Fluid generation, vein formation and the degree of fluid–rock interaction during decompression of high-pressure terranes: the Schistes Lustrés, Alpine Corsica, France

Centimetre‐ to decimetre‐wide quartz+calcite veins in schistes lustrés from Alpine Corsica were formed during exhumation at 30–40 Ma following blueschist facies metamorphism. The δ¹⁸O and δ¹³C values of the veins overlap those of the host schistes lustrés, and the δ¹⁸O values of the veins are much higher than those of other rocks on Corsica. These data suggest that the vein‐forming fluids were derived from the schistes lustrés. Fluids were probably generated by reactions that broke down carpholite, lawsonite, chlorite and white mica at 300–350 °C during decompression between c. 1400 and 800 MPa. However, the δ¹⁸O values of the veins are locally several per mil higher than expected given those of their host rocks. The magnitude of oxygen isotope disequilibrium between the veins and the host rock is inversely proportional to the δ¹⁸O value of the host rock. Additionally, calcite in some schists is in isotopic equilibrium with calcite in adjacent veins, but not with the silicate fraction of the schists. Locally, the schists are calcite bearing only within 1–20 cm of the veins. The vein‐forming fluids may have been preferentially derived from calcite‐bearing, high‐δ¹⁸O rocks that are common within the schistes lustrés and that locally contain abundant (>15%) veins. If the fluids were unable to completely isotopically equilibrate with the rocks, due to relatively rapid flow at moderate temperatures or being confined to fractures, they could form veins with higher δ¹⁸O values than those of the surrounding rocks. Alteration of the host rocks was probably inhibited by isolation of the fluid in ‘quartz‐armoured’ veins. Overall, the veins represent a metre‐ to hectometre‐scale fluid‐flow system confined to within the schistes lustrés unit, with little input from external sources. This fluid‐flow system is one of several that operated in the western Alps during exhumation following high‐pressure metamorphism.     

THE RELATIONSHIP BETWEEN INLAND LAKES EVOLUTION AND CLIMATIC FLUCTUATION IN ARID ZONE

The evolution of the inland lakes in arid and semi-arid zones is accorded with the climatic fluctuation. The humid climate is in harmony with the higher water level and greater lake water quantity budget while arid climate is in correspondence with the lower water level and little water budget. Based on the analysis of the lake fluctuation and lake budget change, with the aid of the data of geom'orphology, palynology, sedimentology and chronology, It is found that the climate experienced a warm and humid period during 7000-3500 yr. B. P. and showed a drying and warming trend in the last century in the Central Asia.     

Geochemical evidence (C,N and Pb isotopes) of recent anthropogenic impact in south‐central Chile from two environmentally distinct lake sediment records

In this paper, we compare the elemental and isotopic (C, N, Pb) geochemistry of lake sediments from two contrasted environments in south‐central Chile. The first lake, Laguna Chica de San Pedro (LCSP), is situated in the urbanised area of the Biobio Region (36°S). The second lake, Lago Puyehue (40° S), is located 400 km to the southeast of LCSP and within an Andean national park. Our aim is to identify environmental impacts associated with increasing industrial activities and land degradation during the last 150 a. In LCSP, shifts in C/N atomic ratios, δ¹³C and δ¹⁵N from 1915–1937 to the late 1980s are attributed to successive land degradation episodes in the lake watershed. Based on a Pb isotopic mixing model, we estimate that up to 20% of lead in LCSP sediments is supplied from urban atmospheric pollution. By contrast, human impact in the watershed of Lago Puyehue is very limited. We observe no change in organic geochemistry during the last 150 a and lead contamination remains lower than 5%, even during the last decades. Although contamination levels are much higher in LCSP than in Lago Puyehue, a peak in anthropogenic Pb is recorded during the same period (1974–1976) at both sites. This maximum contamination level is consistent with increased industrial activity in the vicinity of Concepción. Copyright © 2010 John Wiley & Sons, Ltd.     

A 3600 years paleoclimatic change inferred from organic δ13C and TOC/TN of the Gucheng Lake sediments, southeast China

A 6.2 m thick core of Gucheng Lake sediment provided a 3600 years record of climate change. The contents of the TOC in the core changed from 2.63% to 8.48%, and the δ¹³C values of organic matter were from −21.54% to −27.3%. The TOC/TN ratios indicated that the organic materials in sediments were from lake plankton and land-derived plants. The 2.9–22 m core interval with high TOC/TN ratios, low δ¹³C values and low contents of TOC indicated a cold climate stage. The 6.2–5.5 m and 0.4–0.1 m intervals were characterized by low TOC/TN ratios, high δ¹³C values and high contents of TOC, and reflected temperate climate stages. Project 49372129 supported by NSFC.     

DISSOLVED AND PARTICULATE ORGANIC CARBON IN YANTAI SISHILI BAY AQUICULTURE WATERS

Investigation of dissolved organic carbon (DOC) and particulate organic carbon (POC) at 12 stations in Yantal Sishili Bay in May, August, and November of 1997 and March and May of 1998 showed that DOC concentrations varied from 1.14 mg/L to 5.35 mg/L; that the average values at all staticrLs ineach entise varied from 1.52 mg/L to 2.12 mg/L; that POC concentrafions varied from 0.049 mg/L to 1.411mg/L; and averaged 0.159 mg/L to 0.631 mg/L in each cruise. Horizontal distribution of DOC was influ-enced by factors such as continental input, organism activity, temperature, aquieulture environment, etc. The higher POC concentration occurred along the coast. The vertical distribution of DOC and POC changed obviously in spring and summer, but not obviously in autumn and winter. DOC concentration was highest in summer and POC in spring; both were lowest in winter. The seasonal change of DOC was con-sistent with primary productivity seasonal variation, and that of POC was consistent with ehlorophyll-a sea-sanal variation. The seasonal change trend of the C/N ratio of dissolved organic matter was obvious, but the C/N ratio of particulate organic matter had no such trend.     

利用黄河泥沙围出“渤海湖”的初步设想

本文是一个关于将渤海变成淡水湖的水利工程的构想。让黄河的大量泥沙通过人工导流的方式沿莱州湾南岸与渤海海峡沉积延伸,产生的陆地将渤海封闭并逐渐形成淡水湖。这一工程将陆地连接山东半岛与辽东半岛,并为华北提供巨大淡水库,具有显著的经济、生态效益。具体实施上,可通过两道渔网式围栏促使黄河泥沙定点沉积并阻挡浪潮侵蚀,通过加强汛期水量增加黄河口泥沙。     

洱海近区非潮汐重力变化的研究

本文给出了洱海水体变化对局部重力场影响的解析式和量级,并且将理论结果与实测的水文、流动重力及定点重力分析结果作了比较,结果表明:影响的程度因距洱海的距离而异。在台站重力测量中,由水体变化产生的干扰淹没在零漂之中(约占每日零漂量的2％),潮汐主频段上没有明显的干扰信号;而对流动重力测量,在水体变化大的情况下,部分测点所产生的变化可以达到10×10~(-8)m/s~2。     

Deepwater Ventilation and Stratification in the Neogene South China Sea

Combined data of physical property, benthic foraminifera, and stable isotopes from ODP Sites 1148, 1146, and 1143 are used to discuss deep water evolution in the South China Sea (SCS) since the Early Miocene. The results indicate that 3 lithostratigraphic units, respectively corresponding to 21-17 Ma, 15-10 Ma, and 10-5 Ma with positive red parameter (a*) marking the red brown sediment color represent 3 periods of deep water ventilation. The first 2 periods show a closer link to contemporary production of the Antarctic Bottom Water (AABW) and Northern Component Water (NCW), indicating a free connection of deep waters between the SCS and the open ocean before 10 Ma. After 10 Ma, red parameter dropped but stayed higher than the modern value (a*=0), the CaCO3 percentage difference between Site 1148 from a lower deepwater setting and Site 1146 from an upper deepwater setting enlarged significantly, and benthic species which prefer oxygen-rich bottom conditions dramatically decreased. Coupled with a major negative excursion of benthic δ13C at ~10 Ma, these parameters may denote a weakening in the control of the SCS deep water by the open ocean. Probably they mark the birth of a local deep water due to shallow waterways or rise of sill depths during the course of sea basin closing from south to east by the west-moving Philippine Arc after the end of SCS seafloor spreading at 16-15 Ma. However, it took another 5 Ma before the dissolved oxygen approached close to the modern level. Although the oxygen level continued to stabilize, several Pacific Bottom Water (PBW) and Pacific Deep Water (PDW) marker species rapidly increased since ~6 Ma, followed by a dramatic escalation in planktonic fragmentation which indicates high dissolution especially after ~5 Ma. The period of 5-3 Ma saw the strongest stratified deepwater in the then SCS, as indicated by up to 40% CaCO3 difference between Sites 1148 and 1146. Apart from a strengthening PDW as a result of global cooling and ice cap buildup on northern high latitudes, a deepening sea basin due to stronger subduction eastward may also have triggered the influx of more corrosive waters from the deep western Pacific. Since 3 Ma, the evolution of the SCS deep water entered a modern phase, as characterized by relative stable 10% CaCO3 difference between the two sites and increase in infaunal benthic species which prefer a low oxygenated environment. Thesubsequent reduction of PBW and PDW marker species at about 1.2 Ma and 0.9 Ma and another significant negative excursion of benthic δ13C to a Neogene minimum at ~0.9 Ma together convey a clear message that the PBW largely disappeared and the PDW considerably weakened in the Mid-Pleistocene SCS. Therefore, the true modern mode SCS deep water started to form only during the "Mid-Pleistocene climatic transition" probably due to the rise of sill depths under the Bashi Strait.     

Microscale Simultaneous Measurement of Carbon and Nitrogen Isotopes on Natural Diamond

Simultaneous analysis of carbon and nitrogen isotope ratios by SIMS was applied for the first-time to a natural diamond from the Kelsey Lake kimberlite, State Line Distinct, Colorado (UWD-1). This in situ procedure is faster, reduces sample size for analysis, and measures both isotope ratios from a single ~ 10 μm diameter pit, a critical advantage for zoned diamonds. The carbon isotope ratio (expressed as δ¹³C_VPDB) of the bulk UWD-1 crystal, determined by the conventional combustion method in the present study, is -5.9‰ ± 0.2‰ (VPDB, 2s). Nitrogen mass fraction ([N]) and isotope ratio (expressed as δ¹⁵N_Air) were determined by stepwise combustion and gas-source mass-spectrometry, resulting in 553 ± 64 μg g^-1 and -6.7‰ ± 1.1‰ (Air, 2s), respectively. Secondary ions of ¹²C₂^-, ¹²C¹³C^-, ¹²C¹⁴N^-, and ¹²C¹⁵N^- were simultaneously measured by SIMS using three Faraday cups and one electron multiplier. The spot-to-spot reproducibility of δ¹³C and δ¹⁵N values for the UWD-1 (178 spots on sixteen chips, 10 μm spots), were 0.3‰ and 1.6‰, respectively (2s). While ¹²C¹⁴N^-/¹²C₂^- ratios, which are an indicator for [N], varied up to 12% among these sixteen chips, such variation did not correlate with either δ¹³C or δ¹⁵N values. We propose that UWD-1 is a suitable reference sample for microscale in situ analysis of δ¹³C and δ¹⁵N values in diamond samples.