Natural variability in soil and runoff from small headwater catchments at Storgama, Norway

To provide baseline data for climate manipulation experiments in 11 small (30-268 m2) headwater catchments at Storgama, Telemark County, Southern Norway, we assessed the natural variability in site characteristics and runoff quality. Annual average concentrations in runoff at the sites have coefficients of variation between 26-61%, with the smallest values for total organic carbon (TOC) and carbon to nitrogen (C/N) ratios and the largest for inorganic nitrogen (N). The catchments have between two and five times higher concentrations of inorganic N, TOC, and total phosphorus than the larger (0.6 km2) Storgama watershed nearby. Concentrations of TOC and TON in runoff tend to increase with soil C and N content and with the volume of soil in the catchment. For nitrate (NO3) and ammonium in runoff, the reverse is true. In wet years the proportion of bare rock is a major predictor for the annual average NO3 concentration in runoff.     

Manipulation of snow in small headwater catchments at Storgama, Norway: effects on leaching of total organic carbon and total organic nitrogen

Projected increases in winter temperature due to future climate change may cause decreased snow accumulation at lower and intermediate altitudes in northern temperate regions. The resulting changes in soil temperature and water regime may affect the leaching of total organic carbon (TOC) and total organic nitrogen (TON). We manipulated the snow cover of small headwater catchments in a montane heathland area of southern Norway to quantify its effect on concentrations and fluxes of TOC and TON in runoff. Manipulations included snow removal, to promote soil frost, and insulation, to prevent soil frost. Snow removal resulted in increased TOC and TON concentrations, but decreased fluxes. Insulation caused a slight decrease in concentrations and fluxes of TOC. Our experiments show that a change in snow depth, and thus soil temperature, is not likely to have serious effects on TOC and TON leaching in the montane heathland area studied.     

Projected stream water fluxes of NO3 and total organic carbon from the Storgama headwater catchment, Norway, under climate change and reduced acid deposition

Fluctuations in the 20-year record of nitrate (NO3) and total organic carbon (TOC) concentrations and fluxes in runoff at the small headwater catchment Storgama, southern Norway, were related to climate and acid deposition. The long-term decline in NO3 related to reduced NO3 deposition and increased winter discharge, whereas the long-term increase in TOC related to reduced sulfur deposition. Multiple regression models describing long-term trends and seasonal variability in these records were used to project future concentrations given scenarios of climate change and acid deposition. All scenarios indicated reduced NO3 fluxes and increased TOC fluxes; the largest projected changes for the period 2071-2100 were -86% and +24%, respectively. Uncertainties are that the predicted future temperatures are considerably higher than the historical record. Also, nonlinear responses of ecosystem processes (nitrogen [N] mineralization) to temperature, N-enrichment of soils, and step-changes in environmental conditions may affect future leaching of carbon and N.     

Manipulation of snow in small headwater catchments at Storgama, Norway: effects on leaching of inorganic nitrogen

We have manipulated the winter-time soil temperature regime of small headwater catchments in a montane heathland area of southern Norway to study the possible effects on concentrations and fluxes of inorganic nitrogen in runoff. The experiments included extra insulation of soils in two catchments to prevent subzero temperatures during winter, and removal of snow in two other catchments to promote soil frost. Increased soil temperatures during winter increased the springtime concentrations and fluxes of ammonium (NH4) and nitrate (NO3) in runoff. By contrast, snow removal with development of significant soil frost showed no systematic effects on mean concentrations or fluxes of inorganic N. The results from our experiments suggest that warmer soils during winter caused by exceptionally mild winters, or alternatively a heavy snowpack, imply a greater risk for inorganic N leaching in this region than a possible increase of soil frost events because of reduced snow cover.     

Manipulation of precipitation in small headwater catchments at Storgama, Norway: effects on leaching of organic carbon and nitrogen species

Projected changes in climate in Southern Norway include increases in summer and autumn precipitation. This may affect leaching of dissolved organic matter (DOM) from soils. Effects of experimentally added extra precipitation (10 mm week) during the growing season of 3 years (2004-2006) to small headwater catchments at Storgama (59 degrees 0'N, 550-600 m a.s.l.) on leaching of total organic carbon (TOC) and total organic nitrogen (TON) were assessed. Extra precipitation did not have a significant effect on average TOC and TON concentrations in runoff. Thus, fluxes of TOC and TON increased nearly proportionally with water fluxes. This suggests that a store of adsorbed and potentially mobile TOC and TON in catchment soils buffers the concentration of DOM in runoff. The size and dynamics of the pool of TOC and TON depends on the balance between production and leaching rates. Infrequent short droughts had only small effects on TOC and TON fluxes in runoff from the reference catchments.     

Effect of climate change on fluxes of nitrogen from the Tovdal River basin, Norway, to adjoining marine areas

The mass transport model TEOTIL was used to project nitrate (NO3) fluxes from the Tovdal River basin, southernmost Norway, given four scenarios of climate change. Forests, uplands, and open water currently account for 90% of the NO3 flux. Climate scenarios for 2071-2100 suggest increased temperature by 2-4 degrees C and precipitation by 3-11%. Climate experiments and long-term monitoring were used to estimate future rates of nitrogen (N) leaching. More water will run through the terrestrial catchments during the winter but less will run in the spring. The annual NO3 flux from the Tovdal River to the adjoining Topdalsfjord is projected to remain unchanged, but with more NO3 delivered in the winter and less in the spring. Algal blooms in coastal waters can be expected to occur earlier in the year. Major sources of uncertainty are in the long-term fate of N stored in soil organic matter and the impacts of forest management.     

Increased nitrogen in runoff and soil following 13 years of experimentally increased nitrogen deposition to a coniferous-forested catchment at Gårdsjön, Sweden

Beginning in 1991, we have added nitrogen (N) to the 0.5-ha, N-poor, coniferous-forested catchment G2 NITREX at G?rdsj?n, Sweden, to investigate the consequences of chronic elevated N deposition. We have added 40 kg N ha-1 yr-1 in fortnightly doses of NH4NO3 to the ambient 15 kg N ha-1 yr-1 by means of a sprinkling system. NO3 concentrations in runoff increased during 13 years from<1 to 70 microeq L-1, and in 2004 comprised about 10% of N input. Inhibition of NO3 immobilisation due to increased availability of NH4 might explain the increased leaching of NO3. C and N pools in the forest floor increased but C/N ratio has not changed. The increase in NO3 leaching thus occurred independently of change in C/N ratio. The results from G?rdsj?n demonstrate that increased leaching of inorganic N and decrease in C/N ratio respond to increased N deposition at greatly different time scales.     

Nitrogen Oxide Flux from an Agricultural Soil During Winter Fallow in the Upper Coastal Plain of North Carolina,U.S.A.

Abstract

Incorporation of the remaining crop residue, including the root system, of grain (soybean and corn) and fiber (cotton) crops into the soil following harvest is a common agricultural practice. The crop residue represents a substantial portion of nitrogen initially applied as fertilizer, and thus is a potential source of nitrogen for NO emissions during the winter fallow period. Fluxes of NO and NO₂ were measured from fallow fields from February 7 to March 23, 1994, using a dynamic chamber technique (ambient air as the carrier gas). Average NO flux rates, as a function of previous crop residue, were 9.2 (range –4.2 to 76) ng–N m^–2 s^–1 for soybean, 6.1 (range –11.7 to 110) ng–N m^–2 s^–1 for cotton, and 4.7 (range –0.2 to 40) ng–N m^–2 s^–1 for corn. Maximum NO fluxes were observed in mid–morning when soil temperatures were lowest. Minimum NO flux occurred after mid–afternoon when soil temperature reached a maximum. The decrease in NO flux with increase in soil temperature (5 cm depth) reflected the existence of a NO compensation concentration (i.e., the rate for the NO consumption reactions continued to increase with increase in temperature). NO₂ deposition was calculated for 92% of the data points, with no trend in deposition between the three fields and their corresponding crop residue. These results indicate that significant fluxes of NO are generated from fallow agricultural fields following incorporation of the residue from the previous crop.     

Nitrogen dynamics of a mountain forest on dolomitic limestone--a scenario-based risk assessment

The dominant nitrogen (N) fluxes were simulated in a mountain forest ecosystem on dolomitic bedrock in the Austrian Alps. Based on an existing small-scale climate model the simulation encompassed the present situation and a 50-yr projection. The investigated scenarios were current climate, current N deposition (SC1) and future climate (+2.5 degrees C and +10% annual precipitation) with three levels of N deposition (SC2, 3, 4). The microbially mediated N transformation, including the emission of nitrogen oxides, was calculated with PnET-N-DNDC. Soil hydrology was calculated with HYDRUS and was used to estimate the leaching of nitrate. The expected change of the forest ecosystem due to changes of the climate and the N availability was simulated with PICUS. The incentive for the project was the fact that forests on dolomitic limestone stock on shallow Rendzic Leptosols that are rich in soil organic matter are considered highly sensitive to the expected environmental changes. The simulation results showed a strong effect due to increased temperatures and to elevated levels of N deposition. The outflux of N, both as nitrate (6-25kg Nha(-1)yr(-1)) and nitrogen oxides (1-2kg Nha(-1)yr(-1)), from the forest ecosystem are expected to increase. Temperature exerts a stronger effect on the N(2)O emission than the increased rate of N deposition. The main part of the N emission will occur as N(2) (15kg Nha(-1)yr(-1)). The total N loss is partially offset by increased rates of N uptake in the biomass due to an increase in forest productivity.     

Nitrogen,Phosphorus, Carbon,and Suspended Solids Loads from Forest Clear-Cutting and Site Preparation: Long-Term Paired Catchment Studies from Eastern Finland

The long-term impacts of current forest management methods on surface water quality in Fennoscandia are largely unexplored. We studied the long-term effects of clear-cutting and site preparation on runoff and the export of total nitrogen (total N), total organic nitrogen (TON), ammonium (NH₄-N), nitrate (NO₃-N), total phosphorus (total P), phosphate (PO₄-P), total organic carbon, and suspended solids (SS) in three paired-catchments in Eastern Finland. Clear-cutting and soil preparation were carried out on 34 % (C34), 11 % (C11), and 8 % (C8) of the area of the treated catchments and wide buffer zones were left along the streams. Clear-cutting and soil preparation increased annual runoff and total N, TON, NO₃-N, PO₄-P, and SS loads, except for SS, only in C34. Runoff increased by 16 % and the annual exports of total N, TON, NO₃-N, and PO₄-P by 18, 12, 270, and 12 %, respectively, during the 14-year period after clear-cutting. SS export increased by 291 % in C34, 134 % in C11, and 16 % in C8 during the 14, 6, and 11-year periods after clear-cutting. In the C11 catchment, NO₃-N export decreased by 12 %. The results indicate that while current forest management practices can increase the export of N, P and SS from boreal catchments for many years (>10 years), the increases are only significant when the area of clear cutting exceeds 30 % of catchment area.     

Nitrate in waters from sewage-sludge amended lysimeters

Nitrate nitrogen was measured in runoff and tile-drainage during two years of operation of instrumented, large-scale lysimeters planted to corn (Zea mays L.) and amended with sewage sludge which was applied at rates supplying total N amounting to 2292 kg ha(-) in 1972 and 3286 kg ha(-1) in 1973. Other lysimeters were amended with inorganic fertiliser at the rate of 336 kg N ha(-1) year(-1). Annual losses in runoff and tile-drainage from sludge treatments were 0.9 and 5.1 and 371 and 663 kg NO(3)(-)-N ha(-1). Losses from lysimeters treated with inorganic fertiliser were 1.1 and 3.3 kg NO(3)(-)-N ha(-1) year(-1) in runoff and 31 and 79 kg NO(3)(-)-N ha(-1) year(-1) in tile-drainage. Given the nitrogen inputs accounted for in the study design, unaccounted for losses of 1800 to 2400 kg ha(-1) year(-1) were calculated for sludge and 277 kg ha(-1) year(-1) for inorganic fertiliser treatments. For one year there was a 300 kg ha(-1) increase in N in the lysimeters receiving inorganic fertiliser. Median NO(3)(-)-N concentrations ranged from 8.9 to 14.0 mg litre(-1) in runoff from sludge-treated lysimeters and 3.6 to 5.9 mg litre(-1) in runoff from lysimeters receiving inorganic fertiliser. In tile-drainage the median NO(3)(-)-N concentrations were 148 to 223 mg litre(-1) and 24 to 44 mg litre(-1) for sludge and inorganic fertiliser treatments, respectively. Highest runoff levels occurred in early summer storms, whereas highest tile-drainage concentrations occurred in late winter and early spring.     

Nitrogen deposition in California forests: a review

Atmospheric concentrations and deposition of the major nitrogenous (N) compounds and their biological effects in California forests are reviewed. Climatic characteristics of California are summarized in light of their effects on pollutant accumulation and transport. Over large areas of the state dry deposition is of greater magnitude than wet deposition due to the arid climate. However, fog deposition can also be significant in areas where seasonal fogs and N pollution sources coincide. The dominance of dry deposition is magnified in airsheds with frequent temperature inversions such as occur in the Los Angeles Air Basin. Most of the deposition in such areas occurs in summer as a result of surface deposition of nitric acid vapor (HNO3) as well as particulate nitrate (NO3-) and ammonium (NH4+). Internal uptake of gaseous N pollutants such as nitrogen dioxide (NO2), nitric oxide (NO), HNO3, peroxyacetyl nitrate (PAN), ammonia (NH3), and others provides additional N to forests. However, summer drought and subsequent lower stomatal conductance of plants tend to limit plant utilization of gaseous N. Nitrogen deposition is much greater than S deposition in California. In locations close to photochemical smog source areas, concentrations of oxidized forms of N (NO2, HNO3, PAN) dominate, while in areas near agricultural activities the importance of reduced N forms (NH3, NH4+) significantly increases. Little data from California forests are available for most of the gaseous N pollutants. Total inorganic N deposition in the most highly-exposed forests in the Los Angeles Air Basin may be as high as 25-45 kg ha(-1) year(-1). Nitrogen deposition in these highly-exposed areas has led to N saturation of chaparral and mixed conifer stands. In N saturated forests high concentrations of NO3- are found in streamwater, soil solution, and in foliage. Nitric oxide emissions from soil and foliar N:P ratios are also high in N saturated sites. Further research is needed to determine the ecological effects of chronic N deposition, and to develop appropriate management options for protecting water quality and managing plant nutrient resources in ecosystems which no longer retain excess N.     

Modelling nitrogen saturation and carbon accumulation in heathland soils under elevated nitrogen deposition

A simple model of nitrogen (N) saturation, based on an extension of the biogeochemical model MAGIC, has been tested at two long-running heathland N manipulation experiments. The model simulates N immobilisation as a function of organic soil C/N ratio, but permits a proportion of immobilised N to be accompanied by accumulation of soil carbon (C), slowing the rate of C/N ratio change and subsequent N saturation. The model successfully reproduced observed treatment effects on soil C and N, and inorganic N leaching, for both sites. At the C-rich upland site, N addition led to relatively small reductions in soil C/N, low inorganic N leaching, and a substantial increase in organic soil C. At the C-poor lowland site, soil C/N ratio decreases and N leaching increases were much more dramatic, and soil C accumulation predicted to be smaller. The study suggests that (i) a simple model can effectively simulate observed changes in soil and leachate N; (ii) previous model predictions based on a constant soil C pool may overpredict future N leaching; (iii) N saturation may develop most rapidly in dry, organic-poor, high-decomposition systems; and (iv) N deposition may lead to significantly enhanced soil C sequestration, particularly in wet, nutrient-poor, organic-rich systems.     

Determination of atmospheric nitrogen input to Lake Greenwood, South Carolina: part 2--Gaseous measurements and modeling

The Reedy River branch of Lake Greenwood, SC, has repeatedly experienced summertime algal blooms, upsetting the natural system. A series of experiments were carried out to investigate atmospheric nitrogen (N) input into the lake. N was examined because of the insignificant phosphorus dry atmospheric flux and the unique nutrient demands of the dominant algae (Pithophora oedogonia) contributing to the blooms. Episodic atmospheric measurements during January and March 2001 have shown that the dry N flux onto the lake ranged from 0.9 to 17.4 kg N/ha-yr, and on average is caused by nitric acid (HNO3; 31%), followed by nitrogen dioxide (NO2; 23%), fine ammonium (NH4+; 20%), coarse nitrate (NO3-; 16%), fine NO3 (5%), and coarse NH4+ (5%). Similar measurements in Greenville, SC (the upper watershed of the Reedy River), showed that the dry N deposition flux there ranged from 1.4 to 9.7 kg N/ha-yr and was mostly caused by gaseous deposition (40% NO2 and 40% HNO3). The magnitude of this dry N deposition flux is comparable to wet N flux as well as other point sources in the area. Thermodynamic modeling showed low concentrations of ammonia, relative to the particulate NH4+ concentrations.     

Detrital control on the release of dissolved organic nitrogen (DON) and dissolved inorganic nitrogen (DIN) from the forest floor under chronic N deposition

The role of detrital quantity and quality in forest floor N leaching was investigated in a litter manipulation experiment at a deciduous forest under chronic N deposition. Dissolved inorganic nitrogen (DIN) comprised the bulk of nitrogen leaching from the control except a short period following autumn litterfall. The dominance of DIN was strengthened by litter exclusion, whereas the addition of glucose or fresh litter led to a small increase in dissolved organic nitrogen (DON) and either a temporary or gradual reduction in NO(3)(-) release, respectively. Changes in soluble organic C and microbial C in the forest floor implied that increased availability of C sources might have enhanced microbial immobilization of DIN, either temporarily following glucose application or over the longer term following litter addition. The results suggest that detrital quantity and quality can play a crucial role in determining the balance between DIN and DON in N-enriched forest soils.     

The United Kingdom Acid Waters Monitoring Network: a review of the first 15 years and introduction to the special issue

The United Kingdom Acid Waters Monitoring Network (AWMN) was established in 1988 to determine the ecological impact of acidic emissions control policy on acid-sensitive lakes and streams. AWMN data have been used to explore a range of causal linkages necessary to connect changes in emissions to chemical and, ultimately, biological recovery. Regional scale reductions in sulphur (S) deposition have been found to have had an immediate influence on surface water chemistry, including increases in acid neutralising capacity, pH and alkalinity and declines in aluminium toxicity. These in turn can be linked to changes in the aquatic biota which are consistent with "recovery" responses. A continuation of the current programme is essential in order to better understand apparent non-linearity between nitrogen (N) in deposition and runoff, the substantial rise in organic acid concentrations, and the likely impacts of forecast climate change and other potential constraints on further biological improvement.     

The dynamics of dissolved nitrogen in a blanket peat dominated catchment

Precipitation, soil solution and drainage water were collected from a blanket peat catchment at Moor House National Nature Reserve in the Northern Pennine Uplands, UK, an area of moderately high N deposition. Two tributaries of the main stream were also sampled. Between 1993 and 1995 samples were analysed for NH4+ and NO3- and for part of the period for organic N. Inputs of N in precipitation exceeded outputs in stream water. Organic N represented a small proportion of N inputs while inputs of inorganic N averaged 10.2 kg ha(-1) a(-1). Soil solution from 10 cm depth in the peat was dominated by organic N whereas at 50 cm NH4+ slightly exceeded organic N. NO3- was rarely detected at either depth except during a period of exceptionally warm and dry weather in 1995. Output fluxes in stream water of organic N (5.7 to 6.5 kg ha(-1) a(-1)) were much greater than those of inorganic N (0.6 to 2.2 kg ha(-1) a(-1)). Inorganic N in streams was predominantly NO3- except in the smallest stream which had the largest concentrations of NH4+. This suggests that N transformations, particularly nitrification, may be taking place in the mineral soils adjacent to the streams or within the stream channel of the larger catchment.     

Fluxes of oxidised and reduced nitrogen above a mixed coniferous forest exposed to various nitrogen emission sources

Concentrations of nitrogen gases (NH(3), NO(2), NO, HONO and HNO(3)) and particles (pNH(4) and pNO(3)) were measured over a mixed coniferous forest impacted by high nitrogen loads. Nitrogen dioxide (NO(2)) represented the main nitrogen form, followed by nitric oxide (NO) and ammonia (NH(3)). A combination of gradient method (NH(3) and NO(x)) and resistance modelling techniques (HNO(3), HONO, pNH(4) and pNO(3)) was used to calculate dry deposition of nitrogen compounds. Net flux of NH(3) amounted to -64 ng N m(-2) s(-1) over the measuring period. Net fluxes of NO(x) were upward (8.5 ng N m(-2) s(-1)) with highest emission in the morning. Fluxes of other gases or aerosols substantially contributed to dry deposition. Total nitrogen deposition was estimated at -48 kg N ha(-1) yr(-1) and consisted for almost 80% of NH(x). Comparison of throughfall nitrogen with total deposition suggested substantial uptake of reduced N (+/-15 kg N ha(-1) yr(-1)) within the canopy.     

Deposition of motor vehicle emissions and winter maintenance along roadside assessed by snow analyses

A vertical snow-sampling method, where a sample was taken throughout the snowpack, was used to estimate the pollutant load on a roadside where average daily traffic density was about 9100 motor vehicles. The snow samples were collected at two sites, forest and open field, at two distances of 10 and 30 m from the road. The concentrations of inorganic anions (Cl(-), NO(-)(3), SO(2-)(4)), total N, polycyclic aromatic hydrocarbons (PAHs) and polychlorinated phenols (PCPhs) were analysed. The results suggest that on roadsides there is a deposition caused by road traffic emissions and winter maintenance which exceeds normal background deposition. Inorganic anions mainly in particle form, originating from winter maintenance, are deposited near the road. PAHs with low molecular weight (相似文献   

Plants' use of different nitrogen forms in response to crude oil contamination

In this study, we investigated Phragmites australis’ use of different forms of nitrogen (N) and associated soil N transformations in response to petroleum contamination. ¹⁵N tracer studies indicated that the total amount of inorganic and organic N assimilated by P. australis was low in petroleum-contaminated soil, while the rates of inorganic and organic N uptake on a per-unit-biomass basis were higher in petroleum-contaminated soil than those in un-contaminated soil. The percentage of organic N in total plant-assimilated N increased with petroleum concentration. In addition, high gross N immobilization and nitrification rates relative to gross N mineralization rate might reduce inorganic-N availability to the plants. Therefore, the enhanced rate of N uptake and increased importance of organic N in plant N assimilation might be of great significance to plants growing in petroleum-contaminated soils. Our results suggest that plants might regulate N capture under petroleum contamination.