The “Zero-order Model” revisited: Paul Schindler's influence on the development of trace metal scavenging models

In 1975 Paul Schindler produced the first oceanic trace metal scavenging model to explicitly include the role of surface chemistry as a control on trace metal water column residence times. The eighteen years that have elapsed since the publication of Schindler's seminal paper have seen the development of a variety of oceanic scavenging models; yet, the fundamental insight of his Zero-order Model remains the benchmark. This paper describes the role of Paul Schindler's work on surface chemistry in providing a framework for the current generation of trace element scavenging models.     

Effects of ageing and overconsolidation on the elastic stiffness of a remoulded clay

Summary Results of resonant column tests were used to determine values of low amplitude shear modulus (G ₀) of a remoulded kaolinite clay for different durations of ageing and for different values of consolidation stress (₀) and overconsolidation ratio (OCR). It was found that after completion of primary consolidation the values of G ₀ increased linearly with the logarithm of time and after a week of confinement the value of normalized rate of secondary increase of shear modulus (N _G ) could be reliably estimated. Values of N _G were found to derease linearly with the logarithm of OCR and with the logarithm of ageing duration. This similarity of behaviour provided a basis for establishing an equivalency between age and equivalent overconsolidation ratio (OCR)_eq. The effects of ₀ and OCR on the value of G ₀ were also established in a functional form that indicated a stronger influence compared to that predicted by the Hardin Equation.     

On the physical model of earthquake precursor fields and the mechanism of precursors＇timespace distribution──origin and evidences of the strong body earthquake──generating model

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Monoterpene concentrations in and above a forest of scots pine

Diurnal and vertical ambient air measurements of the monoterpenes have been made in and above a Scots pine (Pinus sylvestris) forest of central Sweden, within the boreal northern coniferous biome. Sampling was done with Tenax TA, and analysis by GC and ion trap detection. Daytime mixing ratios were on the order of tenths of a ppbv from the forest floor to the top of the forest, and a factor of 2 or 3 lower above the forest. Mixing ratios at night were at the ppbv level, highest near the forest floor and the crown, and decreased with height above the forest. The highest total concentration observed was 8 ppbv inside the forest at 3 am (GMT). The average terpene composition was 3-carene 32%, -pinene 29%, limonene 18%, -pinene 10%, -phellandrene 7%, camphene 5%, and sabinene at less than 2%. The 3-carene/-pinene ratio varied with wind direction and speed, relative humidity, and wet/dry vegetation, but not with ozone or NO₂ concentration, solar radiation, or temperature. Variations in the observed terpene composition at the sampling site are mainly caused by the influence of other vegetation in the vicinity of the site. It would seem that wet Scots pine emits more 3-carene relative to -pinene than does dry pine.     

Field calibration and performance of sediment traps in a eutrophic holomictic lake

In wind-stressed and unstratified Lough Neagh low aspect ratio sediment traps, which allow for internal resuspension, collected sediment at a rate close to the natural sediment accumulation rate inferred from dated sediment cores. High aspect ratio traps grossly overestimated the natural rate of sediment accumulation as did, but to a lesser extent, burial rate measurements on an artificial stratigraphic marker. The former type of trap deployed over long exposure periods is therefore recommended as providing the best estimate of net downward particle flux in lakes such as Lough Neagh. However, it is emphasized that all sediment trap types, when operated in shallow turbulent lakes, will to a greater or lesser extent be contaminated by secondary or redeposited material and so will not provide a direct measure of primary sedimentation. Use of tube traps in lakes such as Lough Neagh should not, however, be discounted since they can provide a record of the quality of sedimenting material through time.     

Fluid sources for the La Guitarra epithermal deposit (Temascaltepec district, Mexico): Volatile and helium isotope analyses in fluid inclusions

The La Guitarra deposit (Temascaltepec district, South-Central Mexico), belongs to the low/intermediate sulfidation epithermal type, has a polymetallic character although it is currently being mined for Ag and Au. The mineralization shows a polyphasic character and formed through several stages and sub-stages (named I, IIA, IIB, IIC, IID, and III). The previous structural, mineralogical, fluid inclusion and stable isotope studies were used to constrain the selection of samples for volatile and helium isotope analyses portrayed in this study. The N₂/Ar overall range obtained from analytical runs on fluid inclusion volatiles, by means of Quadrupole Mass Spectrometry (QMS), is 0 to 2526, and it ranges 0 to 2526 for stage I, 0 to 1264 for stage IIA, 0 to 1369 for stage IIB, 11 to 2401 for stage IIC, 19 to 324 for stage IID, and 0 to 2526 for stage III. These values, combined with the CO₂/CH₄ ratios, and N₂-He-Ar and N₂-CH₄-Ar relationships, suggest the occurrence of fluids from magmatic, crustal, and shallow meteoric sources in the forming epithermal vein deposit. The helium isotope analyses, obtained by means of Noble Gas Mass Spectrometry, display R/Ra average values between 0.5 and 2, pointing to the occurrence of mantle-derived helium that was relatively diluted or “contaminated” by crustal helium. These volatile analyses, when correlated with the stable isotope data from previous works and He isotope data, show the same distribution of data concerning sources for mineralizing fluids, especially those corresponding to magmatic and crustal sources. Thus, the overall geochemical data from mineralizing fluids are revealed as intrinsically consistent when compared to each other.The three main sources for mineralizing fluids (magmatic, and both deep and shallow meteoric fluids) are accountable at any scale, from stages of mineralization down to specific mineral associations. The volatile and helium isotope data obtained in this paper suggest that the precious metal-bearing mineral associations formed after hydrothermal pulses of predominantly oxidized magmatic fluids, and thus it is likely that precious metals were carried by fluids with such origin. Minerals from base-metal sulfide associations record both crustal and magmatic sources for mineralizing fluids, thus suggesting that base metals could be derived from deep leaching of crustal rocks. At the La Guitarra epithermal deposit there is no evidence for an evolution of mineralizing fluids towards any dominant source. Rather than that, volatile analyses in fluid inclusions suggest that this deposit formed as a pulsing hydrothermal system where each pulse or set of pulses accounts for different compositions of mineralizing fluids.The positive correlation between the relative content of magmatic fluids (high N₂/Ar ratios) and H₂S suggests that the necessary sulfur to carry mostly gold as bisulfide complexes came essentially from magmatic sources. Chlorine necessary to carry silver and base metals was found to be abundant in inclusion fluids and although there is no evidence about its source, it is plausible that it may come from magmatic sources as well.     

High-resolution sedimentary record of lead in the coastal mud of the East China Sea in the past one hundred and fifty years

In the East China Sea （ECS）, there are some mud areas, including the south coastal mud area, the north coastal mud area, and the mud area to the southwest of Cheju Island. X-ray fluorescence （XRF） techniques and Thermal Ionization Mass Spectrometry （TIMS） were used to study the high-resolution sedimentary record of Pb concentrations and Pb stable isotopic compositions in the past one hundred and fifty years in the coastal mud of the ECS. Pb concentrations of a ^210Pb dating S5 core in the study area have increased rapidly since 1980, and reached the maximal value with 65.08 μg/g in 2000, corresponding to the fast economic development of China since the implementation of the ＂Reform and Open Policy＂ in 1978; ^206Pb/^207Pb ratios generally had stabilized at 1.195 from 1860 to 1966, and decreased gradually from 1966 to 2000, indicating that the anthropogenic source Pb contribution to the ECS has increased gradually since 1966, especially since 1980. Pb concentrations decreased distinctly from 2000 to 2003 and ^206Pb/^207Pb ratios increased from 2001 to 2003, corresponding closely to the ban of lead gasoline from 2000 in China. From 1950 to 2003, there occurred four distinct decrease events of ^206Pb/^207Pb, possibly responding to the Changjiang River （Yangtze River） catastrophic floods in 1998, 1991, 1981 and 1954; from 1860 to 1966, there were two decrease periods of ^206Pb/^207Pb, which may respond to the catastrophic floods of Changjiang River in 1931 and 1935, and 1870. As a result of the erosion and drowning by the catastrophic floods, the anthropogenic lead accumulated in soil and water environments over a long period of time was brought into the Changjiang River, then part of them was finally transported into the ECS, which leads to changes in Pb stable isotopic composition.     

3-D seismic structure of the source area of the 1993 Latur, India, earthquake and its implications for rupture nucleations

The Latur earthquake (M_w 6.1) of 29 September 1993 is a rare stable continental region (SCR) earthquake that occurred on a previously unknown blind fault. In this study, we determined detailed three-dimensional (3-D) P- and S-wave velocity (V_p, V_s) and Poisson's ratio (σ) structures by inverting the first P- and S-wave high-quality arrival time data from 142 aftershocks that were recorded by a network of temporary seismic stations. The source zone of the Latur earthquake shows strong lateral heterogeneities in V_p, V_s and σ structures, extending in a volume of about 90 × 90 × 15 km³. The mainshock occurred within, but near the boundary, of a low-V_p, high-V_s and low-σ zone. This suggests that the structural asperities at the mainshock hypocenter are associated with a partially fluid-saturated fractured rock in a previously unknown source zone with intersecting fault surfaces. This might have triggered the 1993 Latur mainshock and its aftershock sequence. Our results are in good agreement with other geophysical studies that suggest high conductivity and high concentration of radiogenic helium gas beneath the source zone of the Latur earthquake. Our study provides an additional evidence for the presence of fluid related anomaly at the hidden source zone of the Latur earthquake in the SCR and helps us understand the genesis of damaging earthquakes in the SCR of the world.     

双坡面临空岩质边坡滑动破坏模式下的稳定性分析

多数岩质边坡稳定性分析已基本解决了常走向单坡面临空的边坡平面滑动问题。然而,在路堑边坡工程和自然边坡中有很多边坡坡面并不是平面,它包含多个坡面。多坡面边坡包含两个或多个不同走向的坡面。多坡面边坡几何特征不同于单坡面边坡,所以滑动条件也不一样。在赤平投影图上,多坡面的滑动包络线是组成边坡的每个坡面单独投影包络线的组合。为了探讨方便,只讨论了双坡面临空岩质边坡的滑动破坏模式,并将其分为双坡面临空下的平面破坏和楔形体破坏。在赤平投影图上,双坡面滑动区域定义为双坡面边坡滑动包络图中两侧坡面的真倾线之间的面积。如果有一两个节理面真倾向线落在滑动区内,滑动破坏才可能发生。     

Hydrogen isotope of individual n-alkanes from modern sediments and their application to environments

Hydrogen isotopes are commonly fractionated to a much greater extent and as a result display larger variations in δ values, In terms of the hydrogen isotope ratios of individual n-alkanes of 16 samples of modern sediments selected from four different locations in the southern part of Gansu, China, the δD values for most of the n-alkanes varied from -150‰-300‰, Variations in δD also occurred between different ranges of n-alkanes, effects of environmental changes on the hydrogen isotopic compositions of individual n-alkanes have been detected. Besides the δD values of n-alkanes, the δD values of lipids including pristane （Pr）, phytane （Ph） were also examined, by the combination of D/H ratios with molecular fingerprinting, Our results further support the notion that hydrogen isotopes of n-alkanes from modern sediments can act as paleoclimatic and paleoenvironmental proxies and provide invaluable new sources of information in the research of paleoenvironment reconstruction.