the relative importance of sources and control mechanisms on nitrate (NO₃ ⁻) export from five forested watersheds in the Connecticut River watershed. Microbially produced NO₃ ⁻ was the dominant source (82–100%) of NO₃ ⁻ to the sampled streams as indicated by the δ¹⁵N and δ¹⁸O of NO₃ ⁻. Seasonal variations in the δ¹⁸O–NO₃ ⁻ in streamwater are controlled by shifting hydrologic and temperature affects on biotic processing, resulting in a relative increase in unprocessed NO₃ ⁻ export during winter months. Mass balance estimates find that the unprocessed atmospherically derived NO₃ ⁻ stream flux represents less than 3% of the atmospherically delivered wet NO₃ ⁻ flux to the region. This suggests that despite chronically elevated nitrogen deposition these forests are not nitrogen saturated and are retaining, removing, and reprocessing the vast majority of NO₃ ⁻ delivered to them throughout the year. These results confirm previous work within Northeastern U.S. forests and extend observations to watersheds not dominated by a snow-melt driven hydrology. In contrast to previous work, unprocessed atmospherically derived NO₃ ⁻ export is associated with the period of high recharge and low biotic activity as opposed to spring snowmelt and other large runoff events.     

Organic matter quality and management effects on enrichment of soil organic matter fractions in contrasting soils in Zimbabwe

Spatial variability of soil total nitrogen (N), available N (KCl extractable NH₄⁺ and NO₃⁻), and spatial patterns of N mineralization and nitrification at a stand scale were characterized with geostatistical and univariate analysis. Two extensive soil spatial samplings were conducted in an evergreen broadleaf forest in Sichuan province, southwestern China in June and August 2000. In a study area of 90 × 105 m², three soil samples were collected from each 5 × 5 m² plot (n = 378) in June and August, and were analyzed for total N and available N contents. Net N mineralization and nitrification were measured by in situ core incubation and the rates were estimated based on the difference of NH₄⁺ and NO₃⁻ contents between the two sampling dates. Total N, NH₄⁺, and NO₃⁻ were all spatially structured with different semivariogram ranges (from high to low: NH₄⁺, NO₃⁻, and total N). The semivariograms of mineralization and nitrification were not as spatially structured as available N. NH₄⁺ was the dominant soil inorganic N form in the system. Both NH₄⁺ and NO₃⁻ affected spatial patterns of soil available N, but their relative importance switched in August, probably due to high nitrification as indicated by greatly increased soil NO₃⁻ content. High spatial auto-correlations (>0.7) were found between available N and NH4⁺, available N and NO₃⁻ on both sampling dates, as well as total N measurements between both sampling dates. Although significant, the spatial auto-correlation between NH₄⁺ and NO₃⁻ were generally low. Topography had significant but low correlations with mineralization (r = −0.16) and nitrification (r = −0.14), while soil moisture did not. The large nugget values of the calculated semivariograms and high-semivariance values, particularly for mineralization and nitrification, indicate that some fine scale (<5 m) variability may lie below the threshold for detection in this study.     

An Unexpected Nitrate Decline in New Hampshire Streams

Theories of forest nitrogen (N) cycling suggest that stream N losses should increase in response to chronic elevated N deposition and as forest nutrient requirements decline with age. The latter theory was supported initially by measurements of stream NO₃ ⁻ concentration in old-growth and successional stands on Mount Moosilauke, New Hampshire (Vitousek and Reiners 1975; Bioscience 25:376–381). We resampled 28 of these and related streams to evaluate their response to 23 years of forest aggradation and chronic N deposition. Between 1973–74 and 1996–97, mean NO₃ ⁻ concentration in quarterly samples from Mount Moosilauke decreased by 71% (25 μmol/L), Ca²⁺ decreased by 24% (8 μmol/L), and Mg²⁺ decreased by 22% (5 μmol/L). Nitrate concentrations decreased in every stream in every season, but spatial patterns among streams persisted: Streams draining old-growth stands maintained higher NO₃ ⁻ concentrations than those draining successional stands. The cause of the NO₃ ⁻ decline is not evident. Nitrogen deposition has changed little, and although mechanisms such as insect defoliation and soil frost may contribute to the temporal patterns of nitrate loss, they do not appear to fully explain the NO₃ ⁻ decline across the region. Although the role of climate remains uncertain, interannual climate variation and its effects on biotic N retention may be responsible for the synchronous decrease in NO₃ ⁻ across all streams, overriding expected increases due to chronic N deposition and forest aging. Received 4 December 2001; accepted 30 May 2002.     

Pulse additions of soil carbon and nitrogen affect soil nitrogen dynamics in an arid Colorado Plateau shrubland

Biogeochemical cycles in arid and semi-arid ecosystems depend upon the ability of soil microbes to use pulses of resources. Brief periods of high activity generally occur after precipitation events that provide access to energy and nutrients (carbon and nitrogen) for soil organisms. To better understand pulse-driven dynamics of microbial soil nitrogen (N) cycling in an arid Colorado Plateau ecosystem, we simulated a pulsed addition of labile carbon (C) and N in the field under the canopies of the major plant species in plant interspaces. Soil microbial activity and N cycling responded positively to added C while NH₄⁺–N additions resulted in an accumulation of soil NO₃⁻. Increases in microbial activity were reflected in higher rates of respiration and N immobilization with C addition. When both C and N were added to soils, N losses via NH₃ volatilization decreased. There was no effect of soil C or N availability on microbial biomass N suggesting that the level of microbial activity (respiration) may be more important than population size (biomass) in controlling short-term dynamics of inorganic and labile organic N. The effects of C and N pulses on soil microbial function and pools of NH₄⁺–N and labile organic N were observed to last only for the duration of the moisture pulse created by treatment addition, while the effect on the NO₃⁻–N pool persisted after soils dried to pre-pulse moisture levels. We observed that increases in available C lead to greater ecosystem immobilization and retention of N in soil microbial biomass and also lowered rates of gaseous N loss. With the exception of trace gas N losses, the lack of interaction between available C and N on controlling N dynamics, and the subsequent reduction in plant available N with C addition has implications for the competitive relationships between plants species, plants and microbes, or both.