Application of organic petrology and geochemistry to coal waste studies

Coal wastes produced during mining activities are commonly deposited in nearby dumps. These wastes mostly composed of minerals and variable amounts (usually 20-30%) of organic matter start to weather immediately after deposition. Oxidation of the organic matter can lead to self heating and self combustion as a result of organic and mineral matter transformations. The degree of alteration depends on the properties of the wastes, i.e., the maceral and microlithotype composition of the organic matter and its rank.Alteration of wastes also depends on the heating history, i.e., the rate of heating, final heating temperature, duration of heating, and the degree of air access. Although air is probably necessary to initiate and drive the heating processes, these usually take place under relatively oxygen depleted conditions. With slow heating, color of organic matter particles changes, irregular cracks and oxidation rims develop around edges and cracks, and bitumen is expelled. As a result, massive and detritic isotropic and strongly altered organic matter forms. On the other hand, higher heating rates cause the formation of devolatilization pores, oxidation rims around these pores and along cracks, vitrinite-bands-mantling particles, and bitumen expulsions.Organic compounds generated from the wastes include n-alkanes, iso-alkanes, alkylcyclohexanes, acyclic isoprenoids, mainly pristane, phytane and, in some cases, farnesane, sesquiterpanes, tri- and tetracyclic diterpanes, tri- and pentacyclic triterpanes, and steranes, polycyclic aromatic hydrocarbons (mostly with two- to five rings, rarely six rings), and phenols. The compounds formed change during the heating history. The fact that phenols are found in dumps where heating has not yet been completed, but are absent in those where heating ceased previously suggests the presence of water washing. The organic compounds formed may migrate within the dumps. However, when they migrate out of the dumps, they become a hazard to environment.This paper is a review on transformations of organic matter (both maceral composition and reflectance and chemical composition) in coal wastes deposited in coal waste dumps. Immediately after deposition the wastes are exposed to weathering conditions and sometimes undergo self heating processes.     

Book Reviews

Book reviewed in this article:
Westheide, W. & C. O. Hermans (Eds.): The Ultrastructure of Polychaeta. Microfauna Marina, Vol. 4. Ed.: P. Ax, Veröffentl. der Akademie der Wissenschaften u. der Literatur, Mainz. Gustav Fischer Verlag, Stuttgart, New York, 1988. 494 pp., numerous figs. Hard cover; DM 118,—.     

IR calibrations for water determination in olivine,r-GeO<Subscript>2</Subscript>, and SiO<Subscript>2</Subscript> polymorphs

Mineral-specific IR absorption coefficients were calculated for natural and synthetic olivine, SiO₂ polymorphs, and GeO₂ with specific isolated OH point defects using quantitative data from independent techniques such as proton–proton scattering, confocal Raman spectroscopy, and secondary ion mass spectrometry. Moreover, we present a routine to detect OH traces in anisotropic minerals using Raman spectroscopy combined with the “Comparator Technique”. In case of olivine and the SiO₂ system, it turns out that the magnitude of ε for one structure is independent of the type of OH point defect and therewith the peak position (quartz ε = 89,000 ± 15,000 textl textmol_textH2textO^-1 textcm^-2text{l},text{mol}_{{text{H}_2}text{O}}^{-1},text{cm}^{-2}), but it varies as a function of structure (coesite ε = 214,000 ± 14,000 textl textmol_textH2textO^-1 textcm^-2text{l},text{mol}_{{text{H}_2}text{O}}^{-1},text{cm}^{-2}; stishovite ε = 485,000 ± 109,000 textl textmol_textH2textO^-1 textcm^-2text{l},text{mol}_{{text{H}_2}text{O}}^{-1},text{cm}^{-2}). Evaluation of data from this study confirms that not using mineral-specific IR calibrations for the OH quantification in nominally anhydrous minerals leads to inaccurate estimations of OH concentrations, which constitute the basis for modeling the Earth’s deep water cycle.     

Recent insights into the dissolved and particulate fluxes from the Himalayan tributaries to the Ganga River

The Ganga River plays a major role in the transfer of materials from the Indian sub-continent to the Bay of Bengal, both in dissolved and particulate forms. To understand the present elemental dynamics of the Ganga River system, it is important to assess the hydrogeochemical contribution of its tributaries. In this paper, we present an updated database on dissolved and particulate fluxes and denudation rates of the Himalayan tributaries of the Ganga River (Ramganga, Ghaghara, Gandak and Kosi). Dissolved trace element concentrations, their fluxes and suspended sediment-associated elemental fluxes of the Himalayan tributaries have been reported for the first time. Total dissolved flux of the Ramganga, Ghaghara, Gandak and Kosi was estimated as 4, 19.1, 10.3 and 8.8 million tons year^?1 accounting for ~?5.7, ~?27.3, ~?14.7 and ~?12.6%, respectively, of the total annual dissolved load carried by the Ganga River. The total particulate flux of the Ramganga, Ghaghara, Gandak and Kosi was computed as 8.2, 81.6, 30.9 and 19.5 million tons year^?1, respectively. Compared to earlier studies, we have found a significant increase in the total dissolved flux and chemical denudation rate of the studied tributaries. The estimated particulate fluxes were found to be low in comparison to the previous studies. We suggest that a significant increase in the dissolved fluxes and a decrease in the particulate fluxes are an indication of the increasing anthropogenic disturbances in the catchment of these tributaries.     

Implications of trace element composition of syntaxial quartz cements for the geochemical conditions during quartz precipitation in sandstones

A petrographic investigation revealed polyphase quartz cementation in the Finefrau Sandstone (Upper Carboniferous, Western Germany) and the Solling Sandstone (Lower Triassic, Central Germany). Three different cements could be distinguished in each sandstone based on their cathodoluminescence and trace element composition. The first quartz generation is suggested to have been formed during eogenesis due to dissolution and replacement of feldspar. The mesogenetic paragenesis comprises two generations of quartz and illite, which are accompanied by albite in the Solling Sandstone. Sharp luminescence zoning in quartz overgrowths points to distinct episodes of cementation in both sandstones. Significant amounts of Al, Li and H and traces of Ge and B have been detected in the quartz overgrowths. The Al‐content of the quartz cements in the Finefrau Sandstones exceeds that in the quartz cements in the Solling Sandstone by a factor of five. It is suggested that this compositional variation reflects the conditions in the pore‐water, such as temperature and pH. The Al‐concentration is generally correlated to the Li‐content with the exception of the latest quartz generation in the Finefrau Sandstones which is also most enriched in trace elements. The ratio of Li/Al varies between 0·11 and 0·25 in the two sandstones. The Li/H‐ratio, which ranges from 0·12 to 0·3, is controlled by the activity ratio of Li and H in the pore fluid. Clay minerals are the most important source for Li and high salinities favour the mobilization of Li during diagenesis. Thus, a relatively low salinity and low pH are responsible for the low Li/H‐ratio in the Finefrau Sandstone, while high salinity and neutral to alkaline pH results in a high Li/H‐ratio for the Solling Sandstone. The Ge‐contents are generally near the average of detrital quartz and indicate that pressure dissolution is a major source for quartz cementation. Different chemical compositions of distinct quartz generations indicate changes in the physico‐chemical conditions and point to mobilization of silica from different sources (for example, pressure solution and clay mineral transformations).     

On the way to a better state? The role of NGOs in the planning and implementation of protected areas in Brazil

Protected areas are considered some of the most versatile as well as important instruments of nature conservation and environmental policies. The `classic' model of nature conservation aims at the isolation of large areas in order to preserve their `pristine' nature from human interference. However, the transfer of this model to developing countries led to serious conflicts with local people. From a socio-geographical viewpoint, protected areas can be understood as regulative tools for the shaping and controlling of space. This approach helps to recognise the influence of distinct modes of appropriation of space and nature on the emergence and course of conflicts. In the present article it is used to analyse the leading role played by Brazilian NGOs in the transformation of the classic model of protected area management at the beginning of the nineties. Two case studies – dealing with the implementation of the Amazonian Mamirauá Reserve and with the reform of the Brazilian protected area legislation – are used to illustrate not only the success of the new approaches, but also the expectations and contradictions which surround the future development of protected areas in Brazil.     

Aerobic degradation of organic carbon inferred from dinoflagellate cyst decomposition in Southern Ocean sediments

Organic carbon (OC) burial is an important process influencing atmospheric CO₂ concentration and global climate change; therefore it is essential to obtain information on the factors determining its preservation. The Southern Ocean (SO) is believed to play an important role in sequestering CO₂ from the atmosphere via burial of OC. Here we investigate the degradation of organic-walled dinoflagellate cysts (dinocysts) in two short cores from the SO to obtain information on the factors influencing OC preservation. On the basis of the calculated degradation index kt, we conclude that both cores are affected by species-selective aerobic degradation of dinocysts. Further, we calculate a degradation constant k using oxygen exposure time derived from the ages of our cores. The constant k displays a strong relationship with pore-water O₂, suggesting that decomposition of OC is dependent on both the bottom- and pore-water O₂ concentrations.