Lianjun Feng

A New Age Constraint on the Onset of the Neoproterozoic Glaciations in the Yangtze Platform, South China

A sample from the top of the Banxi Group (early Neoproterozoic) in Hunan Province (South China) was dated by the SHRIMP zircon U-Pb method. The resulting age of 725 ± 10 Ma probably solves the debate between the synglacial and the preglacial correlation of the Liantuo Formation and indicates that the Liantuo Formation most likely correlates with the preglacial Banxi Group. Since the Banxi (Danzhou) Group is upwardly transitional to the glacial Jiangkou Group, the age becomes a new maximum age constraint on the onset of the Jiangkou glaciation, which therefore most likely correlates with the Sturtian glaciation.

Hydrothermal origin of elevated iron, manganese and redox-sensitive trace elements in the c. 635 Ma Doushantuo cap carbonate

Abstract: Major and trace element, including REE, concentrations of the Doushantuo cap carbonate (c. 635 Ma) in South China show enrichment in Fe, Mn and redox-sensitive elements and slightly negative Ce anomalies, indicating anoxic environments during cap carbonate precipitation. High FeT/Al ratios but very low concentration of extractable pyrites suggest ferruginous rather than euxinic conditions. The REE + Y patterns of samples show enrichment of heavy REE (HREE), positive Eu anomalies and positive Y anomalies, implying a hydrothermal origin for elevated concentration of Fe, Mn and redox-sensitive elements. The results suggest that ferruginous Ediacaran oceans may have rooted from hydrothermally induced iron accumulation in severely glaciated Cryogenian oceans.

Sulfur and carbon isotopic variations in Neoproterozoic sedimentary rocks from southern China

Abstract A new set of δ34Ssulfide δ34Ssulfate and δ13Ccarbonate values has been reported from Neoproterozoic sedimentary rocks in southern China. The interglacial blackshales of the Datangpo Fm. display higher δ34Ssulfied values with > + 20‰. average, but the postglacial black shales from the Doushantuo Fm. show negative δ34Ccarbonate values. However, the Jinjiadong Fm., the same post-glaciation 3 as the Doushantuo Fm., has positive δ34Ssulfide values, implying that the δ34S value of sedimentary sulfides wouldbe controlled by lithofacies and paleogeographic environments. The δ34Ssulfate values relative to δ13Ccarbonate were obtained by extraction of trace sulfate from the successive carbonate sequences in the Yangtze Gorges sections. A preliminary interpretation suggests that the oceanic environment may fluctuate dramatically at the post-glacial Doushantuo stage and, then, recover its stability at the Dengying stage on the basis of the high resolution δ34S and δ13C corves of seawater.

Variations of sulfur and carbon isotopes in seawater during the Doushantuo stage in late Neoproterozoic

Successive analyses of sulfur and carbon isotopic compositions of carbonates strata in the Doushantuo Formation in the Yangtze area were accomplished through a method of extracting trace sulfate from carbonates. Sulfur and carbon isotopic compositions of coeval seawater were estimated from the samples that show the least diagenetic alteration. A high-resolution age curve of sulfur isotopes in seawater sulfates was obtained in the Doushantuo stage, which reflects the trend of variation in seawater sulfur isotopes after the Neoproterozoic snowball Earth event. Similar characteristics of variation in carbon isotopes were observed in the coeval carbonates. A large positive δ34S excursion over +20‰ occurs in ancient seawater sulfates in the early Doushantuo stage. Simultaneously, the δ13 C values in ancient seawater carbonates exhibit a positive excursion up to 10‰ The maximum δ34S and δ13C values are +46.4‰ and +6.9‰, respectively. In the middle Doushantuo stage, the range of variation in δ34 S values of seawater is relatively narrow, but δ13C values are quite high. Then, δ34S values of seawater become oscillating, and the same occurs in δ13C values. Negative excursions in δ34 S and δ13 C values occur simultaneously at the end of the Doushantuo stage, and the minimum δ34S and δ13C values dropped down to −10.1‰ and –5.7‰, respectively. The characteristics of variations in the sulfur and carbon isotopes of ancient seawater imply strong changes in oceanic environment that became beneficial to inhabitation and propagation of organism. The organic productivity and burial rate of organic carbon once reached a quite high level during the Doushantuo stage. However, the state of environment became unstable after the global glaciation. The global climate and environment possibly were fluctuating and reiterating. The negative excursions in δ34S and δ13C values occurring at the end of the Doushantuo stage may represent a global event, which might be related to oxidation of deep seawater.

Stratigraphic architecture of the Neoproterozoic glacial rocks in the “Xiang-Qian-Gui” region of the central Yangtze Block, South China

Abstract The Yangtze Block in South China is one of the important regions where Neoproterozoic glacial rocks are well developed and studied. However, the classification and correlation of the Neoproterozoic glacial sequences in the central Yangtze Block stillremain controversial among Chinese geologists. The original Sinian sections around the Yangtze Gorges Region became an official standard for classification and correlation since the 1950s. Subsequent regional geologic studies, however, resulted in different classification and correlation, because of its incompleteness. We select one of the complete sections in the bordering areas of Xiang (Hunan). Qian (Guizhou) and Gui (Guangxi). as a standard of classification and correlation. The temporal and spatial distribution, i.e. the stratigraphic architecture, of the glacial rocks in the central Yangtze Block is suggested. Our results indicate that the glacial sequence on the Yangtze Block was deposited during the Nantuo Ice-age, the Datangpo Interglacial-ag...

Simultaneous Determination of 143Nd/144Nd and 147Sm/144Nd Ratios and Sm–Nd Contents from the Same Filament Loaded with Purified Sm–Nd Aliquot from Geological Samples by Isotope Dilution Thermal Ionization Mass Spectrometry

Isotope dilution thermal ionization mass spectrometry (ID-TIMS) is the standard technique used to achieve precise (143)Nd/(144)Nd and (147)Sm/(144)Nd isotope ratios and accurate elemental concentrations of Sm-Nd. However, in previous studies, purified Sm and Nd fractions must be individually loaded onto different filaments for their accurate determination using TIMS because of severe isobaric interferences. Thus, the classical ID-TIMS technique is time consuming and laborious. In this study, a new method is proposed, which is able to acquire both ratios of (143)Nd/(144)Nd and (147)Sm/(144)Nd and concentrations of Sm-Nd simultaneously on the same filament arrangement. The measurement time and filament consumption are reduced by 50% with the current method, and therefore, the operation cost of TIMS is significantly reduced. A mixed (152)Sm-(148)Nd spike was employed to achieve accurate results after spike subtraction and isobaric interference corrections. Results obtained from a series of standard rock samples are in good agreement with recommended values, within ±0.003% for the (143)Nd/(144)Nd ratio and ±1% for the (147)Sm/(144)Nd ratio.

Multiple climate cooling prior to Sturtian glaciations: Evidence from chemical index of alteration of sediments in South China

Investigation of climatic conditions prior to the Sturtian glaciations is critical to understanding the trigger mechanism for the series of Neoproterozoic global glaciations. In this study, we report high-resolution chemical index of alteration (CIA) records in the sediments of South China prior to the Sturtian glaciation (820~720 Ma). Our results showed there occurred multiple climate cooling before the Sturtian glaciations in South China: (1) a series of episodic and possibly global climate cooling periods from ca. 750 Ma to 725 Ma, which also caused some diachronous regional glaciations; (2) a permanent climate cooling period between ca. 800 Ma and 770 Ma, probably contemporaneous to the global “Bitter Springs stage” δ13C negative excursion; (3) a climate cooling period between ca. 815 Ma and 810 Ma. The three stages of climate cooling are also supported by their correspondence to previously reported extremely low δ18O records of igneous/metamorphic minerals from South China. These climate cooling periods also coincide with the magmatism and rifting events in South China. We argue that tectonic movements were the primary control on the climate cooling before the Neoproterozoic global glaciations.

Major and trace element geochemistry of the Neoproterozoic syn-glacial Fulu iron formation, South China

The Fulu iron formation (IF) is an iron-rich unit in the Neoproterozoic glacial successions, South China. The major element data suggest that the iron sources of the Fulu IF are derived from binary mixing from hydrothermal and detrital loads. The Fulu IF is characterized by slightly positive Eu anomalies similar to other Neoproterozoic IFs, indicating that a high-temperature hydrothermal input may contribute little to Neoproterozoic IFs. A shift from non-existent to slightly negative Ce anomalies of the Fulu IF indicates that the IF precipitated across an iron chemocline separating a weakly oxic surface ocean from an oxygen-depleted deep ocean.

Combination of sealed-tube decrepitation with continuous-flow isotope ratio mass spectrometry for carbon isotope analyses of CO2 from fluid inclusions in minerals

A method is presented to perform carbon isotope analyses of CO2 from fluid inclusions in minerals using decrepitation by the sealed tube method followed by cryogenic separation of the resultant CO2 in a high-vacuum line, coupled via a GasBench II to a DELTA V isotope ratio mass spectrometer. The proposed method greatly reduces the sample size and the laboratory time without compromising the precision of the results.

Direct High-Precision Measurements of the 87Sr/86Sr Isotope Ratio in Natural Water without Chemical Separation Using Thermal Ionization Mass Spectrometry Equipped with 1012 Ω Resistors

Thermal ionization mass spectrometry (TIMS) allows excellent precision for determining Sr isotope ratios in natural water samples. Traditionally, a chemical separation procedure using cation exchange resin has been employed to obtain a high purity Sr fraction from natural water, which makes sample preparation time-consuming. In this study, we present a rapid and precise method for the direct determination of the Sr isotope ratio of natural water using TIMS equipped with amplifiers with two 10(12) Ω resistors. To eliminate the (87)Rb isobaric interference, Re ribbons are used as filaments, providing a significant advantage over W ribbons in the inhibition of Rb(+) emission, based on systematically examining a series of NIST SRM987 standard doping with various amounts of Rb using Re and W ribbons. To validate the applicability of our method, twenty-two natural water samples, including different water types (rain, snow, river, lake and drinking water), that show a large range in Sr content variations (2.54-922.8 ppb), were collected and analyzed from North and South China. Analytical results show good precision (0.003-0.005%, 2 RSE) and the method was further validated by comparative analysis of the same water with and without chemical separation. The method is simple and rapid, eliminates sample preparation time, and prevents potential contamination during complicated sample-preparation procedures. Therefore, a high sample throughput inherent to the TIMS can be fully utilized.