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.     

Interactions of Atmospheric Deposition with Coniferous Canopies in Estonia

Throughfall and open field bulk precipitation were measured at three coniferous sites during 1995–2002 in the framework of ICP Integrated Monitoring and at five coniferous sites during 1996–2002 in the framework of ICP Forests (Level II). The coniferous canopies acted as a sink for nitrate and ammonium and as a source for base cations: Ca²⁺, Mg²⁺ and K⁺. The estimated share of SO₄–S dry deposition from total deposition was 1.5–4 times higher for dormant period compared to growing period. During the study period average annual throughfall and bulk deposition of SO₄–S decreased significantly, 2.8 and 2.3 times, respectively. Throughfall enrichment with base cations increased in the order Mg < Na < Ca < K. Using Na as a tracer ion, average dry deposition and canopy leaching were calculated. Leaching was the dominant process for TF enrichment by potassium. Leaching of base cations occurred during growing as well as dormant period. The calculated internal flux of Ca²⁺ and Mg²⁺ varied in the range of 0.6–2.0 and 0.6–1.2 kg ha⁻¹ per year in spruce and pine stands, respectively. The internal circulation of K⁺ was significantly higher (8.9–10.9 kg ha⁻¹ per year) in spruce stands than in pine stands (2.7–4.4 kg ha⁻¹ per year).     

Factors affecting N and P losses from small catchments (Lithuania)

Most of the important factors causing differences in nutrient losses and their interaction were analysed in three small catchments that are located in partially different geographic and climatic conditions in Lithuania. The investigation revealed that climatic factors change the amount and pattern of water discharge over year (larger water discharge during winter in the catchment located closer to the sea), but nutrient leaching is more dependent on land use. Agricultural factors, such as larger cultivated area and excessive fertilisation in one catchment cause larger nitrogen losses (15 kg N ha^–1 year^–1). Large area of non-intensively used grassland leads to very small nitrogen losses (5.7 kg N ha^–1 year^–1) in another catchment. However, larger water discharge combined with loamy sandy soils leads to comparatively high nitrogen losses (12 kg N ha^–1 year^–1). The highest P losses (0.318 kg P ha^–1 year^–1) occurred in the catchment with hilly relief and clay soil texture. In summary, extensive agriculture in the post-Soviet countries has reduced the importance of agricultural activity for the extent of nutrient losses and agricultural factors (cultivation, fertilisation and livestock density) are responsible for the losses only in the region of sufficient agricultural activity (N input – 71.5 kg N ha^–1, livestock density – 0.87 LU ha^–1).     

Monitoring nitrogen deposition in typical forest ecosystems along a large transect in China

The nitrogen (N) deposition fluxes were investigated in eight typical forest ecosystems along the North–South Transect of Eastern China (NSTEC; based on the ChinaFLUX network) by ion-exchange resin (IER) columns from May 2008 to April 2009. Our results demonstrated that the method of IER columns was both labor cost saving and reliable for measuring dissolved inorganic nitrogen (DIN) deposition at the remote forest stations. The deposition of DIN in the throughfall ranged from 1.3 to 29.5 kg N ha^?1 a^?1, increasing from north to south along NSTEC. The relatively high average ratio of ammonium to nitrate in deposition (1.83) indicated that the N deposition along the NSTEC in China mostly originated in farming and animal husbandry rather than in industry and vehicle activities. For seasonal variability, the DIN deposition showed a single peak in the growing season in the northern part of NSTEC, while, in the southern part, it exhibited double-peaks in the early spring and the mid-summer, respectively. On the annual scale, the DIN deposition variations of the eight sites could be mainly explained by precipitation and the distances from forest stations to provincial capital cities.     

Use of forest inventories and geographic information systems to estimate biomass density of tropical forests: Application to tropical Africa

One of the most important databases needed for estimating emissions of carbon dioxide resulting from changes in the cover, use, and management of tropical forests is the total quantity of biomass per unit area, referred to as biomass density. Forest inventories have been shown to be valuable sources of data for estimating biomass density, but inventories for the tropics are few in number and their quality is poor. This lack of reliable data has been overcome by use of a promising approach that produces geographically referenced estimates by modeling in a geographic information system (GIS). This approach has been used to produce geographically referenced, spatial distributions of potential and actual (circa 1980) aboveground biomass density of all forests types in tropical Africa. Potential and actual biomass density estimates ranged from 33 to 412 Mg ha^–1 (10⁶g ha^–1) and 20 to 299 Mg ha^–1, respectively, for very dry lowland to moist lowland forests and from 78 to 197 Mg ha^–1 and 37 to 105 Mg ha^–1, respectively, for montane-seasonal to montane-moist forests. Of the 37 countries included in this study, more than half (51%) contained forests that had less than 60% of their potential biomass. Actual biomass density for forest vegetation was lowest in Botswana, Niger, Somalia, and Zimbabwe (about 10 to 15 Mg ha^–1). Highest estimates for actual biomass density were found in Congo, Equatorial Guinea, Gabon, and Liberia (305 to 344 Mg ha^–1). Results from this research effort can contribute to reducing uncertainty in the inventory of country-level emission by providing consistent estimates of biomass density at subnational scales that can be used with other similarly scaled databases on change in land cover and use.     

Losses of nitrogen and phosphorus from agricultural and forest areas in Finland during the 1980s and 1990s

The temporal changes and spatial variability of phosphorus andnitrogen losses and concentrations in Finland during the period1981–1997 were studied in 15 small agricultural and forestedcatchments. In addition, four coastal river basins with highagricultural land use located in southern Finland were includedin the study in order to assess the representativeness ofagricultural loss estimates from small agricultural catchments.The mean annual loss specific for agricultural land was estimatedto be on average 110 kg km^-2 a^-1 for total phosphorusand 1500 kg km^-2 a^-1 for total nitrogen. The resultsfrom small agricultural catchments were in agreement with thecorresponding loss estimates from rivers, with an average of137 kg km^-2 a^-1 for total phosphorus and 1800 kg km^-2a^-1 for total nitrogen. The results from the studiedagricultural catchments and rivers during the period 1981–1997suggest that weather-driven fluctuation in discharge was usuallythe main reason for changes in nutrient losses, and little or noimpact of changes in agricultural production or managementpractises can be observed. In forested areas the total phosphorusloss (average 9 kg km^-2 a^-1) and total nitrogen loss(average 250 kg km^-2 a^-1) were lower than inagricultural areas. In forested catchments the impact of forestryoperations, such as clear-cutting and fertilization, and theimpact of atmospheric nitrogen deposition can be seen in changesin nutrient losses.     

Sulphate, Nitrogen and Base Cation Budgets at 21 Forested Catchments in Canada, the United States and Europe

To assess the concern over declining base cation levels in forest soils caused by acid deposition, input-output budgets (1990s average) for sulphate (SO₄), inorganic nitrogen (NO₃-N; NH₄-N), calcium (Ca), magnesium (Mg) and potassium (K) were synthesised for 21 forested catchments from 17 regions in Canada, the United States and Europe. Trend analysis was conducted on monthly ion concentrations in deposition and runoff when more than 9 years of data were available (14 regions, 17 sites). Annual average SO₄ deposition during the 1990s ranged between 7.3 and 28.4 kg ha⁻¹ per year, and inorganic nitrogen (N) deposition was between 2.8 and 13.8 kg ha⁻¹ per year, of which 41–67% was nitrate (NO₃-N). Over the period of record, SO₄ concentration in deposition decreased in 13/14 (13 out of 14 total) regions and SO₄ in runoff decreased at 14/17 catchments. In contrast, NO₃-N concentrations in deposition decreased in only 1/14 regions, while NH₄-N concentration patterns varied; increasing at 3/14 regions and decreasing at 2/14 regions. Nitrate concentrations in runoff decreased at 4/17 catchments and increased at only 1 site, whereas runoff levels of NH₄-N increased at 5/17 catchments. Decreasing trends in deposition were also recorded for Ca, Mg, and K at many of the catchments and on an equivalent basis, accounted for up to 131% (median 22%) of the decrease in acid anion deposition. Base cation concentrations in streams generally declined over time, with significant decreases in Ca, Mg and K occurring at 8, 9 and 7 of 17 sites respectively, which accounted for up to 133% (median 48%) of the decrease in acid anion concentration. Sulphate export exceeded input at 18/21 catchments, likely due to dry deposition and/or internal sources. The majority of N in deposition (31–100%; median 94%) was retained in the catchments, although there was a tendency for greater NO₃-N leaching at sites receiving higher (<7 kg ha^-1 per year) bulk inorganic N deposition. Mass balance calculations show that export of Ca and Mg in runoff exceeds input at all 21 catchments, but K export only exceeds input at 16/21 sites. Estimates of base cation weathering were available for 18 sites. When included in the mass balance calculation, Ca, Mg and K exports exceeded inputs at 14, 10 and 2 sites respectively. Annual Ca and Mg losses represent appreciable proportions of the current exchangeable soil Ca and Mg pools, although losses at some of the sites likely occur from weathering reactions beneath the rooting zone and there is considerable uncertainty associated with mineral weathering estimates. Critical loads for sulphur (S) and N, using a critical base cation to aluminium ratio of 10 in soil solution, are currently exceeded at 7 of the 18 sites with base cation weathering estimates. Despite reductions in SO₄ and H⁺ deposition, mass balance estimates indicate that acid deposition continues to acidify soils in many regions with losses of Ca and Mg of primary concern. The U.S. Government's right to retain a non-exclusive, royalty free licence in and to any copyright is acknowledged. The Canadian Crown reserves the right to retain a non-exclusive, royalty free licence in and to any copyright.     

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.     

Nitrate leaching in agriculture to upper groundwater in the sandy regions of the Netherlands during the 1992–1995 period

The Dutch National Monitoring Programme for Effectiveness of the Minerals Policy (LMM) was initiated to allow detection of a statutory reduction in nitrate leaching caused by a decreasing N load. The starting point, or baseline, was taken as the nitrate concentration of the upper metre of groundwater sampled on 99 farms in the 1992–1995 period in the sandy areas of the Netherlands, where predominantly grass and maize grow. We found here that a reduction in nitrate leaching of more than 20% in future would almost certainly be detected with the LMM. Detecting downward trends due to decreasing N load will require nitrate concentrations to also be related to soil drainage, precipitation excess leading to groundwater recharge and to location. Furthermore, we found that about 16% of the N load in the Dutch sandy regions was being leached to the upper metre of groundwater in the 1992–1995 period. The critical N load in approximately 1990 for exceeding the EC limit value for nitrate, NO₃, (50 mg L^–1) in the upper metre of groundwater for the mean situation for grassland, maize and arable land in the sandy area was found to be 210 kg ha^–1 a^–1. Because manure management has been altered, the critical load found will be lower than the current critical load .     

Analysis of Wet Precipitation of Air Pollutants in Mumbai (India)

Bulk precipitation samples at Mumbai (India) were collectedduring the monsoon seasons of 1991 to 1996 and analysed forionic concentrations using an Ion Chromatograph DIONEX model100. The variability of sulphate to nitrate ratio in rainwaterfluctuates in a wide range from 1.5 to 20 and governed by thesulphate concentrations in the sample. The regression analysisof the data reveals that in the bulk precipitation at Mumbai, SO₄ ^2- is becoming increasingly important relative toNO₃ ^-. The role of meteorological influences onscavenging of air pollutants by rain water has been tried toexplain the phenomena. The computed wet deposition rates for Sand N during 1991–1996 show that the S deposition is higherthan N in all the years. There is a wide fluctuation indeposition rates of S ranging from 2 to 55 kg km² per annum.     

Contributions of dry and wet depositions of polychlorinated dibenzo-p-dioxins and dibenzofurans to a contaminated site resulting from a penetachlorophenol manufacturing process

The soils at a factory for manufacturing pentachlorophenol were heavily contaminated by polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs). In order to verify the contributions of dry and wet deposition of PCDD/Fs from the ambient air, the concentration of PCDD/Fs in ambient air and soil were measured, the partition of particle- and gas-phases of atmospheric PCDD/Fs was calculated, and the annual fluxes of total dry and wet PCDD/F depositions were modeled. Average atmospheric PCDD/F concentration was 1.24 ng Nm^???3 (or 0.0397 ng I-TEQ Nm^???3). Moreover, over 92.8% of total PCDD/Fs were in the particle phase, and the dominant species were high chlorinated congeners. The total PCDD/F fluxes of dry and wet deposition were 119.5 ng m^???2 year^???1 (1.34 ng I-TEQ m^???2 year^???1) and 82.0 ng m^???2 year^???1 (1.07 ng I-TEQ m^???2 year^???1), respectively. By scenario simulation, the total fluxes of dry and wet PCDD/F depositions were 87.1 and 68.6 ng I-TEQ, respectively. However, the estimated PCDD/F contents in the contaminated soil were 839.9 ?? g I-TEQ. Hence, the contributions of total depositions of atmospheric PCDD/F were only 0.02%. The results indicated that the major sources of PCDD/F for the contaminated soil could be attributed to the pentachlorophenol manufacturing process.     

An assessment of the relationship between potential chemical indices of nitrogen saturation and nitrogen deposition in hardwood forests in southern Ontario

Southern Ontario receives the highest levels of atmospheric nitrogen (N) deposition in Canada and there are concerns that forests in the region may be approaching a state of ‘N saturation’. In order to evaluate whether potential chemical indices provide evidence of N saturation, 23 hardwood plots were sampled along a modeled N-deposition gradient ranging from 9.3 to 12.8 kg/ha/year. All plots were dominated by sugar maple (Acer saccharum Marsh.) and foliar N and foliar δ¹⁵N were positively correlated with modeled N deposition. However, forest floor N content and the C:N ratio were unrelated to N deposition, but were instead related to soil pH and annual temperature; lower C:N ratios and higher N content in the forest floor were found at the most acidic sites in the cooler, northern part of the study region despite lower N deposition. Likewise, δ¹⁵N values in surface mineral soil and the ¹⁵N enrichment factor of foliage (δ¹⁵N foliage ? δ¹⁵N soil) are correlated to soil pH and temperature and not N deposition. Further, potential N mineralization, ammonification, and nitrification in Ontario maple stands were highest in the northern part of the region with the lowest modeled N deposition. Nitrogen cycling in soil appears to be primarily influenced by the N status of the forest floor and other soil properties rather than N deposition, indicating that chemical indices in soil in these hardwood plots may not provide an early indicator of N saturation.     

Observational and modeling study of dry deposition on surrogate surfaces in a South China city: implication of removal of atmospheric crustal particles

Dry deposition samples collected during 1999–2001 at a South China site using surrogate surfaces were analyzed by capillary electrophoresis. Collector surface properties played important roles to the dry deposition. The deposition velocities for various species ranged from 0.02 to 1.69 cm s^???1, in general agreement with literature values. More than 90% of Ca^2?+? was deposited by sedimentation and its comparable values of dry or wet removal residence times imply that dry deposition is an important atmospheric removal process for the ubiquitous crustal species in South China, compared with precipitation scavenging. Relatively good agreement was found when the species deposition velocities were modeled based on up-to-date knowledge of particle dry deposition. The total depositions for anthropogenic and crustal species in northern China are likely to be much higher than those in the south, including our site where the fluxes of the acidic species SO₄ ^2??? and NO₃ ^??? were 4.4 and 2.2 g m^???2 year^???1, respectively. The sum of dry deposition for cations Na^?+?, Ca^2?+?, Mg^2?+?, and K^?+? contributes 44% of the total flux, which is equivalent to the value estimated in Europe.     

Modelling the contribution of different sources of sulphur to atmospheric deposition in the United Kingdom

In order to understand relationships between sources and receptors of atmospheric deposition, computer models must be used. This paper describes a Lagrangian acid deposition model that represents emissions of trace species across Northern Europe. The chemistry of sulphur dioxide, dimethyl sulphide and hydrogen sulphide is represented and the model tested against estimates of UK wet and dry deposition. Mean UK wet and dry deposition for the period 1992–1994 was 206 and 145 ktonne S yr^-1, respectively. The model predicted wet and dry deposition of 222 and 166 ktonne S yr^-1, in good agreement with measurements. The model has been used to examine the sources of deposited S to the UK. For a base year of 1992, 86% of the UK's SO₂ emissions are exported. The S deposition attributable from mainland European sources was 36% of the UK total S deposition, in good agreement with other UK models but this differs substantially from the calculations of the EMEP model. Natural sources of S deposition from planktonic emissions of dimethyl sulphide, biological emissions of hydrogen sulphide and non-eruptive volcanic emissions of sulphur dioxide contributed approximately 1% of the modelled UK S deposition, of which 95% originated from dimethyl sulphide. The explicit chemical scheme for dimethyl sulphide incorporated into the model showed that 24% of the resultant deposited S was methane sulphonic acid. Boundary conditions of the model were tested and it was found that initialisation of sulphur dioxide and sulphate concentrations to representative ambient conditions had a very small effect. The modelled contribution of UK and European sources to UK S deposition was approximately 40 and 60%, respectively, showing the dramatic change arising from projected UK SO₂ emissions in 2010. This revised version was published online in July 2006 with corrections to the Cover Date.     

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.     

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.     

The Importance of Leaching from Litter Collected in Litterfall Traps

Litterfall (LF) is usually collected by means of opentraps. However, this litter will be subject toleaching by the throughfall which passes through theaccumulated litter in the traps. The nutrients lostduring this leaching are not taken into account in thecalculation of LF nutrient fluxes. We report theresults from a 2-month (August–September) studycarried out in 8 northern coniferous forest stands toassess the possible importance of leaching from litterin LF traps. Compared to throughfall (TF), thelitterfall leachate (LFL_gross), which includes athroughfall component, had significantly (p < 0.05)higher concentrations and fluxes of Ca, Mg, Na and S.The average net LFL (i.e., LFL_net = LFL_gross-TF) fluxes were 21 (Ca), 7 (Mg), 57 (K), 10 (Na), 10 (N), and 19 (S) mg m^-2 mo^-1. LFL_net accounted for 42%, 37% and 50% of the LFL_gross flux, and for 91%, 51% and 49% of the total litterfall flux (i.e.,LF + LFL_net) of Na, S and K, respectively. ForCa, Mg and N, the LFL_net flux accounted for 64%,58% and 29% of the LFL_gross flux, and for< 14% of the total litterfall flux. Compared to TF,LF was the dominant return pathway for Ca, Mg and N tothe forest floor regardless of whether LFL_net wasincluded or not. However, for K and S, takingLFL_net into account determined whether TF or LFwas the dominant pathway. TF remained the dominantpathway for Na even when LFL_net was included.     

Quantifying Carbon Budgets Of Conifer Mediterranean Forest Ecosystems, Turkey

Abstact Aboveground biomass, aboveground litterfall, and leaf litter decomposition of five indigenous tree stands (pure stands ofPinus brutia,Pinus nigra,Cedrus libani,Juniperus excelsa, and a mixed stand ofAbies cilicica,P. nigra, andC. libani) were measured in an eastern Mediterranean evergreen needleleaf forest of Turkey. Measurements were converted to regional scale estimates of carbon (C) stocks and fluxes of forest ecosystems, based on general non-site-specific allometric relationships. Mean C stock of the conifer forests was estimated as 97.8± 79 Mg C ha⁻¹consisting of 83.0 ± 67 Mg C ha⁻¹in the aboveground and 14.8 ± 12 Mg C ha⁻¹in the belowground biomass. The forest stands had mean soil organic carbon (SOC) and nitrogen (SON) stocks of 172.0 ± 25.7 Mg C ha⁻¹and 9.2 ± 1.2 Mg N ha⁻¹, respectively. Mean total monthly litterfall was 376.2± 191.3 kg C ha⁻¹, ranging from 641 ± 385 kg C ha⁻¹forPinus brutiato 286 ± 82 kg C ha⁻¹forCedrus libani. Decomposition rate constants (k) for pine needles were 0.0016 forCedrus libani, 0.0009 forPinus nigra, 0.0006 for the mixed stand, and 0.0005 day⁻¹forPinus brutiaand Juniperus excelsa. Estimation of components of the C budgets revealed that the forest ecosystems were net C sinks, with a mean sequestration rate of 2.0 ± 1.1 Mg C ha⁻¹ yr⁻¹ranging from 3.2 ± 2 Mg C ha⁻¹forPinus brutiato 1.6 ± 0.6 Mg C ha⁻¹forCedrus libani. Mean net ecosystem productivity (NEP) resulted in sequestration of 98.4 ± 54.1 Gg CO₂ yr⁻¹from the atmosphere when extrapolated for the entire study area of 134.2 km²(Gg = 10⁹ g). The quantitative C data from the study revealed the significance of the conifer Mediterranean forests as C sinks     

CH4 and CO emissions from rice straw burning in South East Asia

Atmospheric samples collected during rice straw burning at four different locations in Viet-Nam during the dry (March 1992, February 1993) and wet season (August 1992) were analysed for CO₂, CO, and CH₄. The emission ratios relative to CO₂ for CO and CH₄ for rice straw burning during the dry season were comparable to those observed on samples collected during burning of savanna in Africa or forest in the USA. During the wet season, however the emission ratios for CO and CH₄ relative to CO₂ were 3 to 10 times higher. With these emission ratios and estimates of rice production from Southeastern Asia, we estimated that burning of rice straw emits annually about 2.2 Tmol of CO (26 TgC) and 0.2 Tmol of CH₄ (2.4 TgC) to the atmosphere. Taking into account these new results, CO and CH₄ fluxes from biomass burning could be reevaluated by 5–21% and 5–24%, respectively, in respect with previous estimates of these gas emissions from all biomass burning activities.     

The predicted effect of SO2 emission controls on the water quality of eastern Canadian lakes

Changes in SO _inf4 ^sup2- deposition predicted to occur in response to implementation of announced SO₂ emission control programs in Canada and the U.S.A. have been used as input to water chemistry models thereby giving an estimate of the changes in lake acid neutralizing capacity (ANC) and pH that can be expected from these programs. Eastern Canada has been divided into 22 subregions for the purpose of this analysis. Relative to the current level (1982–86) of SO _inf4 ^sup2- deposition (Scenario 1), the effect of the Canadian SO₂ emission control program alone (Scenario 2) is compared to that obtained when controls are implemented throughout North America (Scenarios 3 and 4). SO₂ emission reduction will effect a shrinkage of the high wet SO _inf4 ^sup2- deposition field in NE North America such that under Scenario 4 conditions, almost no area will remain in Canada that receives >20 kg ha^-1 yr^-1. The greatest decrease in deposition and resulting change in lake chemistry occurs in southern Ontario and southwestern Quebec. ANC distributions shift to higher concentrations and the percentage of lakes having pH<6 decreases in these areas. The Atlantic Provinces will obtain only a minor benefit from the control programs, i.e. experiencing only a small decrease in deposition and improvement in water quality. High sensitivity of the terrain in many parts of Atlantic Canada means that large numbers of lakes will remain acidic (i.e. ANC<0) and/or have pH<6 (an important biological threshold) even after full implementation of the current plans for SO₂ control in Canada and the U.S.