Measurement of ambient air particulate pollutant concentrations and dry depositions for PS-1 combined with dry deposition plate at a wetland site

In this study, the concentrations of ambient total suspended particulates (TSP) and their dry deposition were measured using a PS-1 sampler with dry deposition plates at a wetland sampling site in central Taiwan during a sampling period from October 2016 to December 2016. The PS-1 sampler was fixed at set distances (1.5 and 2 m) from a dry deposition plate, and sampled particulate pollutants were sampled to determine their concentrations and dry deposition rates simultaneously. A dry deposition plate 3 m from the PS-1 sampler was also used to collect dry deposition particulate. This plate was also used to compare dry depositions from ambient air, collected from new device. The results thus obtained indicated that the average dry deposition rates on the dry deposition plates that were 1.5 and 2 m from the sampler were 103.15 and 103.94 µg/m² min, respectively, in October, 83.36 and 100.18 µg/m² min in November, and 171.2 and 157.5 µg/m² min in December. These dry deposition rates were compared with that 3 m away from the PS-1 sampler. The statistical t test revealed no significant differences between the dry depositions on dry deposition plates at 1.5 and 2 m from the sampler. The dry deposition rates at 1.5 and 2 m from the sampler did not differ significantly from that at 3 m from the PS-1 sampler. This study proves that a PS-1 sampler can be combined with a dry deposition plate to measure TSP concentrations and dry depositions simultaneously using a single device.     

Behavior of Gd-DTPA in simulated bank filtration

The behavior of Gd-DTPA during bank filtration was simulated in a 30 m column filled with Pleistocene sand and flushed by surface water from a lakeside in Berlin, Germany. The surface water is about a 1:1 mixture of river water and effluents from a sewage treatment plant. Throughout 34 days this water was continuously spiked with Gd-DTPA at a level of 60 μg/L. The broad plateau of the Gd-DTPA pulse declined by 15.4% within 34 days by transmetallation. Nine percentage of the total decline is caused by Y and rare earth elements; the remaining part is attributed to Cu²⁺ which is the most influential metal in surface water. All other metals also contributing to transmetallation are combined with Cu to Cu equivalents because only the rate constant of transmetallation of Cu²⁺ is known. The analytical results of the column effluents prove the pseudo-first-order kinetics of transmetallation based on reversible sorption of metals by pools in the column sediment and disprove biodegradation at noticeable levels. The mass ratio of water to tracer is <10¹⁰.     

Experimental evidence for mobility of Zr and other trace elements in soils

A Soxhlet extraction was carried out over a period of 27 d on a column comprising 3 cm of quartz overlain by 4 cm of soil from the B horizon and then 1 cm of soil from the A horizon of a granitic podzol. Major and trace elements were leached from the column and accumulated in a reservoir at the base of the column. Total loss of elements from the soil over the course of the experiment ranged from 0.002 to 1 wt% with major elements and the light and heavy rare earth elements (REE) showing the largest percentage losses. Zirconium (0.002%) and then Al (0.008%) showed the lowest percentage loss. The light REE were leached out of the soil preferentially to the mid REE. All elements showed accumulation, by a factor of 2 to 11, in the quartz layers at the base of the column, particularly in the upper first 1 cm of the quartz. Major elements were leached from the column at a rate of 0.02 to 0.59 μmol h⁻¹ whereas Zr, Nd, Sm, Gd, Dy, Rb, and Sr were leached at the rate of 0.5 to 30 × 10⁻⁶ μmol h⁻¹. Concentrations of other REE in the reservoir increased over the duration of the experiment, but they were poorly correlated with time, so leaching rates were not calculated. Normalization of the major element leaching rates to take into account the constant flushing of water through the column, the average annual rainfall in the Allt a’Mharcaidh catchment in Scotland from where the soil was sampled, and the cross-sectional area of the soil in the column, together with the temperature of the soil in the column (70°C) compared with the average annual temperature of the Allt a’Mharcaidh catchment (5.7°C), gave major element release rates from the soil of 0.002 to 0.97 mEq m⁻² yr⁻¹ (depending on the choice of E_a, the dissolution activation energy), which are generally less than those measured in the field of 0.1 to 40.9 mEq m⁻² yr⁻¹.Calculations showed that despite the redistribution and loss of Zr from the column, assumptions of Zr mobility would have had a negligible effect on calculated element release rates of Na, Ca, Fe, and Mg. However, significant underestimates of the release of K (5%), Ti (57%), Al (5%), and Si (10%) as well as some trace elements (e.g., Nd, 23%; Rb, 54%; Sr, 24%) would have occurred. Concentrations of Ca and Sr leached from the column correlated well (RSQ = 0.93, p < 0.01), supporting the idea of the use of Sr release as a proxy for Ca release in weathering rate calculations. The release rates and percentage loss of REE from the soil varied between elements indicating that REE distribution patterns of rocks and soils may not be preserved in drainage waters.     

An in-situ integrated suspended sediment stream sampler (IS3)

An inexpensive, lightweight stream sampler is described which provides a method for continuous collection of suspended stream sediments. The IS^3* sampler collects integrated suspended stream samples, and because the sampler relies on basic sedimentation principles, it can be deployed to collect suspended sediment stream samples for environmental studies or geochemical exploration in remote areas. The sampler trapped from 0.45 to 1.2 g of dry sediment during 7- to 8-d field tests conducted during 1985.     

Formation Laws of Inorganic Gas Pools in the Northern Jiangsu Basin

In the Northern Jiangsu basin there are high pure CO2 gas pools, low condensed oil-containing CO2 gas pools, high condensed oil-containing CO2 gas pools and He-containing natural gas pools, with the δ13Cco2 (PDB) values ranging from -2.87‰ to -6.50‰, 3He/4He 3.71×10-6 to 6.42×10-6, R/Ra 2.64 to 4.5, 40Ar/36Ar 705 to 734, belonging to typical mantle source inorganic gas pools which are related to young magmatic activity. The gas layers occur in two major reservoir-caprock systems, the terrestrial Meso-Cenozoic clastic rock system and the marine Meso-Palaeozoic carbonate rock-clastic rock system. Controlled by the difference in the scale of traps in the two reservoir-caprock systems, large and medium-scale inorganic gas pools are formed in the marine Meso-Palaeozoic Group and only small ones are formed in the terrestrial Meso-Cenozoic strata. Inorganic gas pools in this basin are distributed along the two deep lithospheric faults on the west and south boundaries of the basin. Gas pools are developed     

An inexpensive sampler for obtaining bulk sediment cores

A large-volume core sampler for sediment—muck substrates is described. The sampler can acquire a discrete sediment core of 10 cm in diameter and up to 1.5 m long. Such samplers are needed to collect the volume necessary for analysis of sediments for contaminants, bulk density, or radioactive dating. The sampler consists of a 1- to 2-m length of PVC pipe mounted below a threaded metal pipe air exhaust—intake assembly. This assembly is quick-connected to standard threaded lengths (300 cm) of water pipe (2 cm diam) or electrical conduit so that bottom sediments in water depths of up to 10 m can be sampled. The core sampler is hand-operated and pushed into bottom sediments from a boat. It does not have to be triggered remotely because of the one-way modified check valve in the air exhaust—intake assembly. After the sampler is extracted from the sediment, the extension handle can be quickly removed for ease of sampler handling, and the core can be extruded from the PVC tube by air pressure.Contribution of the National Sedimentation Laboratory, Agricultural Research Service, U.S. Department of Agriculture, Oxford, Mississippi 38655, U.S.A.     

Thiosulphate in surficial geothermal waters, North Island, New Zealand

Thiosulphate is present in hot springs, streams and thermal pools of the Taupo Volcanic Zone and Ngawha, New Zealand, at concentrations of 1.2 (±1.3) × 10⁻⁵ M to 7.05 (±0.12) × 10⁻⁴M. Formed as a metastable product of sulphide oxidation, thiosulphate is buffered in the presence of elemental S according to, . Unless all sulphide present has been bacterially oxidised to sulphate, a steady state concentration of thiosulphate is maintained. As a soft base thiosulphate is capable of complexing several transition metals. The thermodynamically predicted speciation of Ag in Champagne Pool, for example, indicates a Ag(S₂O₃)₂⁻³ activity similar to that of AgCl₂⁻ though less than that of Ag(HS)₂⁻.     

Geochemistry of volatile organic compounds in seawater: Mesocosm experiments with 14C-model compounds

A series of ten radiotracer experiments were conducted in controlled experimental ecosystems (mesocosms) to investigate the behavior of volatile organic compounds (VOC) in seawater. Time-series measurements of the redistribution of ¹⁴C-activity within several major pools—dissolved, particulate, intermediate metabolite, and CO₂—in the ecosystem made possible an evaluation of the rates of processes—volatilization, biodegradation, Sorption and sedimentation—acting to remove VOC from seawater in summer. The behavior of the model ¹⁴C-VOC fell into three categories. Aromatic hydrocarbons (benzene, toluene, naphthalene) were subject to both volatilization and biodegradation, with mineralization dominating in summer. Chlorinated C₂-hydrocarbons (tetrachloroethylene) and chlorinated benzenes (chlorobenzene, 1,4-dichlorobenzene, and 1,2,4-trichlorobenzene) were affected only by volatilization and were relatively resistant to biodegradation. Of all the model VOC studied, only aliphatic hydrocarbons (decane and octadecane) were sorbed onto suspended paniculate matter; however, the primary route of loss from the water column appeared to be biodegradation rather than sedimentation. The mesocosm-derived removal rate constants were then applied to estimate summer VOC residence times in Narragansett Bay, Rhode Island of about 1 day for aromatic hydrocarbons, 1 week for the chlorinated VOC and about 1 day for aliphatic hydrocarbons. Residence times in winter might be on the order of 1 week for all VOC.     

Preferential flow and segregation of porewater solutes in Wetland sediment

Sediment macropores (with effective diameters larger than 100 μm) comprise 11% of the bulk sediment volume in a tidal freshwater wetland vegetated withPeltandra virginica. In order to determine effects of macroporous sediment structure on solute transport, we conducted a solute tracer experiment in the sediment. The effective transport volume (θ_eff, the volume of sediment through which solute was transported normalized to sediment bulk volume) was 0.15 cm³ cm^?3, which is considerably smaller than the total pore space that is potentially available for transport (porosity of sediment is 0.63 cm³ cm^?3). A mean transport time of 13 d was required to flush preferential flow paths inPeltandra hummocks; hydrologic turnover of the volumetrically dominant matrix pores (0.53 cm³ cm^?3) was apparently much slower. Based on porewater sampler design and hydrological principles, we suggest that N₂-purged tension solution samplers and diffusion equilibrators preferentially sample porewater from macropore and matrix domains, respectively. Dissolved ammonium and orthophosphate concentrations were three-fold higher in matrix pores compared to macropores, which is consistent with our finding that more rapid hydrological flushing occurred in macropores compared to matrix pores. Further evaluation of porewater sampler designs in macroporous sediment is needed to improve studies of hydrologic transport and biogeochemical cycling in wetlands.     

A method for the measurement of bedload sediment transport and passive faunal transport on intertidal sandflats

A simple and inexpensive sampler to measure bedload sediment transport in shallow subtidal or intertidal areas is described. The cylindrical sub-sediment trap with an aspect ratio of 20 (height: diameter) is an improvement over conventional bedload samplers which are difficult to use in shallow areas or fail to collect the biological material associated with bedload. Traps deployed on a low-energy intertidal sandflat for six months provided daily estimates of bedload transport (quartz grains: 0.001–40 kg m^?1 d^?1), passive infaunal transport (e.g., the bivalveMya arenaria, max: 800 ind m^?1 d^?1), and organic detrital flux (e.g., macrophyte fragments, max: 400 g dry wt m^?1 d^?1). Bedload rates estimated with traps were compared to predictions from a numerical bedload model to evaluate the trap’s collection and retention efficiency. A significant linear regression between observed (trap) and predicted (model) rates (r²=0.65, p<0.001, n=97) indicated that the traps were useful for the measurement of high- and low-frequency variability in bedload transport. Potential applications of the traps in benthic oceanography include recruitment and recolonization studies.     

Arsenic enrichment in lakes near the smelters at Sudbury,Ontario

Roughly 200 tonnes of arsenic are produced annually with the base metal ores at Sudbury about 125 tonnes of which are released to the ambient environment via the atmosphere. The dispersion of this highly toxic element in lakes around the smelters is described. The total As concentrations in unfiltered lake waters vary from 0.2 to 0.6 ug 1^?1. The suspended particulates in the water column (with As contents of 2–6 ug g^?1) play a major role in the flux of arsenic to the lake sediments. The present-day rates of As accumulation in the sediments are found to be 1.5–6.4 mg m^?2 yr^?1; these rates exceed those of precolonial times by factors of 5–47. The changes in the rates of As flux to the sediments are shown to parallel the history of Cu and Ni production in the district.     

CO2 gas pools in Jiyang sag,China

The CO₂ gas pools of Jiyang sag are located along the Gaoqing–Pingnan fault within a region of alkaline basalts. The concentration of CO₂ in the gas pools is in the range of 68.85–96.99%. All of the geochemical tracers for the CO₂ gas pools support the suggestion that CO₂ was mainly derived from mantle degassing. The δ¹³C values of CO₂ in the gas pools are in the range of −5.67–−3.41‰, which are higher than those of organogenic CO₂, and near to those of abiogenic CO₂. Their ³He/⁴He ratios are 2.80–4.47×10⁶, i.e. the R/Ra ratios are 2.00–3.19, showing that the Jiyang sag had undergone strong mantle degassing. CO₂/³He ratios are 0.59–0.89×10⁹, which are identical to those for N-MORB, indicating that CO₂ in these CO₂ gas pools was mainly derived from the mantle. Accompanying the intrusion of mantle-derived magma, the mantle-derived CO₂ migrated upwards along deep faults and was trapped in advantageous structures forming gas pools.     

卵石推移质采样器试验研究

本文对我国的ＭＢ－２型和美国的ＴＲ－２型卵石推移质采样器的模型的水力特性和采样效率进行了对比试验研究。得到ＭＢ－２的水力效率为０．９１，ＴＲ－２的水力效率为１．０４；仪器置入水中后水流的紊动强度ＴＲ－２比ＭＢ－２大。ＴＲ－２的采校效率平均是ＭＢ－２的１．８４倍，ＴＲ－２的采样效率方差平均是ＭＢ－２的１．６７倍，即前者的采样效率比后者高，但其采样效率的稳定性比后者差。文中还给出了两种仪器的采样效率η     

Reactive transport modelling of mine tailings columns with capillarity-induced high water saturation for preventing sulfide oxidation

A series of laboratory column tests on reactive mine tailings was numerically simulated to study the effect of high water saturation on preventing sulfide mineral oxidation and acid mine drainage (AMD). The approach, also known as an elevated water table (EWT), is a promising alternative to full water covers for the management and closure of sulfidic tailings impoundments and for the long term control of acid mine drainage. The instrumented columns contained reactive tailings from the Louvicourt mine, Quebec, and were overlain by a protective sand cover. Over a 13–19 month period, the columns were exposed to atmospheric O₂ and flushed approximately every month with demineralized water. A free draining control column with no sand cover was also used. During each cycle, water table elevations were controlled by fixing the pressure at the column base and drainage water was collected and analyzed for pH and Eh, major ions, and dissolved metals (Fe, Zn, Cu, Pb, and Mg). The columns were simulated using the multi-component reactive transport model MIN3P which solves the coupled nonlinear equations for transient water flow, O₂ diffusion, advective–dispersive transport and kinetic geochemical reactions. Physical properties and mineralogical compositions for the material layers were obtained from independent laboratory data. The simulated and observed data showed that as the water table elevation increased, the effluent pH became more neutral and SO₄ and dissolved metal concentrations decreased by factors on the order of 10²–10³. It is concluded that water table depths less than or equal to one-half of the air entry value (AEV) can keep mine tailings sufficiently saturated over the long term, thus reducing sulfide oxidation and AMD production.     

Seasonal variations in sediment sulfur cycling in the Ballastplaat mudflat, Belgium

Sulfate reduction rate (SRR) and pools of reduced inorganic sulfur, acid volatile sulfide (AVS), chromium reducible sulfur (CRS), and elemental sulfur (S^o), were studied from June 1990 till March 1992 at two locations on the Ballastplaat mudflat in the Scheldt estuary. The sediment composition at station A was mainly sand with low organic content whereas sediments at station B were dominated by silt and clay with high organic content. SRR was positively related to temperature; more pronounced at station B (Ea=190 kJ mol⁻¹) than at station A (Ea=110 kJ mol⁻¹). The maximum SRR values observed equalled 14 μmol cm⁻³ d⁻¹ at station B and 1 μmol cm⁻³ d⁻¹ at station A. AVS was the dominant radiolabelled end product of the sulfate reduction reaction, except in surface sediments where pyrite and S^o were more dominant. However, CRS was the predominant reduced inorganic sulfur pool in the sediments. Both AVS and CRS pools showed temporal variations out of phase with SRR. SRR peaked in summer, while the concentrations of AVS and CRS were highest in fall. The accumulation of AVS and CRS started late summer after depletion of oxidants, which had accumulated during winter and spring. The estimated annual SRR and thus sulfide production in the upper 15 cm of station B was of the order of 100 mol m⁻² yr⁻¹, and at station A of the order of 12 mol m⁻² yr⁻¹. The sulfur mass balance shows that only a very small fraction, if any, of the produced sulfide is retained as reduced inorganic sulfur in the sediment.     

Calcite dissolution in two deep eutrophic lakes

The calcium cycle, in particular carbonate dissolution, was analyzed in two deep eutrophic lakes, Lago di Lugano (288 m maximum depth) and Sempachersee (87 m) located in Switzerland. A box model approach was used to calculate calcite dissolution in the water column and at the sediment-water interface based on various lake monitoring data such as sediment traps, sediment cores, water and pore-water analysis. A model for stationary conditions allowing the calculation of calcite dissolution in the water column for a given particle size distribution was developed. The relative values of the simulated flux were consistent with sediment trap observations. The best fit of the dissolution rate constant of sinking calcite in Lago di Lugano was on the same order of magnitude (3 · 10⁻¹⁰ kg^1/3 s⁻¹) as published laboratory values for this surface controlled process.Both lakes show a similar specific calcite precipitation rate of 170 g Ca m⁻² a⁻¹. The diffusive flux across the sediment-water interface amounts to about 15 and 10% of total calcite precipitation in Sempachersee and Lago di Lugano, respectively. However, 61% of the precipitated calcite is dissolved in the water column of Lago di Lugano compared to only 13% in Sempachersee. These results point towards the importance of grain size distributions and settling times in stratified deep waters as the two most important factors determining calcite retention in sediments of hard water lakes.     

Consequences of diffuse and channelled porous melt migration on uranium series disequilibria

Magmas erupted at mid-ocean ridges (MORB) result from decompression melting of upwelling mantle. However, the mechanism of melt transport from the source region to the surface is poorly understood. It is debated whether melt is transported through melt-filled conduits or cracks on short time scales (<∼ 10³ yrs), or whether there is a significant component of slow, equilibrium porous flow on much longer time scales (>∼ 10³-10⁴ yrs). Radiogenic excess ²²⁶Ra in MORB indicates that melt is transported from the melting region on time scales less than the half life of ²²⁶Ra (∼1600 yrs), and has been used to argue for fast melt transport from the base of the melting column. However, excess ²²⁶Ra can be generated at the bottom of the melt column, during the onset of melting, and at the top of the melt column by reactive porous flow. Determining the depth at which ²²⁶Ra is generated is critical to interpreting the rate and mechanism of magma migration. A recent compilation of high quality U-series isotope data show that in many young basalts, ²²⁶Ra excess in MORB is negatively correlated with ²³⁰Th excess. The data suggest that ²²⁶Ra excess is generated independently of ²³⁰Th excess, and cannot be explained by “dynamic” or fractional melting, where observed radiogenic excesses are all generated at the base of the melt column. One explanation is that the negative correlation of activity ratios is a result of mixing of slow moving melt that has travelled through reactive, low-porosity pathways and relatively fast moving melt that has been transported in unreactive high-porosity channels. We investigate this possibility by calculating U-series disequilibria in a melting column in which high-porosity, unreactive channels form within a low-porosity matrix that is undergoing melting. The results show that the negative correlation of ²²⁶Ra and ²³⁰Th excesses observed in MORB can be produced if ∼60% of the total melt flux travels through the low-porosity matrix. This melt maintains ²²⁶Ra excesses via chromatographic fractionation of Ra and Th during equilibrium transport. Melt that travels through the unreactive, high-porosity channels is not able to maintain significant ²²⁶Ra excesses because Ra and Th are not fractionated from each other during transport and the transport time for melt in the channels to reach the top of the melt column is longer than the time scale for ²²⁶Ra excesses to decay. Mixing of melt from the high porosity channels with melt from the low-porosity matrix at the top of the melting column can produce a negative correlation of ²²⁶Ra and ²³⁰Th excesses with the slope and magnitude observed in MORB. This transport process can also account for other aspects of the geochemistry of MORB, such as correlations between La/Yb, α_Sm/Nd, and Th/U and ²²⁶Ra and ²³⁰Th excess.     

Variations and net transport of dissolved inorganic nutrients in the South Passage of the Changjiang （Yangtze River） Estuary

Dissolved inorganic nutrient elements were analyzed from the samples collected in the South Passage of the Changjiang (Yangtze River) Estuary in March 2003, including NH4 , NO3-, NO2- and PO43-. The water samples were collected with a Niskin sampler hourly at the near-surface, middle and near-bottom depths at the three stations -A1, A2 and A3-during two complete tidal cycles of neap tide and spring tide. Results showed that 1) the concentrations of NH4 , NO3- and NO2- were a little higher respectively during the neap tide than those during the spring tide, while PO43- showed an opposite trend, and each was higher in the ebb tide than in the flood tide, either for the neap tidal cycle or the spring tidal cycle; 2) higher stratification of the nutrients existed obviously in this area, with the concentrations of which increased from the bottom to the surface, especially for NH4 and NO3-; 3) the coefficient of variation (C.V.) values of all dissolved inorganic nutrients varied from 4.06% to 36.8% beyond different influences of the tidal current and Changjiang runoff; 4) with increasing suspended matter in the water column, the concentrations of PO43- became lower in the filtered water; and 5) the total transport of each tidal cycle was much more in the spring tide than in the neap tide, and the positive values indicated that the nutrients had been exported to the East China Sea. Studies on the variations and net transport of dissolved inorganic nutrients in the South Passage of the Changjiang Estuary will provide the scientific basis for the study of the mechanism of red tide in the East China Sea.     

The role of volcanic eruptions in blocking the drainage leading to the Dead Sea formation

The shrinkage of the Lisan Lake (LL) to form the recent Dead Sea (DS) was mainly a result of the reduction of the catchment area from around 157,000 km² during Late Pleistocene to 43,000 km² presently. The reduction in the catchment area resulted from the eruption and spread of the basalt flows of Jabal Arab-Druz (JAD), which together with the resulting deposition of thick rock debris and gravels occupied the drainage system. The filling of the pre-basalt drainage system, which used to feed the Dead Sea, with basalts and alluvial sediments blocked the inflows from reaching the Dead Sea. Local base levels along the basalt flow boarders such as Azraq Oasis, Sirhan Basin and Damascus Oasis, and numerous pools and mud flats were created.     

Impact of nitrogenous fertiliser-induced proton release on cultivated soils with contrasting carbonate contents: A column experiment

An experimental study was carried out in order to evaluate the impact of nitrogen fertiliser-induced acidification in carbonated soils. Undisturbed soil columns containing different carbonate content were sampled in the field. Fertiliser spreading was simulated by NH₄Cl addition on top of the soil column. Soil solution composition (mainly nitrate and base cations) was studied at the soil column’s base. Nitrification occurred to a different extent depending on soil type. Higher nitrification rates were observed in calcareous soils. In all the soil types, strong correlations between leached base cation and nitrate concentrations were observed. Regression coefficients between base cations, nitrate and chloride were used to determine the dominant processes occurring following NH₄Cl spreading. In non-carbonated soils, nitrogen nitrification induced base cation leaching and soil acidification. In carbonated soils, no change of soil pH was observed. However, fertilisers induced a huge cation leaching. Carbonate mineral weathering led to the release of base cations, which replenished the soil exchangeable complex. Carbonated mineral weathering buffered acidification. Since direct weathering might have occurred without atmospheric CO₂ consumption, the use of nitrogen fertiliser on carbonated soil induces a change in the cation and carbon budgets. When the results of these experiments are extrapolated on a global scale to the surface of fertilised areas lying on carbonate, carbonated reactions with N fertilisers would imply an additional flux of 5.7 × 10¹² mol yr⁻¹ of Ca + Mg. The modifications of weathering reactions in cultivated catchments and the ability of nitrogen fertilisers to significantly modify the CO₂ budget should be included in carbon global cycle assessment.