Pyrite paragenesis and multiple sulfur isotope distribution in late Archean and early Paleoproterozoic Hamersley Basin sediments

The sulfur isotope record in late Archean and early Paleoproterozoic rocks is of considerable importance because it provides evidence for changes in early Earth atmospheric oxygen levels and potentially constrains the origin and relative impact of various microbial metabolisms during the transition from an anoxic to oxic atmosphere. Mass independently fractionated (MIF) sulfur isotopes reveal late Archean and early Paleoproterozoic sulfur sources in different pyrite morphologies in Western Australia's Hamersley Basin. Multiple sulfur isotope values in late Archean pyrite vary according to morphology. Fine grained pyrite has positive sulfur MIF, indicating a reduced elemental sulfur source, whereas pyrite nodules have negative sulfur MIF, potentially derived from soluble sulfate via microbial sulfate reduction. The Hamersley Basin δ³⁴S–Δ³³S record suggests that the extent of oxygenation of the surface ocean fluctuated through the Late Archean from at least 2.6 Ga, more than 150 million yr before the Great Oxidation Event. In the early Paleoproterozoic, there is less distinction between pyrite morphologies with respect to sulfur isotope fractionation, and pyrite from the Brockman Iron Formation trends toward modern sulfur isotope values. An important exception to this is the strong negative MIF recorded in layer parallel pyrite in Paleoproterozoic carbonate facies iron formation. This may suggest that deeper water hydrothermal environments remained anoxic while shallower water environments became more oxidised by the early Paleoproterozoic. The results of the current study indicate that sulfide paragenesis is highly significant when investigating Archean and early Paleoproterozoic multiple sulfur isotope compositions and sulfur sources.     

Volcanic emissions of metals and halogens from White Island (New Zealand) and Erebus volcano (Antarctica) determined with chemical traps

Volcanic emission rates of As, Sb, Pb, Hg, Se, Cl, and F were determined at Erebus volcano, Antarctica and White Island, New Zealand, using chemical traps. The trace metal fluxes were determined by combining the species to S ratios in the solutions with SO₂ emission rates measured by correlation spectrometry at the two volcanoes. At Erebus volcano, fluxes for the metals Pb and Hg were 2.0 × 10^− 4 and 8.1 × 10^− 6 kg s^− 11, respectively. Fluxes for Cl, F, As, Sb and Se (0.35, 0.15, 2.5 × 10^− 4, 1.2 × 10^− 5, and 4.5 × 10^− 6 kg s^− 1, respectively) agreed within error limits for values determined previously by the LiOH impregnated filter method [Zreda-Gostynska, G., Kyle, P., Finnegan, D., Prestbo, K., 1997. Volcanic gas emissions from Mount Erebus and their impact on the Antarctic environment. Journal of Geophysical Research, 102(B7): 15039–15055.], demonstrating the utility of the chemical trap method. A fall in the As/S ratio from 7 × 10^− 4 in 1997/1999 to 3 × 10^− 4 in 2000 at Erebus coincided with a change in the frequency and style of eruptive activity that may have been due to injection of magma into the system. At White Island, chemical trap data indicated fluxes of Cl = 0.90, F = 0.0079, Pb = 2.7 × 10^− 4, Hg = 1.1 × 10^− 5, As = 1.3 × 10^− 4, Sb = 1.9 × 10^− 5 and Se = 1.5 × 10^− 5 kg s^− 1. Samples collected 600 m downwind of the active crater were comparable to samples collected adjacent to the main gas vent, showing that this method can still be used at some distance from a degassing vent.     

基于最终需求的中国出口贸易碳排放研究

以2002年为例,采用投入产出模型,从最终需求的角度对中国出口贸易引起的碳排放(包括直接和间接排放)进行了评估。结果表明,2002年中国为满足对外出口需求而在国内和国外引起的碳排放约288.22~330.49 MtC,其中国内出口排放261.19 MtC,约占当年国内一次能源消费碳排放量的23.45%;大部分部门的出口碳排放主要是由国内排放所贡献,进口再出口排放对总出口排放的平均贡献率在9.38%~20.97%之间。中国单位产值出口的平均碳排放为0.093~0.106 kgC,其中0.084 kgC是在国内排放;碳密集部门多集中于重化工业、交通运输和部分轻工业。将来一方面,中国不宜增加高耗能行业的出口;另一方面,国外发达国家也应积极向中国等发展中国家转让先进生产技术,以减少全球温室气体排放,实现全球减排行动中公平与效率的双赢。     

“7.17”西北夏季沙尘暴数值模拟

 对2005年7月17日发生在西北地区近20 a来夏季最强的沙尘暴过程进行了数值模拟研究,结果得到:①沙尘暴发生前,沙源处于高温控制下;②起沙是水平低涡和垂直涡叠加而成的一种类似于Benard对流泡的系统扫掠沙源的结果;③起沙主要发生在水平低涡移动方向的右部。     

A Study of DMS Oxidation in the Tropics: Comparison of Christmas Island Field Observations of DMS, SO2, and DMSO with Model Simulations

This study reports comparisonsbetween model simulations, based on current sulfurmechanisms, with the DMS, SO₂ and DMSOobservational data reported by Bandy et al.(1996) in their 1994 Christmas Island field study. For both DMS and SO₂, the model results werefound to be in excellent agreement with theobservations when the observations were filtered so asto establish a common meteorological environment. Thisfiltered DMS and SO₂ data encompassedapproximately half of the total sampled days. Basedon these composite profiles, it was shown thatoxidation of DMS via OH was the dominant pathway withno more than 5 to 15% proceeding through Cl atoms andless than 3% through NO₃. This analysis wasbased on an estimated DMS sea-to-air flux of 3.4 ×10⁹ molecs cm^-2 s^-1. The dominant sourceof BL SO₂ was oxidation of DMS, the overallconversion efficiency being evaluated at 0.65 ± 0.15. The major loss of SO₂ was deposition to theocean's surface and scavenging by aerosol. Theresulting combined first order k value was estimated at 1.6 × 10^-5 s^-1. In contrast to the DMSand SO₂ simulations, the model under-predictedthe observed DMSO levels by nearly a factor of 50. Although DMSO instrument measurement problems can notbe totally ruled out, the possibility of DMSO sourcesother than gas phase oxidation of DMS must beseriously considered and should be explored in futurestudies.     

NOx or VOC Limitation in East German Ozone Plumes?

The ozone forming potential of VOCs and NO_x for plumes observed from several cities and a power plant in eastern Germany was investigated. A closed box model with a gas phase photochemical reaction mechanism was employed to simulate several scenarios based upon aircraft observations. In several of the scenarios, the initial concentrations of NO_x, VOCs, and SO₂, were reduced to study the factors limiting the O₃ production. Ozone production was limited by the initial VOC concentrations for all of the simulated plumes. Higher O₃ concentrations were produced with reduced initial NO_x. In one sample with high SO₂ mixing ratios (>100 ppb), SO₂ was also identified as a significant contributor to the production of O₃.     

Methane exchange between coal-bearing basins and the atmosphere: the Ruhr Basin and the Lower Rhine Embayment, Germany

A precise knowledge of methane exchange processes is required to fully understand the recent rise of atmospheric methane concentration. Three of these processes take place at the lithosphere/atmosphere boundary: bacterial consumption of methane and emission of bacterial or thermogenic methane. This study was initiated to quantify these processes on a regional scale in the Ruhr Basin and the Lower Rhine Embayment. Since these areas are subject to bituminous coal and lignite mining, natural and anthropogenically-induced methane exchange processes could be studied. The methane emission and consumption rates and their carbon isotope signal were measured at the lithosphere/atmosphere boundary using flux chambers. On most of the soils studied, methane consumption by bacteria was identified. Thermogenic methane was released only at some of the natural faults examined. In active and abandoned bituminous coal mining areas methane emissions were restricted to small areas, where high emission rates were measured. The carbon isotope composition of methane at natural faults and in mining subsidence troughs was typical of thermogenic methane (−45 to −32 ‰ δ¹³C). Methane exchange balancing revealed that natural methane emissions from these two basins represent no source of atmospheric importance. However, methane release by upcast mining shafts dominates the methane exchange processes and is by about two orders of magnitude greater than methane consumption by bacterial oxidation in the soils.     

Genesis of the Mamut Porphyry Copper Deposit, Sabah, East Malaysia

Abstract: The Mamut deposit of Sabah, East Malaysia, is a porphyry type Cu‐Au deposit genetically related to a quartz monzonite (“adamellite”) porphyry stock associated with upper Miocene Mount Kinabalu plutonism. The genesis of the Mamut deposit is discussed based on petrology of the intrusives in the Mount Kinabalu area combined with ore– and alteration–petrography, fluid inclusion and sulfur isotope studies. Groundmass of the adamellite porphyry at Mamut is rich in K which suggests vapor transport of alkaline elements during the mineralizing magmatic process, while the groundmass of the post‐ore “granodiorite” porphyry at Mamut contains small amounts of normative corundum suggesting depletion in alkaline elements at the root zone of the magma column. Sub‐dendritic tremolitic amphibole rims on hornblende phenocrysts in the Mamut adamellite porphyry suggest interaction between the mineralizing magma and the exsolved fluids. Occurrences of clinopyroxene microphenocrysts and pseudomor‐phic aggregates of shredded biotite and clinopyroxene after hornblende phenocrysts in the barren intrusives imply lower water fugacity and decreasing in water fugacity, respectively. Compositional gap between the core of hornblende phenocrysts and the tremolitic amphibole rims and those in the groundmass of the Mamut adamellite porphyry suggests a decrease in pressure. Higher X_Mg (=Mg/(Mg+Fe) atomic ratio) in the tremolitic amphibole rims in the Mamut adamellite porphyry compared to those of the barren intrusions suggests high oxygen fugacity. High halogen contents of igneous hydrous minerals such as amphiboles, biotite and apatite in the Mamut adamellite porphyry suggest the existence of highly saline fluids during the intrusion and solidification of the mineralizing magma. Fluid inclusions found in quartz veinlet stockworks are characterized by abundant hypersaline polyphase inclusions associated with subordinate amounts of immiscible gaseous vapor. Both Cu and Au are dispersed in disseminated and quartz stockwork ores. Chalcopyrite and pyrrhotite as well as magnetite are the principal ore minerals in the biotitized disseminated ores. Primary assemblage of intermediate solid solution (iss) and pyrrhotite converted to the present assemblage of chalcopyrite and pyrrhotite during cooling. Subsequent to biotitization, quartz veinlet stockworks formed associated with retrograde chlorite alteration. The Cu‐Fe sul–fides associated with stockwork quartz veinlet are chalcopyrite and pyrite. Overlapping Pb and Zn and subsequent Sb mineralizations were spatially controlled by NNE‐trending fractures accompanying the phyllic and advanced argillic alteration envelope. Sulfur isotopic composition of ore sulfides are homogeneous (about +2%) throughout the mineralization stages. These are identical to those of the magmatic sulfides of Mount Kinabalu adamellitic rocks.     

中国氢氟碳化物、全氟化碳和六氟化硫排放源初步估算

通过调研大量资料和统计分析,初步估算出1995年中国氢氟碳化物（HFCs）、全氟化碳（PFCs）和六氟化硫（SF6）这6种温室气体的排放量,分别为2244、2581.2和215t,分别占当年全球排放总量的0.9%、6.45%和3.7%。     

经济层面和技术层面的碳减排研究

相关资料和事实表明,全球气候发生了很大的变化。二氧化碳是温室效应中最重要的温室气体,碳减排工作是缓解温室效应的一项重要措施,为当前科学研究热点之一。本文主要从经济和技术两个方面,较为系统和全面地介绍了当前碳减排方面的研究进展。经济层面的研究,包括数量化模型、碳税机制和碳减排附加效应几个方面。专业技术方面的研究,包括对碳行为的源汇和贮量的计算研究、碳循环研究、以及减少碳排放的工业技术的运用等。文章还简要提出了中国在碳减排研究方面应采取的几点措施。