Depositional environments of Late Eocene lignite-bearing strata, east-central Texas

Late Eocene lignites in the Brazos River Valley area occur in parasequence-scale cycles containing mostly marine sediments. Lignite is present at the base of the marine interval and forms the base of the cycle in a majority of cases. Less frequently, lignite is underlain by a thin interval of nonmarine deposits that form the base of the cycle. In both situations, the lignite is part of a thin transgressive interval. Cycles are separated by an exposure surface, usually marked by plant rooting and/or development of a paleosol in the top of the underlying sediments. Peat accumulated on top of these exposure surfaces and lignite is preserved where marine flooding allowed ocean waters to cover the peat deposits with fine grained sediments, producing high-ash lignite horizons of great lateral extent but variable thickness and quality. This strandplain model of lignite occurrence provides a better understanding of Late Eocene lignites in Texas than the deltaic or fluvial-deltaic models previously used. The strandplain model of lignite occurrence is appropriate for most of the Yegua-Jackson lignites (Middle-Late Eocene) of Texas and should be considered when evaluating depositional conditions of Paleogene lignites in the northern Gulf Coast region. A re-evaluation of Late Eocene stratigraphy of the Brazos Valley area accompanies the documentation of depositional environments.     

Kinetics of organic matter degradation, microbial methane generation, and gas hydrate formation in anoxic marine sediments

Seven sediment cores were taken in the Sea of Okhotsk in a south-north transect along the slope of Sakhalin Island. The retrieved anoxic sediments and pore fluids were analyzed for particulate organic carbon (POC), total nitrogen, total sulfur, dissolved sulfate, sulfide, methane, ammonium, iodide, bromide, calcium, and total alkalinity. A novel method was developed to derive sedimentation rates from a steady-state nitrogen mass balance. Rates of organic matter degradation, sulfate reduction, methane turnover, and carbonate precipitation were derived from the data applying a steady-state transport-reaction model. A good fit to the data set was obtained using the following new rate law for organic matter degradation in anoxic sediments:

     

Fate of microbial biomass-derived amino acids in soil and their contribution to soil organic matter

Soil organic matter (SOM) is important for soil fertility and for the global C cycle. Previous studies have shown that during SOM formation no new compound classes are formed and that it consists basically of plant- and microorganism-derived materials. However, little data on the contribution from microbial sources are available. Therefore, we investigated previously in a model study the fate of C from ¹³C-labelled Gram-negative bacteria in soil (Kindler, R., Miltner, A. Richnow, H.H., Kästner, M., 2006. Fate of gram negative bacterial biomass in soil – mineralization and contribution to SOM. Soil Biology and Biochemistry 38, 2860–2870) and showed that 44% of the bulk ¹³C remained in the soil. Here we present the corresponding data on the fate of amino acids hydrolysed from proteins, which are the most abundant components of microbial biomass. After 224 days incubation, the label in the total amino acids in the soil amended with ¹³C-labelled cells decreased only to >95%. The total amino acids therefore clearly showed a lower turnover than the bulk ¹³C and a surprisingly stable concentration. Proteins therefore have to be considered as being stabilised in soil in dead, non-extractable biomass or cell fragments by known general stabilisation mechanisms. The label in the amino acids in a fraction highly enriched in living microbial biomass decreased to a greater extent, i.e. to 25% of the initially added amount. The amino acids removed from this fraction were redistributed via the microbial food web to non-living SOM. All amino acids in the microbial biomass were degraded at similar rates without a change in isotopic signature. The nuclear magnetic resonance (NMR) spectra of the soils were very similar and indicate that the residues of the degraded microbial biomass were very similar to those of the SOM and are a significant source for the formation of the SOM.     

微生物磷脂脂肪酸单体碳同位素示踪碳循环过程

碳循环对于维持地球生命和调控气候变化具有重要意义。微生物是碳循环的关键驱动者之一,微生物群落结构和碳代谢活动的变化,能够影响温室气体的释放和碳储量,并进一步对气候变化产生反馈作用。在当前全球变化和人类活动加剧的背景下,需要进一步了解不同环境中的微生物群落组成和碳代谢活动的特征和响应。磷脂脂肪酸（PLFA）因其快速的周转速率和多样的分子结构,已经被广泛用于原位识别不同环境中活体微生物的生物量和群落结构。在此基础上,PLFA的单体碳同位素组成进一步指示了微生物利用哪些碳源,以及通过何种方式同化这些碳源,从而揭示微生物介导的碳流通和碳循环过程。本文综述了PLFA单体稳定碳同位素组成（δ¹³C）和放射性碳同位素组成（Δ¹⁴C）在示踪微生物碳循环过程中的应用。对比了农田、草地、森林、湿地以及海洋沉积物中活体微生物的碳源利用和碳同化途径的差异,这些差异可能与不同微生物对碳源的偏好以及不同环境中底物碳的可用性有关。对比了岩石、地下水、表层和深层土壤环境中微生物对化石碳源和年轻碳源的差异利用,化石碳是岩石和地下水环境中活体微生物碳源的重要组成部分,表明现代活体微生物可以直接利用部分老碳;相反,表层和深层土壤微生物倾向于利用现代碳源,这些碳源可能来自根系分泌物和从表面垂直输送的溶解有机碳。随着加速器质谱和单个化合物制备技术的进一步发展,预计PLFA单体放射性碳同位素将在微生物碳循环过程中发挥更重要的作用,值得在不同环境中进一步探索。

     

Volatile organic compounds in coastal seawater

The occurence and temporal variations of a variety of low to medium polarity organic compounds in the volatility range bracketed by n-heptane and n-octadecane have been studied in seawater from a station in Vineyard Sound, Massachusetts, and from a tidal creek in Sippewisset Marsh, Massachusetts. The closed-loop vapor phase stripping method of Grob and Zürcher (J. Chromatogr., v. 117, p. 285–294), high resolution glass capillary gas chromatography, and gas chromatography-mass spectrometry were used. Approximately 50 compounds were found at ≥ 2 ng/kg; most were recovered at less than 10 ng/kg, while the 20 ng/kg level was only rarely exceeded by a few components. The total material recovered was 0.2–1.0 μg organic carbon equivalent/kg seawater. The major compound classes found were normal alkanes, alkenes, aromatic and alkylaromatic hydrocarbons, n-aldehydes, dimethyldisulfide and dimethyltrisulfide, and a few halogenated hydrocarbons. The preliminary results suggest that both biogenic and anthropogenic sources were representted. Also, air-sea gas exchange and other physical processes may be important non-biological sinks.     

Volatile organic compounds in Quaternary sediments

The distribution of volatile organic compounds in surface sediments varies widely with the depositional environment. Oxygen and sulfur compounds, alkenes and arenes, are more abundant than alkanes in strongly reducing sediments such as those from around Walvis Bay, West Africa. Among the compounds identified by GC-MS were toluene, benzene, 2-methyl-2-butene, 3,5-dimethylcyclopentene, 3-menthylfuran, 3-methylfuran, 2-methylbutanol, 3-methylbutanol, 3-pentanone, 2-methylthiophene, 3-methylthiophene and dimethylsulfide. Some of these compounds have the isoprene carbon skeleton.In a less reducing environment such as the Arabian Sea-Persian Gulf area, a more diverse alkene assemblage was observed including ethylene, propylene, pentenes, hexenes, cyclohexene, methylpentenes and dimethylcyclopentenes. Also, the sediments contained a few very specific alkane structures. The gem-dimethyl hydrocarbons (neopentane, neohexane, and neoheptane) were dominant among the branched hydrocarbons. The high concentration of volatile alkenes and oxygen and sulfur compounds is not observed in deep sea drilling samples at depths greater than about 100 m.     

Modeling microbial processes in porous media

 The incorporation of microbial processes into reactive transport models has generally proceeded along two separate lines of investigation: (1) transport of bacteria as inert colloids in porous media, and (2) the biodegradation of dissolved contaminants by a stationary phase of bacteria. Research over the last decade has indicated that these processes are closely linked. This linkage may occur when a change in metabolic activity alters the attachment/detachment rates of bacteria to surfaces, either promoting or retarding bacterial transport in a groundwater-contaminant plume. Changes in metabolic activity, in turn, are controlled by the time of exposure of the microbes to electron acceptors/donor and other components affecting activity. Similarly, metabolic activity can affect the reversibility of attachment, depending on the residence time of active microbes. Thus, improvements in quantitative analysis of active subsurface biota necessitate direct linkages between substrate availability, metabolic activity, growth, and attachment/detachment rates. This linkage requires both a detailed understanding of the biological processes and robust quantitative representations of these processes that can be tested experimentally. This paper presents an overview of current approaches used to represent physicochemical and biological processes in porous media, along with new conceptual approaches that link metabolic activity with partitioning of the microorganism between the aqueous and solid phases. Received, January 1999 · Revised, June 1999, July 1999 · Accepted, October 1999     

Dissolution and transport of manganese by organic acids and their role in sedimentary Mn ore formation

Dissolution experiments of Mn and Fe under natural conditions from fresh basalt, weathered basalt and Mn laterite by different organic acids show that Mn is highly enriched over Fe in solutions from the weathered rocks but that more Fe than Mn is dissolved from the fresh basalt. The enrichment of Mn is caused by sparingly soluble Fe-oxides and hydroxides and more soluble Mn-oxides. In addition from the weathered rocks the Mn concentration dissolved by the organic acids is up to 1000 times higher than in inorganic solutions. Mn enrichment is caused by acid attack, organic reduction of Mn⁴+ to Mn²+ and complexing by the organic acids. The complexed Mn is not attacked as easily by oxidation as free Mn ions. Higher concentrations of manganese in the organic dissolved stage can therefore be transported by rivers over greater distances. Organic complexed Mn, derived from lateritic weathered rocks may therefore contribute to the formation of low iron marine sedimentary Mn deposits.     

Interactions of copper, organic acids, and sulfate in goethite suspensions

Sorption of copper and sulfate onto goethite (-FeOOH) in aqueous solution is examined in Cu---SO₄ binary-sorbate systems and in Cu-SO₄-organic acid (either phthalic acid or chelidamic acid) ternary-sorbate systems. Compared to single-sorbate systems, sorption of Cu onto goethite was enhanced at low pH values in the presence of sulfate. Sorption data for Cu and SO₄ in Cu---SO₄ binary-sorbate systems were described with the Generalized Two Layer Model by proposing formation of a Cu---SO₄ ternary surface complex. Addition of sulfate to a Cu-phthalic acid binary sorbate system had little effect on Cu sorption. However, addition of sulfate to Cu-chelidamic acid binary-sorbate systems resulted in significant reduction of Cu sorption at low pH values, primarily due to competition for surface sites between sulfate and Cu-chelidamic acid ternary surface complexes. While organic acids such as humic substances can potentially influence sorption of metal ions, results from this study suggest that the extent of such influence may be strongly dependent on the presence of other sorbing anions, such as sulfate. Sorption of Cu and SO₄ in Cu---SO₄-organic acid ternary-sorbate systems was predicted reasonably well, based on surface reactions and equilibrium constants derived from fitting of sorption data from single- and binary-sorbate systems. These modeling results provide a validation of the extrapolation of sorption from simple systems to multicomponent systems through surface complexation modeling.     

Proton-binding study of standard and reference fulvic acids, humic acids, and natural organic matter

The acid-base properties of 14 standard and reference materials from the International Humic Substances Society (IHSS) were investigated by potentiometric titration. Titrations were conducted in 0.1 M NaCl under a nitrogen atmosphere, averaging 30 min from start to finish. Concentrations of carboxyl groups and phenolic groups were estimated directly from titration curves. Titration data were also fit to a modified Henderson-Hasselbalch model for two classes of proton-binding sites to obtain “best fit” parameters that describe proton-binding curves for the samples. The model was chosen for its simplicity, its ease of implementation in computer spreadsheets, and its excellent ability to describe the shapes of the titration curves. The carboxyl contents of the IHSS samples are in the general order: terrestrial fulvic acids > aquatic fulvic acids > Suwannee River natural organic matter (NOM) > aquatic humic acids > terrestrial humic acids. Overall, fulvic acids and humic acids have similar phenolic contents; however, all of the aquatically derived samples have higher phenolic contents than the terrestrially derived samples. The acid-base properties of reference Suwannee River NOM are surprisingly similar to those of standard Suwannee River humic acid. Results from titrations in this study were compared with other published results from both direct and indirect titrations. Typically, carboxyl contents for the IHSS samples were in agreement with the results from both methods of titration. Phenolic contents for the IHSS samples were comparable to those determined by direct titrations, but were significantly less than estimates of phenolic content that were based on indirect titrations with Ba(OH)₂ and Ca(OAc)₂. The average phenolic-to-carboxylic ratio of the IHSS samples is approximately 1:4. Models that assume a 1:2 ratio of phenolic-to-carboxylic groups may overestimate the relative contribution of phenolic groups to the acid-base chemistry of humic substances.     

Late Cambrian microbial build-ups,Llano Area,Central Texas: A three-phase morphological evolution

Although Late Cambrian microbial build-ups were recognized in the Point Peak Member of the Wilberns Formation in Central Texas (USA) nearly 70 years ago, only a few studies focused specifically on the build-ups themselves. This study focuses on the interpretation of the regional (15 measured sections described in literature representing an area of 8000 km²) and local (field and drone photogrammetry studies in a 25 km² area from within south Mason County) microbial build-up occurrence, describes their growth phases and details their interactions with the surrounding inter-build-up sediments. The study establishes the occurrence of microbial build-ups in the lower and upper Point Peak members (the Point Peak Member is informally broken up into the lower Point Peak and the upper Point Peak members separated by Plectotrophia zone). The lower Point Peak Member consists of three <1 m thick microbial bioherms and biostrome units, in addition to heterolithic and skeletal/ooid grainstone and packstone beds. One, up to 14 m thick, microbial unit associated with inter-build-up skeletal and ooid grainstone and packstone beds, intercalated with mixed siliciclastic–carbonate silt beds, characterizes the upper Point Peak member. The microbial unit in the upper Point Peak member displays a three-phase growth evolution, from an initial colonization phase on flat based, rip-up clast lenses, to a second aggradation and lateral expansion phase, into a third well-defined capping phase. The ultimate demise of the microbial build-ups is interpreted to have been triggered by an increase of water turbidity caused by a sudden influx of fine siliciclastics. The lower Point Peak member represents inner ramp shallow subtidal and intertidal facies and the upper Point Peak member corresponds to mid-outer ramp subtidal facies. Understanding the morphological architecture and depositional context of these features is of importance for identifying signatures of early life on Earth.     

Supergene processes and uranium ore formation in the Ronneburg ore field,Germany

The Ordovician-Lower Carboniferous sequence of slightly metamorphosed gray carbonate-terrigenous rocks contains the Silurian black cherty shales enriched in carbon (6–9%), pyrite (6–7%), and uranium (∼30 ppm). The uranium ore is localized at the pinch-out of areal and linear zones of the Early Permian supergene (exogenic) oxidation of rocks expressed in reddening (hematitization). U, As, Sb, Cu, Ni, Mo, and Ag have been removed from the oxidized black shales and concentrated in the cementation zone in form of pitchblende and sulfides in wall-rock disseminations and veinlets largely hosted in carbonate-bearing rocks. In the Late Permian, during deposition of the upper Rotliegende and Zechstein, the fractures in the basement were filled with carbonates and sulfates; uranium was partly redeposited along with enrichment in Pb and Zn. Mesozoic and Cenozoic supergene processes altered uranium ore insignificantly.     

Shale depositional processes: Example from the Paleozoic Barnett Shale, Fort Worth Basin, Texas, USA

A long held geologic paradigm is that mudrocks and shales are basically the product of ‘hemipelagic rain’ of silt- and/or clay-sized, detrital, biogenic and particulate organic particles onto the ocean floor over long intervals of time. However, recently published experimental and field-based studies have revealed a plethora of micro-sedimentary features that indicate these common fine-grained rocks also could have been transported and/or reworked by unidirectional currents. In this paper, we add to this growing body of knowledge by describing such features from the Paleozoic Barnett Shale in the Fort Worth Basin, Texas, U.S.A. which suggests transport and deposition was from hyperpycnal, turbidity, storm and/or contour currents, in addition to hemipelagic rain. On the basis of a variety of sedimentary textures and structures, six main sedimentary facies have been defined from four 0.3 meter intervals in a 68m (223 ft) long Barnett Shale core: massive mudstone, rhythmic mudstone, ripple and low-angle laminated mudstone, graded mudstone, clay-rich facies, and spicule-rich facies. Current-induced features of these facies include mm- to cmscale cross- and parallel-laminations, scour surfaces, clastic/biogenic particle alignment, and normal- and inverse-size grading. A spectrum of vertical facies transitions and bed types indicate deposition from waxing-waning flows rather than from steady ‘rain’ of particles to the sea floor. Detrital sponge spicule-rich facies suggests transport to the marine environment as hypopycnal or hyperpycnal flows and reversal in buoyancy by transformation from concentrated to dilute flows; alternatively the spicules could have originated by submarine slumping in front of contemporaneous shallow marine sponge reefs, and then transported basinward as turbidity current flows. The occurrence of dispersed biogenic/organic remains and inversely size graded mudstones also support a hyperpycnal and/or turbidity flow origin for a significant part of the strata. These processes and facies reported in this paper are probably present in other organic-rich shales.     

Volatile organic compounds in open ocean and coastal surface waters

Volatile organic compounds with volatilities ranging between those of n-hexane and n-pentadecane were identified in open ocean and coastal marine surface water samples taken in the north central part of the Gulf of Mexico. Approximately 40 organic compounds were found. The types and concentrations of the compounds found depended upon the extent of anthropogenic and terrestrial influences. Open ocean samples consisted mostly of aromatic hydrocarbons, whereas coastal samples included alkanes, cycloalkanes, cycloalkenes, aromatic hydrocarbons, aldehydes and chlorinated hydrocarbons. Unpolluted open ocean and coastal water samples had individual concentrations rarely exceeding 5 ng/kg; some aromatic hydrocarbons approached 15 ng/kg. n-Pentadecane dominated the hydrocarbons in these samples (50–100 ng/kg). The most polluted coastal water samples had individual volatile organic concentrations as great as 150 ng/kg with total concentrations approaching 1000 ng/kg. The terpene, limonene, was found extensively in the coastal samples (up to 40 ng/kg). Photooxidization of hydrocarbons in industrial/urban atmospheres was considered as a possible source of aldehydes present in coastal water. The dynamic headspace stripping/Tenax-GC adsorption method coupled with packed column gas chromatography, and gas chromatography-mass spectrometry were used for volatile organic analysis.     

The significance of microbial processes in hydrogeology and geochemistry

2 (methanogenesis). In aquifers contaminated by anthropogenic contaminants, an excess of available organic carbon often exists, and microbial metabolism is limited by the availability of electron acceptors. In addition to changes in groundwater chemistry, the solid matrix of the aquifer is affected by microbial processes. The production of carbon dioxide and organic acids can lead to increased mineral solubility, which can lead to the development of secondary porosity and permeability. Conversely, microbial production of carbonate, ferrous iron, and sulfide can result in the precipitation of secondary calcite or pyrite cements that reduce primary porosity and permeability in groundwater systems. Received, January 1999/Revised, July 1999, August 1999/Accepted, October 1999     

Eocene fan delta-submarine fan deposition in the Wagwater Trough, east-central Jamaica

ABSTRACT The Wagwater Trough is a fault-bounded basin which cuts across east-central Jamaica. The basin formed during the late Palaeocene or early Eocene and the earliest sediments deposited in the trough were the Wagwater and Richmond formations of the Wagwater Group. These formations are composed of up to 7000 m of conglomerates, sandstones, and shales. Six facies have been recognized in the Wagwater Group: Facies I-unfossiliferous massive conglomerates; Facies II—channelized, non-marine conglomerates, sandstones, and shales; Facies III-interbedded, fossiliferous conglomerates and sandstones; Facies IV—fossiliferous muddy conglomerates; Facies V—channelized, marine conglomerates, sandstones, and shales; and Facies VI—thin-bedded sheet sandstones and shales. The Wagwater and Richmond formations are interpreted as fan delta-submarine fan deposits. Facies associations suggest that humid-region fan deltas prograded into the basin from the adjacent highlands and discharged very coarse sediments on to a steep submarine slope. At the coast waves reworked the braided-fluvial deposits of the subaerial fan delta into coarse sand and gravel beaches. Sediments deposited on the delta-front slope were frequently remobilized and moved downslope as slumps, debris flows, and turbidity currents. At the slope-basin break submarine fans were deposited. The submarine fans are characterized by coarse inner and mid-fan deposits which grade laterally into thin bedded turbidites of the outer fan and basin floor.     

Petrogenesis of the Barcroft pluton, northern White-Inyo Mountains, east-central California

The White-Inyo Range lies within the regional transition from Paleozoic-Precambrian North American continental basement to outboard Mesozoic and younger accreted terranes and a superimposed Andean-type arc. In the central White Mountains, the metaluminous Barcroft granodiorite invaded a major NE-striking, SE-dipping high-angle reverse fault—the Barcroft break. Because it is a relatively isolated igneous body and is well exposed over an elevation range of 1,500–4,000 m, its thermal history and that of the surrounding superjacent section are clearer than those of nearly coeval, crowded plutons emplaced in the hotter Sierra Nevada belt. The Barcroft pluton was emplaced as a compositionally heterogeneous series of areally scattered melt pulses episodically injected over the approximate interval 167–161 Ma. The oldest dated rocks are relatively quartzofeldspathic, whereas the youngest is more ferromagnesian, suggesting progressive partial fusion of a relatively mafic protolith. Heavy rare earth-enriched zircons indicate that Barcroft melts were derived at mid-crustal depths from a previously emplaced metabasaltic protolith containing plagioclase but lacking garnet. Granodioritic magma genesis involved the possible mixing of mafic and felsic melts, as well as very minor assimilation of country rocks, but mainly by fractional fusion and crystallization. Bulk chemical, rare earth, and isotopic data suggest that analyzed Barcroft rocks are members of a single suite. Granodioritic rocks are slightly more magnetite-rich at higher elevations on the NE, nearer the roof of the pluton. Earlier thermobarometry chronicled cooling and re-equilibration of the Barcroft pluton from its margins inward, as well as from mid-crustal generation depths of ~25 km through ascent and stalling at ~10–12 km. Refractory phase assemblages crystallized along the pluton margins, whereas subsolidus minerals in the interior of the of body continued to exchange with upper crustal deuteric and surficial aqueous fluids during exhumation and cooling.     

Enzymatic and Microbial Degradation of Organic Matter in Lake Hongfeng, Guizhou Province, China

1IntroductionEnzymaticandmicrobialdegradationoforganicmatterhasabearingnotonlyonearlydiagene sis,butalsoonelementcyclingandmicrobedistributioninlakesediments.Somereportsshowedtheabundancevariationsoforganicmatterinsediments (BurdigeandGardner,1998;ArthurandDean ,1998;WanGuojiangetal.,2 0 0 0 ) .However,duetothecomplexchemicalcompositionoforganicmatter,mechanismsofenzymaticandmicrobialdegradationandvariationsofeachchemicalcomponentneedtobestudiedfurther.Underanoxiccondition ,SO2 -4 isanimpo…     

The origin and distribution of HAPs elements in relation to maceral composition of the A1 lignite bed (Paleocene, Calvert Bluff Formation, Wilcox Group), Calvert mine area, east-central Texas

The origin and distribution of twelve potentially Hazardous Air Pollutants (HAPs; As, Be, Cd, Cr, Co, Hg, Mn, Ni, Pb, Sb, Se, and U) identified in the 1990 Clean Air Act Amendments were examined in relation to the maceral composition of the A1 bed (Paleocene, Calvert Bluff Formation, Wilcox Group) of the Calvert mine in east-central Texas. The 3.2 m-thick A1 bed was divided into nine incremental channel samples (7 lignite samples and 2 shaley coal samples) on the basis of megascopic characteristics. Results indicate that As, Cd, Cr, Ni, Pb, Sb, and U are strongly correlated with ash yield and are enriched in the shaley coal samples. We infer that these elements are associated with inorganic constituents in the coal bed and may be derived from a penecontemporaneous stream channel located several kilometers southeast of the mining block. Of the HAPs elements studied, Mn and Hg are the most poorly correlated to ash yield. We infer an organic association for Mn; Hg may be associated with pyrite. The rest of the trace elements (Be, Co, and Se) are weakly correlated with ash yield. Further analytical work is necessary to determine the mode of occurrence for these elements. Overall, concentrations of the HAPs elements are generally similar to or less than those reported in previous studies of lignites of the Wilcox Group, east-central region, Texas. Petrographic analysis indicates the following ranges in composition for the seven lignite samples: liptinites (5–8%), huminites (88–95%), and inertinites (trace amounts to 7%). Samples from the middle portion of the A1 bed contain abundant crypto-eugelinite compared to the rest of the samples; this relationship suggests that the degradation of plant material was an important process during the development of the peat mire. With the exception of Hg and Mn, relatively low levels of the HAPs elements studied are found in the samples containing abundant crypto-eugelinite. We infer that the peat-forming environment for this portion of the coal bed was very wet with minimal detrital input. Relatively high concentrations of crypto-humotelinite were found in samples from the top and base of the coal bed. The presence of abundant crypto-humotefinite in this part of the coal bed suggests the accumulation of wood-rich peat under conditions conducive to a high degree of tissue preservation in the peat mire. Although several of the trace elements (Be, Co, Ni, and Sb) exhibit enrichment in these samples, they are not necessarily chemically associated with humotelinite. We infer that these elements, with the exception of Be, are possibly associated with deposition of the roof and floor rock of the coal bed; however, further analytical work would be necessary to confirm this hypothesis. Beryllium may have an organic origin.     

Diagenesis and reservoir quality of the Aldebaran Sandstone, Denison Trough, east-central Queensland, Australia

The Lower Permian Aldebaran Sandstone is the principal hydrocarbon reservoir in the Denison Trough (Bowen Basin), east-central Queensland, Australia. It accumulated in a wide range of fluvio-deltaic and nearshore marine environments. Detailed petrological study of the unit by thin section, X-ray diffraction, scanning electron microscopy, electron microprobe and isotopic analysis reveals a complex diagenetic history which can be directly related to depositional environment, initial composition and burial-temperature history. Early diagenetic effects included the precipitation of pyrite, siderite and illite-smectite rims (δ¹⁸O (SMOW) =+8.9 to + 11.3‰). Deep burial effects included physico-chemical compaction and the formation of quartz overgrowths, siderite (δ¹³C(PDB) =?34.0 to + 11.5‰, δ¹⁸O =?0.7 to +22.7‰), illite/illite-smectite and ankerite (δ¹³C=?9.3 to ?4.9‰) δ¹⁸O=+ 7.6 to + 14.4‰). Involved fluids were in part ‘connate meteoric’ water derived from compaction of the underlying freshwater Reids Dome beds. Important post-maximum burial effects, controlled by deep meteoric influx from the surface, were ankerite and labile grain dissolution and formation of kaolinite (δ¹⁸O=+7.8 to +8.9‰, δD=?115 to ?99‰), calcite (δ¹³C=?9.5 to +0.9‰, δ¹⁸O=+9.0 to +20.0‰) and dawsonite (δ¹³C=?4.0 to +2.3‰, δ¹⁸O=+9.8 to +19.8‰), the formation of dawsonite reflecting eventual stagnation of the aquifer. Entrapment of contained hydrocarbons was a relatively recent event which may be continuing today. Reservoir quality varies from marginal to good in the west to poor in the east, with predictable trends being directly linked to depositional environment and diagenesis.