Terrestrial carbon-isotope records from coastal deposits (Algarve, Portugal): a tool for chemostratigraphic correlation on an intrabasinal and global scale

ABSTRACT The carbon-isotope signature of terrestrial organic matter (OM) offers a valuable tool to develop stratigraphic correlations for near-shore deposits. A mid-Cretaceous coastal succession of the western Algarve Basin, Portugal, displays a marked negative δ¹³C excursion ranging from − 21.2‰ to − 27.8‰ in the Early Aptian followed by two shifts towards higher values (up to − 19.3‰) during the Early and Late Aptian, respectively. The dominance of cuticle and leaf debris in the bulk OM fraction is confirmed by optical studies, Rock-Eval pyrolysis and by comparison with the δ¹³C signature of four different types of fossilized land-plant particles. Correlation of two terrestrial δ¹³C_bulk OM records from different study sites leads to a significant enhancement of the intrabasinal stratigraphic correlation within the Algarve Basin. Three prominent excursions in the Portuguese records can be correlated with existing δ¹³C curves from pelagic and terrestrial environments. The general carbon-isotope pattern is superimposed by small-scale fluctuations which can be explained by compositional variations within the OM.     

Thermochemical sulphate reduction in the Upper Devonian Cairn Formation of the Fairholme carbonate complex (South-West Alberta, Canadian Rockies): evidence from fluid inclusions and isotopic data

The Fairholme carbonate complex is part of the extensively dolomitized Upper Devonian carbonate reefs in west-central Alberta. The studied formations contain moulds (up to 10 cm in diameter), which are filled partially with (saddle) dolomite, quartz and calcite cements. These cements precipitated from a mixture of brines that acquired high salinity by dissolution of halite and brines derived from evaporated sea water. The fluids were warm (homogenization temperature of primary fluid inclusions of 76 to 200 °C) and saline (20 to 25 wt% NaCl equivalent) and testify to thermochemical sulphate reduction processes. The latter is deduced from S in solid inclusions, CO₂ and H₂S in volatile-rich aqueous inclusions and depleted δ¹³C values down to −26‰ Vienna Pee Dee Belemnite. High ⁸⁷Sr/⁸⁶Sr values (0·7094 to 0·7110) of the cements also indicate interaction of the fluids with siliciclastic sequences. The thermochemical sulphate reduction-related cements probably formed during early Laramide burial. Another (younger) calcite phase, characterized by depleted δ¹⁸O values (−23·9‰ to −13·9‰ Vienna Pee Dee Belemnite), low Na (27 to 37 p.p.m.) and Sr (39 to 150 p.p.m.) concentrations and non-saline (∼0 wt% NaCl equivalent) fluid inclusions, is attributed to post-Laramide meteoric water.     

A distinct δ13C decline in organic lake sediments at the Pleistocene-Holocene transition in southern Sweden

Values of δ¹³C obtained from conventional bulk sediment radiocarbon dates encompassing the Pleistocene Holocene boundary have been compiled and plotted against ¹⁴C age. In all. 286 lake sediment dates from southern Sweden in the range 8.000 to 13.000 BP have been evaluated. A significant decrease in δ¹³C values, initiated shortly before 10.000 RP and amounting to 5%, is distinguished. This change is accompanied by increased limnic productivity. decreased erosive input and increased organic carbon content of the sediments. A probable explanation for the δ¹³C decline in organic material is decreased importance of dissolution of silicates at the transition to the Holocene. During the Late Weichselian. extensive weathering of exposed minerogenic material with subsequent input of bicarbonate to the lake water may have caused a relative enrichment of ¹³C in dissolved inorganic carbon. Furthermore, the early Holocene increase in terrestrial vegetation cover probably led to an increased supply of ¹³C depleted carbon dioxide to the lake water by root respiration. Altered limnic vegetation, presumably towards increased production of phytoplankton. could also have contributed to the observed decreasing δ¹³C trend. The importance of these processes compared to other possible influencing factors. mainly endogenic carbonate production and changes in the global carbon cycle. is discussed.     

Petroleum surface oil seeps from a Palaeoproterozoic petrified giant oilfield

Early Palaeoproterozoic rocks from the Onega Basin in Russian Fennoscandia contain evidence for substantial accumulation and preservation of organic matter (up to 75 wt% total organic carbon) with an estimated original petroleum potential comparable to a modern supergiant oilfield. The basin contains a uniquely preserved petrified oilfield including evidence of oil traps and oil migration pathways. Here, we report the discovery of the surface expression of a migration pathway, along which petroleum was flowing from the sub-surface. This surface oil seep, the first occurrence ever reported from the Palaeoproterozoic, appears as original bitumen clasts redeposited in Palaeoproterozoic lacustrine turbidites. The δ¹³C_org of clastic pyrobitumen ranges between −35.4 and −36.0‰ ( n  = 14), which is within the range of interbed- and vein-trapped fossil oil (−46 and −24‰), suggesting similar source. Biogenic organic matter, whose isotopic composition was modified during thermal maturation, is the likely source for the migrated hydrocarbon.     

Field geometry, petrography and geochemistry of a dolomitization front (Late Jurassic, central Lebanon)

This contribution describes the field geometry, petrography and geochemistry of a well-exposed dolomitization front in Upper Jurassic carbonates, and attempts to highlight the sedimentological, structural and relative sea-level controls on multiphase dolomitization and related diagenetic events. The data presented reflect the superposition of various diagenetic phases which have resulted in a single dolostone body, whose dimensions are well defined in the field. Local microbial intraclastic dolomites of Late Tithonian age accumulated in a hypersaline lagoon during relative sea-level fall. These pre-date beige hydrothermal dolostones (51 to 55 mol% CaCO₃; δ ¹⁸O: −9·3 to −4·0‰ V-PDB; δ ¹³C: −1·5 to +2·1‰ V-PDB; ⁸⁷Sr/⁸⁶Sr: 0·70742; matrix porosity: ≈6%; Klinkenberg permeability: ≈0·5 mD), whose dolomitizing fluid circulated along faults and invaded the nearby facies. First, the burrows were dolomitized, then the bulk rocks, resulting in the investigated 'tongue'-shaped dolomite body. Upon Late Jurassic–Early Cretaceous uplift, near-surface water percolated through – and altered – the underlying beige dolostones. This event was followed by a ferroan dolomite cement phase, which occurred during further burial. This contribution, featuring a well-defined geometric pattern of a dolomitization front with a large petrographic and geochemical data set, may also serve as a case study illustrating the complexity of superimposed diagenetic processes which have to be taken into account in modelling exercises of multiphase hydrothermal dolomitization.     

Anthropogenic CO2 in Southern Ocean surface waters: evidence from stable organic carbon isotopes

We present an approach for tracing the fate of anthropogenic CO₂, compiling a large data set of stable organic carbon isotope ratios from surface sediments, plankton, and sinking matter in the Atlantic Ocean. The δ¹³C values of sinking matter are generally lower by 0.5–4.6‰ compared to the surface sediments. This difference increases with increasing latitude, which is explained by a stronger modern increase in surface water [CO₂ (aq)] in the Southern Ocean relative to the Tropical/Subtropical Ocean. Preindustrial dissolved CO₂ concentrations in Atlantic surface waters, estimated from the δ¹³C_org of surface sediments, are compared to recently measured surface water [CO₂ (aq)] values taken from literature. We obtain only a slight increase in [CO₂ (aq)] at lower latitudes but a significant change of about 7 ± 2 μ m in high latitudinal surface waters which we attribute to anthropogenic perturbation. Our results suggest that CO₂ released by human activities has been stored in Southern Ocean surface waters.     

Nitrogen isotopes in peridotitic diamonds from Fuxian, China: the mantle signature

Nitrogen isotopes in peridotitic diamonds from Fuxian, China, suggest that the upper mantle δ¹⁵N-value has been globally homogeneous since at least the Proterozoic (−5 to −8‰/ATM), with similar values for subcontinental and MORB mantle.
  In addition, Fuxian diamonds retain the memory of a primary nitrogen lower in δ¹⁵N (down to −25‰). For the first time δ¹⁵N- values in diamonds match those of enstatite chondrites, supporting a formation of the Earth from such meteorites and the idea of a heterogeneous accretion of the Earth's volatiles.
  Nitrogen concentrations in diamonds are believed to depend strongly on the rate of the diamond growth and not to be an indicator of C/N ratios of the fluids from which they grew.     

New stratigraphic markers in the late Pleistocene Palouse loess: novel fossil gastropods, absolute age constraints and non-aeolian facies

Four stratigraphic sections in the southern part of the Columbia Basin preserve a sequence of aeolian and non-aeolian sediments ranging in age from 9·43 to >47·0 ¹⁴C ka based on accelerator mass spectrometry radiocarbon dating of fossil molluscs, geochemistry of Cascade Mountain-sourced tephra and association with formally recognized pedostratigraphic units (the Washtucna and Old Maid Coulee soils). Study sections are interpreted as representing concurrent deposition of loess and distal Missoula Flood rhythmites in valleys tributary to main drainages backflooded during the Missoula Floods, and formation of carbonate and iron-rich soils. Sediments belong to the formally recognized L-1 and L-2 loess units established for the Palouse loess, which were deposited in the Columbia Basin subsequent to events of glacial outburst flooding. Sediments associated with the Mount Saint Helens set S and set C tephras in the study sections preserve a fauna of five species of gastropod mollusc which have not been reported previously from sediments of late Pleistocene age in the Palouse region. The fossils comprise two distinct faunules stratigraphically separated by the Mount Saint Helens So tephra. Accelerator mass spectrometry radiocarbon dating of the fossils collected above the tephra in two of the sections yielded ages of 12·48 ± 0·06 and 9·43 ± 0·05 ¹⁴C kyr. These ages suggest that independent determinations of the 13·35 ¹⁴C kyr age of the So tephra in other areas where Missoula Flood sediments are preserved are probably accurate, and help to refine the age of the latest events in the most recent sequence of catastrophic glacial outburst flooding.     

Stable chlorine isotope evidence for non-marine chloride in Badenian evaporites, Carpathian mountain region

Routine trace-element geochemistry suggests that components in putative marine halite evaporites may be partly of nonmarine origin, but such interpretations are commonly ambiguous. Stable chlorine isotopes may provide a less-ambiguous marker of chloride origin where δ³⁷Cl departs from the range predicted for evaporite formation from seawater. Bedded halite with primary sedimentary textures preserves original δ³⁷Cl values. Measurable change in δ³⁷Cl can be generated by incongruent dissolution of halite, but only if less than half the original halite remains. Badenian (middle Miocene) halite from the Forecarpathian and from the East Slovakian and Transcarpathian basins has a δ³⁷Cl range of – 0.2 to 0.8‰. Two phenomena cannot be explained by simple evaporation of 0.0‰ seawater. At Wieliczka, the Shaft Salt has distinctive δ³⁷Cl values (– 0.2 to 0.0‰) relative to neighbouring salt beds (0.2 to  0.6‰), requiring a large, abrupt input of brine with negative δ³⁷Cl. Halite with high (0.6 – 0.8‰) δ³⁷Cl near the base of the East Slovakian and Transcarpathian evaporites requires a large input of chloride with positive δ³⁷Cl into the basins. Expulsion of basin brine with non-0‰δ³⁷Cl into the evaporite basins may account for the nonmarine chloride sources.     

δ30Si and δ29Si Determinations on USGS BHVO-1 and BHVO-2 Reference Materials with a New Configuration on a Nu Plasma Multi-Collector ICP-MS

We report silicon isotopic determinations for USGS rock reference materials BHVO-1 and BHVO-2 using a Nu Plasma multi-collector (MC)-ICP-MS, upgraded with a new adjustable entrance slit, to obtain medium resolution, as well as a stronger primary pump and newly designed sampler and skimmer cones ("B" cones). These settings, combined with the use of collector slits, allowed a resolution to be reached that was sufficient to overcome the ¹⁴N¹⁶O and ¹⁴N₂ interferences overlying the ³⁰Si and the ²⁸Si peaks, respectively, in an earlier set-up. This enabled accurate measurement of both δ³⁰Si and δ²⁹Si. The δ value is expressed in per mil variation relative to the NBS 28 quartz reference material. Based on data acquired from numerous sessions spread over a period of six months, we propose a recommended average δ³⁰Si of −0.33 ± 0.05‰ and −0.29 ± 0.11‰ (2se) for BHVO-1 and BHVO-2, respectively. Our BHVO grand mean silicon isotope composition (δ³⁰Si =−0.31 ± 0.06‰) is significantly more negative than the only published value for BHVO-2, but is in very good agreement with the recently established average value of ocean island basalts (OIB), confirming the conclusion that the OIB reservoir has a distinct isotopic composition from the solar reservoir as sampled by chondrites.     

Long-term (105) or short-term (103) δ13C excursion near the Palaeocene-Eocene transition: evidence from the Tethys

Expanded sedimentary records from the Tethys reveal unique faunal and isotopic changes across the Palaeocene-Eocene (P-E) transition. Unlike in the open oceans, the Tethys exhibits a gradual decrease of 1.5% in δ¹³C values prior to the rapid δ¹³C excursion. Associated with the 6¹³C excursion is a decrease in calcite burial, increase in detrital content and appearance of a unique opportunistic planktic foraminifera1 assemblage (e.g. compressed acarininids). The existence of a prelude decrease in δ¹³C values in the Tethys suggests that the P-E δ¹³C excursion may have occurred in two steps and over a few hundred thousand years, rather than as one step over a few thousand years as previously suggested. This slower excursion rate is readily explained by changing organic carbon weathering or burial rates and avoids the need of invoking ad hoc scenarios.     

Seasonal and interannual variability of Siberian river discharge in the Laptev Sea inferred from stable isotopes in modern bivalves

Stable oxygen and carbon isotope profiles from modern bivalve shells were investigated in order to reconstruct short-term hydrographical changes in the river-shelf system of the Laptev Sea. Oxygen isotopic profiles obtained from the aragonitic species Astarte borealis exhibit amplitude cycles interpreted as annual hydrographical cycles. These records reflect the strong contrast between summer and winter bottom water conditions in the Laptev Sea. The seasonal variations in δ¹⁸O are mainly controlled by the riverine freshwater discharge during summer with 0.5‰ per salinity unit. Corrected for a defined species-dependent fractionation offset of -0.37‰, time-dependent salinity records were reconstructed from these δ¹⁸O profiles. They indicate a good correspondence to seasonal hydrographic changes and synoptical data. Persistent trends with shell growth towards more negative δ¹³C values are observed in all specimens and appear to be related to metabolic changes of the bivalves during ontogeny. In contrast, short-term fluctuations are likely linked to seasonal variabilities of the river water outflow patterns and enhanced phytoplankton productivity during summer. This is corroborated by a clear watermass-related distinction of the various δ¹³C records made on the basis of water depth and distance from the riverine source.     

Stable isotopic signature of a palaeoaquifer, Mississippian Alamogordo Member limestones, Sacramento Mountains, New Mexico, USA

Nine stratigraphic sections, each ≈5 m thick, were sampled from the Alamogordo Member limestones of the Lake Valley Formation, Sacramento Mountains, New Mexico, USA. Four stratigraphic sections consist entirely of lime mudstone and wackestone, whereas the other five sections have a prominent layer of crinoidal packstone about 1 m thick at their base. Stable isotopic analyses reveal that the lime muds in the sections with basal packstone layers show a downward decrease in δ¹⁸O and constant δ¹³C values, whereas those in the sections solely composed of lime mudstone and wackestone have, in general, relatively uniform δ¹⁸O and δ¹³C values. The diagenesis of the Alamogordo Member limestones was previously believed to have been governed by the downward percolation of meteoric water from a regional pre-Pennsylvanian exposure surface ≈100 m above this unit. However, the uniform δ¹³C and downward decrease in δ¹⁸O values in the lime muds in the sections with basal packstones indicate that the meteoric water ascended within the Alamogordo Member, rather than descended from the overlying exposure surface. This indicates that the basal packstones were probably a conduit for meteoric water. This is further supported indirectly by the relatively uniform δ¹⁸O and δ¹³C values of the lime mud in the sections without basal packstones. The implications are that the oxygen isotopic gradients may be used to identify palaeoaquifers, flow directions within these aquifers and that meteoric diagenesis below an exposure surface could be governed by flow through a palaeoaquifer.     

10Be chronology of the last deglaciation of County Donegal, northwestern Ireland

A well-preserved moraine on the northern coast of County Donegal, Ireland, has played a critical role in our understanding of the glacial history of this sector of the Irish Ice Sheet (IIS). Because of a lack of numerical dating of the moraine, however, previous interpretations of its age and significance to the glacial history of this region have varied widely. Here we report eight in situ cosmogenic ¹⁰Be ages on boulders sampled from the moraine. Two of these ages are outliers, with the remaining six ranging from 18.8±1.0 ¹⁰Be kyr to 20.9±1.3 ¹⁰Be kyr, with an uncertainty-weighted mean age of 19.4±0.3 ¹⁰Be kyr (19.4±1.2 kyr accounting for production rate uncertainty). Our results confirm one previous ¹⁰Be age obtained from the moraine, with the combined data ( n =7) constraining the age of initial deglaciation of the IIS from its LGM position on the continental shelf to be 19.3±0.3 ¹⁰Be kyr (19.3±1.2 kyr accounting for production rate uncertainty). These ages are in excellent agreement with calibrated ¹⁴C ages that constrain retreat of the IIS margin from the continental shelf elsewhere in northwestern and western Ireland and the Irish Sea Basin associated with the start of the Cooley Point Interstadial (≥20–≤18.2 cal. kyr BP), suggesting widespread deglaciation of the IIS ∼19.5–20 kyr ago.     

Isotope geochemistry, petrology and depositional environments of the diatomite-dominated Tripoli Formation (Lower Messinian), Sicily

ABSTRACT The Tripoli Formation (Lower Messinian) in Sicily includes diatomites irregularly alternating with marl and carbonate beds and lies, stratigraphically, between the Tortonian pelagic marls and the evaporitic Calcare di base. The relationships between mineralogy, textural features and oxygen-carbon isotopic compositions of carbonate components point to a wide variability of depositional conditions and suggest that Tripoli sedimentation occurred in small basins characterized by periodic and marked restriction from the open sea.
The isotopic values of calcite and dolomite in the diatomites suggest an evolution from normal marine towards more restricted environments. Evaporating conditions are also indicated by the occurrence of anhydrite, length-slow chalcedonic quartz and moulds of gypsum. In a more advanced stage, the precipitation of heavy δ¹⁸0 dolomite in the interstitial pores of fossil-poor diatomites denotes an environment with highly evaporated water. Mixing of meteoric and marine waters, on the other hand, might have favoured the precipitation of a dolomite characterized by relatively low δ¹⁸0 and δ¹³C values.
The deposition of marl and carbonate beds alternating with or overlying the diatomites took place in an environment with highly evaporated marine waters on the basis of δl¹⁸O values of dolomite (up to + 9.10‰) and aragonite (up to + 5.83‰), occurrence of evaporitic minerals and lack of fossils. The presence at these levels of calcite with extremely negative δ¹³C values (down to - 38.40‰), filling gypsum moulds, suggests activity of sulphate-reducing bacteria. Some aragonitic marls, however, bear evidence of deposition in relatively normal marine conditions.     

Boron isotope composition of melt inclusions from porphyry systems of the Central Andes: a reconnaissance study

Quartz-hosted melt inclusions from latite dykes of the Eocene El Salvador copper porphyry system in northern Chile display wide ranges in both boron concentration (15–155 p.p.m. B) and isotope composition (δ¹¹B −7 to +12‰; n  = 10), likely reflecting slab-derived fluid input from seawater-altered oceanic crust. In contrast, the major Miocene tin-silver and tin porphyry systems in the Bolivian back-arc region (Cerro Rico de Potosi, Chorolque, Llallagua) have distinctly different melt inclusion compositions with δ¹¹B of −11.4 ± 2.7‰ ( n  = 10), and magmatic boron enrichment up to several hundred p.p.m. B. The `seawater' signature in the El Salvador melt inclusions explains the oxidized mineral assemblage of the copper porphyry system, as opposed to the more reduced nature of the Bolivian tin porphyry systems, which reflect intracrustal melting of pelitic rocks.     

Holocene deposits from Neptune's Cave, Nordland, Norway: Environmental interpretation and relation to the deglacial and emergence history of the Velfjord–Tosenfjord area

Neptune's Cave in the Velfjord–Tosenfjord area of Nordland, Norway is described, together with its various organic deposits. Samples of attached barnacles, loose marine molluscs, animal bones and organic sediments were dated, with radiocarbon ages of 9840 ± 90 and 9570 ± 80 yr BP being derived for the barnacles and molluscs, based on the superseded but locally used marine reservoir age of 440 years. A growth temperature of c . 7.5 °C in undiluted seawater is deduced from the δ¹³C and δ¹⁸O values of both types of marine shell, which is consistent with their early Holocene age. From the dates, and an assessment of local Holocene uplift and Weichselian deglaciation, a scenario is constructed that could explain the situation and condition of the various deposits. The analysis uses assumed local isobases and sea-level curve to give results: that are consistent with previous data, that equate the demise of the barnacles to the collapse of a tidewater glacier in Tosenfjord, and that constrain the minimum extent of local Holocene uplift. An elk fell into the cave in the mid-Holocene at 5100 ± 70 yr BP, after which a much later single 'bog-burst' event at 1780 ± 70 yr BP could explain the transport of the various loose deposits further into the cave.     

A widespread positive δ13Ccarb anomaly at around 2.33–2.06 Ga on the Fennoscandian Shield: a paradox?

Carbon isotope measurements carried out on 201 carbonate samples from the early Proterozoic of the Kola Peninsula, N. Karelia and Norway yield δ¹³C (PDB) spanning - 20.5% to + 11%. A general δ¹³C secular trend shows that prior to 2.33 Ga values are typically 'normal' marine, averaging around - 3%0. Between 2.33 and 2.06 Ga, in Jatulian time, there follows a rapid excursion to positive δ¹³C of around + 6%. Post-Jatulian time is characterized by δ¹³C of sedimentary carbonates fluctuating between - 5% and +3%; also it is remarkable for the first pronounced development of diagenetic carbonates, which have δ¹³C between - 14 % and - 6% . The c. 6% positive δ¹³C shift with a duration of about 270 Myr coincides with a maximum in the diversity and abundance of stromatolites, and with widespread development of 'red beds', but does not coincide with the maximum of buried C_org mass. The Fennoscandian Shield represents the largest isotoically anomalous carbonate province yet reported, and the positive δ¹³C excursion together with a series of major global palaeoenviromental changes seems to be more intense than the Precambrian/Cambrian transition events. However, it is still not clear what kind of mechanism this phenomenon could be attributed to. An increase of the 'Ronov ratio', and/or 'Broecker ratio' and other possible models are discussed as the target for future investigations.     

Rate of late Quaternary ice-cap thinning on King George Island, South Shetland Islands, West Antarctica defined by cosmogenic 36Cl surface exposure dating

Glacial landforms on the Barton and Weaver peninsulas of King George Island in the South Shetland Islands, West Antarctica were mapped and dated using terrestrial cosmogenic ³⁶Cl methods to provide the first quantitative terrestrial record for late Quaternary deglaciation in the South Shetland Islands. ³⁶Cl ages on glacially eroded and striated bedrock surfaces range from 15.5±2.5 kyr to 1.0±0.7 kyr. The ³⁶Cl ages are younger with decreasing altitude, indicating progressive downwasting of the southwestern part of the Collins Ice Cap at a rate of ∼12 mm yr⁻¹ since 15.5±2.5 kyr ago, supporting the previously published marine records for the timing and estimate of the rate of deglaciation in this region.     

Carbon-isotope stratigraphy in shallow-water carbonates: implications for Cretaceous black-shale deposition

A Barremian to Albian succession on Mount Kanala, part of a Tethyan isolated carbonate platform, was investigated for its δ¹³C variations. The limestone sequence is composed of a series of peritidal shallowing-upward cycles with clear petrographic evidence for strong early diagenetic overprinting related to repeated subaerial exposure. Despite significant impact of diagenesis, the observed changes in δ¹³C can be very well correlated with deep-water sections from different ocean basins and shallow water carbonate platforms in the Middle East. This lends further support to the applicability of δ¹³C variations for stratigraphic purposes in shallow-water limestones. Using the δ¹³C signal, time resolution in Lower Cretaceous platform carbonates can be significantly increased, independent of bio-zonations often hampered by ecological variability.
Cyclostratigraphic analysis of the Aptian part of the section shows that strong positive excursions of the cumulative departure from mean cycle thickness of the peritidal shallowing-upward cycles coincide with global positive δ¹³C excursions. This, and the fact that positive shifts in the δ¹³C record are preserved within shallow water limestones, provide evidence that black-shale accumulation in the ocean basins occurred during sea-level rise and flooding of platform tops. Integration of carbon-isotope-, cyclo- and sequence-stratigraphic results from different carbonate platforms indicate that strong positive global δ¹³C shifts and concurrent organic-carbon burial during black-shale deposition are ultimately caused by rapid rises of eustatic sea level. Hence, the rate of change of eustatic sea level is considered to play a crucial role in black-shale accumulation in the global ocean basins during the Cretaceous.