Mass extinction and Pangea integration during the Paleozoic-Mesozoic transition

The greatest Phanerozoic mass extinction happened at the end-Permian to earliest Triassic.About 95%species,82%genera,and more than half families became extinct,constituting the sole macro-mass extinction in geological history.This event not only caused the great extinction but also destroyed the 200 Myr-long Paleozoic marine ecosystem,prompted its transition to Mesozoic ecosystem,and induced coal gap on land as well as reef gap and chert gap in ocean.The biotic crisis during the Paleozoic-Mesozoic transition was a long process of co-evolution between geospheres and biosphere.The event sequence at the Permian-Triassic boundary(PTB)reveals two-episodic pattern of rapidly deteriorating global changes and biotic mass extinction and the intimate relationship between them.The severe global changes coupling multiple geospheres may have affected the Pangea integration on the Earth’s surface spheres,which include:the Pangea integration→enhanced mountain height and basin depth,changes of wind and ocean current systems;enhanced ocean basin depth→the greatest Phanerozoic regression at PTB,disappearance of epeiric seas and subsequent rapid transgression;the Pangea integration→thermal isolation effect of continental lithosphere and decrease of mid-ocean ridges→development of continental volcanism;two-episode volcanism causing LIPs of the Emeishan Basalt and the Siberian Trap(259–251 Ma)→global warming and mass extinction;continental aridification and replacement of monsoon system by latitudinal wind system→destruction of vegetation;enhanced weathering and CH4emission→negative excursion ofδ13C;mantle plume→crust doming→regression;possible relation between the Illawarra magnetic reversal and the PTB extinction,and so on.Mantle plume produced the Late Permian LIPs and mantle convection may have caused the process of the Pangea integration.Subduction,delamination,and accumulation of the earth’s cool lithospheric material at the"D"layer of CMB started mantle plume by heat compensation and disturbed the outer core thermo-convection,and the latter in turn would generate the mid-Permian geomagnetic reversal.These core and mantle perturbations may have caused the Pangea integration and two successive LIPs in the Permian,and probably finally the mass extinction at the PTB.     

Geological event sequences of the Permian-Triassic transition recorded in the microfacies in Meishan section

The microfacies sequence in the key interval of Beds 24―29 of the Meishan section comprehensively recorded the geological events during the Permian-Triassic transition, including the anoxia, storm disturbance, hard-ground/firm-ground form, volcanic eruption, weathering input, and microbialite development. This investigation of event sequences on the microfacies provided synthetically some clues to clarifying the previously proposed mechanisms of the end-Permian extinction. The deposit succession in Bed 24 o...     

The shift of biogeochemical cycles indicative of the progressive marine ecosystem collapse across the Permian-Triassic boundary: An analog to modern oceans

Global warming, the most severe faunal mass extinction and the shift of biogeochemical cycles were observed in the ocean across the Permian-Triassic boundary about 252 million years ago, providing an analog to understanding the modern oceans. Along with the progressive global warming, the biogeochemical cycle was documented to show a shift from the decoupled processes of carbon, nitrogen and sulfur prior to the mass extinction to the coupled biogeochemical processes during faunal mass extinction. The coupled biogeochemical cycle was further observed to shift from the coupled C-N processes during the first episode of the faunal mass extinction to the coupled C-N-S processes during the second episode, diagnostic of the progressive development of more deteriorated marine environmental conditions and the more severe biotic crisis across the Permian-Triassic boundary. The biogeochemical cycles could thus be an indication to the progressive collapse of marine ecosystems triggered by the global warming in Earth history. In modern oceans, the coupled C-N cycle triggered by the global warming was observed in some regions. If these local C-N processes develop and expand to the global oceans, the coupled C-N-S processes might be brought into existence and the marine ecosystems are inevitable to suffer from complete collapse as observed at 252 million years ago.     

Timing of the terrestrial Permian-Triassic boundary biotic crisis: Implications from U-Pb dating of authigenic zircons

The Late Permian to Early Triassic transition represents one of the most important Phanerozoic mass extinction episodes. The cause of this event is still in debate between catastrophic and gradual mechanisms. This study uses the U-Pb method on zircons from the uppermost Permian/lowermost Triassic clay deposits at Chahe (Guizhou Province, SW China) to examine time constraints for this event. The results of both this and previous studies show that the ages of Bed 68a and 68c (the upper clay bed of the terrestrial Permian-Triassic boundary (PTB)) respectively are 252.6±2.8 and 247.5±2.8 Ma. This age (within the margin of error) almost accords with the upper clay bed (Bed 28) age of Meishan and the eruption age of Tunguss Basalt, and is so far the most accurate age obtained from terrestrial PTB. The claystone of Bed 68 was formed in the earliest Triassic. The biotic crisis occurred at nearly the same time in terrestrial and marine environments during Permian-Triassic interval; however the extinction patterns and processes are different. The extinction pattern of the terrestrial plants shows a major decline at the PTB after long-term evolution, followed by a retarded extinction of the relicts in the earliest Triassic.     

Stratification and mixing of a post-glacial Neoproterozoic ocean: Evidence from carbon and sulfur isotopes in a cap dolostone from northwest China

To improve our knowledge about the geochemical and environmental aftermath of Neoproterozoic global glaciations, we analyzed stable isotopes (δ¹³C, δ¹⁸O, δ³⁴S) and elemental concentrations (Ca, Mg, S, Sr, Fe, and Mn) of the ～ 10-m-thick Zhamoketi cap dolostone atop the Tereeken diamictite in the Quruqtagh area, eastern Chinese Tianshan. Available chemostratigraphic data suggest that the Tereeken diamictite is probably equivalent to the Marinoan glaciation. Our new data indicate that organic and carbonate carbon isotopes of the Zhamoketi cap dolostone show little stratigraphic variations, averaging ? 28.2‰ and ? 4.6‰, respectively. In contrast, sulfur isotopes show significant stratigraphic variations. Carbonate associated sulfate (CAS) abundance decreases rapidly in the basal cap dolostone and δ³⁴S_CAS composition varies between + 9‰ and + 15‰ in the lower 2.5 m. In the overlying interval, CAS abundance remains low while δ³⁴S_CAS rises ～ 5‰ and varies more widely between + 10‰ and + 21‰. The range of δ³⁴S_py of the cap dolostone overlaps with that of δ³⁴S_CAS, but direct comparison shows that δ³⁴S_py is typically greater than δ³⁴S_CAS measured from the same samples. Hypotheses to explain the observations must account for both the remarkable sulfur isotope enrichment of pyrites and the inverse fractionation. We propose that CAS and pyrite were derived from two isotopically distinct reservoirs in a chemically stratified basin or a basin with a sulfate minimum zone. In this model, CAS was derived from shallow, oxic surface waters with moderate sulfate concentration and depleted in ³⁴S due to the post-glacial influx of sulfur from continental weathering. In contrast, pyrite was derived from anoxic bottom waters (or a sulfate minimum zone) with low sulfate concentration and ³⁴S enrichment due to long-term syn-glacial sulfate reduction. The rapid shift in CAS abundance and sulfur isotope composition within the cap dolostone is interpreted to reflect the mixing of the two reservoirs after initial deglaciation. Comparison with other post-Marinoan cap carbonates shows significant spatial heterogeneity in δ³⁴S_CAS, which together with strong temporal variation in δ³⁴S_CAS, points to generally low sulfate concentrations in post-Marinoan oceans.     

On the effect of low-temperature seawater-basalt interaction on the distribution of sulfur in oceanic crust,layer 2

A detailed geochemical-petrological examination of layer 2 basalts recovered during Leg 37 of the DSDP has revealed that the original distribution, form and abundance of igneous sulfide have been profoundly altered during low-grade oxidative diagenesis. The net result appears to have been a rather pervasive remobilization of igneous sulfide to form secondary pyrite accompanied by a bulk loss of sulfur equivalent to about 50–60% of the original igneous value, assuming initial saturation. It is suggested that during infiltration of seawater into the massive crystal-line rock, igneous sulfide has experienced pervasive oxidation, under conditions of limited oxidation potential, to form a series of unstable, soluble sulfur species, primarily in the form of SO₃^2? and S₂O₃^2?. Spontaneous decomposition of these intermediate compounds through disproportionation has resulted in partial reconstitution of the sulfur as secondary pyrite and the generation of SO₄^2? ion, which, due to its kinetic stability, has been lost from the basalt system and ultimately transferred to the ocean. This model not only satisfies the geochemical and petrological observations but also provides a suitable explanation for the highly variable δ³⁴S values which characterize secondary sulfides in deep ocean floor basalts.     

Correlation between the bedded chert sequence of southwest Japan and δ13C excursion of carbonate sequence, and its significance to the Permian-Triassic mass extinction

Abstract Stratigraphic productivity variations of radiolarians below the Permian-Triassic boundary are examined with Ishiga Diagrams in bedded chert sequences of southwest Japan. The diagrams of two different outcrops, drawn from the thickness variation of chert beds, show common stratigraphic variation, which indicates the diagram is a useful tool for correlation of bedded chert sequence. The common stratigraphic productivity variation is also well correlated to a compiled δ¹³C excursion of shallow carbonate sequences. Bedded chert records a dramatic extinction event in a shallow surface zone of oceans below the Permian-Triassic boundary. The Permian-Triassic mass extinction is divided into three intervals based on the Ishiga Diagrams, the stratigraphic lithological variation of bedded chert sequences, and the δ¹³C curve. The preceding extinction interval in the late Djulfian stage was not as serious an event and the biosphere soon recovered. The event of the main extinction interval commenced in the Dorashamian stage and caused a serious destruction of the biosphere. An event of the aftermath interval during the Early Triassic caused a delay in the recovery from the main extinction interval.     

A summary of sulfur dioxide emission rate measuremnts from Guatemalan volcanoes

Measurements of the sulfur dioxide (SO₂) emission rate from three Guatemalan volcanoes provide data which are consistent with theoretical and laboratory studies of eruptive and shallow magma chamber processes. In particular, unerupted magma makes a major contribution to the measured SO₂ emission rates at Santiaguito, a continuously erupting dacitic volcanic dome. Varying shallow magma convection rates can explain the variations in SO₂ emission rates at Santiaguito. At Fuego, a basaltic volcano currently in repose, SO₂ emission rate measurements are consistent with a high level magma body that is crystallizing and releasing volatiles. At Pacaya, a continuously erupting basaltic volcano, recent SO₂ emission rate measurements support laboratory simulation studies of strombolian eruptions; these studies indicate that the majority of gas escapes during eruptions and little gas escapes between eruptions.Average SO₂ emission rates over the last 20 years for Santiaguito, Fuego and Pacaya are 80, 160 and 260 Mg/d, respectively. On a global scale, these three volcanoes account for 1% of the annual global volcanic output of SO₂. Santiaguito and Pacaya, together, emit 6% of the total annual SO₂ emitted by continuously erupting volcanoes.Even though SO₂ measurements at these volcanoes have been made infrequently and by different investigators, the collective data help to establish a useful baseline by which to judge future changes. A more complete record of SO₂ emission rates from these volcanoes could lead to a better understanding of their eruption mechanisms and reduce the impact of their future eruptions on Guatemalan society.     

Sulfur and carbon isotopic systematics of Guadalupian‐Lopingian (Permian) mid‐Panthalassa: δ34S and δ13C profiles in accreted paleo‐atoll carbonates in Japan

Immediately before the extinction of the end‐Guadalupian (Middle Permian; ca 260 Ma), a significant change to the global carbon cycle occurred in the superocean Panthalassa, as indicated by a prominent positive δ¹³C excursion called the Kamura event. However, the causes of this event and its connection to the major extinction of marine invertebrates remain unclear. To understand the mutual relationships between these changes, we analyzed the sulfur isotope ratio of the carbonate‐associated sulfate (CAS) and HCl‐insoluble residue, as well as the carbon isotope ratio of bulk organic matter, for the Middle‐Upper Permian carbonates of an accreted mid‐oceanic paleo‐atoll complex from Japan, where the Kamura event was first documented. We detected the following unique aspects of the stable carbon and sulfur isotope records. First, the extremely high δ¹³C values of carbonate (δ¹³C_carb) over +5 ‰ during the Capitanian (late Guadalupian) were associated with large isotopic differences between carbonate and organic matter (Δ¹³C = δ¹³C_carb ? δ¹³C_org). We infer that the Capitanian Kamura event reflected an unusually large amount of dissolved organic matter in the expanded oxygen minimum zone at mid‐depth. Second, the δ³⁴S values of CAS (δ³⁴S_CAS) were inversely correlated with the δ¹³C_carb values during the Capitanian to early Wuchiapingian (early Late Permian) interval. The Capitanian trend may have appeared under increased oceanic sulfate conditions, which were accelerated by intense volcanic outgassing. Bacterial sulfate reduction with increased sulfate concentrations in seawater may have stimulated the production of pyrite that may have incorporated iron in pre‐existing iron hydroxide/oxide. This stimulated phosphorus release, which enhanced organic matter production and resulted in high δ¹³C_carb. Low δ³⁴S_CAS values under high sulfate concentrations were maintained and the continuous supply of sulfate cannot by explained only by the volcanic eruption of the Emeishan Trap, which has been proposed as a cause of the extinction. The Wuchiapingian δ³⁴S_CAS–δ¹³C_carb correlation, likely related to low sulfate concentration, may have been caused by the removal of oceanic sulfate through the massive evaporite deposition.     

TOMS measurement of the sulfur dioxide emitted during the 1985 Nevado del Ruiz eruptions

The eruptions of Nevado del Ruiz in 1985 were unusually rich in sulfur dioxide. These eruptions were observed with the Nimbus 7 Total Ozone Mapping Spectrometer (TOMS) which can quantitatively map volcanic sulfur dioxide plumes on a global scale. A small eruption, originally believed to be of phreatic origin, took place on September 11, 1985. However, substantial amounts of sulfur dioxide from this eruption were detected with TOMS on the following day. The total mass of SO₂, approximately 9 ± 3 × 10⁴ metric tons, was deposited in two clouds, one in the upper troposphere, the other possibly at 15 km near the stratosphere.The devastating November 13 eruptions were first observed with TOMS at 1150 EST on November 14. Large amounts of sulfur dioxide were found in an arc extending 1100 km from south of Ruiz northeastward to the Gulf of Venezuela and as an isolated cloud centered at 7°N on the Colombia-Venezuela border. On November 15 the plume extended over 2700 km from the Pacific Ocean off the Colombia coast to Barbados, while the isolated mass was located over the Brazil-Guyana border, approximately 1600 km due east of the volcano. Based on wind data from Panama, most of the sulfur dioxide was located at 10–16 km in the troposphere and a small amount was quite likely deposited in the stratosphere at an altitude above 24 km.The total mass of sulfur dioxide in the eruption clouds was approximately 6.6 ± 1.9 × 10⁵ metric tons on November 14. When combined with quiescent sulfur dioxide emissions during this period, the ratio of sulfur dioxide to erupted magma from Ruiz was an order of magnitude greater than in the 1982 eruption of El Chichon or the 1980 eruption of Mount St. Helens.     

Secular geomagnetic variations and volcanic pulses in the Permian-Triassic traps of the Norilsk and Maimecha-Kotui provinces

Detailed paleomagnetic studies have shown that the effusive Permian-Triassic traps in the Kotui River valley were formed as the result of volcanic activity, which occurred in the form of volcanic pulses and individual eruptions with net duration of at most 7000–8000 years, excluding the periods of volcanic quiescence. According to the analysis of the paleomagnetic data earlier obtained by Heunemann and his coauthors [2004b] on the Abagalakh and Listvyanka sections in the Norilsk region, those geological units were formed during 25 volcanic pulses and separate eruptions, which all lasted up to 8000 years altogether, whereas the total time of formation (including the periods of volcanic quiescence) exceeded 10000–100000 years for the Norilsk section and was probably a bit shorter for the Kotui section. Comparison of the positions of virtual geomagnetic poles calculated for the Norilsk and the Kotui sections provides no grounds to suggest that these sections were formed at different geological times. The scatter in the positions of the virtual geomagnetic poles (VGP) for the directional groups and individual directions (58 altogether) jointly for the two sections (more than 160 lava flows) indicates that the secular geomagnetic variations at the Permian-Triassic boundary had similar amplitudes to those that occurred in the past 5 Ma.     

Sulfur isotope ratios of Icelandic lava incrustations and volcanic gases

Sulfur isotope ratios were measured in eight lava incrustations and three volcanic gas samples and their corresponding lava flows. The lava incrustations of sulfate composition are from five recent eruptions and occur as thenardite or as aphtitalite-thenardite mixtures, with abundant trace elements. The incrustations show small sulfur isotope fractionation of 1–2‰ compared with corresponding lavas and the volcanic gas samples. The sulfate incrustations are formed through oxidation of SO₂ from the emitted volcanic gas and subsequent reaction with metal halides. The volcanic gas samples show a distribution of decreasing δ³⁴S through time from +3.4 to −1.8‰; sulfate was preferentially degassed compared to sulfide. The data indicate that sulfate incrustations serve as a late-stage volcanic gas sample with respect to sulfur isotopes.     

Sulfur and chlorine degassing from primitive arc magmas: temporal changes during the 1982–1983 eruptions of Galunggung (West Java, Indonesia)

The 1982–1983 eruptions of Galunggung represent a nine-month period of intermittent volcanic activity with significant changes in explosivity and emission of volatiles. Eruptions started with Vulcanian explosions but changed gradually to Strombolian activity. Compositions of juvenile material changed from basaltic andesite to high-Mg basalt, which are among the most primitive rock types known in the Indonesian arc system. Although bulk compositions suggest a single evolution trend, we infer from the compositions of melt inclusions in olivine phenocrysts that the magmas represent derivatives of a complex spectrum of primary melts. Primitive inclusions in olivine phenocrysts from magma erupted during the Strombolian phase contain up to 2000 ppm sulfur, but concentrations decrease rapidly with increasing SiO₂ down to matrix glass values (50–100 ppm). ‘Vulcanian’ inclusions appear to be degassed before eruption (200 ppm S). Chlorine concentrations increase from 750 to 2200 ppm in Strombolian, and from 800 to 1500 in Vulcanian magmas, whereas matrix glass contains about 1000 ppm in both cases. Ash leachates show two cycles of decreasing S/Cl ratios: from 9.7 to 5.6 at the start of the activity, and from 12.2 to 2.0 after four months. As the second cycle follows upon increased seismic activity at shallow depth, it probably reflects degassing of fresh sulfur-rich magma arriving in the shallow Galunggung reservoir. In contrast to the degassed state of Vulcanian magma, the significant amounts of adsorbed sulfur on the ashes point to an excess source of sulfur, which was most likely derived from intruding Strombolian magma. Hence, the observed sulfur flux of 2 Mt is not in accordance with a petrologic estimate of 0.09 Mt. Using a published value of 550 Mt of erupted material about 0.34 km³ fresh undegassed magma is needed to account for the observed sulfur flux. This is close to the erupted volume of Vulcanian magma (0.26 km³), which presumably was replaced completely by Strombolian magma during the eruption. Using the petrologic method, we calculate a total release of 0.3 Mt chlorine, which agrees well with an output of 0.47 Mt estimated independently from S/Cl ratios of the ash leachates and TOMS sulfur yields. Ash leachates show that about 35% of the sulfur and 30% of the chlorine was scavenged from the eruption plumes. Our results suggest that sulfur and chlorine were largely decoupled during degassing, which resulted in considerable variations in S/Cl ratios during the Galunggung eruptions. We infer that sulfur degassing reflects the arrival of fresh magma at shallow depth, whereas chlorine is largely derived from simultaneously erupted material. As a consequence, the petrologic estimates are more consistent with observed emissions for chlorine than for sulfur.     

Geochemistry of the acid Kawah Putih lake, Patuha Volcano, West Java, Indonesia

Kawah Putih is a summit crater of Patuha volcano, West Java, Indonesia, which contains a shallow, 300 m-wide lake with strongly mineralized acid–sulfate–chloride water. The lake water has a temperature of 26–34°C, pH=<0.5–1.3, S^tot=2500–4600 ppm and Cl=5300–12 600 ppm, and floating sulfur globules with sulfide inclusions are common. Sulfur oxyanion concentrations are unusually high, with S₄O₆²⁻+S₅O₆²⁻+S₆O₆²⁻=2400 – 4200 ppm. Subaerial fumaroles (<93°C) on the lake shore have low molar SO₂/H₂S ratios (<2), which is a favorable condition to produce the observed distribution of sulfur oxyanion species. Sulfur isotope data of dissolved sulfate and native sulfur show a significant ³⁴S fractionation (ΔSO₄–S_e of 20‰), probably the result of SO₂ disproportionation in or below the lake. The lake waters show strong enrichments in ¹⁸O and D relative to local meteoric waters, a result of the combined effects of mixing between isotopically heavy fluids of deep origin and meteoric water, and evaporation-induced fractionation at the lake surface. The stable-isotope systematics combined with energy-balance considerations support very rapid fluid cycling through the lake system. Lake levels and element concentrations show strong seasonal fluctuations, indicative of a short water residence time in the lake as well.Thermodynamic modeling of the lake fluids indicates that the lake water is saturated with silica phases, barite, pyrite and various Pb, Sb, Cu, As, Bi-bearing sulfides when sulfur saturation is assumed. Precipitating phases predicted by the model calculations are consistent with the bulk chemistry of the sulfur-rich bottom sediments and their identified mineral phases. Much of the lake water chemistry can be explained by congruent rock dissolution in combination with preferential enrichments from entering fumarolic gases or brines and element removal by precipitating mineral phases, as indicated by a comparison of the fluids, volcanic rocks and lake bed sediment.Flank springs on the mountain at different elevations vary in composition, and are consistent with local rock dissolution as a dominant factor and pH-dependent element mobility. Discharges of warm sulfate- and chloride-rich water at the highest elevation and a near-neutral spring at lower level may contain a small contribution of crater-lake water. The acid fluid-induced processes at Patuha have led to the accumulation of elements that are commonly associated with volcano-hosted epithermal ore deposits. The dispersal of heavy metals and other potentially toxic elements from the volcano via the local drainage system is a matter of serious environmental concern.     

Multiple sulfur isotope chemostratigraphy across the Permian–Triassic boundary at Chaotian,China: Implications for a shoaling model of toxic deep-waters

Previous studies on multiple sulfur isotopes (³²S, ³³S, and ³⁴S) in sedimentary pyrite at the end-Permian suggested a shoaling of anoxic/sulfidic deep-water contributing to the extinction. This scenario is based on an assumption that the sedimentary sulfur cycle was largely controlled by benthos activity, though a stratigraphic correlation between the sulfur records and ichnofabrics of the sediments at the end-Permian has not yet been examined. We report the multiple sulfur isotopic composition of pyrite in the Permian–Triassic boundary interval at Chaotian, South China. Our data can be generally explained by a mixing of sulfur in sulfide from two different sources: one produced via sulfate reduction in an open system with respect to sulfate and the other produced in a closed system. In particular, the former with the substantially low δ³⁴S (<−40 ‰) and high ∆³³S (up to +0.100 ‰) values was likely produced via water-mass sulfate reduction or via sulfate reduction in oxic sediments with common burrows. The frequent occurrence of small pyrite framboids (mostly <5 μm in diameter) in the Lopingian (Late Permian) Dalong Formation of deep-water facies supports the enhanced water-mass sulfate reduction in an anoxic deep-water mass. The negative ∆³³S values are observed only in the oxic limestones, and no substantial ∆³³S change is observed across the extinction horizon despite of the disappearance of bioturbation. Our results are apparently inconsistent with the previous shoaling model. We expand the model and infer that, when the deep-water was sulfidic and its shoaling rate was high, a substantial amount of hydrogen sulfide (H₂S) was supplied onto the shelf via the shoaling; that resulted in the positive ∆³³S value of the bulk sediments. The observed ∆³³S variation on a global scale suggests a substantial variation in H₂S concentration and/or in upwelling rate of shoaling deep-waters during the Permian–Triassic transition.     

Explosive silicic volcanism in Iceland and the Jan Mayen area during the last 6 Ma: sources and timing of major eruptions

Fifty-three major explosive eruptions on Iceland and Jan Mayen island were identified in 0–6-Ma-old sediments of the North Atlantic and Arctic oceans by the age and the chemical composition of silicic tephra. The depositional age of the tephra was estimated using the continuous record in sediment of paleomagnetic reversals for the last 6 Ma and paleoclimatic proxies (δ¹⁸O, ice-rafted debris) for the last 1 Ma. Major element and normative compositions of glasses were used to assign the sources of the tephra to the rift and off-rift volcanic zones in Iceland, and to the Jan Mayen volcanic system. The tholeiitic central volcanoes along the Iceland rift zones were steadily active with the longest interruption in activity recorded between 4 and 4.9 Ma. They were the source of at least 26 eruptions of dominant rhyolitic magma composition, including the late Pleistocene explosive eruption of Krafla volcano of the Eastern Rift Zone at about 201 ka. The central volcanoes along the off-rift volcanic zones in Iceland were the source of at least 19 eruptions of dominant alkali rhyolitic composition, with three distinct episodes recorded at 4.6–5.3, 3.5–3.6, and 0–1.8 Ma. The longest and last episode recorded 11 Pleistocene major events including the two explosive eruptions of Tindfjallajökull volcano (Thórsmörk, ca. 54.5 ka) and Katla volcano (Sólheimar, ca. 11.9 ka) of the Southeastern Transgressive Zone. Eight major explosive eruptions from the Jan Mayen volcanic system are recorded in terms of the distinctive grain-size, mineralogy and chemistry of the tephra. The tephra contain K-rich glasses (K₂O/SiO₂>0.06) ranging from trachytic to alkali rhyolitic composition. Their normative trends (Ab–Q–Or) and their depleted concentrations of Ba, Eu and heavy-REE reflect fractional crystallisation of K-feldspar, biotite and hornblende. In contrast, their enrichment in highly incompatible and water-mobile trace elements such as Rb, Th, Nb and Ta most likely reflect crustal contamination. One late Pleistocene tephra from Jan Mayen was recorded in the marine sequence. Its age, estimated between 617 and 620 ka, and its composition support a common source with the Borga pumice formation at Sør Jan in the south of the island.     

The oxygen minimum zone (OMZ) off Chile as intense source of CO2 and N2O

The oxygen minimum zones (OMZs) are recognized as intense sources of N₂O greenhouse gas (GHG) and could also be potential sources of CO₂, the most important GHG for the present climate change. This study evaluates, for one of the most intense and shallow OMZ, the Chilean East South Pacific OMZ, the simultaneous N₂O and CO₂ fluxes at the air–sea interface. Four cruises (2000–2002) and 1 year of monitoring (21°–30°–36°S) off Chile allowed the determination of the CO₂ and N₂O concentrations at the sea surface and the analysis of fluxes variations associated with different OMZ configurations. The Chilean OMZ area can be an intense GHG oceanic local source of both N₂O and CO₂. The mean N₂O fluxes are 5–10 times higher than the maximal previous historical source in an OMZ open area as in the Pacific and Indian Oceans. For CO₂, the mean fluxes are also positive and correspond to very high oceanic sources. Even if different coupling and decoupling between N₂O and CO₂ are observed along the Chilean OMZ, 65% of the situations represent high CO₂ and/or N₂O sources. The high GHG sources are associated with coastal upwelling transport of OMZ waters rich in N₂O and probably also in CO₂, located at a shallow depth. The integrated OMZ role on GHG should be better considered to improve our understanding of the past and future atmospheric CO₂ and N₂O evolutions.     

The microfacies and sedimentary responses to the mass extinction during the Permian-Triassic transition at Yangou Section,Jiangxi Province,South China

A Permian-Triassic (P-Tr) boundary section of continuous carbonate facies, which well recorded the biotic and environmental processes through the great P-Tr transition in the shallow non-microbialite carbonate facies, has been studied in Yangou, Leping County, Jiangxi Province. The P-Tr sequence is well correlated with the Meishan section according to the conodont biostratigraphy and the excursion of carbon isotopes. A series of high-resolution thin-sections from the P-Tr boundary carbonate rocks at the Yangou section are studied to explore the interrelation between environmental change and biological evolution during the transitional time. Six microfacies have been identified based upon the observation of the thin-sections under a microscope on the grains and matrix and their interrelation. Combined with the data of fossils and carbon isotopes, Microfacies 4 (MF-4), coated-grain-bearing foraminifer oolitic sparitic limestone, and Microfacies 6 (MF-6), dark shelly micritic limestone, should be the different responses to the two episodes of mass extinction and environmental events that can be correlated throughout South China and even over the world. The oolitic limestone of MF-4 is the first finding from the latest Permian strata in South China and it might be a proxy of an unusual environmental condition of high pCO₂, low sulfate concentration and of microbial blooming in the aftermath of the latest Permian mass extinction. The micritic limestone of MF-6 containing rich micro-gastropods and ostracods probably represents the blooming event of disaster taxa in the earliest Triassic environment. The microfacies analysis at the Yangou section can well reveal the episodic process of the biological evolution and environmental change in the shallow non-microbialite carbonate facies throughout the great P-Tr transition, thus the Yangou section becomes an important complement to the Meishan section.     

Isotopic geochemistry of acid thermal waters and volcanic gases from Zaō volcano in Japan

The chemical composition and D/H, and ratios have been determined for the acid hot waters and volcanic gases discharging from Zaō volcano in Japan. The thermal springs in Zaō volcano issue acid sulfate-chloride type waters (Zaō) and acid sulfate type waters (Kamoshika). Gases emitted at Kamoshika fumaroles are rich in CO₂, SO₂ and N₂, exclusive of H₂O. Chloride concentrations and oxygen isotope data indicate that the Zaō thermal waters issue a fluid mixture from an acid thermal reservoir and meteoric waters from shallow aquifers. The waters in the Zaō volcanic system have slight isotopic shifts from the respective local meteoric values. The isotopic evidence indicates that most of the water in the system is meteoric in origin. Sulfates in Zaō acid sulfate-chloride waters with δ³⁴S values of around +15‰, are enriched in ³⁴S compared to Zaō H₂S, while the acid sulfate waters at Kamoshika contain supergene light sulfate (δ³⁴S = + 4‰) derived from volcanic sulfur dioxide from the volcanic exhalations. The sulfur species in Zaō acid waters are lighter in δ³⁴S than those of other volcanic areas, reflecting the difference in total pressure.     

The effect of volcanic eruptions on the chemistry of surface waters: The 1991 and 2000 eruptions of Mt. Hekla,Iceland

The Mt. Hekla eruptions in 1991 and 2000 have provided a unique opportunity to study the local environmental effects of high latitude volcanic eruptions in the middle of winter. Both eruptions started around sunset at sub-zero temperatures. In order to define better these effects we studied the chemistry of surface waters in the vicinity of the volcano. Additionally, we describe and predict the environmental consequences of these volcanic eruptions on the chemistry of surface waters on land and in the ocean.