Emissions of NO and N2O from soils

Nitric oxide (NO) and nitrous oxide (N₂O) fluxes were measured from agricultural, forest and moorland environments, using chamber techniques. Maximum emissions of NO and N₂O were measured from the agricultural soils shortly after fertiliser application (7 ng NO-N m^–2 s^–1 and 91 ng N₂O-N m^–2 s^–1). For the non-agricultural soils the NO flux ranged from –0.3 to 0.5 ng NO-N m^–2 s^–1 and the N₂O flux ranged from 1 to 2.7 ng N₂O-N m^–2 s^–1. Emissions, however, were increased 2 to 7 fold when N deposition (uplands) and N fixation (alder plantations) contributed to the pool of soil available N. The best predictors of the NO emission were soil NO ₃ ^– and soil temperature, accounting for 60% of the variability observed. The prediction of N₂O was less successful. Only 30% of the variability could be explained by the soil NO ₃ ^– and the soil moisture content, soil temperature did not have a significant effect on the N₂O emission.     

Behaviour and fluxes of trace and toxic elements in creek sediment near Mumbai,India

Studies on marine sediments are extremely important since they act as ultimate sink of anthropogenic pollutants. The present study was conducted near Mumbai city of India to understand andassess the behaviour and fluxes of trace and toxic elements increek sediment. Seven sediment core samples were collected andanalysed for trace and toxic elements such as Fe, Cu, Pb, Zn, Rb and Sr in different sections of the core using EDXRF technique. The fluxes of the elements in each section of the core were calculated using the mass sedimentation rates derivedfrom ²¹⁰Pb dating technique and the sediment density at each location. The estimated depositional fluxes of Fe, Rb and Sr in Zone-1 and Zone-3 are in the ranges of 0.4–0.5% cm^-2yr^-1; 4–6 g cm^-2 yr^-1 and 10–20 g cm^-2 yr^-1 respectively, where as they were about 3–4 times higher in zone-2 for the same elements. The depositionalfluxes of elements Cu (40–60 g cm^-2 yr^-1), Zn (35–43 g cm^-2 yr^-1) and Pb (6–12 g cm^-2 yr^-1) were also found to be higher in zone-2 compared tozone-1 and zone-3 which can be attributed to the release from thenewly developed chemical zone of Thane-Belapur industrial belt.     

Three-year monitoring results of nitrate and ammonium wet deposition in Thailand

Wet deposition is one of the important sources of nitrogen input into the ecosystem. It also contributes to rain acidity in some environments. In this study we reported the annual as well as seasonal trends of nitrogen wet deposition at three locations in Thailand: Bangkok, Chiang Mai and Nan. Comparison of nitrogen wet deposition between in rural and in the urban areas was also made. Daily rainfall was measured and monthly rainwater was collected for nitrogen analysis during 1999–2002. The average NO₃ ^– concentration in rainwater collected from the rural sites (60 km from urban area) was around 0.2–0.3 mg L^–1, while that from the urban areas of Chiang Mai and Nan cities it was 0.4–0.5 mg L^–1. NH₄ ⁺ concentration in rainwater showed the similar ranges to that of NO₃ ^– , except at Nan where concentration was not significantly different between the urban and rural sites. On the other hand, the average concentrations of NO₃ ^– were higher at Bangkok site than other sites, while concentration of NH₄ ⁺ was almost the same between Chiang Mai and Bangkok. Wet deposition of NO₃ ^– at the rural sites of Chiang Mai and Nan ranged from 2.1 to 3.2 kg N ha^–1 yr^–1, while at the urban sites this ranged from about 6 kg N ha^–1 yr^–1 in Chiang Mai and Nan Cities to 8.6 kg N ha^–1 yr^–1 in Bangkok. Wet deposition of NH₄ ⁺ at the rural sites of Chiang Mai and Nan was about 2.4 to 3.6 kg N ha^–1 yr^–1 and at the urban sites of Chiang Mai, Nan and Bangkok this was 7.7, 4.9 and 8.1 kg N ha^–1 yr^–1, respectively. Thus, it was concluded that wet deposition of both nitrogen species was significantly higher at the urban sites than at the rural sites.     

Air pollution impact on Swedish forests-present evidence and future development

Research during the last five years has provided evidence that there is a long-term influence of air pollutants on forest ecosystems also in the southern parts of North Europe. High loads of acidity, sulphur and nitrogen affect soil conditions, trees as well as other organisms.In South and West Sweden changes in soil acidity (pH) have been registered during the last 60 years. The changes not only occur in the humus layer, but also in the lower part of the mineral soil. These latter changes cannot be explained without the action of strong acids originating from anthropogenic air pollution.Losses of elements like magnesium, calcium and potassium occur and phosphorus become less available to plants. An increased demand for plant mutrients is a consequence of the increased fall-out of nitrogen compounds. Nutrient imbalances of trees seem to be the result. Increased sensitivity to frost and drought as well as insects and pathogens is expected.The increased soil acidity and the eutrophication of soils caused by the continued input of nitrogen contributes to changes in plant communities.If we assume that there are no changes in deposition, land-use and management of the forests in SW Sweden, the better forest soils (brown forest soils) will have a continued acidification of humus and mineral soil layers resulting in high levels of aluminium and low levels of calcium. This will create a critical situation for roots and mycorrhiza. Soils that are already acid may not become more acidified, but will still be subject to losses of essential elements.Critical deposition levels or loads of acids (hydrogen ions) and nitrogen rendering no further deterioration of soils and leaching have been set to 0.1–0.2 keq·ha^-1yr^-1 for S Scandinavia (present level 1 keq·ha^-1yr^-1). For nitrogen the critical load is 10–20 kg N ha^-1yr^-1 (present range 10–25 kg ha^-1yr^-1).Contribution from Fourth World Wilderness Congress — Acid Rain Symposium, Denver (Estes Park), Colorado, September 11–18, 1987.     

Fluxes and pools of methane in wetland rice soils with varying organic inputs

Measurements of methane emission rates and concentrations in the soil were made during four growing seasons at the International Rice Research Institute in the Philippines, on plots receiving different levels of organic input. Fluxes were measured using the automated closed chambers system (total emission) and small chambers installed between plants (water surface flux). Concentrations of methane in the soil were measured by collecting soil cores including the gas phase (soil-entrapped methane) and by sampling soil solution in situ (dissolved methane). There was much variability between seasons, but total fluxes from plots receiving high organic inputs (16–24 g CH₄ m^–2) always exceeded those from the low input plots (3–9 g CH₄ m^–2). The fraction of the total emission emerging from the surface water (presumably dominated by ebullition) was greater during the first part of the season, and greater from the high organic input plots (35–62%) than from the low input plots (15–23%). Concentrations of dissolved and entrapped methane in the low organic input plots increased gradually throughout the season; in the high input plots there was an early-season peak which was also seen in emissions. On both treatments, periods of high methane concentrations in the soil coincided with high rates of water surface flux whereas low concentrations of methane were generally associated with low flux rates.     

Background monitoring and long-range transport of atmospheric CFC-11 and CFC-12 at Kosan, Korea

The background concentrations of atmospheric CFC-11 and CFC-12were monitored to assess their impact on stratospheric ozone depletion and global warming from September 1995 to March 1999 at Kosan, Korea, located at eastern margin of the Asian Continent. The concentrations of atmospheric CFC-11 at Kosan have decreased slightly, at a rate of –2.5 pptv yr^-1, over the period in response to the Montreal Protocol. The CFC-12 mixing ratio at Kosan continues to increase in the atmosphere at a rate of 5.7 pptv yr^-1 despite international regulations, because of its extreme atmosphere persistence. Recent trends ofthese two chlorofluorocarbons at Kosan, Korea were concordant with those of the northern hemispheric background monitored unitat Mauna Loa, Hawaii. The maximum seasonal mean mixing ratios of CFC-11 and CFC-12 at Kosan, Korea, were 270±4 pptv inthe spring and 538±9 pptv in the winter, and the corresponding seasonal minima were 267±7 and 529±12 pptv. This occurred in the summer and was due to southeasterlywinds from the northwestern Pacific Ocean. By performing a three-day isentropic backward trajectory analysis, it was shownthat air masses at Kosan, and with the exception of summer, mainly originated from central and northern China. In particular, the mixing ratios of these two contaminant speciesare closely related with their air mass trajectories.     

Methane in ocean waters: Concentration and carbon isotope variability at East Pacific Rise and in the Arabian Sea

Methane concentrations and stable carbon isotope ratios of water samples from the East Pacific Rise (EPR) at 21°S and the Arabian Sea (24°N, 65°E) have been determined. EPR surface water is in equilibrium (ca. 50 nl/L and –50<¹³CH₄<–46) with atmospheric methane. Deep background water has the signature of the remaining fraction of atmospheric methane partially oxidized in the water column by bacteria. Bottom near, hydrothermally influenced vent methane (>100nl/L and –30<¹³CH₄<–22) is detectable only close to the seep site. There is no input of hydrothermal methane into the atmosphere. EPR water is considered to be rather a sink than a source of atmospheric methane. Surface waters of the Arabian Sea are enriched in methane relative to the atmosphere (source for atmospheric methane). Carbon isotope ratios point to a bacterial origin of methane (¹³CH₄<–55) that is generated in the surface waters. Concentration changes and variations of carbon isotope ratios also suggest that methane seeping from the sea floor sediments of the Arabian Sea is oxidized by bacterial activity and does not reach the atmosphere.     

Diurnal variation of methane emissions from an alpine wetland on the eastern edge of Qinghai-Tibetan Plateau

Alpine wetland is a source for CH₄, but little is known about methane emission from such wetland, especially about its diurnal pattern. In this study we tried to probe the diurnal variation in methane emission from alpine wetland vegetation. The average methane emission rate was 9.6 ± 3.4 mg CH₄ m^???2 h^???1. There was an apparent diurnal variation pattern in methane emission with one minor peak at 06:00 and a major one at 15:00. The sunrise peak was consistent with a two-way transport mechanism for plants (convective at daytime and diffusive at night-time). CH₄ emission was found significantly correlated with redox potentials. The afternoon peak could not be explained by diurnal variation in soil temperature, but could be attributable to changes in CH₄ oxidation and production driven by plant gas transport mechanism. The results have important implications for sampling and scaling strategies for estimating methane emission from alpine wetlands.     

Laboratory study of the emission of NO and N2O from some Belgian soils

The NO, NO₂ and N₂O emission was measured, upon application of nitrate, ammonium and both, to four Belgian soils with different characteristics. The addition of NH ₄ ⁺ caused higher NO and N₂O emissions than the addition of no nitrogen, or the addition of NO ₃ ^– . In contrast to the two soils with a pH of approximately 8 the two soils with a pH around 6 showed a considerable delay in production of both NO and N₂O upon the application of the ammonium, probably due to the lag-period of nitrification. The soils with a pH of 8 gave higher emissions on the application of NH ₄ ⁺ than the soils with a pH of 6. The emission of NO₂ was found to be considerably lower than the NO emission from the soils. The NO/NO₂ ratio varied between 5–25 at considerable NO emissions (>50 nmol kg^–1). In the controls of soil 1 and soil 2, which showed very low NO emissions ratios of <1 were observed. The N₂O/NO ratios varied between 5–20 when NO emissions were considerable (>50 nmol kg^–1). Soil 3 and 4 gave lower N₂O/NO ratios than soil 1 and 2. In the controls of soil 1 and soil 2, at low NO emissions, N₂O/NO ratios of >300 were observed. Soil 3 and 4 gave higher NO/NO₂ and lower N₂O/NO ratios than soil 1 and 2.     

Status and Trends of Dissolved Oxygen in Corpus Christi Bay, Texas, U.S.A.

The purpose of this studywas to determine status and long-term trends of dissolved oxygen concentrations (DO) in Corpus Christi Bay, Texas, U.S.A. A 20-year record of randomized stations was used to determine the trend of surface water DO, salinity, and temperature over space and time. A 13-year record of two fixed stations was used to determine the temporal nutrient trends. A 10-year record of fixed stations in the southeastern region of Corpus Christi Bay was used to determine the status of disturbance caused by low DO in bottom waters. From 1982 to 2002, there was a significant decrease in surface water DO at a rate of 0.06 mg L⁻¹ yr⁻¹ and a significant increase in surface water temperature at a rate of 0.07°C yr⁻¹. The southeastern region of Corpus Christi Bay had the lowest average DO, and during July and August, DO are steadily declining at a rate of 0.09 mg L⁻¹ yr⁻¹. It is not likely that eutrophication is causing hypoxia, because freshwater inflow rates have significantly decreased since 1941 and nutrient levels have not changed from 1987 to 2000. Even though long-term trends indicate that average surface DO is decreasing, disturbance by hypoxia appears to be stable, but this may be due to just eight years of data. In fact, if the current trend continues, surface water DO will not meet exceptional aquatic life standards (≤5 mgL⁻¹) in 2032.     

Anthropogenic emissions of methane and nitrous oxide in the Federal Republic of Germany

The anthropogenic emission sources of methane (CH₄) and nitrous oxide (N₂O) in the Federal Republic of Germany were investigated. The object of the recently completed first phase of this research project was to summarize the present knowledge about the emission sources, make a first rough estimate of the emissions, identify the need for further research in the field, and - as far as possible - discuss the existing possibilities to reduce emissions. The main CH₄ emission sources identified are the landfills, stock farming and pit mining, the main N₂O sources are agriculture (including a minor contribution from animal wastes) and the production of adipic acid, the latter possibly being reducible by means of a new catalytic process. The total anthropogenic emissions of CH₄ from Germany are estimated at 5.4 – 7.7 million tonnes per year, contributing a share of roughly 2 % to the world-wide anthropogenic emissions (350 million t/a). Those of N₂O are estimated at 200 000 – 280 000 tonnes per year (world-wide 1.4 – 6.5 million t/a).     

Mega-Development Trends in the Amazon: Implications for Global Change

This paper describes four global-change phenomena that are having major impacts on Amazonian forests. The first is accelerating deforestation and logging. Despite recent government initiatives to slow forest loss, deforestation rates in Brazilian Amazonia have increased from 1.1 million ha yr^–1 in the early 1990s, to nearly 1.5 million ha yr^–1 from 1992–1994, and to more than 1.9 million ha yr^–1 from 1995–1998. Deforestation is also occurring rapidly in some other parts of the Amazon Basin, such as in Bolivia and Ecuador, while industrialized logging is increasing dramatically in the Guianas and central Amazonia.The second phenomenon is that patterns of forest loss and fragmentation are rapidly changing. In recent decades, large-scale deforestation has mainly occurred in the southern and eastern portions of the Amazon — in the Brazilian states of Pará, Maranho, Rondônia, Acre, and Mato Grosso, and in northern Bolivia. While rates of forest loss remain very high in these areas, the development of major new highways is providing direct conduits into the heart of the Amazon. If future trends follow past patterns, land-hungry settlers and loggers may largely bisect the forests of the Amazon Basin.The third phenomenon is that climatic variability is interacting with human land uses, creating additional impacts on forest ecosystems. The 1997/98 El Niño drought, for example, led to a major increase in forest burning, with wildfires raging out of control in the northern Amazonian state of Roraima and other locations. Logging operations, which create labyrinths of roads and tracks in forsts, are increasing fuel loads, desiccation and ignition sources in forest interiors. Forest fragmentation also increases fire susceptibility by creating dry, fire-prone forest edges.Finally, recent evidence suggests that intact Amazonian forests are a globally significant carbon sink, quite possibly caused by higher forest growth rates in response to increasing atmospheric CO₂ fertilization. Evidence for a carbon sink comes from long-term forest mensuration plots, from whole-forest studies of carbon flux and from investigations of atmospheric CO₂ and oxygen isotopes. Unfortunately, intact Amazonian forests are rapidly diminishing. Hence, not only is the destruction of these forests a major source of greenhouse gases, but it is reducing their intrinsic capacity to help buffer the rapid anthropogenic rise in CO₂.     

Consumption of methane by soils

Measurements of the methane flux and methane concentration profiles in soil air are presented. The flux of methane from the soil is calculated by two methods: a) Direct by placing a static open chamber at the soil surface. b) Indirect, using the ²²²Rn concentrations profile and the ²²²Rn flux in the soil surface in parallel with the methane concentration (²²²Rn calibrated fluxes). The methane flux has been determined in two kinds of soils (sandy and loamy) in the surroundings of Málaga (SPAIN). The directly measured methane fluxes at all investigated sites is higher than methane fluxes derived from Rn calibrated fluxes. Atmospheric methane is consumed by soils, mean direct flux to the atmosphere were - 0.33 g m^–2yr-1. The direct methane flux is the same within the measuring error in sandy and loamy soils. The influence of the soil parameters on the methane flux indicates that microbial decomposition of methane is primarily controlled by the transport of methane.     

Soil properties and crop productivity as influenced by flyash incorporation in soil

Field experiments were carried out during 1996–97at Gulawathi, Muthiani and Salarpur Villages, IARI Farm, NewDelhi and NCPP Campus, Dadri to evaluate changes in soilcharacteristics and growth of wheat (Triticum aestivum L.),mustard (Brassica juncea L.), lentil (Lence esculentaMoench.), rice (Oryza sativa L.) and maize (Zea mays L.) byvarying amounts of flyash addition (up to 50t ha^-1) in soils atsowing/transplanting time of crops. Flyash addition in areasadjoining NCPP Thermal Power Plant, Dadri, Ghaziabad, U.P.ranged from 5–12 t ha^-1 yr^-1 in 1995–96. Shoot and root growthand yield of test crops at different locations after flyashincorporation resulted in beneficial effects of flyashaddition in most cases. The silt dominant texture of flyashimproved loamy sand to sandy loam textures of the surfacesoils at the farmers' fields. The increased growth in yield ofcrops with flyash incorporation was possibly due tomodifications in soil moisture retention and transmissioncharacteristics, bulk density, physico-chemical characterssuch as pH and EC and organic carbon content. The response offlyash addition in the soil on soil health and cropproductivity needs to be evaluated on long-term sustainableaspects.     

Deposition and storage of solid-bound heavy metals in the floodplains of the River Geul (the Netherlands)

Because of past mining activities, the floodplains of the River Geul are polluted with heavy metals. The continuous supply of fresh sediments during floods has caused the floodplain soils to exhibit large quality variations in time. By measurements of ¹³⁷Cs deposition rates in part of the floodplain area were determined at 0.4 to 2.7 cm yr^–1. Analysis of soil metal concentrations at various depths at 65 locations, revealed that the upper 40 cm of the soil profile deposited during the past 30–45 yr, exhibit the highest metal levels. The geostatistical interpolation technique kriging was used to map actual and past pollution patterns. It was shown that, as a result of variable deposition rates, the spatial correlation structure of soil metal concentrations becomes less clear with increasing depth/age. Kriged maps of average metal concentrations in the upper 100 cm of the soil profile provided the basis for the calculation of the mass storage of heavy metals.     

Modelling Dissolved Organic Carbon Turnover in Humic Lake Örträsket, Sweden

The organic carbon balance of a lake with high input of allochthonous organic carbon is modelled integrating physical, chemical and biological processes. The physical model captures the behaviour of real thermal stratification in the lake for different flow situations during the period 1993–1997. The dissolved organic carbon model is based on simulated trajectories of water parcels. By tracking parcels, account is kept of environmental factors such as temperature and radiation as well as DOC quality for each parcel. The DOC concentration shows seasonal variations primarily dependent on inflow. The organic matter degradation (bacterial- and photodegradation) in the lake amounts to 1.5–2.5 mg C l^–1 yr^–1, where photooxidation is responsible for approximately 10%. The estimated DIC production in the lake is large compared to sediment mineralisation and primary production. The main conclusion is that the model with the selected parameterisations of the degradation processes reasonably well describes the DOC dynamics in a forest lake.     

Lead Levels in the Airborne Dust Particulates of an Urban City of Central India

The dust fall-out rate, distribution pattern andconcentration of lead in the particulate fall-outmatters in urban Raipur city covering an area of 160 km² during one hydrological year i.e. November1996–June 1997, has been described. The entire cityhas been divided into 6 zones comprising ofindustrial, commercial, residential and heavy trafficareas. A monthly collection and analysis of dustfall-out rate between 3.0(±0.1) and91.3(±1.2) metric tonnes km^-2 month^-1 wereobserved at all 6 sampling sites. The total annualflux of lead in the fall-out of the city at differentzones is in the range 0.0065–0.4304 kg km^-2yr^-1. The results show that dust fall-out and thelead levels both are at higher magnitudes in winterand autumn. These large levels of air pollutants havealso been correlated with some meteorological parameters like relative humidity and temperature, and strong positive correlations have been observed.     

Nitrous oxide emission out of grassland

Grazed grassland which received 295 kg ha^–1 N-fertilizer (NH₄NO₃), split-applied, was used to measure nitrous oxide emission. The closed box method was used. At the same time, also soil cores were taken for incubation in the presence of acetylene. During 280 days in 1992, a total emission of 8.4 kg N₂O-N ha^–1 was found. This was close to 50 % of the total denitrification, which was 18.7 kg (N₂O+N₂)-N ha^–1 over 280 days. A variability study on N₂O emission was carried out on a surface of 1, 100 and 10,000 m², respectively. This study confirmed the lognormal distribution of data with variation coefficients of 20 to 25%. It was also found that the effect of application of 200 kg KNO₃-N on N₂O emission was limited to 2 weeks upon fertilization. It more than doubled the emission rate during this period.     

Estimates of animal methane emissions

The enteric methane emissions into the atmospheric annually from domestic animals total about 77 Tg. Another 10 to 14 Tg are likely released from animal manure disposal systems. About 95% of global animal enteric methane is from ruminants, a consequence of their large populations, body size and appetites combined with the extensive degree of anaerobic microbial fermentation occurring in their gut. Accurate methane estimates are particularly sensitive to cattle and buffalo census numbers and estimated diet consumption. Since consumption is largely unknown and must be predicted, accuracy is limited often by the information required, i.e., distribution of animals by class, weight and productivity. Fraction of the diet lost as enteric methane mostly falls into the range of 5.5–6.5% of gross energy intake for the world's cattle, sheep and goats. Manure methane emissions are heavily influenced by fraction of disposal by anaerobic lagoon. Non-ruminants, i.e., swine, become major contributors to these emissions.     

Baseline Concentrations of Trace Elements in Surface Soils of the Torrelles and Sant Climent Municipal Districts (Catalonia,Spain)

An investigation was conducted to study the baseline levels of Ba, Cd, Cu, Cr, Ni, Pb, Sr, V and Zn (aqua regia-extractable) based on 51 representative soils of the Torrelles and Sant Climent Municipal Districts (Catalonia, Spain). The baseline concentrations of those elements were (mg kg⁻¹): Ba 73.9–617.9, Cr 9.2–120.2, Cu 4.0–111.6, Ni 6.1–118.6, Pb 5.6–217.5, Sr 19.6–128.8, V 12.1–101.2, and Zn 16.8–326.8, respectively.Forty-nine samples were reported as having less than the 0.67 mg kg⁻¹ detection limit for cadmiun and were therefore not useful for baseline determination; however, these results suggest that the baseline average is probably below 0.67 mg kg⁻¹.Upper baseline values for most of the elements corresponded with those reported in the literature, except for Pb and Zn, which were two to four times greater.Soil properties, including clay fraction, OC, CEC and pH_w were related to metal concentration using correlation and factorial analysis. R-mode factor analysis separates the soil analysis data into three factors. These factors explain 67.3% of the total variance, suggesting that metal concentration was controlled by soil composition.