High resolution simulation of recent Arctic and Antarctic stratospheric chemical ozone loss compared to observations

Simulations of polar ozone losses were performed using the three-dimensional high-resolution (1^∘ × 1^∘) chemical transport model MIMOSA-CHIM. Three Arctic winters 1999–2000, 2001–2002, 2002–2003 and three Antarctic winters 2001, 2002, and 2003 were considered for the study. The cumulative ozone loss in the Arctic winter 2002–2003 reached around 35% at 475 K inside the vortex, as compared to more than 60% in 1999–2000. During 1999–2000, denitrification induces a maximum of about 23% extra ozone loss at 475 K as compared to 17% in 2002–2003. Unlike these two colder Arctic winters, the 2001–2002 Arctic was warmer and did not experience much ozone loss. Sensitivity tests showed that the chosen resolution of 1^∘ × 1^∘ provides a better evaluation of ozone loss at the edge of the polar vortex in high solar zenith angle conditions. The simulation results for ozone, ClO, HNO₃, N₂O, and NO _y for winters 1999–2000 and 2002–2003 were compared with measurements on board ER-2 and Geophysica aircraft respectively. Sensitivity tests showed that increasing heating rates calculated by the model by 50% and doubling the PSC (Polar Stratospheric Clouds) particle density (from 5 × 10⁻³ to 10⁻² cm⁻³) refines the agreement with in situ ozone, N₂O and NO _y levels. In this configuration, simulated ClO levels are increased and are in better agreement with observations in January but are overestimated by about 20% in March. The use of the Burkholder et al. (1990) Cl₂O₂ absorption cross-sections slightly increases further ClO levels especially in high solar zenith angle conditions. Comparisons of the modelled ozone values with ozonesonde measurement in the Antarctic winter 2003 and with Polar Ozone and Aerosol Measurement III (POAM III) measurements in the Antarctic winters 2001 and 2002, shows that the simulations underestimate the ozone loss rate at the end of the ozone destruction period. A slightly better agreement is obtained with the use of Burkholder et al. (1990) Cl₂O₂ absorption cross-sections.     

Surface Energy Balance Measurements Above an Exurban Residential Neighbourhood of Kansas City,Missouri

Previous measurements of urban energy balances generally have been limited to densely built, central city sites and older suburban locations with mature tree canopies that are higher than the height of the buildings. In contrast, few data are available for the extensive, open vegetated types typical of low-density residential areas that have been newly converted from rural land use. We made direct measurements of surface energy fluxes using the eddy-covariance technique at Greenwood, a recently developed exurban neighbourhood near Kansas City, Missouri, USA, during an intensive field campaign in August 2004. Energy partitioning was dominated by the latent heat flux under both cloudy and near clear-sky conditions. The mean daytime Bowen ratio (β) values were 0.46, 0.48, and 0.47 respectively for the cloudy, near clear-sky and all-sky conditions. Net radiation (R _n ) increased rapidly from dawn (−34 and −58W m⁻²) during the night to reach a maximum (423 and 630W m⁻²) after midday for cloudy and near clear-sky conditions respectively. Mean daytime values were 253 and 370W m⁻², respectively for the cloudy and near clear-sky conditions, while mean daily values were 114 for cloudy and 171W m⁻² for near clear-sky conditions, respectively. Midday surface albedo values were 0.25 and 0.24 for the cloudy and near clear-sky conditions, respectively. The site exhibited an angular dependence on the solar elevation angle, in contrast to previous observations over urban and suburban areas, but similar to vegetated surfaces. The latent heat flux (Q _E ), sensible heat flux (Q _H ), and the residual heat storage ΔQ _s terms accounted for between 46–58%, 21–23%, and 18–31% of R _n , respectively, for all-sky conditions and time averages. The observed albedo, R _n , and Q _E values are higher than the values that have been reported for suburban areas with high summer evapotranspiration rates in North America. These results suggest that the rapidly growing residential areas at the exurban fringe of large metropolitan areas have a surface energy balance that is more similar to the rural areas from which they were developed than it is to the older suburbs and city centres that make up the urban fabric to which they are being joined.     

Cloud Transmission Estimates of UV-B Erythemal Irradiance

Summary Two UV-Biometer 501A instruments were used to estimate global erythemal irradiance at two locations in southwest Sweden; the Earth Sciences Centre, University of G?teborg (57.69° N; 11.92° E) and the island of Nordkoster, 200 km to the north (58.83° N; 10.72° E). A semi-empirical radiative transfer model was used to calculate the global erythemally effective irradiance under clear skies. A ratio of the hourly measured to clear-sky modelled irradiance was then derived for zenith angles 35–70°. Subsequent comparisons were then made with routine measurements of sunshine duration at G?teborg and sunshine duration, cloud cover, type and height at Nordkoster. Cloud transmission of UV-B irradiance decreases with increasing solar zenith angle, with cloud attenuation being 8% stronger at Nordkoster Island for zenith angles >>;60°. Transmission also decreases with increasing cloud cover such that overcast cloud conditions reduce transmissions by an average of 75%. In addition, cloud type affects the amount of ground incident irradiant flux. Fractus cloud afforded the least UV-B transmission (0.16), while cirrus filaments afforded the most (0.95). The spatial and temporal distribution of clouds appears tobe non-random. Under conditions of 1 to 3 octas, sky cover, clouds appear to be concentrated in line with the sensor and Sun on more occasions than that expected given a random cloud distribution. The same cloud cover condition also resulted in many instances of ground incident irradiance above clear-sky values. The presence of cumuliform clouds appears to increase the likelihood of the latter phenomena. Received January 4, 1998     

Measurement and investigation of chamber radical sources in the European Photoreactor (EUPHORE)

It is essential to quantify the background reactivity of smog-chambers, since this might be the major limitation of experiments carried out at low pollutant concentrations typical of the polluted atmosphere. Detailed investigation of three chamber experiments at zero-NO _x in the European Photoreactor (EUPHORE) were carried out by means of rate-of-production analysis and two uncertainty analysis tools: local uncertainty analysis and Monte Carlo simulations with Latin hypercube sampling. The chemical mechanism employed was that for methane plus the inorganic subset of the Master Chemical Mechanism (MCMv3.1). Newly installed instruments in EUPHORE allowed the measurement of nitrous acid and formaldehyde at sub-ppb concentrations with high sensitivity. The presence of HONO and HCHO during the experiments could be explained only by processes taking place on the FEP Teflon walls. The HONO production rate can be described by the empirical equation W(HONO)_EUPHORE ^dry = a × j _{NO 2}× exp (− T ₀/T) in the low relative humidity region (RH < 2%, a = 7.3×10²¹ cm⁻³, T ₀ = 8945K), and by the equation W(HONO)_EUPHORE ^humid = W(HONO)_EUPHORE ^dry+ j _{NO 2}× b × RH ^q in the higher relative humidity region (2% < RH < 15%, b = 5.8×10⁸ cm⁻³ and q = 0.36, and RH is the relative humidity in percentages). For HCHO the expression W(HCHO)_EUPHORE = c × j _{NO 2}exp (− T′₀/T) is applicable (c = 3.1×10¹⁷ cm⁻³ and T′₀ = 5686 K). In the 0–15% relative humidity range OH production from HONO generated at the wall is about a factor of two higher than that from the photolysis of 100 ppb ozone. Effect of added NO₂ was found to be consistent with the dark HONO formation rate coefficient of MCMv3.1.     

Clear-sky aerosol radiative forcing effects based on multi-site AERONET observations over Europe

Summary One of the great unknowns in climate research is the contribution of aerosols to climate forcing and climate perturbation. In this study, retrievals from AERONET are used to estimate the direct clear-sky aerosol top-of-atmosphere and surface radiative forcing effects for 12 multi-site observing stations in Europe. The radiative transfer code sdisort in the libRadtran environment is applied to accomplish these estimations. Most of the calculations in this study rely on observations which have been made for the years 1999, 2000, and 2001. Some stations do have observations dating back to the year of 1995. The calculations rely on a pre-compiled aerosol optical properties database for Europe. Aerosol radiative forcing effects are calculated with monthly mean aerosol optical properties retrievals and calculations are presented for three different surface albedo scenarios. Two of the surface albedo scenarios are generic by nature bare soil and green vegetation and the third relies on the ISCCP (International Satellite Cloud Climatology Project) data product. The ISCCP database has also been used to obtain clear-sky weighting fractions over AERONET stations. The AERONET stations cover the area 0° to 30° E and 42° to 52° N. AERONET retrievals are column integrated and this study does not make any seperation between the contribution of natural and anthropogenic components. For the 12 AERONET stations, median clear-sky top-of-atmosphere aerosol radiative forcing effect values for different surface albedo scenarios are calculated to be in the range of −4 to −2 W/m². High median radiative forcing effect values of about −6 W/m² were found to occur mainly in the summer months while lower values of about −1 W/m² occur in the winter months. The aerosol surface forcing also increases in summer months and can reach values of −8 W/m². Individual stations often have much higher values by a factor of 2. The median top-of-atmosphere aerosol radiative forcing effect efficiency is estimated to be about −25 W/m² and their respective surface efficiency is around −35 W/m². The fractional absorption coefficient is estimated to be 1.7, but deviates significantly from station to station. In addition, it is found that the well known peak of the aerosol radiative forcing effect at a solar zenith angle of about 75° is in fact the average of the peaks occurring at shorter and longer wavelengths. According to estimations for Central Europe, based on mean aerosol optical properties retrievals from 12 stations, the critical threshold of the aerosol single scattering albedo, between cooling and heating in the presence of an aerosol layer, is close between 0.6 and 0.76.     

Relationship between Net Radiation and Broadband Solar Radiation in the Tibetan Plateau

The characteristics of net radiation (R_n)(0.3--10 μm) in Lhasa and Haibei in the Tibetan Plateau were analyzed based on long-term in-situ measurements of surface radiation data. The monthly average of daily R_n reached a minimum during the winter period followed by an increase until May and then a decline until January. This variation is consistent with solar activity. The annual mean daily total R_n values were 0.92 MJ m^-2 d^-1 and 0.66 MJ m^-2d^-1 in Lhasa and Haibei, respectively. A relationship between R_n and broadband solar radiation (R_s) was demonstrated by a good linear correlation at the two sites. R_n can be an accurate estimate from R_s. The estimated R_n values were similar to the observed values, and the relative deviations between the estimates and measurements of R_n were 2.8% and 3.8% in Lhasa and Haibei, respectively. The application of the R_n estimating model to other locations showed that it could provide acceptable estimated R_n values from the R_s data. Furthermore, we analyzed the influence of clouds on R_n by different clear index (K_s), defined as the ratio of R_s to the extraterrestrial solar irradiance on a horizontal surface. The results indicate that more accurate results are associated with increased cloudy conditions. The influence of the albedo was also considered, but its inclusion in the model resulted in only a slight improvement. Because surface albedo is not usually measured, an expression based solely on global solar radiation could be of more extensive use.     

Acid rain and alkalization in southwestern China: chemical and strontium isotope evidence in rainwater from Guiyang

A comprehensive study on the chemical compositions of rainwater was carried out from June 2007 to December 2008 in Guiyang, a city located on the acid rain control zone of southwest China. All samples were analyzed for pH, major anions (F⁻, Cl⁻, NO₃⁻, SO₄²⁻), major cations (K⁺, Na⁺, Ca²⁺, Mg²⁺, NH₄⁺), Sr²⁺ and Sr isotope. The pH increase is due to the result of neutralization caused by the alkaline dust which contain large amount of CaCO₃. It was observed that Ca²⁺ was the most abundant cation with a volume-weighted mean (VWM) value of 217.6 μeq/L (52.7–1928 μeq/L), accounting for 66% (39%–88%) of the total cations. SO₄²⁻ was the most abundant anion with VWM value of 237.8 μeq/L (49.6-1643 μeq/L). SO₄²⁻ and NO₃⁻ were dominant among the anions, accounting for 66%–97% of the total measured anions. The Sr concentrations vary from 0.01 to 0.92 μmol/L, and strontium isotopic ratios vary in the range of 0.707684–0.710094, with an average of 0.708092. The elements ratios and the ⁸⁷Sr/⁸⁶Sr ratios showed that the solutes of rainwater mainly come from weathering of carbonate and secondary dust input. Moreover, urbanization results in the calcium-rich dust increased and the high concentrations of alkaline ions (mainly Ca²⁺) have played an important role to neutralize the acidity of rainwater, leading to the increase of arithmetic pH mean value by 0.5 units since 2002. It is worth noting that the emission of SO₂ and NO_x from the automobile exhaust is increasing and is becoming another important precursor of acid rain now.     

Measurement of the photodissociation coefficient of NO2 in the atmosphere: I. Method and surface measurements

An instrument, specifically designed for measurements from a balloon platform in the stratosphere, has been used to obtain ground-level values of the atmospheric photodissociation coefficient of nitrogen dioxide, J _{NO 2}.A typical clear-sky value is 8.0×10^-3 s^-1 when the solar zenith angle is 40°. Measurements were made as a function of solar zenith angle and correlated with a calibrated Eppley UV radiometer. It is shown that J _{NO 2}may be expressed as a simple function of the radiometer output so that estimates of J _{NO 2}can be made using just an upward looking radiometer to an accuracy of about 20%. The measurements are also found to be in good agreement with calculations of J _{NO 2}using a simplified isotropic multiple scattering computer routine.     

Atmospheric inorganic nitrogen in marine aerosol and precipitation and its deposition to the North and South Pacific Oceans

Aerosol and rain samples were collected between 48°N and 55°S during the KH-08-2 and MR08-06 cruises conducted over the North and South Pacific Ocean in 2008 and 2009, to estimate dry and wet deposition fluxes of atmospheric inorganic nitrogen (N). Inorganic N in aerosols was composed of ~68% NH₄⁺ and ~32% NO₃^– (median values for all data), with ~81% and ~45% of each species being present on fine mode aerosol, respectively. Concentrations of NH₄⁺ and NO₃⁻ in rainwater ranged from 1.7–55 μmol L⁻¹ and 0.16–18 μmol L⁻¹, respectively, accounting for ~87% by NH₄⁺ and ~13% by NO₃⁻ of total inorganic N (median values for all data). A significant correlation (r = 0.74, p < 0.05, n = 10) between NH₄⁺ and methanesulfonic acid (MSA) was found in rainwater samples collected over the South Pacific, whereas no significant correlations were found between NH₄⁺ and MSA in rainwater collected over the subarctic (r = 0.42, p > 0.1, n = 6) and subtropical (r = 0.33, p > 0.5, n = 6) western North Pacific, suggesting that emissions of ammonia (NH₃) by marine biological activity from the ocean could become a significant source of NH₄⁺ over the South Pacific. While NO₃⁻ was the dominant inorganic N species in dry deposition, inorganic N supplied to surface waters by wet deposition was predominantly by NH₄⁺ (42–99% of the wet deposition fluxes for total inorganic N). We estimated mean total (dry + wet) deposition fluxes of atmospheric total inorganic N in the Pacific Ocean to be 32–64 μmol m⁻² d⁻¹, with 66–99% of this by wet deposition, indicating that wet deposition plays a more important role in the supply of atmospheric inorganic N than dry deposition.     

CLIMAP SSTs re-revisited

Since the 1976 publication of the CLIMAP ice age sea surface temperature (SST) reconstruction showing a 1–2 ^∘C tropical cooling a substantial debate has arisen as to whether tropical SSTs may instead have been 4–5^∘ colder than present. Herein I review the arguments for large SST variations and question a number of key findings, particularly the validity of ice-age coral SST estimates and “down-projecting” tropical snowline changes to the surface. GCM results indicate that an intermediate solution requiring ∼2.5 ^∘C warm pool cooling is consistent with most quantitative low elevation surface land data and is small enough to allow the persistence of tropical biota in the ocean during glacial times. The proposal reduces estimated ice-age climate sensitivity (for a doubling of CO₂) from a “high-end” sensitivity of about 4.5 ^∘C (for a 5–6 ^∘C tropical cooling) to a “mid-range” sensitivity of about 3.0 ^∘C for a 2.5 ^∘C warm-pool decrease. Received: 28 July 1999 /Accepted: 12 August 1999     

Effect of clouds on UV and total irradiance at Paradise Bay, Antarctic Peninsula, from a summer 2000 campaign

Summary ?The analysis of ground-based measurements of solar erythemal ultraviolet (UV) irradiance with a Solar Light 501 biometer, and total (300–3000 nm) irradiance with an Eppley B&W pyranometer at the Argentine Antarctic Base “Almirante Brown”, Paradise Bay (64.9° S, 62.9° W, 10 m a.s.l.) is presented. Measurement period extends from February 16 to March 28 2000. A relatively high mean albedo and a very clean atmosphere characterise the place. Sky conditions were of generally high cloud cover percentage. Clear-sky irradiance for each day was estimated with model calculations, and the effect of the cloudiness was studied through the ratio of measured to clear-sky value (r). Two particular cases were analysed: overcast sky without precipitation and overcast sky with rain or slight snowfall, the last one presenting frequently dense fog. Total irradiance was more attenuated than UV by the homogeneous cloudiness, obtaining mean r values of 0.54 for erythemal irradiance and 0.30 for total irradiance in the first case (without precipitation) and 0.27 and 0.17 respectively in the second case (with precipitation). Mean r values for the complete period were 0.58 for erythemal irradiance and 0.43 for total irradiance. Erythemal and total daily insolations reduce quickly at this epoch due to the increase of the noon solar zenith angle and the decrease of daylight time. Additionally, they were strongly modulated by cloudiness. Measured maxima were 2.71 kJ/m² and 18.42 MJ/m² respectively. Measurements were compared with satellite data. TOMS-inferred erythemal daily insolation shows the typical underestimation with respect to ground measurements at regions of high mean albedo. Measured mean total daily insolation agrees with climatological satellite data for the months of the campaign. Received August 9, 2002; revised January 4, 2003; accepted January 28, 2003 Published online May 20, 2003     

Micrometeorological Conditions for Dust-Devil Occurrence in the Atacama Desert

We report on field observations in January 2009 (austral summer) of atmospheric dust devils in the northern part of the Atacama Desert in South America (≈20^◦S). An extremely high level of dust-devil activity over the study site has been observed, dependent on local meteorological conditions. We found a high correlation between the dust-devil frequency of occurrence and the Obukhov length scale, L, calculated from meteorological gradient measurements, with a clear tendency for this frequency to increase with decreasing −L. The upper threshold values of −L ≈ 20–30 m, and the 2-m mean wind speed, V ₂ ≈ 8m s⁻¹, for dust-devil occurrence have been found, but the minimal V ₂ threshold was not observed. Parallel routine meteorological measurements enabled us to calculate the main constituents of the surface energy balance, to obtain direct estimates of the surface albedo (α ≈ 0.21 at the solar noon) and to summarize the local conditions.     

Rainfall variability and kinetic energy in Southern Nigeria

A decreasing trend of rainfall has been observed in West Africa, where rainfall erosivity is also considered to be high. Therefore, this study was carried out to evaluate the variability of rainfall and its erosivity in two contrasting zones in southern Nigeria between 1977 and 1999 to understand the implications of climate variability on rainfall erosivity. The study sites were Ibadan, a sub-humid zone, and Port-Harcourt, a humid zone. Time of occurrence of rainfall, rainfall amount (A), intensity (I ₁₅ and I ₃₀), kinetic energy (E) and rainfall erosivity factor (R), were evaluated. Kinetic energy was estimated with Brown–Foster (BF) equation, making the rainfall erosivity (product of kinetic energy and intensity) to be designated as EI ₃₀-BF and EI ₁₅-BF. The frequency of rainfall during daylight (06:00–18:00 h) was 48% for Ibadan and 69% for Port-Harcourt. There were time-specific differences in daily rainfall occurrence between the zones, suggesting a strong influence of local effects on rainfall generation, such as, relief in Ibadan and proximity to the sea in Port-Harcourt. Annual E was 213 MJ ha⁻¹for Ibadan and 361 MJ ha⁻¹ for Port-Harcourt. Ibadan had a significantly higher daily E than Port-Harcourt because of higher intensity while Port-Harcourt had significantly higher annual E than Ibadan because of higher annual rainfall amount. Annual erosivity at Ibadan using the EI ₃₀-BF was 9,742 MJ mm ha⁻¹ h⁻¹ whereas it was 15,752 MJ mm ha⁻¹ h⁻¹ at Port-Harcourt. Using the EI ₁₅-BF, Ibadan had an annual value of 14,806 MJ mm ha⁻¹ h⁻¹ while Port-Harcourt had 20,583 MJ mm ha⁻¹ h⁻¹. Thus, annual rainfall erosivity was significantly higher in the humid than the sub-humid zone because of higher amount of rainfall but the reverse was the case with daily erosivity because of higher intensities in the sub-humid zone. Rainfall intensity was, therefore, a key measure of erosivity. There was a strong positive relationship between rainfall erosivity and rainfall amount. Between 1977 and 1988, 50–88% of the 12 years had rainfall erosivity which exceeded the long-term average but rainfall erosivity was less than the long-term average between 1989 and 1999. This suggested a decreasing trend in erosivity due to the decreasing trend in rainfall amount in West Africa. However, the trend did not imply lesser soil erosion and environmental degradation risks.     

Uptake of the NO <Subscript>3</Subscript> Radical on Aqueous Surfaces

Using a single drop experiment, the uptake of NO₃ radicals on aqueous solutions of the dye Alizarin Red S and NaCl was measured at 293 K. Uptake coefficients in the range (1.7–3.1) ⋅ 10^{− 3} were measured on Alizarin Red S solutions. The uptake coefficients measured on NaCl solutions were in the range of (1.1–2.0) ⋅ 10⁻³ depending on the salt concentration. Both experiments lead to a consistent result for the mass accommodation coefficient of α_NO3 = (4.2_{− 1.7}^+2.2)⋅ 10⁻³. The product H(D_l k_Cl−^II)^0.5 for the NO₃ radical was determined to be (1.9 ± 0.2) M atm^{− 1} cm s^−0.5 M^−0.5 s^−0.5 by fitting the uptake data for the NaCl solutions to the so-called resistance model. The yield of the chemical NO₃ radical source was characterized using UV-VIS and FT-IR spectroscopy. The amount of gas-phase NO₃ radicals measured at elevated humidities was less than expected. Instead, a rise of the gas-phase HNO₃ concentration was found indicating a conversion of gas-phase NO₃ radicals to gas-phase HNO₃ on the moist reactor walls.     

基于地基宽带辐射观测资料的云检测算法改进

利用地表太阳总辐射和散射辐射对Long and Ackerman (2000)的云检测算法进行了改进,提高了云判别的准确率.首先采用比值概率密度峰值法,初步选出晴天时刻.然后根据晴天时刻的地表太阳总辐射和太阳天顶角余弦值,拟合得到该日晴天总辐射近似表达式.在此基础上,计算各时刻实际观测值与用该拟合式估计的总辐射的比值,...     

Variations in Vegetation Net Primary Production in the Qinghai-Xizang Plateau, China, from 1982 to 1999

Vegetation net primary production (NPP) derived from a carbon model (Carnegie–Ames–Stanford Approach, CASA) and its interannual change in the Qinghai-Xizang (Tibetan) Plateau were investigated in this study using 1982–1999 time series data sets of normalized difference vegetation index (NDVI) and paired ground-based information on vegetation, climate, soil, and solar radiation. The 18-year averaged annual NPP over the plateau was 125 g C m⁻² yr⁻¹, decreasing from the southeast to the northwest, consistent with precipitation and temperature patterns. Total annual NPP was estimated between 0.183 and 0.244 Pg C over the 18 years, with an average of 0.212 Pg C (1 Pg = 10¹⁵ g). Two distinct periods (1982–1990 and 1991–1999) of NPP variation were observed, separated by a sharp reduction during 1990–1991. From 1982 to 1990, annual NPP did not show a significant trend, while from 1991 to 1999 a marked increase of 0.007 Pg C yr⁻² was observed. NPP trends for most vegetation types resembled that of the whole plateau. The largest annual NPP increase during 1991–1999 appeared in alpine meadows, accounting for 32.3% of the increment of the whole region. Changes in solar radiation and temperature significantly influenced NPP variation, suggesting that solar radiation may be one of the major factors associated with changes in NPP.     

Long-term modeling of soil C erosion and sequestration at the small watershed scale

The soil C balance is determined by the difference between inputs (e.g., plant litter, organic amendments, depositional C) and outputs (e.g., soil respiration, dissolved organic C leaching, and eroded C). There is a need to improve our understanding of whether soil erosion is a sink or a source of atmospheric CO₂. The objective of this paper is to discover the long-term influence of soil erosion on the C cycle of managed watersheds near Coshocton, OH. We hypothesize that the amount of eroded C that is deposited in or out of a watershed compares in magnitude to the soil C changes induced via microbial respiration. We applied the erosion productivity impact calculator (EPIC) model to evaluate the role of erosion–deposition processes on the C balance of three small watersheds (∼1 ha). Experimental records from the USDA North Appalachian Experimental Watershed facility north of Coshocton, OH were used in the study. Soils are predominantly silt loam and have developed from loess-like deposits over residual bedrock. Management practices in the three watersheds have changed over time. Currently, watershed 118 (W118) is under a corn (Zea mays L.)–soybean (Glycine max [L.] Merr.) no till rotation, W128 is under conventional till continuous corn, and W188 is under no till continuous corn. Simulations of a comprehensive set of ecosystem processes including plant growth, runoff, and water erosion were used to quantify sediment C yields. A simulated sediment C yield of 43 ± 22 kg C ha⁻¹ year⁻¹ compared favorably against the observed 31 ± 12 kg C ha⁻¹ year⁻¹ in W118. EPIC overestimated the soil C stock in the top 30-cm soil depth in W118 by 21% of the measured value (36.8 Mg C ha⁻¹). Simulations of soil C stocks in the other two watersheds (42.3 Mg C ha⁻¹ in W128 and 50.4 Mg C ha⁻¹ in W188) were off by <1 Mg C ha⁻¹. Simulated eroded C re-deposited inside (30–212 kg C ha⁻¹ year⁻¹) or outside (73–179 kg C ha⁻¹ year⁻¹) watershed boundaries compared in magnitude to a simulated soil C sequestration rate of 225 kg C ha⁻¹ year⁻¹ and to literature values. An analysis of net ecosystem carbon balance revealed that the watershed currently under a plow till system (W128) was a source of C to the atmosphere while the watersheds currently under a no till system (W118 and W188) behaved as C sinks of atmospheric CO₂. Our results demonstrate a clear need for documenting and modeling the proportion of eroded soil C that is transported outside watershed boundaries and the proportion that evolves as CO₂ to the atmosphere.     

Chemical characterization of water-soluble aerosols in different residential environments of semi aridregion of India

This paper deals with the atmospheric concentrations of PM₅ and PM_2.5 particulate matter and its water soluble constituents along with the size distribution of ions and spatial variation at three different residential environments in a semiarid region in India. Samples were collected from the indoors and outdoors of urban, rural and roadside sites of Agra during October 2007–March 2008. The mean concentrations of PM_2.5 indoors and outdoors were 178 μgm⁻³ and 195 μgm⁻³ while the mean concentrations of PM₅ indoors and outdoors were 231.8 μgm⁻³ and 265.2 μgm⁻³ respectively. Out of the total aerosol mass, water soluble constituents contributed an average of 80% (33% anions, 50% cations) in PM₅ and 70% (29% anions, 43% cations) in PM_2.5. The indoor–outdoor ratio of water soluble components suggested additional aerosol indoor sources at rural and roadside sites. Indoor–outdoor correlations were also determined which show poor relationships among concentrations of aerosol ions at all three sites. Univariate Pearson correlation coefficients among water soluble aerosols were determined to evaluate the relationship between aerosol ions in indoor and outdoor air.     

Compositions and source apportionments of atmospheric aerosol during Asian dust storm and local pollution in central Taiwan

A study has been carried out on water soluble ions, trace elements, as well as PM_2.5 and PM_2.5–10 elemental and organic carbon samples collected daily from Central Taiwan over a one year period in 2005. A source apportionment study was performed, employing a Gaussian trajectory transfer coefficient model (GTx) to the results from 141 sets of PM_2.5 and PM_2.5–10 samples. Two different types of PM₁₀ episodes, local pollution (LOP) and Asian dust storm (ADS) were observed in this study. The results revealed that relative high concentrations of secondary aerosols (NO₃⁻, SO₄²⁻ and NH₄⁺) and the elements Cu, Zn, Cd, Pb and As were observed in PM_2.5 during LOP periods. However, sea salt species (Na⁺ and Cl⁻) and crustal elements (e.g., Al, Fe, Mg, K, Ca and Ti) of PM_2.5–10 showed a sharp increase during ADS periods. Anthropogenic source metals, Cu, Zn, Cd, Pb and As, as well as coarse nitrate also increased with ADS episodes. Moreover, reconstruction of aerosol compositions revealed that soil of PM_2.5–10 elevated approximately 12–14% in ADS periods than LOP and Clear periods. A significantly high ratio of non-sea salt sulfate to elemental carbon (NSS-SO₄²⁻/EC) of PM_2.5–10 during ADS periods was associated with higher concentrations of non-sea-salt sulfates from the industrial regions of China. Source apportionment analysis showed that 39% of PM₁₀, 25% of PM_2.5, 50% of PM_2.5–10, 42% of sulfate and 30% of nitrate were attributable to the long range transport during ADS periods, respectively.     

基于地面短波辐射观测资料计算淡积云的辐射强迫及水平尺度方法研究

本文根据不同类型云影响地面短波辐射的差异,提出利用地面短波总辐射变化检测识别淡积云以及计算淡积云水平尺度的方法,并对该算法进行误差分析,统计内蒙古草原地区夏季淡积云的水平尺度及其辐射强迫。结果表明:淡积云检测方法能比较好地识别、筛选出淡积云天。淡积云水平尺度和淡积云所在高度的风速成正比,风速测量的准确性直接影响淡积云水平尺度估算准确性;淡积云水平与垂直尺度比对计算淡积云水平尺度影响最大;云移动经过遮挡太阳直射辐射的时段内,太阳天顶角变化的影响可以忽略不计。内蒙古草原地区夏季淡积云短波辐射强迫小时平均为-134.1 W m-2,水平尺度平均值为1129 m,水平尺度的概率密度呈幂指数分布。