Spatio-temporal variations of respirable particles at residential areas located in the vicinity of opencast coal projects,India: a case study

The objective of the study is to investigate spatio-temporal variations of PM₁₀, PM_2.5, and PM₁ concentrations at seven residential sites, located in the vicinity of opencast coal projects, Basundhara Garjanbahal Area (BGA), India. Meteorological parameters such as wind speed, wind direction, relative humidity, and temperature were collected simultaneously with PM concentrations. Mean concentrations of PM₁₀ in the range 215 ± 169–526 ± 412 μg m^?3, PM_2.5 in the range of 91 ± 79–297 ± 107 μg m^?3, PM₁ in the range of 68 ± 60–247 ± 84 μg m^?3 were obtained. Coarse fractions (PM_2.5–10) varied from 27 to 58% whereas fine fractions (PM_1–2.5 and PM₁) varied in the range of 51–73%. PM_2.5 concentration was 41–74% of PM₁₀ concentration, PM₁ concentration was 31–62% of PM₁₀ concentration, and PM₁ concentration was 73–83% of PM_2.5 concentration. Role of meteorology on PM concentrations was assessed using correlation analysis. Linear relationships were established among PM concentrations using least square regression analysis. With the aid of principal component analysis, two components were drawn out of eight variables, which represent more than 75% of variance. The results indicated that major sources of air pollutants (PM₁₀, PM_2.5, PM₁, CO, CO₂) at the residential sites are road dust raised by vehicular movement, spillage of coal generated during transportation, spontaneous combustion of coal, and biomass burning in village area.     

Geochemical features of aerosols in Santiago de Chile from time series analysis

Santiago, the capital of Chile, suffers from high air pollution levels, especially during winter. An extensive particulate matter (PM) monitoring and analysis program was conducted to quantify elemental concentrations of PM. Size-resolved PM samples (PM_2.5 and PM_10–2.5) from the La Paz and Las Condes stations in Santiago (2004–2005) were analyzed using ICP-MS. Most trace element concentrations (Cu, Pb, Zn, Mn, V, Sb, Pb and As) were higher during winter than during summer and were also higher at the La Paz station than at the Las Condes station. During the highest pollution events, As concentrations in PM_2.5 (16 ng m^?3) exceeded the annual average standard value (6 ng m^?3). A 10-year time series showed decreasing Pb and As concentrations and slightly increasing Zn, Cu and Mn concentrations. Concentrations of Cr and Ni remained relatively constant. The implementation of new public policies in 1998 may explain the decreasing concentrations of Pb and As. Enrichment factor (EF) calculations identified two principal groups: elements with EF < 10 (Mg, Y, Zr, U Sr, Ca, Ti, and V) and EF > 10 (Rb, K, Cs, Fe, P, Ba, Mn, Ni, Cr, Co, Zn, Sn, Pb, Cu, Mo, Cd, As, Ag, and Sb), which were related to natural and anthropogenic PM sources, respectively. Three main PM sources were identified using factor analysis: a natural source (crustal matter and marine aerosol), combustion and copper smelting. Three other sources were identified using rare earth elements: fluid catalytic crackers, oil-fired power production and catalytic converters.     

Development of low-cost passive sampler from cow bone char for sampling of volatile organic compounds

A simple and low-cost passive sampler for collection of volatile organic compounds, specifically benzene, toluene, ethylbenzene and xylene (BTEX), from the ambient air has been developed by using cow bone char (CBC) as an adsorbent with desorption by solvent extraction prior to analysis by gas chromatography–mass spectrometry (GC–MS). The laboratory-made CBC was prepared by calcination process in a partially oxidative atmosphere. The developed passive sampler was tested for a suitable amount of CBC used, diffusion tube type and size, and sampling duration, in a closed chamber saturated with each of the BTEX vapors. With the optimum amount of 250 mg CBC packed in a glass bottle (82.6 mm height × 11.1 mm i.d.) and the exposure time of 168 h, detection limits (µg/m³) for BTEX determination using this developed sampler together with GC–MS were 0.28 (benzene), 0.79 (toluene), 0.58 (ethylbenzene), 0.28 (p-xylene) and 0.54 (o-xylene). The proposed method was applied to sampling BTEX from selected petrol stations, traffic congestion areas and a rural area in Chiang Mai Province, Thailand. The BTEX concentrations detected were well correlated with their sources as they were the highest at the petrol station sites, lower at the traffic congestion area sites and the lowest at the rural area site. The laboratory-made passive sampler containing CBC has thus opened up a possibility of having a simple and effective device for sampling of BTEX in the ambient air.     

Study of the water saving potential of an irrigation area based on a remote sensing evapotranspiration model

To estimate the water saving potential of an irrigation area and create a scientific water saving plan, the irrigation water use efficiency and water productivity of the Hulanhe irrigation area for 2007–2014 were calculated, and the water saving potentials of different water saving plans were determined from the perspectives of engineering and crop water saving. The results showed that the evapotranspiration calculated from the surface energy balance algorithm for land model (SEBAL) agreed well with the measured results. The irrigation water use efficiency in the Hulanhe irrigation area was positively correlated with precipitation of irrigated land and was negatively correlated with the net irrigation water volume. The engineering water saving potential ranges for periods of 5, 8, 11, and 15 years were (1.702?×?10⁸, 5.103?×?10⁸) m³, (1.783?×?10⁸, 5.184?×?10⁸) m³, (1.865?×?10⁸, 5.266?×?10⁸) m³, and (2.301?×?10⁸, 5.702?×?10⁸) m³, respectively, and the water saving potential increased year over year. Low amounts of precipitation of irrigated land corresponded with small amounts of net irrigation water and greater water saving potential. Based on the cumulative frequency of the water productivity calculated for the Hulanhe irrigation area from 2007 to 2014, the target water productivity for short (50% of the multi-year average cumulative water productivity) and long (70% of the multi-year average cumulative water productivity) terms were 1.03 kg/m³ and 1.22 kg/m³, respectively, and the cumulative crop water saving potentials for short and long terms were 1.18?×?10⁸ and 2.74?×?10⁸ m³, respectively. These results provided a theoretical reference for creating water saving plans for irrigation areas.     

Oxidation of methane in the water column of Lake Baikal

The rate of aerobic oxidation of methane was calculated based on average profiles of the tritiumhelium age of the Baikal waters and concentrations of the dissolved methane in the water column. In the deep lake zone (>200 m), the intensity of oxidation vertically decreases and is (2–0.3) × 10^?2 nl CH₄l^?1 days^?1 in southern and central Baikal and (2.8–1.0) × 10^?2 nl CH₄ l^?1 days^?1 in northern Baikal. The effective coefficient of the oxidation rate in the lake depressions is 3.6 × 10^?4, 3.3 × 10^?4, and 3.7 × 10^?4 days^?1, respectively. At current methane concentrations in the water column, about 80 t of methane is oxidized per year. Oxidation of the dissolved methane in the water column was estimated at a possible increase of its concentration.     

Cryosphere as a temporal sink and source of microplastics in the Arctic region

Microplastics (MPs) pollution has become a serious environmental issue of growing global concern due to the increasing plastic production and usage. Under climate warming, the cryosphere, defined as the part of Earth’s layer characterized by the low temperatures and the presence of frozen water, has been experiencing significant changes. The Arctic cryosphere (e.g., sea ice, snow cover, Greenland ice sheet, permafrost) can store and release pollutants into environments, making Arctic an important temporal sink and source of MPs. Here, we summarized the distributions of MPs in Arctic snow, sea ice, seawater, rivers, and sediments, to illustrate their potential sources, transport pathways, storage and release, and possible effects in this sentinel region. Items concentrations of MPs in snow and ice varied about 1–6 orders of magnitude in different regions, which were mostly attributed to the different sampling and measurement methods, and potential sources of MPs. MPs concentrations from Arctic seawater, river/lake water, and sediments also fluctuated largely, ranging from several items of per unit to >40,000 items m^?3, 100 items m^?3, and 10,000 items kg^?1 dw, respectively. Arctic land snow cover can be a temporal storage of MPs, with MPs deposition flux of about (4.9–14.26) × 10⁸ items km^?2 yr^?1. MPs transported by rivers to Arctic ocean was estimated to be approximately 8–48 ton/yr, with discharge flux of MPs at about (1.65–9.35) × 10⁸ items/s. Average storage of MPs in sea ice was estimated to be about 6.1×10¹⁸ items, with annual release of about 5.1×10¹⁸ items. Atmospheric transport of MPs from long-distance terrestrial sources contributed significantly to MPs deposition in Arctic land snow cover, sea ice and oceanic surface waters. Arctic Great Rivers can flow MPs into the Arctic Ocean. Sea ice can temporally store, transport and then release MPs in the surrounded environment. Ocean currents from the Atlantic brought high concentrations of MPs into the Arctic. However, there existed large uncertainties of estimation on the storage and release of MPs in Arctic cryosphere owing to the hypothesis of average MPs concentrations. Meanwhile, representatives of MPs data across the large Arctic region should be mutually verified with in situ observations and modeling. Therefore, we suggested that systematic monitoring MPs in the Arctic cryosphere, potential threats on Arctic ecosystems, and the carbon cycle under increasing Arctic warming, are urgently needed to be studied in future.     

Distribution of heavy metals in soils of Port Harcourt and its environs,Niger Delta,Nigeria

Geochemical evaluation of the distribution of heavy metals in soils of Port Harcourt and its environs in the Niger Delta region is presented in respect of anthropogenic factor and index of geoaccumulation. Sixteen (16) soil samples were collected from two horizons (0-10 cm and 100 cm) from the various grids and analyzed. The geo-chemical analyses showed the vertical and horizontal distributions of heavy metals. The results showed the ranges of the metals determined as follows: Pb (6.86-2.49)×10-6, with an average of 4.63×10-6; Cd (0.05-0.00)×10-6, with an average of 0.02×10-6, As (0.01-0.00)×10-6, with an average of 0.00×10-6. Cu (15.36-10.80) ×10-6, with an average of 13.36×10-6, and V (1.36-0.20)×10-6, with an average of 0.94×10-6. Quantification of the degree of pollution was carried out using anthropogenic factor (AF) and index of geoaccumulation (Igeo). The Igeo values of 0.06, 0.02 and 0.00 for Pb, Cd and As, respectively indicate low-level contamination while Zn (1.14) and V (1.40) show me-dium-level contamination. The sources of contamination are attributed to urbanized anthropogenic activities. The majority of the samples analyzed show that the AF values are less than 1 with the exception of vanadium (V) whose AF values range from 2.73 to 13.60×10-6. Vanadium is more enriched than As, Cd, Pb, and Cu. The order of degrees of anthropogenic contamination and index of geoaccumulation in the soil is V >Zn >Pb >Cu >Cd >AS. Metals were retained near the top soil and their concentrations in the deepest horizons were lower and normal for uncontaminated soils. Metal concentrations in the top soil horizons were significantly related to distance from the industrial and hu-man activities.     

Gas generation and expulsion characteristics of Middle–Upper Triassic source rocks,eastern Kuqa Depression,Tarim Basin,China: implications for shale gas resource potential

Frontier exploration in the Kuqa Depression, western China, has identified the continuous tight-sand gas accumulation in the Lower Cretaceous and Lower Jurassic as a major unconventional gas pool. However, assessment of the shale gas resource in the Kuqa Depression is new. The shale succession in the Middle–Upper Triassic comprises the Taliqike Formation (T₃t), the Huangshanjie Formation (T₃h) and the middle–upper Karamay Formation (T_2–3k), with an average accumulated thickness of 260 m. The high-quality shale is dominated by type III kerogen with high maturity and an average original total organic carbon (TOC) of about 2.68 wt%. An improved hydrocarbon generation and expulsion model was applied to this self-contained source–reservoir system to reveal the gas generation and expulsion (intensity, efficiency and volume) characteristics of Middle–Upper Triassic source rocks. The maximum volume of shale gas in the source rocks was obtained by determining the difference between generation and expulsion volumes. The results indicate that source rocks reached the hydrocarbon expulsion threshold of 1.1% VR and the hydrocarbon generation and expulsion reached their peak at 1.0% VR and 1.28% VR, with the maximum rate of 56 mg HC/0.1% TOC and 62.8 mg HC/0.1% TOC, respectively. The volumes of gas generation and expulsion from Middle–Upper Triassic source rocks were 12.02 × 10¹² m³ and 5.98 × 10¹² m³, respectively, with the residual volume of 6.04 × 10¹² m³, giving an average gas expulsion efficiency of 44.38% and retention efficiency of 55.62%. Based on the gas generation and expulsion characteristics, the predicted shale gas potential volume is 6.04 × 10¹² m³, indicating a significant shale gas resource in the Middle–Upper Triassic in the eastern Kuqa Depression.     

Geochemical,isotopic and hydrological mass balance approaches to constrain the lake water–groundwater interaction in Dal Lake,Kashmir Valley

It is important to have qualitative as well as quantitative understanding of the hydraulic exchange between lake and groundwater for effective water resource management. Dal, a famous urban fresh water lake, plays a fundamental role in social, cultural and economic dynamics of the Kashmir Valley. In this paper geochemical, isotopic and hydrological mass balance approaches are used to constrain the lake water–groundwater interaction of Dal Lake and to identify the sources of lake water. Water samples of precipitation (n = 27), lake water (n = 18) and groundwater (n = 32) were collected across the lake and its catchment for the analysis of δ¹⁸O and δ²H. A total of 444 lake water samples and 440 groundwater samples (springs, tube wells and dug wells) were collected for the analysis of Ca²⁺, Mg²⁺, HCO₃ ^?, SO₄ ^2?, Cl^?, NO₃ ^?, Na⁺ and K⁺. Water table and lake water level were monitored at 40 observation locations in the catchment. Water table map including pH and EC values corroborate and verify the gaining nature of the Dal Lake. Stable isotopes of lake water in Boddal and Gagribal basins showed more deviation from the global meteoric water line than Hazratbal and Nigeen basins, indicating the evaporation of lake water. The isotopic and geochemical mass balance suggested that groundwater contributes a significant proportion (23–40%) to Dal Lake. The estimated average groundwater contribution to Dal Lake ranged from 31.2 × 10³ to 674 × 10³ m³ day^?1 with an average of 276 × 10³ m³ day^?1. The study will be useful to delineate the possible sources of nutrients and pollutants entering the lake and for the management of lake water resources for sustainable development.     

Electrical conduction and polarization of calcite single crystals

The electrical conductivity and polarization properties of calcite single crystals with three orientations, namely, a (00.1) plane perpendicular to the crystallographic c axis (10.0) plane parallel to the crystallographic c axis, and a (10.4) cleavage plane, were studied by both complex impedance and thermally stimulated depolarization current (TSDC) measurements. Conductivities for (00.1)-, (10.0)-, and (10.4)-oriented single calcite crystals at 400–600?°C were 1.16?×?10^?7?–?1.05?×?10^?5, 7.40?×?10^?8?–?4.27?×?10^?6, and 4.27?×?10^?7?–?2.86?×?10^?5 Ω^?1 m^?1, respectively, and the activation energies for conduction were 112, 103, and 101?kJ?mol^?1, respectively. The TSDC spectra verified the electrical polarizability of calcite crystals. The activation energy for depolarization, estimated from TSDC spectra, of the (00.1)-, (10.0)-, and (10.4)-oriented calcite substrates were 112, 119, and 114?kJ?mol^?1, respectively. Considering the correlation between the processes of conduction and electric polarization, we proposed the mechanisms of conduction and polarization in calcite on the assumption of oxide ion transport.     

Chemical characterization and sources of PM2.5 at 12-h resolution in Guiyang,China

The increasing emission of primary and gaseous precursors of secondarily formed atmospheric particulate matter due to continuing industrial development and urbanization are leading to an increased public awareness of environmental issues and human health risks in China. As part of a pilot study, 12-h integrated fine fraction particulate matter (PM_2.5) filter samples were collected to chemically characterize and investigate the sources of ambient particulate matter in Guiyang City, Guizhou Province, southwestern China. Results showed that the 12-h integrated PM_2.5 concentrations exhibited a daytime average of 51 ± 22 µg m^?3 (mean ± standard deviation) with a range of 17–128 µg m^?3 and a nighttime average of 55 ± 32 µg m^?3 with a range of 4–186 µg m^?3. The 24-h integrated PM_2.5 concentrations varied from 15 to 157 µg m^?3, with a mean value of 53 ± 25 µg m^?3, which exceeded the 24-h PM_2.5 standard of 35 µg m^?3 set by USEPA, but was below the standard of 75 µg m^?3, set by China Ministry of Environmental Protection. Energy-dispersive X-ray fluorescence spectrometry (XRF) was applied to determine PM_2.5 chemical element concentrations. The order of concentrations of heavy metals in PM_2.5 were iron (Fe) > zinc (Zn) > manganese (Mn) > lead (Pb) > arsenic (As) > chromium (Cr). The total concentration of 18 chemical elements was 13 ± 2 µg m^?3, accounting for 25% in PM_2.5, which is comparable to other major cities in China, but much higher than cities outside of China.     

Chloride as tracer of solute transport in the aquifer–aquitard system in the Pearl River Delta,China

A 1D numerical model is constructed to investigate the impact of sedimentation and sea level changes on transport of Cl^? in the aquifer–aquitard system in the Pearl River Delta (PRD), China. The model simulates the evolution of the vertical Cl^? concentration profiles during the Holocene. Sedimentation is modeled as a moving boundary problem. Chloride concentration profiles are reconstructed for nine boreholes, covering a wide area of the PRD, from northwest to southeast. Satisfactory agreement is obtained between simulated and measured Cl^? concentration profiles. Diffusion solely is adequate to reproduce the vertical Cl^? concentration profiles, which indicates that diffusion is the regionally dominant vertical transport mechanism across the aquitards in the PRD. The estimated effective diffusion coefficients of the aquitards range from 2.0?×?10^–11 to 2.0?×?10^–10 m²/s. The effective diffusion coefficients of the aquifers range from 3.0?×?10^–11 to 4.0?×?10^–10 m²/s. Advective transport tends to underestimate Cl^? concentrations in the aquitard and overestimate Cl^? concentrations in the basal aquifer. The results of this study will help understand the mechanisms of solute transport in the PRD and other deltas with similar geological and hydrogeological characteristics.     

Effect of confining pressure on the diffusion of HTO, 36Cl− and 125I− in a layered argillaceous rock (Opalinus Clay): diffusion perpendicular to the fabric

The through- and out-diffusion of HTO, ³⁶Cl⁻ and ¹²⁵I⁻ in Opalinus Clay, an argillaceous rock from the northern part of Switzerland, was studied under different confining pressures between 4 and 15 MPa. The direction of diffusion and the confining pressure were perpendicular to the bedding. Confining pressure had only a small effect on diffusion. An increase in pressure from 4 to 15 MPa resulted in a decrease of the effective diffusion coefficient of ∼20%. Diffusion accessible porosities were not measurably affected. The values of the effective diffusion coefficients, D_e, ranged between (5.6±0.4)×10⁻¹² and (6.7±0.4)×10⁻¹² m² s⁻¹ for HTO, (7.1±0.5)×10⁻¹³ and (9.1±0.6)×10⁻¹³ m² s⁻¹ for ³⁶Cl⁻ and (4.5±0.3)×10⁻¹³ and (6.6±0.4)×10⁻¹³ m² s⁻¹ for ¹²⁵I⁻. The rock capacity factors, α, measured were circa 0.14 for HTO, 0.040 for ³⁶Cl⁻ and 0.080 for ¹²⁵I⁻. Because of anion exclusion effects, anions diffuse slower and exhibit smaller diffusion accessible porosities than the uncharged HTO. Unlike ³⁶Cl⁻, ¹²⁵I⁻ sorbs weakly on Opalinus Clay resulting in a larger rock capacity factor. The sorption coefficient, K_d, for ¹²⁵I⁻ is of the order of 1–2×10⁻⁵ m³ kg⁻¹. The effective diffusion coefficient for HTO is in good agreement with values measured in other sedimentary rocks and can be related to the porosity using Archie's Law with exponent m=2.5.     

A search for small-scale clumpiness in dense cores of molecular clouds

We have analyzed HCN(1-0) and CS(2-1) line profiles obtained with high signal-to-noise ratios toward distinct positions in three selected objects in order to search for small-scale structure in molecular cloud cores associated with regions of high-mass star formation. In some cases, ripples were detected in the line profiles, which could be due to the presence of a large number of unresolved small clumps in the telescope beam. The number of clumps for regions with linear scales of ～0.2–0.5 pc is determined using an analytical model and detailed calculations for a clumpy cloud model; this number varies in the range: ～2 × 10⁴–3 × 10⁵, depending on the source. The clump densities range from ～3 × 10⁵–10⁶ cm^?3, and the sizes and volume filling factors of the clumps are ～(1–3) × 10^?3 pc and ～0.03–0.12. The clumps are surrounded by inter-clump gas with densities not lower than ～(2–7) × 10⁴ cm^?3. The internal thermal energy of the gas in the model clumps is much higher than their gravitational energy. Their mean lifetimes can depend on the inter-clump collisional rates, and vary in the range ～10⁴–10⁵ yr. These structures are probably connected with density fluctuations due to turbulence in high-mass star-forming regions.     

Coarse and fine particulates, Hg(p)-bound particulate concentrations and compositions study at Sha-Lu, central Taiwan

Ambient air and coarse, fine and particulate-bound mercury (Hg(p)) pollutants were collected and analyzed from March 17 to May 22 and September 3, 2009 to March 5, 2010 at a highway traffic site located in Sha-Lu, central Taiwan. This study has the following objectives: (1) to measure the coarse and fine particulates concentrations and the particulate-bound mercury Hg(p) which was attached to these particulate; (2) to determine the average Hg(p) compositions in coarse and fine particulates and (3) to compare the Hg(p) concentrations and compositions particulate in this study to the those obtained in other studies. The results obtained in this study indicated that the average ambient air PM_2.5, PM_2.5–10 and PM₁₀ were 18.79 ± 6.71, 11.22 ± 4.93 and 30.01 ± 10.27 μg/m³, respectively. The ranges of concentrations for Hg(p) in PM_2.5 were from 0.0016 to 0.0557 ng/m³, from 0.0006 to 0.0364 ng/m³ in PM_2.5–10 and from 0.0022 to 0.0862 ng/m³ in PM₁₀. In addition, the highest particle-bound mercury compositions in PM_2.5 were 16.85 ng/g and the lowest particle-bound mercury concentrations were 0.55 ng/g. The highest particle-bound mercury compositions in PM_2.5–10 were 13.88 ng/g and the lowest particle-bound mercury in PM_2.5–10 were 0.22 ng/g.     

Perchlorate mobilization of metals in serpentine soils

Natural processes and anthropogenic activities may result in the formation and/or introduction of perchlorate (ClO₄⁻) at elevated levels into the environment. Perchlorate in soil environments on Earth and potentially in Mars may modify the dynamics of metal release and their mobilization. Serpentine soils, known for their elevated metal concentrations, provide an opportunity to assess the extent that perchlorate may enhance metal release and availability in natural soil and regolith systems. Here, we assess the release rates and extractability of Ni, Mn, Co and Cr in processed Sri Lankan serpentine soils using a range of perchlorate concentrations (0.10–2.50 w/v ClO₄⁻) via kinetic and incubation experiments. Kinetic experiments revealed an increase of Ni, Mn, Co and Cr dissolution rates (1.33 × 10⁻¹¹, 2.74 × 10⁻¹¹, 3.05 × 10⁻¹² and 5.35 × 10⁻¹³ mol m⁻² s⁻¹, respectively) with increasing perchlorate concentrations. Similarly, sequential and single extractions demonstrated that Ni, Mn, Co and Cr increased with increasing perchlorate concentrations compared to the control soil (i.e., considering all extractions: 1.3–6.2 (Ni), 1.2–126 (Mn), 1.4–34.6 (Co) and 1.2–6.4 (Cr) times greater than the control in all soils). Despite the oxidizing capability of perchlorate and the accelerated release of Cr, the dominant oxidation state of Cr in solution was Cr(III), potentially due to low pH (<2) and Cr(VI) instability. This implies that environmental remediation of perchlorate enriched sites must not only treat the direct hazard of perchlorate, but also the potential indirect hazard of related metal contamination.     

Geochemical characteristics of the Xuanwei Formation in West Guizhou: Significance of sedimentary environment and mineralization

The Upper Permian Xuanwei Formation widely occurs in western Guizhou, unconformably overlying the Emeishan basalts, and mainly consists of black shales. It is ∼170 m thick at Cuyudong Village, Weining County, West Guizhou, China, where the samples of black shale and sandy shale were collected and analyzed. The shales mainly contain SiO₂, 18.9%–44.1%, Al₂O₃, 14.8%–52.8%, Fe₂O₃, 1.0%–41.2%, LOI, 3.2%–21.1%, TiO₂, 1.0%–6.7%, and MgO, 0.2%–2.5%. The contents of all other major elements are lower than 1.0%. It is shown that the black shales have higher contents of Fe₂O₃ and LOI than normal shales. The siderites occurred in the black shales with higher contents of Fe₂O₃, which may be attributed to hydrothermal activities on seafloor. All analyzed shale samples have extremely high Ga, 47.8×10⁻⁶–109.9×10⁻⁶ (70.5×10⁻⁶ on average), higher than the industrial mining standard of Ga Resource Industry Standard. The total contents of rare-earth elements (REE) of 9 black shale samples vary from 213×10⁻⁶ to 1460×10⁻⁶, suggesting that these black shales are enriched in REE. The shale-normalized REE patterns display both positive and negative Ce anomalies (Ce/Ce* from 0.5 to 1.7), revealing that the Xuanwei shales were precipitated under oxic and anoxic conditions. The Rb-Sr chronological diagram of 6 shale samples in the Xuanwei Formation shows an age of 255±12 Ma. Strontium isotopic ratios (⁸⁷Sr/⁸⁶Sr)_t0 range from 0.70635 to 0.70711, suggesting that these Xuanwei black shales might be derived from chemical weathering of the Emeishan basalts.     

Estimation of methane emission from whole waste landfill site using correlation between flux and ground temperature

A methodology to estimate a methane emission in a waste landfill site was developed. The methane flux at a waste landfill site in summer, autumn, and winter was within the following ranges: from −1.3×10⁻² to 16, from −6.4×10⁻² to 7.5, and from −1.6×10⁻³ to 1.5×10⁻² g-CH₄ m⁻² h⁻¹, respectively. In those seasons, the mean methane emission rate and coefficient of variation were 1.1 g-CH₄ m⁻² h⁻¹ ±290%, 0.57 g-CH₄ m⁻² h⁻¹ ±347%, and 5.4×10⁻² g-CH₄ m⁻² h⁻¹ ±370%, respectively. These results simultaneously showed that fluctuations of methane emission from the landfill surface were both of spatial and temporal variability. In each season, an exponential relationship was observed between the methane flux density and the ground temperature. Total methane emissions were estimated to be 5.7×10⁻², 7.1×10⁻³, and 1.7×10⁻³ g-CH₄ m⁻² h⁻¹ in the summer, autumn, and winter surveys, respectively, using a temperature surrogated-kriging method. The results of this study would improve upon the labor-intensive closed-chamber method, and could be a more practical way to estimate methane emissions from waste landfills.     

Regional evaluation of hydraulic properties in variably fractured rock using a hydrostructural domain approach

A hydrostructural domain approach was tested and validated in fractured bedrock aquifers of the Gulf Islands, British Columbia (BC), Canada. Relative potential hydraulic properties for three hydrostructural domains in folded and faulted sedimentary rocks were derived using stochastically generated fracture data and hybrid discrete fracture network-equivalent porous media (DFN-EPM) modelling. Model-derived relative potential transmissivity values show good spatial agreement with transmissivity values obtained from pumping tests at selected sites. A spatial pattern of increasing transmissivity towards the southeast along the island chain is consistent between both datasets. Cluster analysis on relative potential permeability values obtained from a larger dataset for the region identified four clusters with geometric means of 9?×?10^?13, 4?×?10^?13, 2?×?10^–13, and 3?×?10^–14 m². The general trend is an increase in relative potential permeability toward the southeast, emulating the trends identified in the site-specific analyses. Relative potential permeability values increase with proximity to the hinge line of a regional northwest-trending asymmetric fault propagation fold structure, and with proximity to superimposed high-angle north- and northeast-trending brittle faults. The results are consistent with documented patterns of structurally controlled fluid flow and show promise for use in regional characterization of fractured bedrock aquifers.