四川盆地东部垫江凹陷三叠系嘉陵江组岩盐氯同位素特征与成钾指标研究

垫江凹陷位于四川盆地东部,是四川盆地三叠纪时期重要的成盐凹陷之一,但当时古卤水是否达到钾盐沉积阶段,是否具备形成海相钾盐的良好条件,一直存在争议。本文通过对垫江凹陷长平3井、高探1井和ZK001井嘉陵江组岩盐样品进行化学成分分析,以及对长平3井典型岩盐样品进行氯同位素分析来判断古卤水沉积阶段和成钾条件。结果发现垫江凹陷三叠系嘉陵江组岩盐δ37 Cl值均为负值,均小于-0.32‰,最低达到-1.18‰,绝大部分岩盐样品溴氯系数大于0.31,有很大一部分样品溴氯系数超过0.45,进一步表明垫江凹陷在嘉陵江期古卤水浓缩已达到钾石盐析出阶段,与岩盐包裹体成分分析结果一致。综合气候-物源-构造因素,认为垫江凹陷三叠纪嘉陵江期气候条件炎热,物质来源丰富,存在次级凹陷,古构造条件优越,具备良好的成钾潜力。     

Variations in the quantity and composition of seston from an estuary in southern Chile on different temporal scales

Estuaries are characterised by highly variable environmental conditions largely driven by tidal and atmospheric forces. This study investigates variation in the physical environment and the composition of the seston on various temporal scales in the Quempillén estuary, southern Chile. The water column was sampled throughout the tidal cycle at various times of the year. Total particulate matter, particulate inorganic matter, particulate organic matter, particle numbers, total particle volume, proximate biochemical composition and energy content of the seston, chlorophyll a and chloropigments were routinely measured. In each of the months in which sampling took place, two or three tidal cycles were examined. The information not only helps to explain the dynamics of the estuary, but is essential for an understanding of the physiology and ecology of the suspension-feeders which exploit the seston as a food source, the most dominant being the gastropod Crepipatella dilatata. Temperature and salinity were generally highest during summer, but seston quality, defined by energy content and biochemical composition (lipid, protein and carbohydrate) was higher at the end of winter and during spring. Chlorophyll a values were greatest in late spring (November). Many of the variables studied changed frequently according to the phase of the tidal cycle, and in several cases significant differences were observed among tidal cycles from the same month of the same year. In general the variables measured did not exhibit consistent patterns linked to the tidal cycle, possibly because any such patterns were masked by atmospheric conditions (wind and rain) that dominate the region and greatly influence the estuary. The quantity and quality of the seston available to suspension-feeders is largely determined by these atmospheric forces, which cause an influx of terrigenous material from adjacent areas and also resuspend bottom sediment. These effects are magnified by the shallowness of the estuary (<2 m depth). The food supply for C. dilatata and other suspension-feeders therefore varies on temporal scales varying from hourly (tidal cycle) to daily/weekly (atmospheric forces) to monthly (seasonal influences), but inhibition of feeding by low salinity sometimes limits the ability of C. dilatata to exploit fully the available organic matter.     

Cadmium and phosphorus cycling in the water column of the South China Sea: The roles of biotic and abiotic particles

The concentrations of cadmium, phosphorus, and aluminum in size-fractionated phytoplankton, zooplankton, and sinking particles are determined using ICPMS to evaluate the roles of biotic and abiotic particles on the cycling and ratios of Cd and P in the water column. Plankton were collected with a filtration apparatus equipped with 10-, 60-, and 150-μm aperture plankton nets on two occasions (2002 and 2006), and sinking particles were sampled by moored sediment traps deployed at depths of 120, 600, and 3500 m from 2004 to 2005. In contrast to what our previous study revealed, i.e., that most of the other bioactive trace metals in plankton were strongly correlated with abiotic Al and adsorbed on phytoplankton [Ho, T.Y., Wen, L.S., You, C.F., Lee, D.C., 2007. The trace metal composition of size-fractionated plankton in the South China Sea: biotic versus abiotic sources. Limnol Oceanogr 52, 1776–88.], Cd/P ratios, ranging from 0.12 to 0.34 mmol/mol P, did not vary with Al and exhibited fairly consistent values among different sizes of plankton, showing that Cd was mostly incorporated on an intracellular basis. In terms of the sinking particles, fluxes in Cd and P as well as in Cd/P ratios were strongly influenced by both biotic and abiotic particles. Overall, the Cd/P ratios in the sinking particles ranged from 0.03 to 1.2 mmol/mol, with the highest value observed in traps at 120 m during the productive season. The lowest value was observed in deep water during high flux periods for lithogenic particles. At surface depth, flux and Cd/P ratios were elevated during the most productive season in the region. The elevated ratios in the traps at 120 m were most likely related to preferential uptake of Cd for the dominant species (coccolithophores) during the productive period. Relatively, Cd/P ratios sharply decreased with increasing Al flux in deep water and ratios were much lower than the expected Cd/P ratios obtained from the relative portion of lithogenic and biogenic particles, indicating that the adsorption of soluble P into lithogenic particles was significant in the deep water during high lithogenic particle flux periods. Using averaged annual fluxes and standing stock in the water column, the residence time of biogenic Cd and P are 0.10 and 0.20, 250 and 100, and 9100 and 5000 years respectively in the top 120 m, 600 m, and water column as a whole, also showing preferential removal for Cd in the euphotic zone but relatively higher removal rates for P in the deep water. Our study suggests that the shift in microalgal community structure along with input of lithogenic minerals are both potentially important factors in influencing Cd/P ratios in oceanic water on a geological time scale.     

Advection in plankton models with variable elemental ratios

As ocean biogeochemical models evolve to permit the elemental composition of plankton populations and dissolved organic matter to vary, each element is normally assigned a separate state variable, which is advected and mixed independently of the others. In a population of cells with varying elemental quotas, the proper currency of the advection operator is subpopulations of similar cells. The spatial gradient in total C, N, or P summed over the spectrum of such subpopulations is identical to that calculated for the population means, so treating the various elements as independent should generally be a valid approximation. However, errors can arise in high-order advection schemes with nonlinear corrector terms, which are not additive across the subpopulations. Some numerical examples indicate that these errors are relatively small [O(10⁻³–10⁻⁴)] but can be as high as O(10⁻²) in certain cases. As grid resolution varies, the error scales approximately to the Courant number.     

A darkling beetle population in West Texas during the 1997–1998 El Niño

We examined the abundance and distribution of Eleodes extricata (Tenebrionidae) in a semi-arid region of West Texas. During the 2-year study, climatic conditions were extreme but opposite, with 1997 being unusually wet and mild, and 1998 being unusually dry and hot. These conditions were associated with striking differences in the population structure of the beetles. Under identical pitfall-sampling efforts, we captured 1562 and 671 individuals in 1997 and 1998, respectively. Capture rates were lowest in grassland, and highest in sand shinnery oak, and within the latter, they were lowest in blowouts, intermediate along the edges of blowouts, and highest under vegetative cover. Sex ratios were consistently female-biased, and the degree of bias increased from spring through fall in both years. These increases were more pronounced in 1998, with the sex ratios of early and late sampling periods differing by over four-fold, from 1·15 to 5·00. Females were heavier than males, and the dry masses of both sexes increased from spring though fall in both years. As with sex ratios, these increases were more pronounced in 1998. Only the largest beetles survived the drought, illustrating how extreme conditions can exert especially strong directional selection, and affect sex ratios in populations with sexual size dimorphism.     

Remineralization Ratios in the Subtropical North Pacific Gyre

Based on a new mixing model of two end-members, the water column remineralization ratios of P/N/C_org - O₂ = 1/13 ± 1/135 ± 18/170 ± 9 are obtained for the Hawaii Ocean Time-series (HOT) data set at station ALOHA. The traditional Redfield ratios of P/N/C_org/–O₂ = 1/16/106/138 have standard deviations of more than 50%, when they are based on the average composition of phytoplankton. Apparently, the remineralization processes in the water column have smoothed out the observed large variability of plankton compositions. A new molar formula for the remineralized plankton may be written as ₁₃₅H₂₈₀O₁₀₅N₁₃P or C₂₅(CH₂O)₁₀₁(CH₄)₉(NH₃)₁₃(H₃PO₄). Oxidation of this formula results inC₂₅(CH₂O)₁₀₁(CH₄)₉(NH₃)₁₃(H₃PO₄) + 170O₂ 135CO₂ + 132H₂O + 13NO₃ ^- + H₂PO₄ ^- + 14H⁺.For comparison, remineralization using Redfield's formula gives:(CH₂O)₁₀₆(NH₃)₁₆(H₃PO₄) + 138O₂ 106CO₂ + 122H₂O + 16NO₃ ^-+ H₂PO₄ ^- + 17H⁺     

Carbon isotope ratios of C_4 plants in loess areas of North China

Recent stable carbon isotope studies have shown that the occurrence of C4 plants on the Earth was much later than that of C3 plants and there was a global ex-pansion of C4 biomass around 5―8 million years ago[1]. Although far fewer species use the C4 pat…     

A technique for atmospheric measurements of stable carbon isotope ratios of isoprene,methacrolein, and methyl vinyl ketone

A technique was developed to measure stable carbon isotope ratios (¹³C/¹²C) of light volatile organic compounds (VOCs) such as isoprene, methacrolein (MACR) and methyl vinyl ketone (MVK) using gas chromatography combustion isotope ratio mass spectrometry (GCC-IRMS). An automated sampling and cryofocussing system allowed for the extraction of VOCs from air samples of up to 140 L of air collected over 3 h, and the subsequent ¹³C/¹²C analysis of the VOCs by GCC-IRMS. Chromatography using selective transfer between two columns was used to improve the separation for selected compounds, increasing peak resolution and attaining less noisy baselines. Still, some target compounds could not be completely separated from co-eluting peaks. To reduce the bias of isotope ratio determinations, which can result from incomplete peak resolution, a peak-fitting procedure has been developed. In cases of overlapping peaks or substantial baseline drift, this peak fitting allows more accurate determination of isotope ratios than conventional integration schemes. Comparisons between off-line IRMS measurements and a peak-evaluation procedure using a prepared VOC gas-phase standard show that isotope ratios derived from large (>1 ng of carbon per peak) and well-resolved peaks have a reproducibility of ±0.3‰. With smaller masses in the range of 0.1–1 ng of carbon, reproducibility decreased to ±(0.5–0.8)‰. For a 140 L sample of air, such small masses of carbon correspond to mixing ratios in the low pptV range. The developed measurement technique was applied to a small set of ambient air samples taken during hot, sunny periods from late May to early August, 2005, at Forschungszentrum Jülich, Germany, a semi-rural area. The range of δ¹³C values determined for isoprene, benzene, and toluene are consistent with those reported in the literature. GCC-IRMS results of δ¹³C for ambient samples of isoprene, MACR, and MVK, measured at mixing ratios of 15–280 pptV, are presented and discussed.     

Evaluation of Simultaneous Analyte Leaching/Vapour Phase Introduction for Direct Osmium Isotope Ratio Measurements in Solid Samples by Double-Focusing Sector Field ICP-MS

The analytical performance of a method for Os isotope ratio measurement by double‐focusing, sector field ICP‐MS (ICP‐SFMS) was evaluated. The method is based on several optimised, concurrent processes: Os extraction from samples in hot concentrated nitric acid; separation of Os from the digest solution by the formation of volatile osmium tetroxide accelerated by continuous hydrogen peroxide addition; transport of analyte vapour by an oxygen flow into the ICP; and isotopic determination by ICP‐SFMS. Due to the very efficient utilisation of analyte (approaching 0.5‰), Os isotope ratio measurement could be performed at low pg levels. Combined with an ability to process sample sizes up to 2 g (up to 50 g if the organic matrix of biological or botanical samples is eliminated by ashing), materials with Os concentrations in the low, or even sub pg g^?1 range could be determined by this method. Given that two complete digestion/distillation systems were available for interchangeable use, throughputs of up to fifteen samples per 8 hour shift could be achieved. The method precision, evaluated as the long‐term reproducibility of ¹⁸⁷ Os/¹⁸⁸Os ratio measurements in a commercial Os reference sample containing 0.5 ng Os, was 0.16% relative standard deviation (RSD, 1s). The method has been applied to perform replicate ¹⁸⁷ Os/¹⁸⁸ Os ratio measurements on a suite of fifty reference materials of various origins and matrix compositions, with Os concentrations varying from < 0.1 pg g^?1 to > 100 ng g^?1, yielding an average precision of 3% RSD. Though none of the materials tested are certified for Os content or Os isotope composition, comparison of the obtained data with published Os isotope information for similar sample types revealed close agreement between the two. The method can also be used for the simultaneous, semi‐quantitative determination of Os concentrations.