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Mudstones from the Argiles de Châtillon Formation exposed in the Boulonnais region of Northern France represent a proximal lateral equivalent of the organic-rich Kimmeridge Clay Formation. The Argiles de Châtillon Formation is composed of two subunits that straddle the Kimmeridgian–Tithonian boundary. Each subunit contains an organic-rich interval. The two conspicuous organic-rich intervals have been linked to either periods of high sea level or greenhouse warming. Here, we use palynology to further understand climate and environmental mechanisms that drove organic matter enrichment. We use bulk organic carbon isotope records (δ13Corg) to correlate the Boulonnais sections with those of the Kimmeridge Clay Formation. The palynological results suggest that the stratigraphically lower organic-rich interval (Kimmeridgian) was deposited under suboxic to anoxic stratified conditions. A large-scale climate shift from cooler/humid to warmer/arid conditions marked the Kimmeridgian–Tithonian boundary, influencing organic matter enrichment in the stratigraphically higher organic-rich interval (Tithonian). In contrast with the lower organic-rich interval, there are no indications of stratified conditions for the higher organic-rich interval. Within this thicker organic-rich interval, cyclic variations in amorphous organic matter distribution, total organic carbon and δ13Corg trends on a 2 m scale are observed. They co-occur with fluctuations of the palynological assemblages, indicative of more humid versus arid climate conditions, likely alternating on a ∼100 kyr eccentricity timescale. Our results show that under the most humid phases of these overall arid climate conditions, sulfurization of carbohydrates was the dominant control on organic matter preservation. This climate-controlled process that drives organic matter enrichment in the Tithonian can be recognized on a basin-wide scale.

Tubular carbonate concretions of up to 1 m in length and perpendicular to bedding, occur abundantly in the Upper Pliensbachian (upper Amaltheus margaritatus Zone, Gibbosus Subzone) in outcrops (Fontaneilles section) in the vicinity of Rivière-sûr-Tarn, southern France. Stable isotope analyses of these concretions show negative δ13C values that decrease from the rim to the center from −18.8‰ to −25.7‰ (V-PDB), but normal marine δ18O values (−1.8‰). Carbon isotope analyses of Late Pliensbachian bulk carbonate (matrix) samples from the Fontaneilles section show clearly decreasing C-isotope values across the A. margaritatus Zone, from +1‰ to −3‰ (V-PDB). Isotope analyses of coeval belemnite rostra do not document such a negative C-isotope trend with values remaining stable around +2‰ (V-PDB). Computer tomographic (CT) scanning of the tubular concretions show multiple canals that are lined or filled entirely with pyrite. Previously, the formation of these concretions with one, two, or more central tubes, has been ascribed to the activity of an enigmatic organism, possibly with annelid or arthropod affinities, known asTisoa siphonalis. Our results suggest tisoan structures are abiogenic. Based on our geochemical analyses and sedimentological observations we suggest that these concretions formed as a combination of the anaerobic oxidation of methane (AOM) and sulfate reduction within the sediment. Fluids rich in methane and/or hydrocarbons likely altered local bulk rock carbon isotope records, but did not affect the global carbon cycle. Interestingly, Tisoa siphonalis has been described from many locations in the Grands Causses Basin in southern France, and from northern France and Luxemburg, always occurring at the same stratigraphic level. Upper Pliensbachian authigenic carbonates thus possibly cover an area of many thousand square kilometers. Greatly reduced sedimentation rates are needed to explain the stabilization of the sulfate-methane transition zone in the sedimentary column in order for the tubular concretions to form. Late Pliensbachian cooling, reducing run-off, and/or the influx of colder water and more vigorous circulation could be responsible for a halt in sedimentation. At the same time (thermogenic) methane may have destabilized during a major phase of Late Pliensbachian sea level fall. As such Tisoa siphonalis is more than a geological curiosity, and its further study could prove pivotal in understanding Early Jurassic paleoenvironmental change.

The Triassic–Jurassic (T–J) mass-extinction event is marked by isotope anomalies in organic (δ 13 Corg) and carbonate carbon (δ 13 Ccarb) reservoirs. These have been attributed to a (rapid) 4-fold rise in pCO2 as a result of massive flood basalt volcanism and/ or methane hydrate dissociation. Here we examine the response of marine photosynthetic phytoplankton to the proposed perturbation in the carbon cycle. Our high-resolution micropalaeontological analysis of T–J boundary beds at St Audrie's Bay in Somerset, UK, provides evidence for a bio-calcification crisis that is characterized by (1) extinction and malformation in calcareous nannoplankton and (2) contemporaneous blooms of organic-walled, green algal ‘disaster’ species which comprise in one case N70% of the total palynomorph fraction. Blooms of prasinophytes and acritarchs occur at the onset and in association with a prominent negative shift in δ 13 Corg values close to the first appearance of the Early Jurassic ammonite Psiloceras planorbis. Across the same interval we obtained palaeotemperature and palaeosalinity estimates from oyster low-Mg calcite based on Mg/Ca, Sr/Ca and δ 18 O records. The results of our palynological and geochemical analyses strongly suggest that shallow marine basins in NW Europe during this period became salinity stratified, inducing anoxic conditions. The T–J boundary event shows similarities with the Permian–Triassic (P–T) mass-extinction event, which was also marked by extensive flood basalt volcanism, negative excursions in carbon isotope records, a bio-calcification crisis, the development of shallow-marine anoxia and mass abundances of acritarchs in the Early Triassic. This leads us to suggest that the proliferation of green algal phytoplankton may be symptomatic of elevated carbon dioxide levels in the atmosphere and oceans during mass-extinction events. © 2007 Published by Elsevier B.V.

Tubular carbonate concretions of up to 1 m in length and perpendicular to bedding, occur abundantly in the Upper Pliensbachian (upper Amaltheus margaritatus Zone, Gibbosus Subzone) in outcrops (Fontaneilles section) in the vicinity of Rivière-sûr-Tarn, southern France. Stable isotope analyses of these concretions show negative &delta13C values that decrease from the rim to the center from −18.8‰ to −25.7‰ (V-PDB), but normal marine δ18O values (−1.8‰). Carbon isotope analyses of Late Pliensbachian bulk carbonate (matrix) samples from the Fontaneilles section show clearly decreasing C-isotope values across the A. margaritatus Zone, from +1‰ to −3‰ (V-PDB). Isotope analyses of coeval belemnite rostra do not document such a negative C-isotope trend with values remaining stable around +2‰ (V-PDB). Computer tomographic (CT) scanning of the tubular concretions show multiple canals that are lined or filled entirely with pyrite. Previously, the formation of these concretions with one, two, or more central tubes, has been ascribed to the activity of an enigmatic organism, possibly with annelid or arthropod affinities, known as Tisoa siphonalis. Our results suggest tisoan structures are abiogenic. Based on our geochemical analyses and sedimentological observations we suggest that these concretions formed as a combination of the anaerobic oxidation of methane (AOM) and sulfate reduction within the sediment. Fluids rich in methane and/or hydrocarbons likely altered local bulk rock carbon isotope records, but did not affect the global carbon cycle. Interestingly, Tisoa siphonalis has been described from many locations in the Grands Causses Basin in southern France, and from northern France and Luxemburg, always occurring at the same stratigraphic level. Upper Pliensbachian authigenic carbonates thus possibly cover an area of many thousand square kilometers. Greatly reduced sedimentation rates are needed to explain the stabilization of the sulfate-methane transition zone in the sedimentary column in order for the tubular concretions to form. Late Pliensbachian cooling, reducing run-off, and/or the influx of colder water and more vigorous circulation could be responsible for a halt in sedimentation. At the same time (thermogenic) methane may have destabilized during a major phase of Late Pliensbachian sea level fall. As such Tisoa siphonalis is more than a geological curiosity, and its further study could prove pivotal in understanding Early Jurassic paleoenvironmental change.

[1] Profiles of Mo/total organic carbon (TOC) through the Lower Toarcian black shales of the Cleveland Basin, Yorkshire, United Kingdom, and the Posidonia shale of Germany and Switzerland reveal water mass restriction during the interval from late tenuicostatum Zone times to early bifrons Zone times, times which include that of the putative Early Toarcian oceanic anoxic event. The degree of restriction is revealed by crossplots of Mo and TOC concentrations for the Cleveland Basin, which define two linear arrays with regression slopes (ppm/%) of 0.5 and 17. The slope of 0.5 applies to sediment from the upper semicelatum and exaratum Subzones. This value, which is one tenth of that for modern sediments from the Black Sea (Mo/TOC regression slope 4.5), reveals that water mass restriction during this interval was around 10 times more severe than in the modern Black Sea; the renewal frequency of the water mass was between 4 and 40 ka. The Mo/TOC regression slope of 17 applies to the overlying falciferum and commune subzones: the value shows that restriction in this interval was less severe and that the renewal frequency of the water mass was between 10 and 130 years. The more restricted of the two intervals has been termed the Early Toarcian oceanic anoxic event but is shown to be an event caused by basin restriction local to NW Europe. Crossplots of Re, Os, and Mo against TOC show similar trends of increasing element concentration with increase in TOC but with differing slopes. Together with modeling of 187 Os/ 188 Os and d 98 Mo, the element/TOC trends show that drawdown of Re, Os, and Mo was essentially complete during upper semicelatum and exaratum Subzone times (Mo/TOC regression slope of 0.5). Drawdown sensitized the restricted water mass to isotopic change forced by freshwater mixing so that continental inputs of Re, Os, and Mo, via a low-salinity surface layer, created isotopic excursions of up to 1.3% in d 98 Mo and up to 0.6% for 187 Os/ 188 Os. Restriction thereby compromises attempts to date Toarcian black shales, and possibly all black shales, using Re-Os chronology and introduces a confounding influence in the attempts to use d 98 Mo and initial 187 Os/ 188 Os for palaeo-oceanographic interpretation.

[1] The Triassic-Jurassic boundary mass-extinction event (T-J; 199.6 Ma) is associated with major perturbations in the carbon cycle recorded in stable carbon isotopes. Two rapid negative isotope excursions in bulk organic carbon (δ13Corg) occur within the immediate boundary interval at multiple locations and have been linked to the outgassing of 12C-enriched CO2 from the Central Atlantic Magmatic Province. In British Columbia, a positive δ13Corg excursion of +5‰ (Vienna Peedee belemnite (V-PDB)) spans part or all of the subsequent Hettangian stage. Here, we examine the significance of these carbon isotope excursions as records of global carbon cycle dynamics across the T-J boundary and test the link between carbon cycle perturbation-stabilization and biotic extinction-recovery patterns. A combination of δ13Corg and palynological analyses from the Late Triassic to Early Jurassic in the Mingolsheim core (Germany) suggests that organic carbon isotope variations are best explained as the result of both compositional changes in terrestrial versus marine input and disturbance and recovery patterns of major terrestrial plant groups across the T-J boundary. A new high-resolution δ13Ccarb record from the Val Adrara section in the Southern Alps (Italy) spanning from the uppermost Rhaetian through Lower Sinemurian does not exhibit a negative excursion at the T-J boundary but does record a large positive δ13Ccarb excursion of +4‰ (V-PDB) in bulk carbonate that begins at the T-J boundary and reaches a local maximum at the Early Late Hettangian boundary. Values then gradually decrease reaching +0.5‰ at the Hettangian-Sinemurian boundary and remain relatively constant into the Early Sinemurian. Complementary δ13Ccarb data from 4 more sections that span the Hettangian-Sinemurian boundary support carbon cycle stabilization within the Upper Hettangian. Our analyses suggest that isotope changes in organic carbon reservoirs do not necessarily require a shift in the global exogenic carbon reservoir and that the positive excursion in the carbonate carbon isotope record is best explained as the combined result of an increase in atmospheric pCO2 leading to accelerated carbon cycling, decreased skeletal carbonate production, and increased organic carbon burial lasting several hundred thousand years. The termination of the positive inorganic carbon isotope excursion coincides with the recovery of marine skeletal carbonate producers and coeval changes in terrestrial vegetation and reflects the gradual reduction in pCO2 and the stabilization of the global carbon cycle during the Sinemurian.

Two hypotheses have been proposed to explain simultaneous large negative excursions (up to 7% PeeDee belemnite) in bulk carbonate (delta(13)C(carb)) and organic carbon isotope records (delta(13)C(org)) from black shales marking the Toarcian oceanic anoxic event (T-OAE). The first explanation envisions recycling of dissolved inorganic carbon (DIC) with a light isotopic signature into the photic zone from the lower levels of a salinity-stratified water mass, essentially requiring a regional paleoceanographic driver of the carbon cycle. The second involves the rapid and massive dissociation of methane from gas hydrates that effectively renders the T-OAE a global perturbation of the carbon cycle. We present C isotope records from belemnites (delta(13)C(bel)) sampled from two localities, calibrated with high-resolution ammonite biostratigraphy and Sr isotope stratigraphy, in Yorkshire (England) and Dotternhausen (Germany), that can be used to assess which model best explains the observed changes in carbon isotopes. Our records of the delta(13)C composition of belemnite calcite do not show the large negative C isotope excursions shown by coeval records of delta(13)C in sedimentary organic matter or bulk sedimentary carbonate. It follows that isotopically light carbon cannot have dominated the ocean-atmosphere carbon reservoir during the Toarcian OAE, as would be required were the methane release hypothesis correct. On the basis of an evaluation of available carbon isotope records we discuss a model in which the recycling of DIC from the deeper levels of a stratified water body, and shallowing of anoxic conditions into the photic zone, can explain all isotopic profiles. In particular, the model accounts for the higher C isotope values of belemnites that are characteristic of open ocean, well-mixed conditions, and the lower C isotope values of neritic phytoplankton communities that recorded the degree of density stratification and shallowing of anoxia in the photic zone.