Simulation of global warming potential (GWP) from rice fields in the Tai-Lake region,China by coupling 1:50,000 soil database with DNDC model

Quantifying greenhouse gas (GHG) emissions from wetland ecosystems is a relatively new issue in global climate change studies. China has approximately 22% of the world's rice paddies and 38% of the world's rice production, which are crucial to accurately estimate the global warming potential (GWP) at regional scale. This paper reports an application of a biogeochemical model (DeNitrification and DeComposition or DNDC) for quantifying GWP from rice fields in the Tai-Lake region of China. For this application, DNDC is linked to a 1:50,000 soil database, which was derived from 1107 paddy soil profiles compiled during the Second National Soil Survey of China in the 1980–1990s. The simulated results show that the 2.34 Mha of paddy soil cultivated in rice–wheat rotation in the Tai-Lake region emitted about ?1.48 Tg C, 0.84 Tg N and 5.67 Tg C as CO₂, N₂O, and CH₄ respectively, with a cumulative GWP of 565 Tg CO₂ equivalent from 1982 to 2000. As for soil subgroups, the highest GWP (26,900 kg CO₂ equivalent ha^?1 yr^?1) was linked to gleyed paddy soils accounting for about 4.4% of the total area of paddy soils. The lowest GWP (5370 kg CO₂ equivalent ha^?1 yr^?1) was associated with submergenic paddy soils accounting for about 0.32% of the total area of paddy soils. The most common soil in the area was hydromorphic paddy soils, which accounted for about 53% of the total area of paddy soils with a GWP of 12,300 kg CO₂ equivalent ha^?1 yr^?1. On a regional basis, the annual averaged GWP in the polder, Tai-Lake plain, and alluvial plain soil regions was distinctly higher than that in the low mountainous and Hilly soil regions. As for administrative areas, the average annual GWP of counties in Shanghai city was high. Conversely, the average annual GWP of counties in Jiangsu province was low. The high variability in soil properties throughout the Tai-Lake region is important and affects the net greenhouse gas emissions. Therefore, the use of detailed soil data sets with high-resolution digital soil maps is essential to improve the accuracy of GWP estimates with process-based models at regional and national scales.     

Net ecosystem CO2 exchange over a larch forest in Hokkaido, Japan

Larch forests are distributed extensively in the east Eurasian continent and are expected to play a significant role in the terrestrial ecosystem carbon cycling process. In view of the fact that studies on carbon exchange for this important biome have been very limited, we have initiated a long-term flux observation in a larch forest ecosystem in Hokkaido in northern Japan since 2000. The net ecosystem CO₂ exchange (NEE) showed large seasonal and diurnal variation. Generally, the larch forest ecosystem released CO₂ in nighttime and assimilated CO₂ in daytime during the growing season from May to October. The ecosystem started to become a net carbon sink in May, reaching a maximum carbon uptake as high as 186 g C m⁻² month⁻¹ in June. With the yellowing, senescing and leaf fall, the ecosystem turned into a carbon source in November. During the non-growing season, the larch forest ecosystem became a net source of CO₂, releasing an average of 16.7 g C m⁻² month⁻¹. Overall, the ecosystem sequestered 141–240 g C m⁻² yr⁻¹ in 2001. The NEE was significantly influenced by environmental factors. Respiration of the ecosystem, for example, was exponentially dependent on air temperature, while photosynthesis was related to the incident PAR in a manner consistent with the Michaelis–Menten model. Although the vapor pressure deficit (VPD) was scarcely higher than 15 hPa, the CO₂ uptake rate was also depressed when VPD surpassed 10 hPa.     

Continuous observations of carbon dioxide at Mace Head,Ireland from 1995 to 1999 and its net European ecosystem exchange

A 5-yr record of continuous high-frequency carbon dioxide CO₂ observations over the 1995–1999 period for the Mace Head Atmospheric Research Station has been examined to reveal a complex interplay between local- and regional-scale sources and sinks. During the winter months, an additional CO₂ source, over and above fossil fuel combustion, is required to support the observed concentrations of CO₂ in European regionally polluted air masses. During the summer months, an additional CO₂ sink is required. Over the entire study period, the additional net European ecosystem exchange source–sink required is –0.36±0.4 Gtonne C yr⁻¹.     

Ozone, nitric acid, and ammonia air pollution is unhealthy for people and ecosystems in southern Sierra Nevada, California

Two-week average concentrations of ozone (O₃), nitric acid vapor (HNO₃) and ammonia (NH₃) were measured with passive samplers during the 2002 summer season across the central Sierra Nevada Mountains, California, along the San Joaquin River drainage. Elevated concentrations of the pollutants were determined with seasonal means for individual sites ranging between 62 and 88 ppb for O₃, 1.0-3.8 μg m⁻³ for HNO₃, and 2.6-5.2 μg m⁻³ for NH₃. Calculated O₃ exposure indices were very high, reaching SUM00-191 ppm h, SUM60-151 ppm h, and W126-124 ppm h. Calculated nitrogen (N) dry deposition ranged from 1.4 to 15 kg N ha⁻¹ for maximum values, and 0.4-8 kg N ha⁻¹ for minimum values; potentially exceeding Critical Loads (CL) for nutritional N. The U.S., California, and European 8 h O₃ human health standards were exceeded during 104, 108, and 114 days respectively, indicating high risk to humans from ambient O₃.     

Long-term effects of clear-cutting and selective cutting on soil methane fluxes in a temperate spruce forest in southern Germany

Based on multi-year measurements of CH₄ exchange in sub-daily resolution we show that clear-cutting of a forest in Southern Germany increased soil temperature and moisture and decreased CH₄ uptake. CH₄ uptake in the first year after clear-cutting (−4.5 ± 0.2 μg C m⁻² h⁻¹) was three times lower than during the pre-harvest period (−14.2 ± 1.3 μg C m⁻² h⁻¹). In contrast, selective cutting did not significantly reduce CH₄ uptake. Annual mean uptake rates were −1.18 kg C ha⁻¹ yr⁻¹ (spruce control), −1.16 kg C ha⁻¹ yr⁻¹ (selective cut site) and −0.44 kg C ha⁻¹ yr⁻¹ (clear-cut site), respectively. Substantial seasonal and inter-annual variations in CH₄ fluxes were observed as a result of significant variability of weather conditions, demonstrating the need for long-term measurements. Our findings imply that a stepwise selective cutting instead of clear-cutting may contribute to mitigating global warming by maintaining a high CH₄ uptake capacity of the soil.     

Temporal variability of soil-atmospheric CO2 and CH4 fluxes from different land uses in mid-subtropical China

Different land uses in subtropics play an important role in regulating the global environmental changes. To reduce uncertainties of greenhouse gas (GHG) emissions of agricultural soils in subtropical ecosystem, a four years campaign was started to determine the temporal GHG (CO₂ and CH₄) fluxes from seven sites of four land use types (1 vegetable field, 3 uplands, 2 orchards, 1 pine forest). The mean annual budgets of CO₂, and CH₄ were 6.5～10.5 Mg CO₂ ha^?1 yr^?1, and +0.47 ～ ?2.37 kg CH₄ ha^?1 yr^?1, respectively. Pine forest had significantly lower CO₂ emission and higher CH₄ uptake than agriculture land uses. Tilled orchard emitted more CO₂ and oxidized less CH₄ than non-tilled orchard. Upland crops had higher CO₂ emissions than orchards, while abrupt differences of CH₄ uptake were observed between upland crops and orchards. Every year, the climate was warm and wet from April to September (the hot–humid season) and became cool and dry from October to March (the cool–dry season). Driven by seasonality of temperature and WFPS, CO₂ fluxes were significantly higher in the hot–humid season than in cool–dry season. Soil temperature, WFPS, NO₃^?–N and NH₄⁺–N contents interactively explained CH₄ uptake which was significantly higher in cool–dry season than in hot–humid season. We conclude that soil C fluxes from different land uses are strongly under control of different climatic predictors along with soil nutrient status, which interact in conjunction with each other to supply the readily available substrates.     

Characteristics influencing the variability of urban CO2 fluxes in Melbourne,Australia

Urban areas are significant contributors to global carbon dioxide emissions. Vehicle emissions and other anthropogenic related activities are a frequent source of CO₂ to the atmosphere, contributing to global warming. Micrometeorological techniques used for observations in Northern Hemisphere cities have found that urban CO₂ fluxes are consistently a source. This study investigates CO₂ fluxes in an Australian city, adding to the global database of CO₂ fluxes in a bid to aid in future development of planning policies concerning reductions in CO₂ emissions. Using the eddy covariance approach, fluxes of CO₂ were measured at a suburban site (Preston) in Melbourne, Australia from February 2004 to June 2005 to investigate temporal variability. A second site (Surrey Hills) with differing surface characteristics (in particular, greater vegetation cover) was also established in Melbourne and ran simultaneously for 6 months (February 2004–July 2004). Results showed that both sites were a net source of CO₂ to the atmosphere. Diurnal patterns of fluxes were largely influenced by traffic volumes, with two distinct peaks occurring at the morning and evening traffic peak hours, with the winter morning peak averaging 10.9 μmol m⁻² s⁻¹ at Preston. Summer time fluxes were lower than during winter due to greater vegetative influence and reduced natural gas combustion. Vegetation limited the source of CO₂ in the afternoon, yet was not enough to combat the strong local anthropogenic emissions. Surrey Hills showed higher fluxes of CO₂ despite greater vegetation cover because of higher local traffic volumes. Annual emissions from Preston were estimated at 84.9 t CO₂ ha⁻¹ yr⁻¹. Magnitudes and patterns of suburban CO₂ fluxes in Melbourne were similar to those observed in Northern Hemisphere suburban areas.     

Effect of land-use change on CH4 and N2O emissions from freshwater marsh in Northeast China

The wetlands play an important role in global carbon and nitrogen storage, and they are also natural sources of greenhouse gases such as methane (CH₄) and nitrous oxide (N₂O). Land-use change is an important factor affecting the exchange of greenhouse gases between wetlands and the atmosphere. However, few studies have investigated the effect of land-use change on CH₄ and N₂O emissions from freshwater marsh in China. Therefore, a field study was carried out over a year to investigate the seasonal changes of the emissions of CH₄ and N₂O at three sites (Deyeuxia angustifolia marsh, dryland and rice field) in the Sanjiang Plain of Northeast China. Marsh was the source of CH₄ showing a distinct temporal variation. Maximum fluxes occurred in June and the highest value was 20.69 ± 2.57 mg CH₄ m^?2 h^?1. The seasonal change of N₂O fluxes from marsh was not obvious, consisted of a series of emission pulses. The marsh acted as a N₂O sink during winter, while became a N₂O source in the growing season. The results showed that gas exchange between soil/snow and the atmosphere in the winter season contributed greatly to the annual budgets. The winter season CH₄ flux was about 3.24% of the annual flux and the winter uptake of N₂O accounted for 13.70% of the growing-season emission. Conversion marsh to dryland resulted in a shift from a strong CH₄ source to a weak sink (from 199.12 ± 39.04 to ?1.37 ± 0.68 kg CH₄ ha^?1 yr^?1), while increased N₂O emissions somewhat (from 4.07 ± 1.72 to 4.90 ± 1.52 kg N₂O ha^?1 yr^?1). Conversion marsh to rice field significantly decreased CH₄ emission from 199.12 ± 39.04 to 94.82 ± 9.86 kg CH₄ ha^?1 yr^?1 and N₂O emission from 4.07 ± 1.72 to 2.09 ± 0.79 kg N₂O ha^?1 yr^?1.     

A preliminary climatology of trajectories related to atmospheric CO2 measurements at Alert and Mould bay

An attempt is made to establish a climatological relationship between anomalous CO₂ values observed at Alert and Mould Bay and trajectories of air parcels arriving at these stations. Measured atmospheric CO₂ values from 1981 to 1984 inclusive were used to obtain climatological winter and summer distributions of 5-day back trajectory origins associated with positive and negative CO₂ deviations relative to a ‘typical’ smoothed seasonal cycle obtained by a simple composite averaging process.Based on a climatological distribution of positive and negative trajectory origins, there are two basic ‘air masses’ over the Arctic Ocean with different CO₂ concentration levels which influence CO₂ deviation values at Alert and Mould Bay.     

Fenton-like oxidation and mineralization of phenol using synthetic Fe(II)–Fe(III) green rusts

Background, aim, and scope  

In literature, the environmental applications of green rust (GR) have mainly been pointed out through the reduction of inorganic contaminants and the reductive dechlorination of chlorinated organics. However, reactions involving GR for the oxidation and mineralization of organic pollutants remain very scantly described. In this study, the ability of three synthetic Fe(II)–Fe(III) green rusts, GR(CO₃²⁻), GR(SO₄²⁻), and GR(Cl⁻), to promote Fenton-like reaction was examined by employing phenol as a model pollutant. Unlike the traditional Fenton’s reagent (dissolved Fe(II) + H₂O₂), where the pH values have to be lowered to less than 4, the proposed reaction can effectively oxidize the organic molecules at neutral pH and could avoid the initial acidification which may be costly and destructive for the in situ remediation of contaminated groundwater and soils. The green rust reactivity towards the oxidative transformation of phenol was thoroughly evaluated by performing a large kinetic study, chemical analyses, and spectroscopic investigations.     

Nitrous oxide emissions from mineral and organic soils of a Norway spruce stand in South–West Germany

Due to the high temporal and spatial variability of N₂O fluxes, estimates of N₂O emission from temperate forest ecosystems are still highly uncertain, particularly at larger scales. Although highest N₂O emissions with up to 7.0 kg N ha⁻¹ yr⁻¹ were mainly reported for soils affected by stagnant water, most of the reported gas flux measurements were performed at forest sites with well-aerated soils yielding mostly to low mean annual emission rates less than 1.0 kg N ha⁻¹ yr⁻¹. This study compares N₂O fluxes from upland (Cambisols) and temporally water-logged (Gleysols, Histosols) soils of the Central Black Forest (South-West Germany) over a period of 2 yr. Mean annual N₂O fluxes from investigated soils ranged between 0.2 and 3.9 kg N ha⁻¹ yr⁻¹. The fluxes showed a large variability between the different soil types. Emissions could be clearly ranked in the following order: Cambisols (0.26–0.75 kg N ha⁻¹ yr⁻¹)<Gleysols (1.37–2.68 kg N ha⁻¹ yr⁻¹)<Histosol (3.66–3.95 kg N ha⁻¹ yr⁻¹). Although the Cambisols cover two-thirds of the investigated area, only about half of the overall N₂O is emitted from this soil type. Therefore, regional or national N₂O fluxes from temperate forest soils are underestimated if soils characterised by intermediate aeration conditions are disregarded.     

A new look at atmospheric carbon dioxide

Carbon dioxide is increasing in the atmosphere and is of considerable concern in global climate change because of its greenhouse gas warming potential. The rate of increase has accelerated since measurements began at Mauna Loa Observatory in 1958 where carbon dioxide increased from less than 1 part per million per year (ppm yr^?1) prior to 1970 to more than 2 ppm yr^?1 in recent years. Here we show that the anthropogenic component (atmospheric value reduced by the pre-industrial value of 280 ppm) of atmospheric carbon dioxide has been increasing exponentially with a doubling time of about 30 years since the beginning of the industrial revolution (～1800). Even during the 1970s, when fossil fuel emissions dropped sharply in response to the “oil crisis” of 1973, the anthropogenic atmospheric carbon dioxide level continued increasing exponentially at Mauna Loa Observatory. Since the growth rate (time derivative) of an exponential has the same characteristic lifetime as the function itself, the carbon dioxide growth rate is also doubling at the same rate. This explains the observation that the linear growth rate of carbon dioxide has more than doubled in the past 40 years. The accelerating growth rate is simply the outcome of exponential growth in carbon dioxide with a nearly constant doubling time of about 30 years (about 2%/yr) and appears to have tracked human population since the pre-industrial era.     

Decadal changes in atmospheric CO2 concentration and δ13C over two seas and two oceans: Italy to New Zealand

Continuous measurements of the CO₂ concentration were repeatedly carried out from 1996 to 2007 between Italy and New Zealand by means of a Siemens Ultramat 5E analyzer assembled for shipboard use. Along the ship routes discrete air samples were collected from 1998 to 2005 using four-litre Pyrex flasks. The δ¹³C of the CO₂ from the flask air samples was measured according to well-established techniques. The decadal changes of these two variables can now be evaluated from these results. Large variations of the CO₂ concentration were normally recorded in the Mediterranean and the Red Sea. Completely different trends of the CO₂ concentration were observed in the Red Sea (30° N to about 13° N) between 2007 (a marked southward decrease) and 2005 and 2003 when a marked southward increase is apparent, at least between 23° and 13° N. A further difference among different expeditions is related to the decrease or increase of the CO₂ concentration in the Gulf of Aden. The backward trajectories of the air masses help to explain, at least partially, these differences. In the Indian Ocean and Southern Ocean a decrease of a few ppmv of the CO₂ concentration takes place from Cape Guardafui (Northern Somaliland) to southern New Zealand, particularly during 2005 and 2007. The yearly rate of increase of the CO₂ concentration between 1996 and 2007 for the Indian Ocean is of about 1.9 ppmv yr^?1, in excellent agreement with the NOAA/CMDL measurements carried out during the same period at Mahé Isld. (Indian Ocean) and Cape Grim (Tasmania). The δ¹³C results obtained from the CO₂ of flask samples collected in the Mediterranean show the effect of anthropogenic emissions, though this is considerably smaller than expected. This inconsistency may be related to the large terrestrial biospheric sink of CO₂ in the Northern Hemisphere. The results obtained from the Red Sea are quite variable through time and space, particularly in its southern section; their interpretation is not easy. The Indian Ocean and the Southern Ocean show rather homogeneous δ¹³C results even though a variable carbon isotope shift can be calculated from period/cruise to period/cruise. In the case of the Indian Ocean the mean δ¹³C value from the flask air samples collected in 2005 is ?8.29‰ and the calculated rate of the carbon isotope shift between 1998 and 2005 is ?0.034‰ yr^?1, considerably larger than that calculated at the closest NOAA station (Mahé Isld.) of ?0.026‰ yr^?1. This discrepancy may be, at least partially, caused by the small number of measurements carried out at sea. However, the atmosphere over the Indian Ocean is less affected by anthropogenic emissions than in other areas.     

Short-term effect of increasing nitrogen deposition on CO2, CH4 and N2O fluxes in an alpine meadow on the Qinghai-Tibetan Plateau,China

An increasing nitrogen deposition experiment (2 g N m^?2 year^?1) was initiated in an alpine meadow on the Qinghai-Tibetan Plateau in May 2007. The greenhouse gases (GHGs), including CO₂, CH₄ and N₂O, was observed in the growing season (from May to September) of 2008 using static chamber and gas chromatography techniques. The CO₂ emission and CH₄ uptake rate showed a seasonal fluctuation, reaching the maximum in the middle of July. We found soil temperature and water-filled pore space (WFPS) were the dominant factors that controlled seasonal variation of CO₂ and CH₄ respectively and lacks of correlation between N₂O fluxes and environmental variables. The temperature sensitivity (Q₁₀) of CO₂ emission and CH₄ uptake were relatively higher (3.79 for CO₂, 3.29 for CH₄) than that of warmer region ecosystems, indicating the increase of temperature in the future will exert great impacts on CO₂ emission and CH₄ uptake in the alpine meadow. In the entire growing season, nitrogen deposition tended to increase N₂O emission, to reduce CH₄ uptake and to decrease CO₂ emission, and the differences caused by nitrogen deposition were all not significant (p < 0.05). However, we still found significant difference (p < 0.05) between the control and nitrogen deposition treatment at some observation dates for CH₄ rather than for CO₂ and N₂O, implying CH₄ is most susceptible in response to increased nitrogen availability among the three greenhouse gases. In addition, we found short-term nitrogen deposition treatment had very limited impacts on net global warming potential (GWP) of the three GHGs together in term of CO₂-equivalents. Overall, the research suggests that longer study periods are needed to verify the cumulative effects of increasing nitrogen deposition on GHG fluxes in the alpine meadow.     

Trace elements in aerosol and precipitation at New Castle,NH, USA

Concentrations of a suite of trace elements (Al, Ag, As, Cd, Co, Cr, Cu, Fe, Ni, Pb, Sr, V, Zn) were measured in aerosol and precipitation samples collected at a coastal site in New Castle, NH, from August 1996, through July 1997. Metal concentrations in aerosol and precipitation exhibit a high degree of temporal variability over the annual cycle, varying by approximately one order of magnitude or less for aerosol metals and by ∼2–3 orders of magnitude in precipitation. Estimates of the total annual atmospheric deposition of metals to the Gulf of Maine range from ∼10³ kg yr⁻¹ for Ag, ∼10⁴–10⁵ kg yr⁻¹ for the majority of metals, and ∼10⁶ kg yr⁻¹ for the crustal elements Al and Fe.     

Greenhouse gas emissions from dairy open lot and manure stockpile in northern China: A case study

The open lots and manure stockpiles of dairy farm are major sources of greenhouse gas (GHG) emissions in typical dairy cow housing and manure management system in China. GHG (CO₂, CH₄ and N₂O) emissions from the ground level of brick-paved open lots and uncovered manure stockpiles were estimated according to the field measurements of a typical dairy farm in Beijing by closed chambers in four consecutive seasons. Location variation and manure removal strategy impacts were assessed on GHG emissions from the open lots. Estimated CO₂, CH₄ and N₂O emissions from the ground level of the open lots were 137.5±64.7 kg hd^-1 yr^-1, 0.45±0.21 kg hd^-1 yr^-1 and 0.13±0.08 kg hd^-1 yr^-1, respectively. There were remarkable location variations of GHG emissions from different zones (cubicle zone vs. aisle zone) of the open lot. However, the emissions from the whole open lot were less affected by the locations. After manure removal, lower CH₄ but higher N₂O emitted from the open lot. Estimated CO₂, CH₄ and N₂O emissions from stockpile with a stacking height of 55±12 cm were 858.9±375.8 kg hd^-1 yr^-1, 8.5±5.4 kg hd^-1 yr^-1 and 2.3±1.1 kg hd^-1 yr^-1, respectively. In situ storage duration, which estimated by manure volatile solid contents (VS), would affect GHG emissions from stockpiles. Much higher N₂O was emitted from stockpiles in summer due to longer manure storage.

Implications: This study deals with greenhouse gas (GHG) emissions from open lots and stockpiles. It’s an increasing area of concern in some livestock producing countries. The Intergovernmental Panel on Climate Change (IPCC) methodology is commonly used for estimation of national GHG emission inventories. There is a shortage of on-farm information to evaluate the accuracy of these equations and default emission factors. This work provides valuable information for improving accounting practices within China or for similar manure management practice in other countries.     

A study of seasonal and yearly modulation of carbon dioxide sources and sinks,with a particular attention to the Boreal Atlantic Ocean

With the intention of identifying and monitoring space and time patterns of carbon dioxide sources and sinks, the seasonal fields of atmospheric CO₂ concentration over an area covering Europe, the Boreal Atlantic, and North Africa have been computed by using CO₂ observations measured at one or two remote sites in conjunction with the backward air trajectories crossing the same observation sites.The air trajectories have been calculated by means of the wind speed fields provided by the ECMWF (European Centre of Medium-range Weather Forecast, of Reading, UK) analyses (T213/L31 model) on a regular grid, while the atmospheric CO₂ concentrations have been measured at two alpine European stations, located in the free atmosphere, far from the influence of local industrial pollution.A modified version of the statistical receptor-to-source-oriented-model (hereafter, source-oriented model) of Stohl (Atmos. Environ. 30 (1998) 947), using the above-mentioned air trajectories, has then been applied to reconstruct the spatial distribution fields of atmospheric CO₂.This source-oriented methodology belongs to a family of models which are simpler and easier to use than the more powerful and widespread inverse models and can allow a reliable deduction of the location of sources and sinks of gas tracers.We have applied this kind of model in order to identify source and sink macro-regions of CO₂ over the above-mentioned area in the period 1993–1998. The CO₂ observing stations of Plateau Rosà (3480 m a.s.l., in the western Alps) and Zugspitze (2937 m, in the eastern Alps) have been considered particularly fit for this purpose, because of their location in high orography areas, allowing to monitor values of atmospheric CO₂ concentrations representative of fairly well-mixed air, not affected by some local influences (industries, urban emissions, etc.). In this way, it can be assumed that possible maxima or minima observed in the trend of measured gas concentration can be due to contaminations of the air mass during its whole travel, at some specific locations identified by the source-oriented model.The most interesting result obtained in this study is the seasonal cycle of the atmospheric CO₂ concentration found over the mid- and sub-tropical latitudes of the Boreal Atlantic Ocean and evident in all simulations. This cycle appears to be clearly related to the seasonal trend of the SST, particularly in the tropical and subtropical Atlantic regions, and is particularly evident during the warmest months (during Spring, Autumn and particularly in Summer).     

Analysis of 3-year observations of CFC-11, CFC-12 and CFC-113 from a semi-rural site in China

In-situ measurements of atmospheric chlorofluorocarbons (CFCs) can be used to the assess their global and regional emissions and to check for compliance with phase-out schedules under Montreal protocol and its amendments. The atmospheric mixing ratios of CFC-11 (CCl₃F), CFC-12 (CCl₂F₂) and CFC-113 (CCl₂F–CClF₂) have been measured by an automated in-situ GC-ECDs system at the regional Chinese Global Atmosphere Watch (GAW) station Shangdianzi (SDZ), from November 2006 to October 2009. The time series for these three principal CFCs showed large episodic events and background conditions occurred for approximately 30% (CFC-11), 52% (CFC-12) and 56% (CFC-113) of the measurements. The mean background mixing ratios for CFC-11, CFC-12 and CFC-113 were 244.8 ppt (parts per trillion, 10^?12, molar) 539.6 ppt and 76.8 ppt, respectively, for 2006–2009. The enhanced CFC mixing ratios compared to AGAGE sites such as Trinidad Head (THD), US and Mace Head (MHD), Ireland suggest regional influences even during background conditions at SDZ, which is much closer to highly-populated areas. Between 2006 and 2009 background CFCs exhibited downward trends at rates of ?2.0 ppt yr^?1 for CFC-11, ?2.5 ppt yr^?1 for CFC-12 and ?0.7 ppt yr^?1 for CFC-113. De-trended 3-year average background seasonal cycles displayed small fluctuations with peak-to-trough amplitudes of 1.0 ± 0.02 ppt (0.4%) for background CFC-11, 1.3 ± 2.1 ppt (0.3%) for CFC-12 and 0.2 ± 0.4 ppt (0.3%) for CFC-113. On the other hand, during pollution periods these CFCs showed much larger seasonal cycles of 11.2 ± 10.7 ppt (5%) for CFC-11, 7.5 ± 6.5 ppt (2%) for CFC-12 and 1.0 ± 1.2 ppt (1.2%) for CFC-113, with apparent winter minima and early summer maxima. This enhancement was attributed to prevailing wind directions from urban regions in summer and to enhanced anthropogenic sources during the warm season. In general, horizontal winds from northeast showed negative contribution to atmospheric CFCs loading, whereas South Western advection (urban sector: Beijing) had positive contributions.     

Agricultural ammonia emissions inventory and spatial distribution in the North China Plain

An agricultural ammonia (NH₃) emission inventory in the North China Plain (NCP) on a prefecture level for the year 2004, and a 5 × 5 km² resolution spatial distribution map, has been calculated for the first time. The census database from China's statistics datasets, and emission factors re-calculated by the RAINS model supported total emissions of 3071 kt NH₃-N yr⁻¹ for the NCP, accounting for 27% of the total emissions in China. NH₃ emission from mineral fertilizer application contributed 1620 kt NH₃-N yr⁻¹, 54% of the total emission, while livestock emissions accounted for the remaining 46% of the total emissions, including 7%, 27%, 7% and 5% from cattle, pigs, sheep and goats, and poultry, respectively. A high-resolution spatial NH₃ emissions map was developed based on 1 × 1 km land use database and aggregated to a 5 × 5 km grid resolution. The highest emission density value was 198 kg N ha⁻¹ yr⁻¹.     

Study on dissolved organic carbon in precipitation in Northern China

Dissolved organic carbon (DOC) was measured in 483 precipitation samples collected at 10 sites in Northern China from December 2007 to November 2008. The annual volume-weighted mean (VWM) concentrations and wet deposition fluxes of DOC for 10 sites ranged from 2.4 to 3.9 mg C/L and 1.4 to 2.7 g C m^?2 yr^?1, respectively. The proportion of DOC to total organic carbon (TOC) was 79% on average, suggesting that a significant fraction of TOC was present as insoluble particulate organic carbon. Due to intensive domestic coal use for house heating and smaller dilution of scavenged organic carbon, higher VWM concentrations of DOC were observed during winter and spring than during summer and autumn. When precipitation events were classified via air mass back-trajectories, the mixed trajectories from SE and NW always corresponded to significantly higher DOC than those from SE or NW alone, coinciding with the centre of a low pressure system moved eastward and the wind direction changed from southeast to northwest. The results also showed that each site had a similar seasonal variation for DOC wet deposition flux. The largest flux occurred during the rainy season, and the lowest flux appeared during winter months. The product of the TC/DOC ratio and the DOC flux yielded an average TC wet deposition flux of 3.2 g C m^?2 yr^?1 in Northern China, accounting for 8.6% and 22% of the carbon sink magnitude (37 g C m^?2 yr^?1) in terrestrial ecosystems and anthropogenic carbon emissions (14 g C m^?2 yr^?1), respectively. This indicates that atmospheric wet deposition of TC is a significant carbon flux that cannot be neglected in regional models of the carbon cycle, and should be considered along with dry deposition in the removal mechanism for carbon from regional atmosphere.