Lockdown as an Empirical Strategy to Curb Air Pollution: Evidence from a Quasi-Natural Experiment

In this study, three approaches namely parallel, sequential, and multiple linear regression are applied to analyze the local air quality improvements during the COVID-19 lockdowns. In the present work, the authors have analyzed the monitoring data of the following primary air pollutants: particulate matter (PM₁₀ and PM_2.5), nitrogen dioxide (NO₂), sulfur dioxide (SO₂), and carbon monoxide (CO). During the lockdown period, the first phase has most noticeable impact on airquality evidenced by the parallel approach, and it has reflected a significant reduction in concentration levels of PM₁₀ (27%), PM_2.5 (19%), NO₂ (74%), SO₂ (36%), and CO (47%), respectively. In the sequential approach, a reduction in pollution levels is also observed for different pollutants, however, these results are biased due to rainfall in that period. In the multiple linear regression approach, the concentrations of primary air pollutants are selected, and set as target variables to predict their expected values during the city's lockdown period.The obtained results suggest that if a 21-days lockdown is implemented, then a reduction of 42 µg m⁻³ in PM₁₀, 23 µg m⁻³ in PM_2.5, 14 µg m⁻³ in NO₂, 2 µg m⁻³ in SO₂, and 0.7 mg m⁻³ in CO can be achieved.     

Horizontal and vertical fluxes of particulate matter during wind erosion on arable land in the province La Pampa,Argentina

A detailed analysis of horizontal and vertical particulate matter (PM) fluxes during wind erosion has been done, based on measurements of PM smaller than 10, 2.5, and 1.0 μm, at windward and leeward positions on a measuring field. The three fractions of PM measurement are differently influenced by the increasing wind and shear velocities of the wind. The measured concentrations of the coarser fractions of the fine dust, PM₁₀, and PM_2.5, increase with wind and shear velocity, whereas the PM_1.0 concentrations show no clear correlation to the shear velocity. The share of PM_2.5 on PM₁₀ depends on the measurement height and wind speed and varies between 4 and 12 m/s at the 1 m height ranging from 25% to 7% (average 10%), and at the 4 m height from 39% to 23% (average 30%). Although general relationships between wind speed, PM concentration, and horizontal and vertical fluxes could be found, the contribution of the measuring field was very low, as balances of incoming and outgoing fluxes show. Consequently, the measured PM concentrations are determined from a variety of sources, such as traffic on unpaved roads, cattle drives, tillage operations, and wind erosion, and thus, represent all components of land use and landscape structure in the near and far surroundings of the measuring field. The current results may reflect factors from the landscape scale rather than the influence of field-related variables. The measuring devices used to monitor PM concentrations showed differences of up to 20%, which led to considerable deviations when determining total balances. Differences up to 67% between the calculated fluxes prove the necessity of a previous calibration of the devices used.     

Source apportionment and secondary organic aerosol estimation of PM2.5 in an urban atmosphere in China

PM2.5 is the key pollutant in atmospheric pollution in China.With new national air quality standards taking effect,PM2.5 has become a major issue for future pollution control.To effectively prevent and control PM2.5,its emission sources must be precisely and thoroughly understood.However,there are few publications reporting comprehensive and systematic results of PM2.5 source apportionment in the country.Based on PM2.5 sampling during 2009 in Shenzhen and follow-up investigation,positive matrix factorization(PMF)analysis has been carried out to understand the major sources and their temporal and spatial variations.The results show that in urban Shenzhen(University Town site),annual mean PM2.5 concentration was 42.2μg m?3,with secondary sulfate,vehicular emission,biomass burning and secondary nitrate as major sources;these contributed30.0%,26.9%,9.8%and 9.3%to total PM2.5,respectively.Other sources included high chloride,heavy oil combustion,sea salt,dust and the metallurgical industry,with contributions between 2%–4%.Spatiotemporal variations of various sources show that vehicular emission was mainly a local source,whereas secondary sulfate and biomass burning were mostly regional.Secondary nitrate had both local and regional sources.Identification of secondary organic aerosol(SOA)has always been difficult in aerosol source apportionment.In this study,the PMF model and organic carbon/elemental carbon(OC/EC)ratio method were combined to estimate SOA in PM2.5.The results show that in urban Shenzhen,annual SOA mass concentration was 7.5μg m?3,accounting for 57%of total organic matter,with precursors emitted from vehicles as the major source.This work can serve as a case study for further in-depth research on PM2.5 pollution and source apportionment in China.     

Sand dunes as potential sources of dust in northern China

While saltation bombardment of sand grains on a fine substrate can produce considerable dust, the well-sorted nature of sand dunes tends to preclude them from consideration as major dust sources. Recent research, however, has revealed that sand dunes can, in some cases, be large sources of dust. We used the PI-SWERL(Portable In-Situ Wind Erosion Laboratory) to measure in the field the potential of sand dunes and other desert landforms to emit particulate matter 10 μm(PM-10) dust in the Tengger, Ulan Buh, and Mu Us deserts of northern China. Combined with high resolution particle size measurements of the dune sand, an assessment of sand dunes as a dust source can be made. Large active transverse dunes tend to contain little to no stored PM-10, yet they produce a low dust flux. Coppice dunes stabilized by vegetation contain appreciable PM-10 and have very high dust emission potential. There is a positive correlation between the amount of PM-10 stored in a dune and its potential dust flux. Saltation liberates loose fines stored in dunes, making them very efficient dust emitters compared to landforms such as dry lake beds and washes where dust particles are unavailable for aeolian transport due to protective crusts or sediment cohesion. In cases where large dunes do not store PM-10 yet emit dust when active, two hypotheses can be considered:(1) iron-oxide grain coatings are removed during saltation, creating dust, and(2) sand grains collide during saltation, abrading grains to create dust. Observations reveal that iron oxide coatings are present on some dune sands. PI-SWERL data suggests that low dust fluxes from dunes containing no stored dust may represent an estimate for the amount of PM-10 dust produced by removal of iron oxide coatings. These results are similar to results from dunes in the United States. In addition, PI-SWERL results suggest that dust-bearing coppice dunes, which cover vast areas of China's sandy deserts, may become major sources of dust in the future if overgrazing, depletion of groundwater, or drought destabilizes the vegetation that now partially covers these dunes.     

SALTATING PARTICLES,PLAYA CRUSTS AND DUST AEROSOLS AT OWENS (DRY) LAKE,CALIFORNIA

As part of the multinational Lake Owens Dust Experiment (LODE), we have studied the generation of dust storms on the south sand sheet of Owens (dry) Lake, California, an anthropogenically desiccated playa reported to be the single greatest source of particulate matter in North America. During March 1993, we performed an intensive field study including eight significant dust storms, building on our prior work (1978–1984) and preliminary studies (1991–1992). We studied sources and magnitude of coarse saltating particles, the meteorological conditions that allow them to become mobile across the flat playa of Owens (dry) Lake, and how the motion of saltating particles across different types of playa surfaces results in the generation of PM₁₀ dusts (aerosol particles smaller than 10 μm aerodynamic diameter). Saltating grains of lacustrine sand and broken crust abrade and disaggregate the playa surface into fine aerosols, and the resulting PM₁₀ concentrations recorded during major dust storms are among the highest ever recorded in North America. On 23 March 1993, we measured a 2 h concentration on the playa of 40 620 μg m⁻³, as far as we can determine the highest ambient PM₁₀ value ever recorded in the U.S.A. Abrasion of salt-silt-clay crusts by saltation is shown to be responsible for all but a small part of one dust storm. The quantity ‘sand run’, saltating particle transport multiplied by wind run, is shown to be very closely correlated with dust aerosol concentration. Finally, we have established that on-lake bed studies are essential for quantitative prediction of dust events on the Owens (dry) Lake bed, despite the difficult conditions encountered.     

The factors influencing the abrasion efficiency of saltating grains on a clay‐crusted playa

The entrainment and subsequent transport of PM₁₀ (particulate matter <10 µm) has become an important and challenging focus of research for both scientific and practical applications. Arid and semi‐arid environments are important sources for the atmospheric loading of PM₁₀, although the emission of this material is often limited by surface crusts. It has been suggested that the primary mechanisms through which PM₁₀ is released from a crusted surface are abrasion by saltating grains or disturbance by agricultural and recreational activities. To examine the importance of saltation abrasion in the emission of PM₁₀, a series of field wind tunnel tests were conducted on a clay‐crusted surface near Desert Wells, Arizona. In a previous part of this study it was found that the emission rate varies linearly with the saltation transport rate, although there can be considerable variation in this relationship. This paper more closely examines the source of the variability in the abrasion efficiency, the amount of PM₁₀ emitted by a given quantity of saltating grains. The abrasion efficiency was found to vary with the susceptibility of the surface to abrasion, the ability of the sand to abrade that surface and the availability of material with a caliper size <10 µm within the crust. Specifically, the results of the study show that the abrasion efficiency is related to the crust strength, the amount of surface disturbance and the velocity of the saltating grains. It is concluded that the spatial and temporal variability of these controls on the abrasion efficiency imposes severe contextual limitations on experimentally derived models, and can make theoretical models too complex and impractical to be of use. Copyright­© 2001 John Wiley & Sons, Ltd.     

Correlation between plasmid DNA damage induced by PM10 and trace metals in inhalable particulate matters in Beijing air

Based on the study of Beijing PM₁₀ bioreactivity with the newly developed plasmid DNA assay method, and analysis for trace elements of PM₁₀, the cause of plasmid DNA damage by PM₁₀ was investigated. The study showed that plasmid DNA oxidative damages by PM₁₀ are of difference in different seasons at various areas. The concentrations of TM50 of PM₁₀ in whole samples respectively collected at urban and comparison sites during winter were 900 μg mL⁻¹ and 74 μg mL⁻¹, while those in their corresponding soluble fractions were 540 μg mL⁻¹ and 86 μg mL⁻¹. In contrast, TM50 contents of PM₁₀ from summer whole samples at urban areas and comparison sites were 116 μg mL⁻¹ and 210 μg mL⁻¹, whereas those in their soluble fractions were 180 μg mL⁻¹ and 306 μg mL⁻¹. The difference of bioreactivity of Beijing PM₁₀ resulted from the variation of trace elements. The oxidative damage of plasmid DNA caused by Pb, Zn, As in PM₁₀ (whole sample) was relatively strong. TM50 and Mn, V, Zn display stronger correlation in the soluble fraction. It implies that Zn could be the major trace element in Beijing PM₁₀ which contributes to oxidative damage to plasmid DNA.     

A reassessment of current volcanic emissions from the Central American arc with specific examples from Nicaragua

The Central American volcanic arc supplies a significant proportion of the persistent annual global sulphur dioxide emissions from volcanoes. In November/December 2003, we completed a survey of the arc section from Mombacho to San Cristóbal in Nicaragua recording individual mean fluxes of 800, 530 and 220 Mg day^− 1 in the plumes from San Cristóbal, Telica and Masaya, respectively. An assessment of fluxes published since 1997 along the entire Central America arc yields a mean total arc flux of SO₂ of 4360 Mg day^− 1 or 8–16% of the annual estimated global volcanic SO₂ flux to the troposphere. New field data shows that Masaya volcano continues to show stable HCl/SO₂ and HF/SO₂ ratios, suggesting a sustained flux of these components of ∼ 220 and 30 Mg day^− 1, respectively (1997 to 2004). Masaya's plume composition also appears to have been stable, between 2001 and 2003, with respect to all the particulate species measured, with significant fluxes of SO₄²⁻ (4 Mg day^− 1), Na⁺ (0.9–1.3 Mg day^− 1) and K⁺ (0.7 Mg day^− 1). Extrapolating the Masaya plume species ratios to the entire Central American arc gives mean HCl and HF fluxes of 1300 and 170 Mg day^− 1 and a particulate sulphate flux of 40 Mg day^− 1 for 1997 to 2004, although without further understanding of the degassing processes and sources at depth of these different volatiles, these arc-scale estimates should be treated with caution. Combining our arc scale mean SO₂ flux with published measurements of volcanic gas compositions with respect to CO₂ and H₂O allows us to estimate mean CO₂ fluxes of 4400–9600 Mg day^− 1 and H₂O fluxes of 70,000–78,000 Mg day^− 1 for the arc. Preliminary comparisons of these estimates of outgassing rates with published volatile input fluxes into the Central American subduction zone, suggest that Cl is more efficiently recycled through the subduction zone than CO₂. The results for H₂O are inconclusive.     

Inorganic carbon and nutrient fluxes on the Arctic Shelf

Historic data from the Russian-American Hydrochemical Atlas of Arctic Ocean together with data from the TRANSDRIFT II 1994 and TUNDRA 1994 cruises have been used to assess the spatial and inter-annual variability of carbon and nutrient fluxes, as well as air–sea CO₂ exchange in the Laptev and western East Siberian Seas during the summer season. Budget computations using summer data of dissolved inorganic phosphate (DIP), dissolved inorganic nitrogen (DIN) and dissolved inorganic carbon (DIC) gives that the Laptev Sea shelf is a net sink of DIP and DIN of 2.5×10⁶, 23.2×10⁶ mol d⁻¹, respectively, while it is a net source of DIC (excluding air–sea exchange) of 1249×10⁶ mol d⁻¹. In the East Siberian Seas the budget computations give 0.5×10⁶, −11.4×10⁶ and −173×10⁶ mol d⁻¹ (minus being a sink) for DIP, DIN, and DIC, respectively. In summers, the Laptev Sea Shelf is net autotrophic while the East-Siberian Sea Shelf is net heterotrophic, and both systems are weak net denitrifying. The Laptev Sea Shelf takes up 2.1 mmol CO₂ m⁻² d⁻¹ from atmosphere, whereas the western part of the East-Siberian Sea Shelf loose 0.3 mmol CO₂ m⁻² d⁻¹ to the atmosphere. The variability of DIP, DIN and DIC fluxes during summer in the different regions of the Laptev and East Siberian Seas depends on bottom topography, river runoff, exchange with surrounding seas and wind field.     

Spatial and seasonal variability of sediment oxygen consumption and nutrient fluxes at the sediment water interface in a sub-tropical lagoon (New Caledonia)

In order to quantify the spatial and seasonal variations of sediment oxygen consumption and nutrient fluxes, we performed a spatial survey in the south west lagoon of New Caledonia during the two major seasons (dry and wet) based on a network of 11 sampling stations. Stations were selected along two barrier reef to land transects representing most types of sediments encountered in the lagoon. Fluxes were measured using ex-situ sediment incubations and compared to sediment characteristics. Sediment oxygen consumption (SOC) varied between 500 and 2000 μmol m⁻² h⁻¹, depending on season and stations. Nutrient effluxes from sediment were highly variable with highest fluxes measured in muddy sediments near the coast. Inter-sample variability was as high as seasonal differences so that no seasonally driven temperature effect could be observed on benthic nutrient fluxes in our temperature range. Nutrient fluxes, generally directed from the sediment to the water column, varied between −5.0 and 70.0 μmol m⁻² h⁻¹ for ammonia and between −2.5 and +12.5 μmol m⁻² h⁻¹ for PO₄ and NO₂₊₃. SOC and nutrient fluxes were compared to pelagic primary production rates in order to highlight the tight coupling existing between the benthic and pelagic compartments in this shallow tropical lagoon. Under specific occasions of low pelagic productivity, oxygen sediment consumption and related carbon and nutrient fluxes could balance nearly all net primary production in the lagoon. These biogeochemical estimates point to the functional importance of sediment biogeochemistry in the lagoon of New Caledonia.     

Lithological and hydrological controls on water composition: evaporite dissolution and glacial weathering in the south central Andes of Argentina (33°–34°S)

Lithological and hydrological influence on fluvial physical and chemical erosion was studied in a glacierized sedimentary basin with high evaporite presence. Suspended particulate matter (SPM), total dissolved solids (TDS) and major ion concentrations were analysed for 2 years of different hydrologic condition: (i) 2009–2010, Q = 100% average; and (ii) 2010–2011, Q = 60% average. Annual hydrograph was simple regime‐type with one peak in summer related to snow melting. The intra‐annual SPM and TDS variations were directly and inversely associated to Q, respectively. Snow chemistry showed continental influence (Na⁺/Ca²⁺ = 0.17), and atmospheric input of TDS was <1% of the total exported flux. River water was highly concentrated in Ca²⁺ and SO₄²⁻ (~4 mmol l⁻¹) and in Na⁺ and Cl⁻ (~3 mmol l⁻¹). Ca²⁺/SO₄²⁻ and Na⁺/Cl⁻ molar ratios were ~1 and related to Q, directly and inversely, respectively. Major ion relationships suggest that river chemistry is controlled by evaporite (gypsum and halite) dissolution having a summer input from sulfide oxidation and carbonate dissolution, and a winter input from subsurface flow loaded with silicate weathering products. This variation pattern resulted in nearly chemostatic behaviour for Ca⁺, Mg²⁺ and SO₄²⁻, whereas Na⁺, Cl⁻ and SiO₂ concentrations showed to be controlled by dilution/concentration processes. During the 2009–2010 hydrological year, the fluxes of water, SPM and TDS registered in the snow melting–high Q season were, respectively, 71%, 92% and 67% of the annual total, whereas for equal period in 2010–2011, 56% of water, 86% of SPM and 54% of TDS annual fluxes were registered. The SPM fluxes for 2009–2010 and 2010–2011 were 1.19 × 10⁶ and 0.79 × 10⁶ t year⁻¹, whereas TDS fluxes were 0.68 × 10⁶ and 0.55 × 10⁶ t year⁻¹, respectively. Export rates for 2009–2010 were 484 t km² year⁻¹ for SPM and 275 t km² year⁻¹ for TDS. These rates are higher than those observed in glacierized granite basins and in non‐glacierized evaporite basins, suggesting a synergistic effect of lithology and glaciers on physical and chemical erosion. Copyright © 2014 John Wiley & Sons, Ltd.     

Simulations of spatial variability in particle‐size emissions during wind erosion events

This study simulates how spatial variations in particle‐size emissions from a playa affect bulk and size‐resolved dust concentration profiles during two contrasting wind erosion events (a small local and a large regional event) in the Channel Country, Lake Eyre Basin, Australia. The regional event had higher dust concentration as a result of stronger frontal winds and higher erodibility across the playa. For each event, two emission scenarios are simulated to determine if measured size‐resolved dust concentration profiles can be explained by spatial variability in source area emissions. The first scenario assumes that particle‐size emissions from source areas occur at a uniform rate, while the second scenario assumes that particle‐size emissions vary between and within source areas. The uniform emission scenario, reproduced measured bulk dust concentration profiles (R² = 0·93 regional and R² = 0·81 local), however simulated size‐resolved dust concentration profiles had poor statistical fits to measured size‐resolved profiles for each size class (the highest were R² = 0·5 regional and R² = 0·3 local). For the differential particle‐size emission scenario, the fit to the measured bulk dust concentration profiles is improved (R² = 0·97 regional and R² = 0·83 local). However, the fit to the size‐resolved profiles improved dramatically, with the lowest being R² = 0·89 (regional) and R² = 0·80 (local). Particle‐size emission models should therefore be tested against both bulk and size‐resolved dust concentration profiles, since if only bulk dust concentration profiles are used model performance may be over‐stated. As the source areas in the first 90 m upwind of the tower were similar for both events, the percentage contributions of each particle‐size class to total emissions can be compared. The contribution of each particle‐size class was similar even though the wind speed, turbulence and dust concentrations were significantly different; suggesting that the contribution of each particle‐size to the total emitted dusts is not related to wind speed and turbulence. Copyright © 2012 John Wiley & Sons, Ltd.     

Average mass concentrations of TSP, PM10 and PM2.5 in Erzurum urban atmosphere, Turkey

In this study, particulate matters (TSP, PM₁₀, PM_2.5 and PM_10–2.5) which are hazardous for environment and human health were investigated in Erzurum urban atmosphere at a sampling point from February 2005 to February 2006. During sampling, two low volume samplers were used and each sampling period lasted approximately 24 h. In order for detection of representative sampling region and point of Erzurum, Kriging method was applied to the black smoke concentration data for winter seasons. Mass concentrations of TSP, PM₁₀ and PM_2.5 of Erzurum urban atmosphere were measured on average, as 129, 31 and 13 μg/m³, respectively, in the sampling period. Meteorological factors, such as temperature, wind speed, wind direction and rainfall were typically found to be affecting PMs, especially PM_2.5. Air temperature did not seem to be significantly affecting TSP and PM₁₀ mass concentrations, but had a considerably negative induction on PM_2.5 mass concentrations. However, combustion sourced PM_2.5 was usually diluted from the urban atmosphere by the speed of wind, soil sourced coarse mode particle concentrations (TSP, PM₁₀) were slightly affected by the speed of wind. Rainfall was found to be decreasing concentrations to 48% in all fractions (TSP, PM₁₀, PM_10–2.5, PM_2.5) and played an important role on dilution of the atmosphere. Fine mode fraction of PM (PM_2.5) showed significant daily and seasonal variations on mass concentrations. On the other hand, coarse mode fractions (TSP, PM₁₀ and PM_10–2.5) revealed more steady variations. It was observed that fine mode fraction variations were affected by the heating in residences during winter seasons.     

Eddy covariance imaging of diffuse volcanic CO<Subscript>2</Subscript> emissions at Mammoth Mountain,CA, USA

Use of eddy covariance (EC) techniques to map the spatial distribution of diffuse volcanic CO₂ fluxes and quantify CO₂ emission rate was tested at the Horseshoe Lake tree-kill area on Mammoth Mountain, California, USA. EC measurements of CO₂ flux were made during September–October 2010 and ranged from 85 to 1,766 g m⁻² day⁻¹. Comparative maps of soil CO₂ flux were simulated and CO₂ emission rates estimated from three accumulation chamber (AC) CO₂ flux surveys. Least-squares inversion of measured eddy covariance CO₂ fluxes and corresponding modeled source weight functions recovered 58–77% of the CO₂ emission rates estimated based on simulated AC soil CO₂ fluxes. Spatial distributions of modeled surface CO₂ fluxes based on EC and AC observations showed moderate to good correspondence (R ² = 0.36 to 0.70). Results provide a framework for automated monitoring of volcanic CO₂ emissions over relatively large areas.     

Simultaneous water and vapour transfer in an unsaturated mudstone in badlands terrain,southwestern Taiwan

The simultaneous transfer of pore fluid and vapour was studied in the unsaturated shallow subsurface of a Plio-Pleistocene marine mudstone badland slope in southwestern Taiwan during the dry season using field monitoring data and numerical simulations. Data from field monitoring show mass-basis water contents of ~0.05 to ~0.10 that decrease towards the unsaturated ground surface and were invariant during the middle part of the dry season, except for daily fluctuations. In addition, the observed daily fluctuations in water content correlate with fluctuations in bedrock temperature, especially at depths of 2.5–5.0 cm. Periodic increases in water content occurred most notably during the day, when the bedrock temperature showed the greatest increase. Water contents then decreased to the previous state as bedrock temperature decreased during the night. Calculated vapour fluxes within the mudstone during the day increased up to 6 × 10⁻⁶–1 × 10⁻⁵ kg m⁻² s⁻¹, deriving a 0.01–0.02 increase in mass-basis water content at 2.5 cm depth for a 12-h period. This agrees with field monitoring data, suggesting that increases in water content occurred due to vapour intrusions into the bedrock. Pore water electrical conductivity (EC) showed periodic variations due to vapour intrusion, and gradually increased between the ground surface and depths of 2.5–5.0 cm. In contrast, pore water EC gradually decreased between 15 and 40 cm depth. Calculated water fluxes at depths of 2.5–40.0 cm varied from −4 × 10⁻⁶ to −2 × 10⁻⁹ kg m⁻² s⁻¹. These fluxes generated an increase in solute concentrations at the ground surface, with negative values of water flux indicating an upwards movement of water towards the surface. We show that the increase in solute content due to solute transfer from depth is highly dependent on variations in water flux with depth. © 2020 John Wiley & Sons, Ltd.     

Health impact assessment of marine emissions in Pearl River Delta region

Global marine vessels emissions are adversely affecting human health particularly in southeast Asia. But health burdens from both ocean- and river-going vessels in Pearl River Delta (PRD) regions are not quantified. We estimated the potential health impacts using pooled relative risks of mortality and hospital admissions in China, and the model derived concentrations of sulfur dioxide (SO₂), particulate matter (PM₁₀), nitrogen dioxide (NO₂) and ozone (O₃) due to vessels emissions. SO₂ concentrations due to marine emissions in Hong Kong were 13.6 μgm^?3 compared with 0.7 μgm^?3 in PRD regions that were far from the marine vessels. In PRD regions, the estimated annual numbers (per million people) of excess deaths from all natural causes and hospital admissions from cardiorespiratory causes attributable to SO₂, NO₂, O₃ and PM₁₀ combined from marine emissions were 45 and 265 respectively. Marine emission control measures could contribute a large reduction in mortality and hospital admissions in PRD regions especially in Hong Kong.     

Volatile emissions and gas geochemistry of Hot Spring Basin,Yellowstone National Park,USA

We characterize and quantify volatile emissions at Hot Spring Basin (HSB), a large acid-sulfate region that lies just outside the northeastern edge of the 640 ka Yellowstone Caldera. Relative to other thermal areas in Yellowstone, HSB gases are rich in He and H₂, and mildly enriched in CH₄ and H₂S. Gas compositions are consistent with boiling directly off a deep geothermal liquid at depth as it migrates toward the surface. This fluid, and the gases evolved from it, carries geochemical signatures of magmatic volatiles and water–rock reactions with multiple crustal sources, including limestones or quartz-rich sediments with low K/U (or ^40?Ar/^4?He). Variations in gas chemistry across the region reflect reservoir heterogeneity and variable degrees of boiling. Gas-geothermometer temperatures approach 300 °C and suggest that the reservoir feeding HSB is one of the hottest at Yellowstone. Diffuse CO₂ flux in the western basin of HSB, as measured by accumulation-chamber methods, is similar in magnitude to other acid-sulfate areas of Yellowstone and is well correlated to shallow soil temperatures. The extrapolation of diffuse CO₂ fluxes across all the thermal/altered area suggests that 410 ± 140 t d^− 1 CO₂ are emitted at HSB (vent emissions not included). Diffuse fluxes of H₂S were measured in Yellowstone for the first time and likely exceed 2.4 t d^− 1 at HSB. Comparing estimates of the total estimated diffuse H₂S emission to the amount of sulfur as SO₄²⁻ in streams indicates ~ 50% of the original H₂S in the gas emission is lost into shallow groundwater, precipitated as native sulfur, or vented through fumaroles. We estimate the heat output of HSB as ~ 140–370 MW using CO₂ as a tracer for steam condensate, but not including the contribution from fumaroles and hydrothermal vents. Overall, the diffuse heat and volatile fluxes of HSB are as great as some active volcanoes, but they are a small fraction (1–3% for CO₂, 2–8% for heat) of that estimated for the entire Yellowstone system.     

Contemporary rates of chemical denudation and atmospheric CO2 sequestration in glacier basins: an Arctic perspective

This paper presents new estimates of solute fluxes from five high Arctic glacier basins in Svalbard. These estimates are combined with data from two other glacier basins to assess the effectiveness of chemical denudation on Svalbard and to estimate rates of temporary (or transient) CO₂ drawdown. We use a solute provenance model to partition solutes into marine, aerosol, atmospheric and crustal components and to estimate their annual fluxes. Crustally derived solute fluxes are equivalent to a mean chemical denudation rate of 350 Σmeq⁺ m⁻² a⁻¹ for Svalbard (range: 160–560 Σmeq⁺ m⁻² a⁻¹), which lies within the global range of 94–4200 Σmeq⁺ m⁻² a⁻¹ for 21 glacier basins in the northern hemisphere, and is close to the continental average of 390 Σmeq⁺ m⁻² a⁻¹. Specific annual discharge is the most significant control upon chemical denudation in the glacierized basins, and basin lithology is an important secondary control, with carbonate‐rich and basaltic lithologies currently showing the greatest chemical denudation rates. Estimates of transient CO₂ drawdown are also directly associated with specific annual discharge and rock type. On Svalbard transient CO₂ drawdown lies in the range 110–3000 kg C km⁻² a⁻¹, whilst the range is 110–13000 kg C km⁻² a⁻¹ for the northern hemisphere glacial data set. Transient CO₂ drawdown is therefore usually low in the Svalbard basins unless carbonate or basalt rocks are abundant. The analysis shows that a large area of uncertainty in the transient CO₂ drawdown estimates exists due to the non‐stoichiometric release of solute during silicate hydrolysis. Silicate hydrolysis is particularly non‐stoichiometric in basins where the extent of glacierization is high, which is most probably an artefact of high flushing rates through ice‐marginal and subglacial environments where K‐feldspars are undergoing mechanical comminution. Copyright © 2000 John Wiley & Sons, Ltd.     

城市景观湖泊不同时间尺度CH4通量特征及影响因素分析——以南京市莫愁湖为例

城市景观湖泊对温室气体的收支发挥着重要作用。本文以南京市莫愁湖为研究对象,采用静态箱—温室气体分析仪法实时监测湖泊水—气界面CH₄通量,分析湖泊主要温室气体CH₄在日尺度和季节尺度上因冒泡和扩散排放方式不同对其通量的影响,探究影响湖泊CH₄通量的因素。结果表明:(1)在日尺度上,四季24 h内CH₄均呈排放状态,受白天冒泡影响,四季CH₄总通量均存在白天高于夜间的日变化特征。(2)在季节尺度上,莫愁湖CH₄排放通量呈现显著的时空异质性,受冒泡通量的影响夏季CH₄通量明显高于春、秋、冬三季;B区的CH₄总通量(6.04 nmol/(m²·s))显著高于A区(3.82 nmol/(m²·s)),水体的营养化程度和离岸距离是空间变化的主要影响因素。A、B两区CH₄排放夏季以冒泡排放为主,春、秋、冬以扩散排放为主。(3)在日尺度上,CH₄