Geochemical Characteristics of Oil from Oligocene Lower Ganchaigou Formation Oil Sand in Northern Qaidam Basin,China

Oil from the Oligocene oil sands of the Lower Ganchaigou Formation in the Northern Qaidam Basin and the related asphaltenes was analyzed using bulk and organic geochemical methods to assess the organic matter source input, thermal maturity, paleo-environmental conditions, kerogen type, hydrocarbon quality, and the correlation between this oil and its potential source rock in the basin. The extracted oil samples are characterized by very high contents of saturated hydrocarbons (average 62.76%), low contents of aromatic hydrocarbons (average 16.11%), and moderate amounts of nitrogen–sulfur–oxygen or resin compounds (average 21.57%), suggesting that the fluid petroleum extracted from the Oligocene oil sands is of high quality. However, a variety of biomarker parameters obtained from the hydrocarbon fractions (saturated and aromatic) indicate that the extracted oil was generated from source rocks with a wide range of thermal maturity conditions, ranging from the early to peak oil window stages, which are generally consistent with the biomarker maturity parameters, vitrinite reflectance (approximately 0.6%), and T_max values of the Middle Jurassic carbonaceous mudstones and organic-rich mudstone source rocks of the Dameigou Formation, as reported in the literature. These findings suggest that the studied oil is derived from Dameigou Formation source rocks. Furthermore, the source- and environment-related biomarker parameters of the studied oil are characterized by relatively high pristane/phytane ratios, the presence of tricyclic terpanes, low abundances of C₂₇ regular steranes, low C₂₇/C₂₉ regular sterane ratios, and very low sterane/hopane ratios. These data suggest that the oil was generated from source rocks containing plankton/land plant matter that was mainly deposited in a lacustrine environment and preserved under sub-oxic to oxic conditions, and the data also indicate a potential relationship between the studied oil and the associated potential source rocks. The distribution of pristane, phytane, tricyclic terpanes, regular steranes and hopane shows an affinity with the studied Oligocene Lower Ganchaigou Formation oil to previously published Dameigou Formation source rocks. In support of this finding, the pyrolysis–gas chromatography results of the analyzed oil asphaltene indicate that the oil was primarily derived from type II organic matter, which is also consistent with the organic matter of the Middle Jurassic source rocks. Thus, the Middle Jurassic carbonaceous mudstones and organic rock mudstones of the Dameigou Formation could be significantly contributing source rocks to the Oligocene Lower Ganchaigou Formation oil sand and other oil reservoirs in the Northern Qaidam Basin.

     

Characterization of Late Cretaceous to Miocene source rocks in the Eastern Mediterranean Sea: An integrated numerical approach of stratigraphic forward modelling and petroleum system modelling

Stratigraphic forward modelling was used to simulate the deposition of Upper Cretaceous, Eocene and Oligo‐Miocene source rocks in the Eastern Mediterranean Sea and, thus, obtain a process‐based 3D prediction of the quantity and quality distribution of organic matter (OM) in the respective intervals. Upper Cretaceous and Eocene models support the idea of an upwelling‐related source rock formation along the Levant Margin and the Eratosthenes Seamount (ESM). Along the margin, source rock facies form a narrow band of 50 km parallel to the palaeo shelf break, with high total organic carbon (TOC) contents of about 1% to 11%, and HI values of 300–500 mg HC/g TOC. On top of the ESM, TOC contents are mainly between 0.5% and 3% and HI values between 150 and 250 mg HC/g TOC. At both locations, TOC and HI values decrease rapidly towards the deeper parts of the basin. In the Oligo‐Miocene intervals, terrestrial OM makes up the highest contribution to the TOC content, as marine organic matter (OM) is diluted by high‐sedimentation rates. In general, TOC contents are low (<1%), but are distributed relatively homogenously throughout the whole basin, creating poor quality, but very thick source rock intervals of 1–2 km of cumulative thickness. The incorporation of these source rock models into a classic petroleum system model could identify several zones of thermal maturation in the respective source rock intervals. Upper Cretaceous source rocks started petroleum generation in the late Palaeocene/early Eocene with peak generation between 20 and 15 Ma ca. 50 km offshore northern Lebanon. Southeast of the ESM, generation started in the early Eocene with peak generation between 18 and 15 Ma. Eocene source rocks started HC generation ca. 25 Ma ago between 50 and 100 km southeast of the ESM and reached the oil to wet gas window at present day. However, until today they have converted less than 20% of their initial kerogen. Although the Miocene source rocks are mostly immature, Oligocene source rocks lie within the oil window in the southern Levant Basin and reached the onset of the wet gas window in the northern Levant Basin. However, only 10%–20% of their initial kerogen have been transformed to date.     

Molecular fingerprinting of wetland organic matter using pyrolysis-GC/MS: an example from the southern Cape coastline of South Africa

Pyrolysis–gas chromatography mass spectrometry (py-GC/MS) allows the characterisation of complex macromolecular organic matter. In lakes and wetlands this can potentially be used to assess the preservation/diagenesis and provenance of sediment organic matter. It can complement palaeoenvironmental investigations utilising ‘bulk’ sediment variables such as total organic carbon (TOC) and TOC/total nitrogen ratios. We applied py-GC/MS analyses to a ~32,000-year sediment record from the southern Cape coastline of South Africa. We used the results to evaluate the sources and extent of degradation of organic matter in this semi-arid environment. Marked down-core changes in the relative abundance of multiple pyrolysis products were observed. Correspondence analysis revealed that the major driver of this down-core variability in OM composition was selective preservation/degradation. Samples comprising highly degraded OM are primarily confined to the lower half of the core, older than ~12,000 years, and are characterised by suites of low-molecular-weight aromatic pyrolysis products. Samples rich in organic matter, e.g. surface sediments, are characterised by products derived from fresh emergent or terrestrial vegetation, which include lignin monomers, plant-derived fatty acids and long-chain n-alkanes. Pyrolysates from the late glacial-early Holocene period, approximately mid-way down the core are characterised by distinct suites of long-chain n-alkene/n-alkane doublets, which may reflect the selective preservation of recalcitrant aliphatic macromolecules and/or enhanced inputs of the algal macromolecule algaenan/polymerised algal lipids. Increased TOC, lower δ¹³C and increased abundance of more labile lignin and fatty acid products at the same depths suggest this period was associated with increased lake primary productivity and enhanced inputs of terrestrial OM. TOC is the only ‘bulk’ parameter correlated with the correspondence analysis axes extracted from the py-GC/MS data. Distinct fluctuations in TOC/total nitrogen ratio are not explained by variation in organo-nitrogen pyrolysis products. Notwithstanding, the study suggests that py-GC/MS has potential to complement palaeolimnological investigations, particularly in regions such as southern Africa, where other paleoenvironmental proxy variables in sediments may be lacking or equivocal.     

Application of210Pb in soils

The spectroscopic measurement of soil samples is described.²¹⁰Pb data from a soil survey in western-Europe are briefly reviewed. The average²¹⁰Pb flux from the atmosphere, as determined from²¹⁰Pb _exc soil inventories, is 90 Bq m^–2a^–1. A simple one-dimensional box-chain model is described. The model simulates the vertical, post depositional transport of natural and fall-out radionuclides in the soil. Simulation of measured²¹⁰Pb _exc ,¹³⁴Cs,¹³⁷Cs, and²⁴¹Am soil profiles shows that mixing (bioturbation) is a very efficient transport mechanism. Lead seems to be strongly fixed to organic and clay particles. It is transported by the displacement of the organic and clay carrier substances. The mean residence time of lead, caesium, plutonium and americium in organic rich forest soils is in the order of 250–1000 years. An applicability study in investigate the use of²¹⁰Pb in erosion problems showed erosion rates from 60–180 g m^–2a^–1 on organic rich forest and meadow sites with 10°–25° slopes.This is the eighth of a series of papers to be published by this journal following the 20 ^th anniversary of the first application of²¹⁰Pb dating of lake sediments. Dr P. G. Appleby is guest editing this series.     

Numerical modelling of the hydrocarbon generation of Tertiary source rocks intruded by doleritic sills in the Zhanhua depression,Bohai Bay Basin,China

An igneous hydrocarbon reservoir had been found in the Zhanhua depression, Bohai Bay Basin, eastern China. Two doleritic sills successively intruded into the immature source rock of the third member of the Shahejie Formation (Es3). The heat released from the magma changed the mineral composition of wall rocks and accelerated the maturity of organic matter. Thin hornfels and carbargilite zones were found next to the sills. The vitrinite reflectances (%R_o) of these heated wall rocks increased to at least 1.4% near the contacts (<50 m), and accumulation of oil was found in the hornfels zone and dolerite bodies. With the aim of understanding the influence of the sills on the hydrocarbon generation process, a complex heat conduction model was used to simulate the thermal history of the organic‐rich wall rocks, in which both the latent heat of crystallization of intrusions and vapourization heat of pore water in wall rocks were considered. The simulation results suggested that the cooling of each sill continued for about 0.1 Ma after its emplacement and the temperature of wall rocks was considerably raised. The peak temperature (T_peak) that wall rocks experienced can reach 460–650°C in the region of 10 m away from the contacts. The thermal model was qualitatively verified by comparing the experimental data of vitrinite reflectances and mineral geothermometers of the wall rocks with the simulation results. Furthermore, we modelled the hydrocarbon generation of the source rocks based on the simulated thermal history. In the region of about 100 m from the contacts, the organic matter was heated and partially transformed into hydrocarbon within only a few 1000 years, which was significantly faster than the normal burial generation process.     

Rates of peat accumulation over the past 200 years in fiveSphagnum-dominated peatlands in the United States

Using²¹⁰Pb-dating of peat cores, corroborated by pollen and acid-insoluble ash approaches, rates of vertical height growth, dry mass accumulation, and organic matter accumulation were determined for fiveSphagnum-dominated peatland sites (one in Minnesota, one in Pennsylvania, one on the Maryland/West Virginia border, two in West Virginia), spanning a mean annual temperature range of 4.5 °C and differing in total annual precipitation by a factor of almost 2. Site differences in rates of vertical height growth and dry mass accumulation were documented, but both within-core and between-site differences in bulk density and ash concentrations of peat confound efforts to relate vertical height growth and dry mass accumulation to net organic matter accumulation. Taking bulk densities and ash concentrations into account, rates of net organic matter accumulation over the past 150–200 years were strikingly similar at four of the five sites, an unexpected result given the general trend that with decreasing latitude, peat deposits become older, thinner, and more highly decomposed. More comprehensive studies are needed in which net organic matter accumulation is determined at several locations within a single peatland, at several peatlands within a particular geographic/climatic region, and at peatland sites in different geographic/climatic regions. If additional studies confirm that recent (past 200 years) net organic matter accumulation is relatively insensitive to broad-scale regional climatic differences, boreal and subarctic peatlands may continue to function as a net sink for atmospheric CO₂ and a net source of atmospheric CH₄ with no change in rates of net organic matter accumulation, even under predicted scenarios of global climate change.This publication is the third paper in a series of papers presented at the session on Past Climatic Change and the Development of Peatlands at the ASLO and SWS Meetings in Edmonton, Canada, May 30–June 3, 1993. Dr P. Kuhry and Dr S. C. Zoltai are serving as Guest Editors.     

Evolution of clay mineral assemblages and organic matter in the late glacial-Holocene sedimentary infill of Lake Annecy, (northwestern Alps): paleoenvironmental implications

The basin fill of Lake Annecy was investigated from a 44 m core which reached down to glacial sediments of the last glaciation (called Würm in the alpine areas). We analyzed three main parameters: sediment texture (optical microscopy and laser microgranulometry), clay mineral assemblages (CMA by XRD), and organic matter (OM by Rock-Eval pyrolysis). Settling of suspended load, under variable hydrodynamic conditions is the main depositional process. Both CMA and OM provenances can be recognized for the different sedimentary and igneous-metamorphic formations (Carboniferous to Quaternary, and older crystalline basement) and corresponding areas, in the surrounding region of Lake Annecy. Oligocene-Miocene molasses, Early Cretaceous marls, and Early-Middle Jurassic marls and shales are the main sedimentary sources. Two distinct processes were operating: destruction of glacial sediments (till sensu largo) and reworking, or direct erosion and run-off from ice-free catchment areas. Clay minerals related to pedogenesis, and non-reworked terrestrial and lacustrine OM, were progessively added to these primary sources during the Late Würmian/Holocene transition to warmer climatic conditions. Rapid modifications of CMA and OM sources during the earlier phase of sedimentary infilling (Unit 2) suggest that valley glaciers connected to the lake basin almost completely disappeared within a few centuries.     

Flood pattern and weather determine Populus leaf litter breakdown and nitrogen dynamics on a cold desert floodplain

Patterns and processes involved in litter breakdown on desert river floodplains are not well understood. We used leafpacks containing Fremont cottonwood (Populus deltoides subsp. wislizenii) leaf litter to investigate the roles of weather and microclimate, flooding (immersion), and macroinvertebrates on litter organic matter (OM) and nitrogen (N) loss on a floodplain in a cool-temperate semi-arid environment (Yampa River, northwestern Colorado, USA). Total mass of N in fresh autumn litter fell by 20% over winter and spring, but in most cases there was no further N loss prior to termination of the study after 653 days exposure, including up to 20 days immersion during the spring flood pulse. Final OM mass was 10–40% of initial values. The pattern of OM and N losses suggested most N would be released outside the flood season, when retention within the floodplain would be likely. The exclusion of macroinvertebrates modestly reduced the rate of OM loss (by about 10%) but had no effect on N dynamics over nine months. Immersion in floodwater accelerated OM loss, but modest variation in litter quality did not affect the breakdown rate. These results are consistent with the concept that decomposition on desert floodplains progresses much as does litter processing in desert uplands, but with periodic bouts of processing typical of aquatic environments when litter is inundated by floodwaters. The strong dependence of litter breakdown rate on weather and floods means that climate change or river flow management can easily disrupt floodplain nutrient dynamics.     

Biomarker and stable carbon isotope analyses of sedimentary organic matter from Lake Tswaing: evidence for deglacial wetness and early Holocene drought from South Africa

Comparing the organic matter (OM) composition of modern and past lake sediments contributes to the understanding of changes in lacustrine environments over time. We investigate modern plant and lake-water samples as well as modern and ancient sediment samples from the Tswaing Crater in South Africa using biomarker and stable carbon isotope analyses on bulk OM and specific biomarker compounds. The characteristic molecular markers for higher land plants (predominantly C3-type deciduous angiosperms) in Lake Tswaing are long-chain n-alkanes (n-C₂₇₋₃₃), n-alkanols (n-C₂₈₊₃₀), stigmasterol, β-sitosterol, β-amyrin, α-amyrin and lupeol. The C₁₇ n-alkane, tetrahymanol, gammaceran-3-one and C₂₉ sterols dominate the lipid fraction of autochthonously produced OM. By comparing stable carbon isotope analyses on bulk OM and the characteristic biomarkers, we follow the modern carbon cycle in the crater environment and find indications for methanotrophic activity in the lake from isotopically depleted moretene. A comparative study of core sediments reveals changes in the terrestrial (C3 versus C4) and aquatic bioproductivity and allows insights into the variability of the carbon cycle under the influence of changing climatic conditions for the time from the end of the last glacial (Termination I) to the late Holocene, ca. 14,000–2,000 calibrated years before present (years BP). The most pronounced changes occur in the aquatic realm after ca. 10,000 years BP when our results imply climate swings from more humid to more arid and after 7,500 years BP to gradually more humid conditions again, which can be related to a shift in the position of the Inter-Tropical Convergence Zone or to changes in the tropical atmosphere–ocean interaction. Long-chain alkenones (LCAs) have been identified in ancient lake sediments from Africa for the first time. They occur in samples older than 7,500 years BP and their distribution (dominance of C₃₈ and of tri- over tetra-unsaturated LCAs) is distinctly different from other published records suggesting a to date unknown source organism.     

Evaluation of Upper Triassic T3x5 Source Rocks (Western Sichuan Depression, Sichuan Basin) and their Hydrocarbon Generation and Expulsion Characteristics: Implication for Tight-Sand Gas and Shale Gas Accumulation Potential Assessment

An unconventional, continuous petroleum system consists of an accumulation of hydrocarbons that is found in low-matrix-permeability rocks and contain large amounts of hydrocarbons. Tight-sand gas in the Jurassic and shale gas within the fifth member of Xujiahe Formation (T₃x⁵) are currently regarded as the most prolific emerging unconventional gas plays in China. The conventional and systematical evaluation of T₃x⁵ source rocks was carried out for the first time in the western Sichuan basin (WSD). Hydrocarbon generation and expulsion characteristics (including intensity, efficiency, and amount) of T₃x⁵ source rocks were investigated. Results show that T₃x⁵ source rocks are thick (generally >200 m), have high total organic content (TOC, ranging from 2.5 to 4.5 wt%), and dominated by III-type kerogen. These favorable characteristics result in a great hydrocarbon generating potential under the high thermal evolution history (R _o > 1.2%) of the area. An improved hydrocarbon generation potential methodology was applied to well data from the area to unravel the hydrocarbon generation and expulsion characteristics of T₃x⁵ source rocks in the WSD. Results indicate that the source rocks reached hydrocarbon expulsion threshold at 1.06% R _o and the comprehensive hydrocarbon expulsion efficiency was about 60%. The amount of generation and expulsion from T₃x⁵ source rocks was 3.14 × 10¹⁰ and 1.86 × 10¹⁰ t, respectively, with a residual amount of 1.28 × 10¹⁰ t within the source rocks. Continuous-type tight-sand gas was predicted to develop in the Jurassic in the Chengdu Sag of the WSD because of the good source-reservoir configuration (i.e., the hydrocarbon generation and expulsion center was located in Chengdu Sag), the Jurassic sandstone reservoirs were tight, and the gas expelled from the T₃x⁵ source rocks migrated for very short distances vertically and horizontally. The amount of gas accumulation in the Jurassic reservoirs derived from T₃x⁵ source rocks is up to 9.3 × 10⁸ t. The T₃x⁵ gas shale has good accumulation potential compared with several active US shale-gas plays. Volumetrically, the geological resource of shale gas is up to 1.05 × 10¹⁰ t. Small differences between the amounts calculated by volumetric method compared with that by hydrocarbon generation potential methodology may be due to other gas accumulations present within interbedded sands associated with the gas shales.     

Stable carbon isotope ratios in lake and swamp sediments as a proxy for prehistoric forest clearance and crop cultivation in the Neotropics

Close correspondence between stable carbon isotope ratios ( ¹³ C), pollen, and charcoal profiles in sediment cores from Laguna Zoncho and Machita swamp, Costa Rica, shows that prehistoric forest clearance and crop cultivation can be detected in the stable carbon isotope ratios of total organic carbon ( ¹3C _TOC ). Analyses of δ 13C _TOC complement evidence from pollen, charcoal, and phytoliths and provide a proxy that is sensitive to the intensity and/or proximity to core sites of prehistoric forest clearance and agriculture in watersheds. Stable carbon isotope analyses are particularly useful in situations in which other evidence of forest clearance and agriculture is limited.     

Mechanisms for Organic Matter and Phosphorus Burial in Sedimentsof a Shallow, Subtropical, Macrophyte-Dominated Lake

We studied the role that submersed aquatic vegetation (SAV) plays in the sedimentation of organic matter (OM) and phosphorus (P) in Lake Panasoffkee, Florida (USA), a shallow, hard-water, macrophyte-dominated water body. Carbon/Nitrogen ratios (C/N) and stable isotope signatures (δ¹³C and δ¹⁵N) in algae, higher plants, and surface sediments were measured to identify sources of OM to the lake mud. Pollen, plant macrofossils, and geochemistry in sediment cores indicated that primary productivity and SAV abundance in Lake Panasoffkee increased in the late 1800s, probably as a response to increased P loading from human settlement and forest clearance. SAV and associated periphyton served as temporary sinks for soluble P, maintaining relatively clear-water, low-nutrient conditions in the lake. P accumulation in Lake Panasoffkee sediments increased together with indicators for greater SAV presence. This suggests that SAV and associated epiphytes promote P burial and retention in sediments. Although it might be assumed that rooted submersed macrophytes are directly responsible for P uptake from water and transfer to sediments, C/N and stable carbon isotope results argue for the importance of other macrophyte growth forms, and perhaps epiphytic algae, in permanent OM and P sequestration. For instance, high rates of photosynthesis by epiphytes in hard-water systems consume CO₂ and promote CaCO₃ precipitation. Sloughing of accumulated carbonates from macrophyte leaves transfers epiphytes and associated P to the sediment. Our paleolimnological findings are relevant to restoration efforts in the Florida Everglades and support the claim that constructed SAV wetlands remove P from waters effectively.     

Lacustrine organic matter and the Holocene paleoenvironmental record of Lake Albano (central Italy)

A combined bulk and detailed geochemical study of the sedimentary organic matter in Lake Albano, central Italy, provides critical data to track the response of this aquatic system to the environmental changes of variable amplitude that occurred during the Holocene. RockEval pyrolysis of this predominantly laminated, organic carbonrich sedimentary sequence shows changes in hydrogen and oxygen indices that are related to variations in the dominance of the primary producers. These variations are further confirmed by the pigments and the carbon isotopic composition of bulk organic matter showing that cyanobacteria dominated the lake waters during the early and late Holocene whereas diatoms have been the main producers during the middle Holocene. Sharp decreases in productivity, 2–3 centuries long, are identified at ca. 8.2, 6.4 and 3.8 ka. B.P. Changes in temperature and/or effective moisture are suggested as the most probable causes, although human impact cannot be ruled out for the latest part of the Holocene.     

Late glacial environment and climate development in northeastern China derived from geochemical and isotopic investigations of the varved sediment record from Lake Sihailongwan (Jilin Province)

Total organic carbon (TOC) content, total nitrogen (TN) content, stable nitrogen isotope (δ¹⁵N) and stable organic carbon isotope (δ¹³C_org) ratios were continuously analysed on a high resolution sediment profile from Lake Sihailongwan (SHL), covering the time span between 16,500 and 9,500 years BP. Strong variations of the investigated proxy parameters are attributed to great climatic fluctuations during the investigated time period. Variations in organic carbon isotope ratios and the ratio of TOC/TN (C/N ratio) are discussed with respect to changing proportions of different organic matter (OM) sources to bulk sedimentary OM. Phases of high TOC content, high TN content, depleted δ¹³C_org values and high δ¹⁵N values are interpreted as times with increased productivity of lacustrine algae in relation to input of terrigenous organic matter. Two distinct phases of enriched nitrogen isotope ratios from 14,200 to 13,700 and 11,550 to 11,050 years BP point towards a reduced phytoplankton discrimination against ¹⁵N due to a diminished dissolved inorganic nitrogen pool. The combination of geochemical (TOC, TN, C/N ratio) and isotopic (δ¹³C_org, δ¹⁵N) proxy parameters points to a division of climate development into four stages. A cold and dry stage before 14,200 years BP, a warm optimum stage with high phytoplankton productivity from 14,200 to 12,450 BP, a colder and drier stage from 12,450 to 11,600 BP and a stage of climatic amelioration with high variability in TOC and TN contents after 11,600 BP. These results are discussed in relation to monsoon variability and Northern Hemisphere climate development of the late glacial.     

CLIMATIC CONTROL OF pH BUFFERING IN THE A AND B HORIZONS OF UNITED STATES SOILS

In previous studies, models of the climatic controls on pH in the A (pHA) and B horizons (pHB) of U.S. soils were developed which differ in the functional forms and variables incorporated into each model. This study suggests that the differences in the models are explained by climate's control over the soil properties that determine pH buffering. Climatic control of pHA and pHB buffering in most acid soils is through its control over clay mineralogy. However in very acid soils, organic matter content (OM) is a stronger buffer of pHA than is clay mineralogy because in these highly leached soils, OM contents are very high and most OM is concentrated in the A horizon. In basic soils, climate dominates buffering through its control over the chemical reactions involving calcium carbonate (CaCO₃) formation. The pHA model suggests that in basic soils as moisture decreases CaCO₃ content increases causing pHA buffering to increase. In contrast, the pHB model suggests that as moisture decreases pHB buffering decreases. Although leaching of basic soils is limited, when it occurs a highly-concentrated pulse of calcium (Ca²⁺) is illuviated to the B horizon, causing pHB to increase. As leaching decreases, the magnitude of this pulse of Ca²⁺ increases because more Ca ²⁺ is available for leaching and depth of leaching of Ca²⁺ decreases. Studies of basic soils support only the results of the pHA model, but they are based mainly on laboratory studies which do not consider the influence of climate on B horizon chemistry. [Key Words: Soil acidity, pH buffering, climate, modeling, U.S. soils.]     

Isotopic fingerprints on lacustrine organic matter from Laguna Potrok Aike (southern Patagonia, Argentina) reflect environmental changes during the last 16,000 years

A combination of carbon-to-nitrogen ratios (TOC/TN), Rock Eval-analyses, and stable isotope values of bulk nitrogen (δ¹⁵N) and organic carbon (δ¹³C_org) was used to characterize bulk organic matter (OM) of a piston core from the Patagonian maar lake Laguna Potrok Aike (Argentina) for the purpose of palaeoenvironmental reconstruction. Sedimentary data were compared with geochemical signatures of potential OM sources from Laguna Potrok Aike and its catchment area to identify the sources of sedimentary OM. Correlation patterns between isotopic data and TOC/TN ratios allowed differentiation of five distinct phases with different OM composition. Before 8470 calibrated ¹⁴C years before present (cal. yrs BP) and after 7400 cal. yrs BP, isotopic and organo-geochemical fingerprints indicate that the sediments of Laguna Potrok Aike consist predominantly of soil and diatom OM with varying admixtures of cyanobacterial and aquatic macrophyte OM. For a short phase of the early Holocene (ca. 8470–7400 cal. yrs BP), however, extremely high input of soil OM is implied by isotopic fingerprints. Previous seismic and geochronological results indicate a severe lake-level drop of 33 m below present-day shortly before 6590 cal. yrs BP. It is suggested that this lake level drop was accompanied by increased erosion of shore banks and channel incision enhancing soil OM deposition in the lake basin. Thus, isotopic data can be linked to hydrological variations at Laguna Potrok Aike and allow a more precise dating of this extremely low lake level. An isotopic mixing model was used including four different sources (soil, cyanobacteria, diatom and aquatic macrophyte OM) to model OM variations and the model results were compared with quantitative microfossil data.     

Deep Natural Gas Resources

From a geological perspective, deep natural gas resources generally are defined as occurring in reservoirs below 15,000 feet, whereas ultradeep gas occurs below 25,000 feet. From an operational point of view, deep may be thought of in a relative sense based on the geologic and engineering knowledge of gas (and oil) resources in a particular area. Deep gas occurs in either conventionally trapped or unconventional (continuous-type) basin-center accumulations that are essentially large single fields having spatial dimensions often exceeding those of conventional fields.Exploration for deep conventional and continuous-type basin-center natural gas resources deserves special attention because these resources are widespread and occur in diverse geologic environments. In 1995, the U.S. Geological Survey estimated that 939 TCF of technically recoverable natural gas remained to be discovered or was part of reserve appreciation from known fields in the onshore areas and state waters of the United States. Of this USGS resource, nearly 114 trillion cubic feet (Tcf) of technically recoverable gas remains to be discovered from deep sedimentary basins. Worldwide estimates of deep gas also are high. The U.S. Geological Survey World Petroleum Assessment 2000 Project recently estimated a world undiscovered conventional gas resource outside the U.S. of 844 Tcf below 4.5 km (about 15,000 feet).Less is known about the origins of deep gas than about the origins of gas at shallower depths because fewer wells have been drilled into the deeper portions of many basins. Some of the many factors contributing to the origin and accumulation of deep gas include the initial concentration of organic matter, the thermal stability of methane, the role of minerals, water, and nonhydrocarbon gases in natural gas generation, porosity loss with increasing depth and thermal maturity, the kinetics of deep gas generation, thermal cracking of oil to gas, and source rock potential based on thermal maturity and kerogen type. Recent experimental simulations using laboratory pyrolysis methods have provided much information on the origins of deep gas.Technologic problems are among the greatest challenges to deep drilling. Problems associated with overcoming hostile drilling environments (e.g. high temperatures and pressures, and acid gases such as CO₂ and H₂S) for successful well completion, present the greatest obstacles to drilling, evaluating, and developing deep gas fields. Even though the overall success ratio for deep wells (producing below 15,000 feet) is about 25%, a lack of geological and geophysical information continues to be a major barrier to deep gas exploration.Results of recent finding-cost studies by depth interval for the onshore U.S. indicate that, on average, deep wells cost nearly 10 times more to drill than shallow wells, but well costs and gas recoveries differ widely among different gas plays in different basins.Based on an analysis of natural gas assessments, deep gas holds significant promise for future exploration and development. Both basin-center and conventional gas plays could contain significant deep undiscovered technically recoverable gas resources.     

Loss on ignition: a qualitative or quantitative method for organic matter and carbonate mineral content in sediments?

Since the publication of the paper of , loss on ignition (LOI) has been widely used as a method to estimate the amount of organic matter and carbonate mineral content (and indirectly of organic and inorganic carbon) in sediments. The relationships between LOI at 550 °C (LOI₅₅₀) and organic carbon (OC) content and between LOI at 950 °C (LOI₉₅₀) and inorganic carbon (IC) content are currently accepted as a standard. However, the comparison of 150 analyses of samples of diverse lithologies, collected from a single core, reveals that these relationships are affected by sediment composition (presence of clays, salts, and the variable content of organic carbon). This results in an incremental error on the estimation of carbon content from LOI values that invalidates the use of LOI values as a quantitative method for estimating carbon content. Conversely, the general trends of LOI₅₅₀ and LOI₉₅₀ show a good correlation with carbon content (both organic and inorganic) allowing use of LOI as a qualitative test for carbon content. Similarly, in our case, LOI at 105 °C (LOI₁₀₅) is a good qualitative proxy for the trends in gypsum content.     

Stable isotope (δ13C and δ15N) signatures of sedimented organic matter as indicators of historic lake trophic state

We explored the use of carbon and nitrogen isotopes (¹³C and ¹⁵N) in sedimented organic matter (OM) as proxy indicators of trophic state change in Florida lakes. Stable isotope data from four ²¹⁰Pb-dated sediment cores were compared stratigraphically with established proxies for historical trophic state (diatom-inferred limnetic total phosphorus, sediment C/N ratio) and indicators of cultural disturbance (sediment total P and ²²⁶Ra activity). Diatom-based limnetic total P inferences indicate a transition from oligo-mesotrophy to meso-eutrophy in Clear Lake, and from eutrophy to hypereutrophy in Lakes Parker, Hollingsworth and Griffin. In cores from all four lakes, the carbon isotopic signature of accumulated OM generally tracks trophic state inferences and cultural impact assessments based on other variables. Oldest sediments in the records yield lower diatom-inferred total limnetic P concentrations and display relatively low ¹³C values. In the Clear, Hollingsworth and Parker records, diatom-inferred nutrient concentrations increase after ca. AD 1900, and are associated stratigraphically with higher ¹³C values in sediment OM. In the Lake Griffin core, both proxies display slight increases before ~1900, but highest values occur over the last ~100 years. As Lakes Clear, Hollingsworth and Parker became increasingly nutrient-enriched over the past century, the ¹⁵N of sedimented organic matter decreased. This reflects, in part, the increasing relative contribution of nitrogen-fixing cyanobacteria to sedimented organic matter as primary productivity increased in these waterbodies. The Lake Griffin core displays a narrow range of both ¹³C and ¹⁵N values. Despite the complexity of carbon and nitrogen cycles in lakes, stratigraphic agreement between diatom-inferred changes in limnetic total P and the stable isotope signatures of sedimented OM suggests that ¹³C and ¹⁵N reflect shifts in historic lake trophic state.     

Holocene records of carbon and hydrogen isotope ratios of organic matter in annually laminated sediments of Lake Korttajärvi, central Finland

An 11.6 m long continuous succession of annually laminated sediments from Lake Korttajärvi in central Finland was investigated for the isotopic composition of carbon and hydrogen in organic matter. The sequence covers a time period of 9590 years, and the varve chronology has been thoroughly described in earlier studies. From 7100 to 4400 BC the lake was part of the Ancient Lake Päijänne, but in 4400 BC it became separated and formed the present independent lake system. Two organic fractions were investigated. One fraction obtained by HCl-treatment was analyzed for δ¹³C and another HCl-HF-digested organic fraction was analyzed for both δ¹³C and δD. The isotopic data were compared to atomic C/N ratios, carbon contents, diatom-inferred pH values and other environmental parameters. The diatom-inferred pH values and organic carbon contents provide evidence for a long-term change towards more acidic conditions and lower productivity in Lake Korttajärvi. The inferred pH values decrease from 7.0 to 6.1, followed by a slight increase during the last millennia. Variations in pH are accompanied by an increase in the δ¹³C_HCl-HF values of organic matter from ?31.6 to $-29.2\permilleAn 11.6 m long continuous succession of annually laminated sediments from Lake Korttaj?rvi in central Finland was investigated for the isotopic composition of carbon and hydrogen in organic matter. The sequence covers a time period of 9590 years, and the varve chronology has been thoroughly described in earlier studies. From 7100 to 4400 BC the lake was part of the Ancient Lake P?ij?nne, but in 4400 BC it became separated and formed the present independent lake system. Two organic fractions were investigated. One fraction obtained by HCl-treatment was analyzed for δ¹³C and another HCl-HF-digested organic fraction was analyzed for both δ¹³C and δD. The isotopic data were compared to atomic C/N ratios, carbon contents, diatom-inferred pH values and other environmental parameters. The diatom-inferred pH values and organic carbon contents provide evidence for a long-term change towards more acidic conditions and lower productivity in Lake Korttaj?rvi. The inferred pH values decrease from 7.0 to 6.1, followed by a slight increase during the last millennia. Variations in pH are accompanied by an increase in the δ¹³C_HCl-HF values of organic matter from −31.6 to , followed by a subtle decrease to . The changes in pH and δ¹³C_HCl-HF are closely related (r = − 0.91, P < 0.01), and apparently reflect changing environmental conditions in the lake and in its catchment area. δD values show a marked shift to higher values during the early Holocene, which may be partly related to a climatic amelioration leading to the Holocene Climatic Optimum in 6000–2500 BC. The Medieval Warm Period in AD 980–1250 is associated with a local maximum in δD, lending support for a significant warming during that time.