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1.
In order to understand spatial variations of stable isotope geochemistry in the Quruqtagh basin (northwestern China) in the aftermath of an Ediacaran glaciation, we analyzed carbonate carbon isotopes (δ13Ccarb), carbonate oxygen isotopes (δ18Ocarb), carbonate associated sulfate sulfur (δ34SCAS) and oxygen isotopes (δ18OCAS), and pyrite sulfur isotopes (δ34Spy) of a cap dolostone atop the Ediacaran Hankalchough glacial diamictite at four sections. The four studied sections (YKG, MK, H and ZBS) represent an onshore-offshore transect in the Quruqtagh basin. Our data show a strong paleobathymetry-dependent isotopic gradient. From the onshore to offshore sections, δ13Ccarb values decrease from −2‰ to −16‰ (VPDB), whereas δ18Ocarb values increase from −4‰ to −1‰ (VPDB). Both δ34SCAS and δ34Spy show stratigraphic variations in the two onshore sections (MK and YKG), but are more stable in the two offshore sections (H and ZBS). δ18OCAS values of onshore samples are consistent with terrestrial oxidative weathering of pyrite. We propose that following the Hankalchough glaciation seawater in the Quruqtagh basin was characterized by a strong isotopic gradient. The isotopic data may be interpreted using a three-component mixing model that involves three reservoirs: deep-basin water, surface water, and terrestrial weathering input. In this model, the negative δ13Ccarb values in the offshore sections are related to the upwelling of deep-basin water (where anaerobic oxidation of dissolved organic carbon resulted in 13C-depleted DIC), whereas sulfur isotope variations are strongly controlled by surface water sulfate and terrestrial weathering input derived from oxidative weathering of pyrite. The new data provide evidence for the oceanic oxidation following the Hankalchough glaciation.  相似文献   

2.
Studies of carbonate carbon isotope of loess/paleosol (δ13Ccarb) in the Chinese Loess Plateau (CLP) have shown δ13Ccarb less negative in loess and more negative in paleosol, which is opposite to that of bulk organic matter. Although some mechanisms have been proposed to explain this inconsistency, few studies have been conducted to investigate how carbonate migration could affect the reliability of utilizing δ13Ccarb as an effective indicator. Here, a loess/paleosol profile with a nodule horizon intercalated in the loess layer, located on the southeastern edge of the CLP, was investigated to understand the influence of carbonate eluviation and reprecipitation on δ13Ccarb along the section. The mean grain size and magnetic susceptibility generally conform to the field observed loess/paleosol stratigraphy. However, carbonate content shows distinct differences in the two sides of the nodule horizon, clearly indicating eluviation along the section. The variation of carbon and oxygen isotopic compositions of soil carbonate (δ13CSC and δ18OSC) and nodule carbonate (δ13CNC and δ18ONC) along the profile does not present a clearly meaningful picture. Generally, δ13CSC and δ18OSC have a similar change trend along the profile and are positively correlated, but there is no apparent relationship between δ13CNC and δ18ONC. More importantly, δ18ONC values fall in the range of δ18OSC, whereas δ13CNC values are much more positive than δ13CSC. Detailed analyses of the data indicate migration of carbonate along the profile, which is an important factor that determines that loess/paleosol δ13Ccarb could not be employed as a high-resolution paleovegetational and paleoenvironmental indicator in the CLP, at least on or below the glacial/interglacial scales.  相似文献   

3.
In order to examine the causal relationships between the carbon cycle in a shallow euphotic zone and the environmental changes in a relatively deep disphotic zone at the end-Guadalupian (Middle Permian), isotopic compositions of carbonate carbon (δ13Ccarb) of the Guadalupian–Lopingian (Upper Permian) rocks were analyzed in the Chaotian section in northern Sichuan, South China. By analyzing exceptionally fresh drill core samples, a continuous chemostratigraphic record was newly obtained. The ca. 65 m-thick analyzed carbonate rocks at Chaotian comprise three stratigraphic units, i.e., the Limestone Unit of the Guadalupian Maokou Formation, the Mudstone Unit of the Maokou Formation, and the lower part of the Wuchiapingian (Lower Lopingian) Wujiaping Formation, in ascending order. The Limestone Unit of the Maokou Formation is characterized by almost constant δ13Ccarb values of ca. +4‰ followed by an abrupt drop for 7‰ to −3‰ in the topmost part of the unit. In the Mudstone Unit of the Maokou Formation, the δ13Ccarb values are rather constant around +2‰, although distinct three isotopic negative excursions for 3‰ from ca. +2 to −1‰ occurred in the upper part of the unit. In the lower part of the Wujiaping Formation, the δ13Ccarb values monotonously increase for 5‰ from ca. 0 to +5‰. The present data newly demonstrated four isotopic negative excursions in the topmost part of the Maokou Formation in the Capitanian (Late Guadalupian) at Chaotian. It is noteworthy that these negative excursions are in accordance with the emergence of an oxygen-depleted condition on the relatively deep disphotic slope/basin on the basis of litho- and bio-facies characteristics. They suggest multiple upwelling of oxygen-depleted waters with dissolved inorganic carbon of relatively low carbon isotope values along the continental margin, from the deeper disphotic slope/basin to the shallower euphotic shelf, slightly before the end-Guadalupian extinction. Although the negative excursions at Chaotian are apparently correlated with the previously proposed large negative excursion in the middle Capitanian in South China, the age difference according to the biostratigraphic constraints clearly exclude this interpretation. The isotopic negative excursions at Chaotian are unique and no similar isotopic signal in the same period has been reported elsewhere. The multiple upwelling of oxygen-depleted waters onto the euphotic shelf may have represented local phenomena that occurred solely around northwestern South China.  相似文献   

4.
Carbon isotope chemostratigraphy has been used worldwide for stratigraphic correlation.In this study,δ13Ccarb values are estimated for the Early Cambrian Sugaitebulake section in the Tarim Basin,Xinjiang Autonomous Region,China.As a result,one positive and two negative carbon isotope excursions in the studied section were iden-tified.The δ13Ccarb values reached the maximum negative excursion(N1:-12.39‰) at the basal of the Yuertusi For-mation,and then increased to P1.After P1,δ13Ccarb values sharply decreased to about-7.06‰(N2) in the studied section.The pattern of δ13Ccarb in the Early Cambrian is comparable to the synchronous records of other sections,such as the Laolin section,the Xiaotan section and the Anjiahe section of the Yangtze Platform.It is concluded that the Early Cambrian Yuertusi Formation from the Tarim Basin is within the Nemakit-Daldynian stage,and the lower strata of the Yuertusi Formation may belong to the Zhujiaqing Formation(Meishucun Formation) of the Yangtze Platform.The Ediacaran/Cambrian boundary of the Tarim Block should be located in cherts and phosphorites suc-cessions at the basal of the Yuertusi Formation.The δ13Ccarb negative excursion N1 is just across the PC/C boundary,and may be related to certain biomass extinction due to anoxic sedimentary environment,transgression and/or the oceanic overturn.The second δ13Ccarb negative excursion N2 may account for the sea-level falling in the Early Cam-brian.  相似文献   

5.
Isotopic compositions of organic (δ13C-Corg) and carbonate (δ13C-Ccarb) carbon were analyzed in the particulate matter (hereafter, particulates) and sediments from the North and Middle Caspian basins. Isotopic composition of Corg was used for assessing proportions of the allochthonous and autochthonous organic matter in the particulates. Difference between the δ13C-Corg values in surface sediments and particulates is explained by the aerobic and anaerobic diagenetic transformations. Isotopic composition of Corg in sediments may be used as a tool for reconstructing the Quaternary transgressive-regressive history of the Caspian Sea.  相似文献   

6.
The latest Permian was a time of major change in ocean chemistry, accompanying the greatest mass extinction of the Phanerozoic. To examine the nature of these changes, samples from two well-studied marine sections that span the Permian-Triassic boundary have been analyzed: the Meishan and Shangsi sections located in Southern China. Isotopic analysis of the carbonate-associated sulfate in these samples provides a detailed record of several isotopic shifts in δ34SCAS approaching and across the PTB, ranging from +30 to −15‰ (VCDT), with repeated asynchronous fluctuations at the two locations. We interpret the patterns of isotopic shifts, in conjunction with other data, to indicate a shallow unstable chemocline overlying euxinic deep-water which periodically upwelled into the photic zone. These chemocline upward excursion events introduced sulfide to the photic zone stimulating a bloom of phototrophic sulfur oxidizing bacteria. We hypothesize that elemental sulfur globules produced by these organisms and 34S-depleted pyrite produced in the euxinic water column were deposited in the sediment; later oxidation led to incorporation as CAS. This created the large changes to the δ34SCAS observed in the latest Permian at these locations.  相似文献   

7.
Carbon and oxygen isotope records for Shangsi Section in Northwest Sichuan Basin, South China can help investigating depositional environments and processes, including the burial rate and possible contribution of hydrothermal events. Samples from the lower Chihsian Formation show δ13CPDB and δ18OPDB values close to those of typical marine limestone. However, the overlying Permian middle-upper Chihsian, Wujiaping, and Maokou Formation samples reveal negative δ18OSMOW values and strong positive δ13CPDB values. These indicate high biological productivity and rapid burial of organic carbon. Samples from the Dalong Formation present both negative δ13CPDB and negative δ18OPDB values, which are quite different from the underlying Permian strata. These abnormal carbon and oxygen isotope characteristics in the Dalong Formation may suggest that hydrothermal processes contributed to deposition.  相似文献   

8.
《Gondwana Research》2014,25(3-4):1276-1282
Concentrations of total organic matter (TOC), carbon isotopic compositions of carbonate and organic matter (δ13Ccarb, δ13Corg), and sulfur isotopic compositions of carbonate associated sulfate (δ34Ssulfate) across the Guadalupian–Lopingian (G–L) boundary were analyzed from identical samples of Tieqiao section, Laibin, Guangxi province, South China. The δ13Ccarb values show a positive excursion from − 0.45‰ to the peak of 3.80‰ in the Laibin limestone member of the Maokou Formation, followed by a drastic drop to − 2.60‰ in the lowest Heshan formation, then returned to about 1.58‰. Similar to the trends of the δ13Ccarb values, Δ13Ccarb–org values also show a positive excursion followed by a sharp negative shift. The onset of a major negative carbon isotope excursion postdates the end Guadalupian extinction that indicates subsequent severe disturbance of the ocean–atmosphere carbon cycle. The first biostratigraphic δ34Ssulfate values during the G–L transition exhibit a remarkable fluctuation: a dramatic negative shift followed by a rapid positive shift, ranging from 36.88‰ to − 37.41‰. These sulfate isotopic records suggest that the ocean during the G–L transition was strongly stratified, forming an unstable chemocline separating oxic shallow water from anoxic/euxinic deep water. Chemocline excursions, together with subsequent rapid transgression and oceanic anoxia, were likely responsible for the massive diversity decline of the G–L biotic crisis.  相似文献   

9.
Carbonate concretions can form as a result of organic matter degradation within sediments. However, the ability to determine specific processes and timing relationships to particular concretions has remained elusive. Previously employed proxies (e.g., carbon and oxygen isotopes) cannot uniquely distinguish among diagenetic alkalinity sources generated by microbial oxidation of organic matter using oxygen, nitrate, metal oxides, and sulfate as electron acceptors, in addition to degradation by thermal decarboxylation. Here, we employ concentrations of carbonate-associated sulfate (CAS) and δ34SCAS (along with more traditional approaches) to determine the specific nature of concretion authigenesis within the Miocene Monterey Formation.Integrated geochemical analyses reveal that at least three specific organo-diagenetic reaction pathways can be tied to concretion formation and that these reactions are largely sample-site specific. One calcitic concretion from the Phosphatic Shale Member at Naples Beach yields δ34SCAS values near Miocene seawater sulfate (～+22‰ VCDT), abundant CAS (ca. 1000 ppm), depleted δ13Ccarb (～?11‰ VPDB), and very low concentrations of Fe (ca. 700 ppm) and Mn (ca. 15 ppm)—characteristics most consistent with shallow formation in association with organic matter degradation by nitrate, iron-oxides and/or minor sulfate reduction. Cemented concretionary layers of the Phosphatic Shale Member at Shell Beach display elevated δ34SCAS (up to ～+37‰), CAS concentrations of ～600 ppm, mildly depleted δ13Ccarb (～?6‰), moderate amounts of Mn (ca. 250 ppm), and relatively low Fe (ca. 1700 ppm), indicative of formation in sediments dominated by sulfate reduction. Finally, concretions within a siliceous host at Montaña de Oro and Naples Beach show minimal CAS concentrations, positive δ13C values, and the highest concentrations of Fe (ca. 11,300 ppm) and Mn (ca. 440 ppm), consistent with formation in sediments experiencing methanogenesis in a highly reducing environment. This study highlights the promise in combining CAS analysis with more traditional techniques to differentiate among diagenetic reactions as preserved in the geologic record and shows potential for unraveling subsurface biospheric processes in ancient samples with a high degree of specificity.  相似文献   

10.
This study is a comprehensive, stable isotope survey of the marine carbonate-dominated, upper Paleo- to lower Neoproterozoic stratigraphy of Jixian County, China. Carbonate-associated sulfate (CAS) was extracted and measured for δ34SCAS using the same samples analyzed for δ13Ccarbonate. This integrated proxy approach is a step towards a more comprehensive picture of secular variation in the composition of Proterozoic seawater. We specifically sampled marine carbonate intervals from the lower section of the Chuanlinggou Formation, Changcheng Group (ca. 1700 Ma) to the top of the Jingeryu Formation, Qingbaikou Group (ca. 800 Ma). δ13Ccarbonate values are mostly negative in the upper Paleoproterozoic Changcheng Group, with an ascending trend from −3‰ to 0‰. We observed variation of approximately 0 ± 1‰ in the Mesoproterozoic Jixian Group, and positive values of +2 ± 2‰ characterize the lower Neoproterozoic Qingbaikou Group. Stratigraphic variations in δ34SCAS are more remarkable in their ranges and magnitudes, including conspicuously high values exceeding +30‰ in the three intervals at ca. 1700 Ma, 1300-1100 Ma, and 1000-900 Ma. In the Changcheng Group, δ34SCAS values are typically higher than +25‰, with only a few values of less than +15‰. In contrast, most of the data spanning from the Mesoproterozoic Tieling Formation of the Jixian Group to the lower Neoproterozoic Jingeryu Formation of the Qingbaikou Group are highly variable between +10‰ and +25‰, with some values exceeding +25‰.In the late Paleoproterozoic (1700-1600 Ma), a >10‰ decrease in δ34SCAS and ∼3‰ increase in δ13Ccarbonate are coincident with, and likely related to, the breakup of Columbia, a supercontinent that predated Rodinia. Carbon and sulfur isotope data from the Mesoproterozoic, when global tectonic activity was comparatively weaker, fall mostly in the ranges of +15 ± 10‰ and 0 ± 1‰, respectively, but fluctuations of >20‰ for δ34SCAS and >3‰ for the δ13Ccarbonate at ca. 1450-1400 Ma may reflect subduction and large-scale magmatic activity in island arcs marking the end of Columbia breakup. From the late Mesoproterozoic (ca. 1300-1100 Ma) to the early Neoproterozoic (ca. 800 Ma), the δ13C and δ34S of seawater increased gradually with increasing variability. Most impressive areδ34SCAS values that exceed +30‰ in two intervals at ca. 1300-1100 Ma and ca. 1000-900 Ma, which may reflect the assembly and early breakup of Rodinia. Although gaps in the record remain, and studies of even higher resolution are warranted, our results suggest that changes in paleoceanographic conditions linked to global tectonics strongly influenced the biogeochemical cycles of C and S. Furthermore, periods of the Proterozoic previously noted for their isotopic invariability show clear isotopic expressions of this tectonic activity.  相似文献   

11.
In order to better understand the paleoceanographic sedimentary environment of the Lower Cambrian black shales extensively distributed in South China, outcropped along the present southern margin of the Yangtze Platform with a width of ca. 200-400 km and a length of more than 1500 km, we present new paired δ13C data on carbonates (δ13Ccarb) and associated organic carbon (δ13Corg) and δ34Spy data on sedimentary pyrite in black shales from three sections (Ganziping, Shancha and Xiaohekou) located in NW Hunan, China. In these sections, a total of 82 Lower Cambrian black shale samples have δ13Ccarb values ranging from -4.0‰ to 1.7‰ with an average value of -2.1‰, and δ13Corg values between -34.9‰ and -28.8‰, averaging -31.9‰. The ?34Spy values of 16 separated sedi-mentary pyrite samples from the black shales vary between +10.2‰ and +28.7‰ with an average value of +19.5‰, presenting a small isotope fractionation between seawater sulfate and sedimentary sulfide. The model calculation based on credible data from the paired analyses for δ13Ccarb and δ13Corg of 11 black shale samples shows a high CO2 concentration in the Early Cambrian atmosphere, about 20 times higher than pre-industrial revolution values, consis-tent with previous global predictions. The small sulfur isotope fractionation between seawater sulfate and sedimen-tary sulfide in black shales, only 15.5‰ on average, implies a low sulfate level in the Early Cambrian seawater around 1 mmol. In combination with a high degree of pyritization (DOP) in the black shales, it is suggested that sul-fidic deep-ocean water could have lingered up to the earliest Cambrian in this area. The black shale deposition is envisaged in a stratified marine basin, with a surface euphotic and oxygenated water layer and sulfidic deeper water, controlled by a continental margin rift.  相似文献   

12.
High resolution carbon isotope analyses of carbonate and organic carbon from Meishan, South China showed that the variation of δ13Ccarb is marked by three large positive excursions during the Changhsingian (end-Permian). Carbon isotope stratigraphy during this stage shows three cyclic intervals in δ13Ccarb, with two cycles corresponding to the lower (Paleofusulinid minima Zone) and one corresponding to the upper Changhsingian (P. sinensis Zone). The large positive δ13Ccarb excursions indicate episodes of enhanced burial of isotopically light or-ganic carbon, presumably in response to deep-water anoxia episodically extending into shallow water with the rise of sea level. The organic carbon during the Changhsingian is distinguished into two groups, and the δ13Corg of each group parallels (separately) the more detailed profile of δ13Ccarb, strongly showing that the values of fractionation Δ13Ccab-org remain relatively constant, with only two intervals with anomaly. The enhanced fractionation Δ13Ccab-org with large negative δ13Corg excursions apparently indicates significant inputs from sulfide-oxidizing bacteria and green sulfur bacteria, notably at bed 24 just predating mass extinction. Our evidence appears to support that the ex-tended euxinic water is possible for the main pulse of mass extinction at the end-Permian.  相似文献   

13.
This paper investigates kerogen carbon isotopes, the difference between carbonate and kerogen carbon isotopes (Δ13Ccarb-kero = δ 13Ccarb − δ 13Ckero) and the difference between carbonate and n-C19 alkane compound-specific carbon isotopes (Δ13Ccarb-n-C19 = δ 13Ccarb − δ 13C n-C19) during the Permian–Triassic transition at Meishan, South China. The results show that kerogen carbon isotopes underwent both gradual and sharp shifts in beds 23–25 and 26–29, respectively. The differences between carbonate and organic carbon isotopes, both the Δ13Ccarb-kero and Δ13Ccarb-n-C19, which are mainly affected by CO2-fixing enzyme and pCO2, oscillated frequently during the Permian–Triassic transition. Both the variations of Δ13Ccarb-n-C19 and Δ13Ccarb-kero coupled with the alternation between cyanobacteria and green sulfur bacteria indicated by biomarkers. The episodic low values of Δ13Ccarb-n-C19 corresponded to episodic blooms of green sulfur bacteria, while the episodic high values of Δ13Ccarb-n-C19 corresponded to episodic blooms of cyanobacteria. The relationships between the variation of carbon isotopes and biota show that the microbes which flourished after the extinction of macroorganism affected the carbon isotope fractionation greatly. Combining the carbon isotope compositions and the pattern of size variation of the conodont Neogondolella, this paper supposes that anoxia of the photic zone at bed 24 was episodic and it would be caused by the degradation of terrigenous organic matters by sulfate reducing bacteria in the upper water column. Considered together with results from previous research, the high resolution variation of the biogeochemistry presents the sequence of the important geo-events during the Permian–Triassic crisis.  相似文献   

14.
The 2.33–2.06 Ga positive δ13Ccarb excursion, associated with environmental change and the breakup of the Kenorland or Superia supercontinent, is called the Lomagundi or Jatulian Event or Great Oxidation Event, and has been reported in many Early Precambrian cratons, but not yet in the Sino-Korean craton. The Guanmenshan Formation of the Liaohe Group occurs in the northeastern part of the Sino-Korean craton. δ13Ccarb and δ18O values in 42 samples from this formation range from 3.5–5.9‰ (V-PDB), and 15.4–24.8‰ (V-SMOW), respectively, showing a clear positive δ13Ccarb excursion that characterizes the Lomagundi Event. Thirty-five of the 42 samples with less hydrothermal alteration have higher δ13Ccarb and δ18Ocarb values than the other 7 samples obviously affected by fluid flow, confirming that it was fluid flow that reduced the δ13Ccarb and δ18Ocarb values. This positive δ13Ccarb excursion places deposition of the Guanmenshan Formation within the age range of 2.33–2.06 Ga.  相似文献   

15.
Large carbon cycle perturbations associated with the Middle Permian (Capitanian) mass extinction have been widely reported, but their causes and timing are still in dispute. Low resolution carbon isotope records prior to this event also limit the construction of a Middle Permian chemostratigraphic framework and global or local stratigraphic correlation, and hence limit our understanding of carbon cycle and environmental changes. To investigate these issues, we analyzed the 13Corg values from the Middle Permian chert-mudstone sequence (Gufeng Formation) in the Lower Yangtze deep-water basin (South China) and compared them with published records to build a chemostratigraphic scheme and discuss the underlying environmental events. The records show increased δ13Corg values from late Kungurian to early Guadalupian, followed by a decrease to the late Wordian/early Capitanian. The early-mid Capitanian was characterized by elevated δ13Corg values suggesting the presence of the “Kamura Event”: an interval of heavy positive values seen in the δ13Ccarb record. We propose that these heavy Capitanian δ13C values may be a response to a marked decline in chemical weathering rates on Pangea and associated reduction in carbonate burial, which we show using a biogeochemical model. The subsequent negative δ13C excursion seen in some carbonate records, especially in shallower-water sections (and in a muted expression in organic carbon) coincide with the Capitanian mass extinction may be caused by the input of isotopically-light carbon sourced from the terrestrial decomposition of organic matter.  相似文献   

16.
The redox sensitive elements, molybdenum (Mo) and uranium (U), in marine sediments from the latest Permian Dalong (大隆) Formation at the Shangsi (上寺) Section, Northeast Siehuan (四川), South China, were analyzed by inductively coupled plasma mass spectrometry (ICP-MS) to determine their response to a range of redox conditions, and to estimate the organic carbon burial rate. On the basis of the correlation between authigenic Mo abundance and organic carbon content in modern oceans, the organic carbon burial rates were calculated for the rocks at Dalong Formation, ranging from 0.48-125.83 mmol/(m2-d), which shows a larger range than the mineralization rate of organic carbon at the continental margins (1.6-4.23 mmol/(m2.d)). The Zr-normalized Mo and U abundances show large fluctuations in the entire section. The maxima of Zr-normalized Mo abundance and thus the maxima of the organic carbon burial rates were observed at the interval between the 155th and 156th beds (404-407 m above the base of Middle Permian). A decrease (the minimum) in U/Mo ratios is present in this interval. It is speculated that the oxygen-limited conditions and ultimately anoxia or euxinia may develop within this depth interval. In contrast, an enhanced enrichment of Zr-normallzed U abundance is found, in association with less enrichment in Zr-normnllzed Mo abundance in the interval from the I51st to 154th beds (395-404 m above the base of Middle Permian), inferring the dominance of a suboxic/anoxic depositional condition (denitrifying condition), or without free H2S. The presence of small quantities of dissolved oxygen may have caused the solubilization and loss of Mo from sediments. It is proposed that the multiple cycles of abrupt oxidation and reduction due to the upwelllng at this interval lead to the enhanced accumulation of authigenic U, but less enrichment of Mo. A decrease in the contents of U, Mo, and TOC is found above the 157th bed (407 m above the base of Middle Permian), in association with the enhanced U/Mo ratio, suggesting the overall oxic conditions at the end of the Dalong Formation.  相似文献   

17.
The strongly deformed Middle Devonian-Lower Carboniferous metasedimentary-volcanic successions of the Trevone Basin (SW England) contain stratiform and Pb-Sb vein deposits that reveal a wide variation in δ34S and δ13C, reflecting mineral deposition during diagenesis, regional metamorphism and basin inversion. Pre-Variscan metasedimentary sulphide (δ34S=−33.7 to −26.7‰) and metabasite sulphide (δ34S=+4.0 to +10.8‰) suggest two accessible source reservoirs for sulphur which were available for Sb-As-(Au) and Pb-Zn-(Ag) mineralisation (δ34S=−3.3 to −15.0‰) during late Variscan semiductile-brittle shear. On the basis of pressure-corrected fluid inclusion temperatures, the calculated composition of fluid sulphur reveals an enrichment in δ34SH2S in the individual vein parageneses and depletion of the fluid sulphur reservoir during evolution of the vein systems. Carbonates in the same veins are partly contemporaneous with Pb-Sb mineralisation and late tensional deformation; their isotopic composition (δ13C=−3.2 and −13.4‰) appears strongly influenced by the host formation. Fluid inclusions in post-tensional quartz show a marked reduction in CO2, suggesting that episodes of CO2 degassing in response to punctuated reductions in pressure during uplift and brittle deformation was an important mechanism for vein carbonation. An origin for the Pb-Sb mineralisation involving local remobilisation of sulphur from the mixed metasedimentary-volcanic succession is probably inseparable from processes connected with Variscan metamorphism and deformation. Although the N Cornish Variscan deformation is part of a spatially large-scale event, the isotopic evidence suggests compartmentalisation of sulphur and carbon isotope features and short distances between sources and sinks. Received: 15 August 1998 / Accepted: 8 October 1999  相似文献   

18.
Bulk δ 34Srock values, sulfur contents, and magnetic susceptibility were determined for 12 gold-related granitoid intrusions in southwestern New Brunswick, the Canadian Appalachians. The sulfur isotope compositions of sulfide minerals in some of the granitoid samples were also analyzed. This new dataset was used to characterize two distinctive groups of granitoids: (1) a Late Devonian granitic series (GS) and (2) a Late Silurian to Early Devonian granodioritic to monzogranitic series (GMS). The GS rocks have a large range in δ 34S values of −7.1‰ to +13‰ with an average of 2.2 ± 5.0‰ (1σ), low bulk-S contents (33 to 7,710 ppm) and low magnetic susceptibility values (<10−4 SI), consistent with reduced ilmenite-series granites. The GMS rocks have a relatively narrower variation in δ 34S values of −4.4‰ to +7.3‰ with an average 1.2 ± 2.9‰ but with larger ranges in bulk-S contents (45 to 11,100 ppm) and high magnetic susceptibility values (>10−3 SI), indicative of oxidized magnetite-series granites. The exceptions for the GMS rocks are the Lake George granodiorite and Tower Hill granite that display reduced characteristics, which may have resulted from interaction of the magmas forming these intrusions with graphite- or organic carbon-bearing sedimentary rocks. The bulk δ 34S values and S contents of the GMS rocks are interpreted in terms of selective assimilation–fractional crystallization (SAFC) processes. Degassing processes may account for the δ 34S values and S contents of some GS rocks. The characteristics of our sulfur isotope and abundance data suggest that mineralizing components S and Au in intrusion-related gold systems are dominantly derived from magmatic sources, although minor contaminants derived from country rocks are evident. In addition, the molar sulfate to sulfide ratio in a granitic rock sample can be calculated from the δ 34Srock value of the whole-rock sample and the δ 34Ssulfide (or δ 34Ssulfate) value of sulfide and/or sulfate mineral in the sample on the basis of S-isotope fractionation and mass balance under the condition of magmatic equilibrium. This may be used to predict the speciation of sulfur in granitic rocks, which can be a potential exploration tool for intrusion-related gold systems.  相似文献   

19.
Strontium and carbon isotope stratigraphy was applied to a 202 m-thick shallow marine carbonate section within the Late Jurassic Bau Limestone at the SSF quarry in northwest Borneo, Malaysia, which was deposited in the western Palaeo-Pacific. Strontium isotopic ratios of rudist specimens suggest that the SSF section was formed between the latest Oxfordian (155.95 Ma) and the Late Kimmeridgian (152.70 Ma), which is consistent with previous biostratigraphy. The δ13Ccarb values of bulk carbonate range from −0.10 to +2.28‰ and generally show an increasing upward trend in the lower part of the section and a decreasing upward trend in the upper part of the section. A comparable pattern is preserved in the δ13Corg isotope record. Limestone samples of the SSF section mainly preserve the initial δ13Ccarb values, except for the interval 84–92 m, where an apparent negative anomaly likely developed as a result of meteoric diagenesis. Comparing with the Tethyan δ13Ccarb profile, a negative anomaly in the lower SSF section can be correlated with the lowered δ13C values around the Oxfordian/Kimmeridgian boundary. In addition, δ13Ccarb values of the Bau Limestone are generally ∼1‰ lower than the Tethyan values, but comparable with the values reported from Scotland and Russia, located in Boreal realm during the Late Jurassic. This suggests that either the Tethyan record or the other records have been affected by the δ13C values of regionally variable dissolved inorganic carbon (DIC). The Late Jurassic δ13CDIC values are thought to have been regionally variable as a result of their palaeoceanographic settings. This study shows that δ13C chemostratigraphy of the Palaeo-Pacific region contributes to an improved understanding of global carbon cycling and oceanography during this time period.  相似文献   

20.
A major late Paleozoic depocentre, the Sverdrup Basin, Canadian High Arctic, has been largely left out of the latest Permian extinction debate, as early workers presumed Middle to Late Permian strata were absent. Basin-scale sequence-stratigraphic and chemostratigraphic correlations indicate Late Permian strata are only missing on the basin margins, where they were removed by sub-Triassic erosion, whereas continuous deposition is recorded in the basin centre. The varying degree of sub-Triassic erosion has significant impact on the carbon-isotope record across the Latest Permian Extinction event, where both the apparent rate and magnitude of carbon-isotope shift vary as a function of basin position. The intrabasin variability in apparent δ13Corg shift across the event is equivalent to that observed globally. In contrast to the abrupt isotope shifts recorded on the basin margin, similar to many records reported globally, the basin centre section shows a systematic shift associated with the Latest Permian Extinction. The Earth likely underwent a prolonged period of increasing environmental stress leading up to the event.  相似文献   

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