Outburst floods from glacial Lake Missoula

The Pleistocene outburst floods from glacial Lake Missoula, known as the “Spokane Floods”, released as much as 2184 km³ of water and produced the greatest known floods of the geologic past. A computer simulation model for these floods that is based on physical equations governing the enlargement by water flow of the tunnel penetrating the ice dam is described. The predicted maximum flood discharge lies in the range 2.74 × 10⁶−13.7 × 10⁶ m³ sec⁻¹, lending independent glaciological support to paleohydrologic estimates of maximum discharge.     

Solid bitumen reflectance and Rock-Eval Tmax as maturation indices: an example from the “Nordegg Member”, Western Canada Sedimentary Basin

Marine, organic-rich rock units commonly contain little for vitrinite reflectance (VR₀) measurement, the most commoly used method of assessing thermal maturity. This is true of the Lower Jurassic “Nordegg Member”, a type I/II, sulphur-rich source rock from the Western Canada Sedimentary Basin. This study examines the advantages and pitfalls associated with the use of Rock-Eval T_max and solid bitumen reflectance (BR₀) to determined maturity in the “Nordegg”. Vitrinite reflectance data from Cretaceous coals and known coalification gradients in the study area are used to extrapolate VR₀ values for the “Nordegg”.T_max increases non-linearly with respect to both BR₀ and extrapolated VR₀ values. A sharp increase in the reflectaance of both solid bitumen and vitrinite occurs between T_max 440–450°C, and is coincident with a pronounced decrease in Hydrogen Index values and the loss of solid bitumen and telalginite fluorescence over the same narrow T_max interval. This T_max range is interpreted as the main zone of hydrocarbon generation in the “Nordegg”, and corresponds to extrapolated VR₀ values of 0.55–0.85%. The moderate to high sulphur contents in the kerogen played a significant role in determining the boundaries of the “Nordegg” oil window.A linear relationship between BR₀ and extrapolated VR₀, as proposed elsewhere, is not true for the “Nordegg”. BR₀ increases with respect to extrapolated VR₀ according to Jacob's (1985) formula (VR₀=0.618×(BR₀)+0.40) up to VR₀≈0.72% (BR₀≈0.52%). Beyond this point, BR₀ increases sharply relative to extrapolated VR₀, according to the relatioship VR₀ = 0.277 × (BR₀) + 0.57 (R² = 0.91). The break in the BR₀−VR₀ curve at 0.72%VR₀ is thought to signifiy the peak of hydrocarbon generation and represents a previously unrecognized coalification jump in the solid bitumen analogous to the first coalification jump of liptinites.     

Evidence for cyclic reactions between andalusite, “sericite” and sillimanite, mount franks area, willyama complex N.S.W

In the Mt. Franks area of the Willyama Complex, microfabric evidence suggests that the alteration of andalusite to sillimanite has taken place by a process similar to that suggested by Carmichael (1969). Andalusite is pre- to syn-S₂ in age. Alteration to “sericite” has resulted in the formation of “sericite” laths, some of which are crenulated about S₂, and some which are syn- and post-S₂. “Fibrolite” occurs in these andalusite—“sericite” aggregates within the sillimanite zone and is wholly embedded in “sericite”. “Fibrolite” is pre- to syn-S₂ in age. This evidence is interpreted as suggesting that the formation of sillimanite from andalusite took place via a “sericite” phase.Further microfabric observations are interpreted to imply constant volume for the reaction aluminosilicate → “sericite”. This suggests a situation in which Al³⁺ is relatively mobile but Al⁴⁺ is relatively immobile. This suggestion differs from Carmichael's (1969) idea of Al³⁺ immobility.     

The optical features and hydrocarbon-generating model of “barkinite” from Late Permian coals in South China

Leping coal is known for its high content of “barkinite”, which is a unique liptinite maceral apparently found only in the Late Permian coals of South China. “Barkinite” has previously identified as suberinite, but on the basis of further investigations, most coal petrologists conclude that “barkinite” is not suberinite, but a distinct maceral. The term “barkinite” was introduced by (State Bureau of Technical Supervision of the People's Republic of China, 1991, GB 12937-91 (in Chinese)), but it has not been recognized by ICCP and has not been accepted internationally.In this paper, elemental analyses (EA), pyrolysis-gas chromatography, Rock-Eval pyrolysis and optical techniques were used to study the optical features and the hydrocarbon-generating model of “barkinite”. The results show that “barkinite” with imbricate structure usually occurs in single or multiple layers or in a circular form, and no definite border exists between the cell walls and fillings, but there exist clear aperture among the cells.“Barkinite” is characterized by fluorescing in relatively high rank coals. At low maturity of 0.60–0.80%R_o, “barkinite” shows strong bright orange–yellow fluorescence, and the fluorescent colors of different cells are inhomogeneous in one sample. As vitrinite reflectance increases up to 0.90%R_o, “barkinite” also displays strong yellow or yellow–brown fluorescence; and most of “barkinite” lose fluorescence at the maturity of 1.20–1.30%R_o. However, most of suberinite types lose fluorescence at a vitrinite reflectance of 0.50% Ro, or at the stage of high volatile C bituminous coal. In particular, the cell walls of “barkinite” usually show red color, whereas the cell fillings show yellow color under transmitted light. This character is contrary to suberinite.“Barkinite” is also characterized by late generation of large amounts of liquid oil, which is different from the early generation of large amounts of liquid hydrocarbon. In addition, “barkinite” with high hydrocarbon generation potential, high elemental hydrogen, and low carbon content. The pyrolysis products of “barkinite” are dominated by aliphatic compounds, followed by low molecular-weight aromatic compounds (benzene, toluene, xylene and naphthalene), and a few isoprenoids. The pyrolysis hydrocarbons of “barkinite” are mostly composed of light oil (C₆–C₁₄) and wet gas (C₂–C₅), and that heavy oil (C₁₅⁺) and methane (C₁) are the minor hydrocarbon.In addition, suberinite is defined only as suberinized cell walls—it does not include the cell fillings, and the cell lumens were empty or filled by corpocollinites, which do not show any fluorescence. Whereas, “barkinite” not only includes the cell walls, but also includes the cell fillings, and the cell fillings show bright yellow fluorescence.Since the optical features and the hydrocarbon-generating model of “barkinite” are quite different from suberinite. We suggest that “barkinite” is a new type of maceral.     

Rates of Deglaciation during the Last Glaciation and Holocene in the Cordillera Vilcanota-Quelccaya Ice Cap Region, Southeastern Perú

Moraine chronology is combined with digital topography to model deglacial rates of paleoglacier volumes in both the Huancané Valley on the west side of the Quelccaya Ice Cap and the Upismayo Valley on the northwest side of the Cordillera Vilcanota. The fastest rates of deglaciation (39×10⁻⁵ to 114×10⁻⁵ km³ yr⁻¹ and 112×10⁻⁵ to 247×10⁻⁵ km³ yr⁻¹ for each valley, respectively) were calculated for the most recent paleoglaciers, corresponding to the last few centuries. These results are consistent with observations in the Venezuelan Andes showing high rates of deglaciation since the Little Ice Age. These rates also fall within the range of 20th century rates of deglaciation measured on the Quelccaya Ice Cap (29×10⁻⁵ to 220×10⁻⁵ km³ yr⁻¹, Brecher and Thompson, 1993; Thompson, 2000). These results imply that rates of deglaciation may fluctuate significantly over time and that high rates of deglaciation may not be exclusive to the late 20th century. Equilibrium line altitude (ELA) depressions for the ice volumes of the last glaciation modeled here were computed as 230 m for the Quelccaya Ice Cap and 170 m for the Cordillera Vilcanota. Maximum ELA depressions are lower than previously published: <500 m for the Cordillera Vilcanota and <400 m for the Quelccaya Ice Cap. These lower values could imply a topographic control over paleoglacier extent.     

Dislocation generation, slip systems, and dynamic recrystallization in experimentally deformed plagioclase single crystals

Three samples of gem quality plagioclase crystals of An60 were experimentally deformed at 900 °C, 1 GPa confining pressure and strain rates of 7.5–8.7×10⁻⁷ s⁻¹. The starting material is effectively dislocation-free so that all observed defects were introduced during the experiments. Two samples were shortened normal to one of the principal slip planes (010), corresponding to a “hard” orientation, and one sample was deformed with a Schmid factor of 0.45 for the principal slip system [001](010), corresponding to a “soft” orientation. Several slip systems were activated in the “soft” sample: dislocations of the [001](010) and 110(001) system are about equally abundant, whereas 110{111} and [101] in ( 31) to ( 42) are less common. In the “soft” sample plastic deformation is pervasive and deformation bands are abundant. In the “hard” samples the plastic deformation is concentrated in rims along the sample boundaries. Deformation bands and shear fractures are common. Twinning occurs in close association with fracturing, and the processes are clearly interrelated. Glissile dislocations of all observed slip systems are associated with fractures and deformation bands indicating that deformation bands and fractures are important sites of dislocation generation. Grain boundaries of tiny, defect-free grains in healed fracture zones have migrated subsequent to fracturing. These grains represent former fragments of the fracture process and may act as nuclei for new grains during dynamic recrystallization. Nucleation via small fragments can explain a non-host-controlled orientation of recrystallized grains in plagioclase and possibly in other silicate materials which have been plastically deformed near the semi-brittle to plastic transition.     

Radiocaesium dispersion and fixation in the lagoon systems of “Ria de Aveiro”, Portugal

Radiocaesium (¹³⁷Cs) dispersion and Cs⁺ fixation were studied in the sediments collected from the lagoon systems of “Ria de Aveiro”. The Cs⁺ sorption was tested for the fine mica grains and for the < 2 μm clay fractions extracted from silty clays. The Cs⁺ exchange is found strongly onto mica-rich fractions than smectite-rich fractions. The distribution coefficient increases if the silty material is constituted by rich-mica clay fractions or if the non-clay minerals are removed from the silty-clay material. The samples studied behave as multisite ion exchange, where Cs⁺ engages in ion-exchange reactions with hydrated cations on planar sites on expansible layer silicates. Higher concentrations of the ¹³⁷Cs were found associated with mica-rich silty clays. The ¹³⁷Cs ranges from 3.2 to 3.9 Bq kg^− 1 in the < 38 μm fractions and from 2.9 to 3.3 Bq kg^− 1 in the < 64 μm fractions.     

Lower Eocene carbonate-cemented “chimney” structures (Varna, Bulgaria) — Control of seepage rates on their formation and stable isotopic signature

The genesis of Lower Eocene calcite-cemented columns, “pisoid”-covered structures and horizontal interbeds, clustered in dispersed outcrops in the Pobiti Kamani area (Varna, Bulgaria) is related to fossil processes of hydrocarbon migration. Field observations, petrography and stable isotope geochemistry of the cemented structures and associated early-diagenetic veins, revealed that varying seepage rates of a single, warm hydrocarbon-bearing fluid, probably ascending along active faults, controlled the type of structure formed and its geochemical signature. Slow seepage allowed methane to oxidize within the sediment under ambient seafloor conditions (δ¹⁸O = − 1 ± 0.5‰ V-PDB), explaining columns' depleted δ¹³C ratios of − 43‰. Increasing seepage rates caused methane to emanate into the water column (δ¹³C = − 8‰) and raised precipitation temperatures (δ¹⁸O = − 8‰). Calcite-cemented conduits formed and upward migrating fluids also affected interbed cementation. Even higher-energy fluid flow and temperatures likely controlled the formation of “pisoids”, whereby sediment was whirled up and cemented.     

Surface carbonate and land-derived clastic marine sediments from southern Chile: mineralogical and geochemical investigation

Surface carbonate and land-derived deposits in the sea off southern Chile were investigated for their mineralogical and geochemical composition. The data were related to environmental features and compared with those of similar temperate and polar carbonate deposits from Tasmania, New Zealand, Arctica, and Antarctica. The mineralogy of the siliciclastic fraction is typical of cold areas and is mainly composed of chlorite, mica, quartz, feldspars and amphibole. The CaCO₃ content varies from 30 to 90%; carbonate mineralogy is made up of low-Mg calcite, high-Mg calcite and minor amounts of aragonite. The Ca, Mg, Sr, Fe, and Mn contents of bulk carbonates and some selected skeletal hard parts are comparable to those of carbonates from Tasmania. The elemental composition is mainly related to carbonate mineralogy, skeletal components, and seawater conditions. The δ¹³C and δ¹⁸O values of carbonates are positive, and their field falls between the “seafloor diagenesis” and “upwelling water” trend lines, because the sediments are likely to be in equilibrium with waters of Antarctic origin. The mineralogical, elemental, and isotopic compositions of carbonates from southern Chile show better similarities with the “temperate” carbonates from Tasmania and New Zealand than with the “polar” carbonates from Arctica and Antarctica. Carbonate deposition is allowed by the low terrigenous input, the low SPM concentration and, probably, the upwelling of seawater from Antarctica.     

The political-economy of Blair’s “New Regional Policy”

The “region” and “regional change” have been elusive ideas within political and economic geography, and in essence require a greater understanding of their dynamic characteristics. Trailing in the backwaters of the devolution to the Celtic nations of Britain, the contemporary era of New Labour’s political-economic ideology, manifest through “third-way” governance in England places the region and its functional capacity into the heart of geographical inquiry. Drawing upon a new regionalist epistemology, this paper seeks to recover a sense of (regional) political economy through a critical investigation of the development and formulation of Blair’s “New Regional Policy” (NRP). I address how New Labour has attempted to marry economic regionalisation on the one hand, and democratic regionalism on the other. This paper specifically questions the wisdom of such a marriage of politically distinct ideologies through a critical investigation of the underlying contradictions of their strategy from both a theoretical and empirical standpoint. Demonstrated both in the North East “no” vote in 2004, and in the post-mortem undertaken by the ODPM Select Committee in 2005, the paper illustrates how a loss of political drive gradually undermined the capacity of devolution to deliver in England. Finally, I argue that through the lens of the NRP we can speculate on some of the wider issues and implications for the study of regional governance.     

Oxidation of As-bearing gold ore—a comparison of batch and column experiments

This study deals with the experimental determination of the rate of weathering and As release from Au-bearing sulfide ores of the Mokrsko-West deposit (Czech Republic). The elevated As contents in the ore and the possible As mobilisation must be taken into account due to the close proximity of the deposit to the Vltava River, a source of drinking water for Prague. Crushed and homogenized ore material was divided into four grain-size fractions showing uniform chemical and mineralogical composition and subjected to batch and column leaching experiments. The most important reactions controlling metal leaching include (i) oxidation of sulfides, (ii) carbonate equilibrium and (iii) precipitation of hydrated ferric oxides (HFO). Hydrated ferric oxides were found to be important sorbents of mobilized As. The highest concentration of As in the leachates was obtained from the 64–1000 μm fraction. The oxidation rate in the agitated batch experiment calculated on the basis of sulfate concentrations is an order of magnitude higher (3.8×10⁻⁹ to 4.4×10⁻⁸ mol SO₄²⁻ h⁻¹ g⁻¹) than in the static column experiment (9.6×10⁻¹⁰ to 7.4×10⁻⁹ mol SO₄²⁻ h⁻¹ g⁻¹). The higher oxidation rate of batch experiments is explained by abrasion of oxidation products (mainly HFO) and by further exposition of reaction surfaces of the sulfide grains.     

Laboratory and field evidence in support of the electrogeochemically enhanced migration of ions through glaciolacustrine sediment

Ionic aureoles, overlying or contiguous to massive sulphide occurrences, are postulated to have been emplaced as a result of natural galvanic forces. The occurrences of these galvanic forces, most commonly referred to as the self-potential or spontaneous polarization phenomena, are well documented, but ionic migration in response to these electrical forces remained to be proven conclusively.The purpose of this study was to attempt to document ionic migration attributable solely to electrogeochemical transport. Pleistocene glaciolacustrine sediments rich in clay-size particles was the geological substrate chosen to minimize migration processes other than those of electrogeochemical transport.Laboratory experiments which simulated a field situation and utilized the radioisotope ⁶⁵Zn as a tracer, revealed a readily detectable diffusion of Zn²⁺ into glaciolacustrine clay; the distance of penetration of the Zn²⁺ being significantly increased by the application of a DC electrical potential, similar in magnitude to a natural self-potential. The rate of diffusion was greatest around the margins of the cathodic electrode located at the base of the clay layers; the areas shown to have the greatest current density. The resulting pattern of Zn penetration into the clay, when viewed in a vertical section, showed a double peaked increase in Zn concentration on either side, and a distinct decrease in Zn penetration directly above this cathode. Extrapolation of the average diffusion coefficient found for Zn²⁺ (D₀ = 6.3 × 10⁻⁹cm s⁻¹) to other ions commonly associated with base metal deposits, revealed that only H⁺ could be expected to move through appreciable thicknesses (>20 m) of clay in the 8000 years since sediment deposition.The hypothesis that H⁺ would diffuse through varved clay, and that the resulting pattern would be predictably modified by a self-potential field generated by an oxidizing sulphide body, was tested over the Magusi River volcanogenic massive sulphide deposit near Noranda, Quebec. The organic soil horizon (H) and top of the clay soil layer (C) were sampled and analyzed for conductivity, pH, and other major and minor elements. The mineral horizon revealed distinct changes in conductivity, pH, Ca, Mg, and Fe above the contacts of the hanging wall and footwall of the sulphide horizon, thus producing a double-peaked “rabbit-ear” anomalous pattern. The H soil horizon, when corrections for variable “total” element and carbon concentrations were applied, showed clear anomalies in Fe and other pH sensitive elements. A ratio of EDTA Fe/TOTAL Fe to total organic carbon revealed the best “rabbit-ear” anomaly above the sulphide horizoon. The use of organic horizon geochemistry as a method of evaluating EM conductors overlain by water-saturated lacustrine sediments is recommended.     

Water losses from the Ričice reservoir built in the Dinaric karst

The Ričice reservoir was built in 1987 in the central part of the bare Dinaric karst region in Croatia, on the border with Bosnia and Herzegovina. The reservoir water level rise rapidly after rainfall, but due to high water-loss rates the water remains impounded for a very short time. The reservoir volume at the spillway altitude is 18.4 × 10⁶ m³. Due to water losses, the mean annual water volume in the 1989–1995 period was 6.5 × 10⁶ m³. Interdisciplinary analyses and investigations of geological, hydrological and hydrogeological factors which caused water losses from the Ričice reservoir have been carried out. Water losses from the reservoir are defined using a water budget equation. An assessment of the calculation of hydraulic conductivity, and a definition of the groundwater level below the Ričice reservoir, using Darcy's equation for vertical flow, is carried out. It may be concluded that the water losses from the Ričice reservoir are mainly controlled by the water level in the reservoir.     

“Traditional” women, “modern” water: Linking gender and commodification in Rajasthan, India

In this paper, I analyze the connections made between women and water in a Rajasthani drinking water supply project as a significant part of drinking water’s commodification. For development policy makers, water progressing from something free to something valued by price is inevitable when moving economies toward modernity and development. My findings indicate that water is not commodified simply by charging money for it, but through a series of discourses and acts that link it to other “modern” objects and give it value. One of these objects is “women”. I argue that through women’s participation activities that link gender and modernity to new responsibilities and increased mobility for village women involving the clean water supply, a “traditional” Rajasthani woman becomes “modern”. Water, in parallel, becomes “new”, “improved” and worth paying for. Women and water resources are further connected through project staff’s efforts to promote latrines by targeting women as their primary users. The research shows that villagers applied their own meanings to latrines, some of which precluded women using them. This paper fills a gap in feminist political ecology, which often overlooks how gender is created through natural resource interventions, by concerning itself with how new meanings of “water” and “women” are mutually constructed through struggles over water use and its commodification. It contributes to critical development geography literatures by demonstrating that women’s participation approaches to natural resource development act as both constraints and opportunities for village constituents. It examines an under-explored area of gender and water research by tracing village-level struggles over meanings of latrines.     

Deep structure under Yellowstone National Park U.S.A.: A continental “hot spot”

In order to understand the origin of long-lived loci of volcanism (sometimes called “hot spots”) and their possible role in global tectonic processes, it is essential to know their deep structure. Even though some work has been done on the crustal, upper-mantle, and deep-mantle structure under some of these “hot spots”, the picture is far from clear. In an attempt to study the structure under the Yellowstone National Park U.S.A., which is considered to be such a “hot spot”, we recorded teleseisms using 26 telemetered seismic stations and three groups of portable stations. The network was operated within a 150 km radius centered on the Yellowstone caldera, the major, Quaternary volcanic feature of the Yellowstone region. Teleseismic delays of about 1.5 sec are found inside the caldera, and the delays remain high over a 100 km wide area around the caldera. The spatial distribution and magnitude of the delays indicate the presence of a large body of low-velocity material with horizontal dimensions corresponding approximately to the caldera size (40 km × 80 km) near the surface and extending to a depth of 200–250 km under the caldera. Using ray-tracing and inversion techniques, it is estimated that the compressional velocity inside the anomalous body is lower than in the surrounding rock by about 15% in the upper crust and by 5% in the lower crust and upper mantle. It is postulated that the body is partly composed of molten rock with a high degree of partial melting at shallow depths and is responsible for the observed Yellowstone volcanism. The large size of the partially molten body, taken together with its location at the head of a 350 km zone of volcanic propagation along the axis of the Snake River Plain, indicates that the volcanism associated with Yellowstone has its origin below the lithosphere and is relatively stationary with respect to plate motion. Using our techniques, we are unable to detect any measurable velocity contrast in the mantle beneath the low-velocity body, and, hence, we are unable to determine whether the Yellowstone melting anomaly is associated with a deep heat source or with any deep phenomenon such as a convection plume, chemical plume, or gravitational anchor.     

The role of “excess” CO2 in the formation of trona deposits

The prevailing theory for the formation of trona [Na₃(CO₃)(HCO₃) · 2(H₂O)] relies on evaporative concentration of water produced by silicate hydrolysis of volcanic rock or volcaniclastic sediments. Given the abundance of closed drainage basins dominated by volcanics, it is puzzling that there are so few trona deposits and present-day lakes that would yield dominantly Na–CO₃ minerals upon evaporation. Groundwater in the San Bernardino Basin (southeastern Arizona, USA and northeastern Sonora, Mexico) would yield mainly Na–CO₃ minerals upon evaporation, but waters in the surrounding basins would not. Analysis of the chemical evolution of this groundwater shows that the critical difference from the surrounding basins is not lithology, but the injection of magmatic CO₂. Many major deposits of trona and Na–CO₃-type lakes appear to have had “excess” CO₂ input, either from magmatic sources or from the decay of organic matter. It is proposed that, along with the presence of volcanics, addition of “excess” CO₂ is an important pre-condition for the formation of trona deposits.     

The use of “loam” concentrates in geochemical exploration in deeply weathered arid terrains

This paper reviews some aspects of the use of “loam” (soil) concentrates in geochemical surveys in arid, deeply weathered environments.An orientation survey at a small Ni-Cu-Co prospect in Western Australia has shown that discrimination between mineralized and unmineralized samples could be achieved using Ni, Cu, Co, Cr, Zn, As, Sn, Sc, Ti, Yb and Y in the coarse fraction of heavy concentrates. However, at the same prospect the best contrast for Ni, Cu and Co in surface samples was provided by analysis of the same fraction following a cold ammonium citrate/hydroxylamine hydrochloride digestion.At a nearby, larger prospect, some 54 km² in area, concentrates were separated, by jigging, from bulk soil samples, themselves composites of representative subsamples. Sampling at a density of 4 samples per km² revealed 1–2 km² size anomalies of Cu, Ni, Co, Cr, As and Au which could be related, variously, to known Ni-Cu and Au mineralization.In Botswana, analysis of concentrates, separated by tabling from samples collected at a density of 1 sample per 7.5 km² over an area of 5400 km², identified distinctive geochemical districts. Enhanced values of Au and of Cu-Ni in the concentrates were relatable to known mineralization and the results suggested that there were also Sn-W-Mo-Bi (granitoid) and Au-Pb-Zn-Bi-Sn (volcanogenic) associations which could lead to new prospecting targets. Anomalies of certain elements (for example, Cu in an ultramafic environment) may be more readily detected in surface material by “enrichment indexing” the concentrate data.     

Sources and transport of carbon and nitrogen in the River Sava watershed, a major tributary of the River Danube

Carbon and nitrogen dynamics were examined throughout the River Sava watershed, a major tributary of the River Danube, in 2005 and 2006. The River Sava exported 2.1 × 10¹¹ mol C/yr as dissolved inorganic carbon (DIC), and emitted 2.5 × 10¹⁰ mol C/yr as CO₂ to the atmosphere. Stable carbon isotope ratios indicate that up to 42% of DIC originated from carbonate weathering and 23% from degradation of organic matter. Loads of dissolved and particulate organic carbon increased with discharge and export rates were calculated to be 2.1 × 10¹⁰ mol C/yr and up to 4.1 × 10⁹ mol C/yr, respectively. Isotopic compositions (δ¹³C and δ¹⁵N) and C/N ratios indicated that soil organic matter was the dominant source of particulate organic matter for 59% of the samples. Eighteen percent of the samples were dominated by plankton, 12% by periodic inputs of fresh terrestrial plant detritus with C/N > 15, and about 11% of the samples were dominated by the contribution of aquatic vascular plants. Nitrate inputs were controlled by land use in the River Sava watershed. δ¹⁵N_NO3 values <6‰ were found in predominantly forested watersheds, while values >6‰ typically represented watersheds with a higher percentage of agricultural and/or urban land use. Elevated δ¹⁵N_NO3 values (up to +25.5‰) at some sites were probably due to the combined effects of low-flow and inputs from sewage and/or animal waste.     

Petrologic and geochemical characteristics of “barkinite” from the Dahe mine, Guizhou Province, China

Although “barkinite” has long been studied by many geologists, its geochemical characteristics and environment of deposition are still not known in detail. In order to study the petrography and geochemical characteristics of “barkinite”, coal samples from two Permian coal seams were taken from the Dahe mine, Guizhou Province. The samples were separated into maceral fractions, and then analyzed by microscopical, isotopic, Rock-Eval, and geochemical methods. The microscopical results indicate that “barkinite” occurs as four main types. According to their relationship to other maceral groups, “barkinite” is ostensibly formed under variably dry–wet or oxidizing–reducing conditions. The extract yield, isotope data and Rock-Eval values of “barkinite” are different from other macerals. Microscopical and geochemical results indicate that “barkinite” forms part of the liptinite group.