Enhancing pentachlorophenol degradation by vermicomposting associated bioremediation

Vermicomposting is an effective and environmentally friendly approach for soil organic contamination clean-up. This study investigated the roles and mechanisms of earthworm (Eisenia foetida) on soil pentachlorophenol (PCP) degradation with sterile and non-sterile soil-compost treatment. Limited soil PCP degradation was observed in the control and sterile compost treatments, whereas the synergetic effects of earthworm and compost contributed to the PCP biodegradation acceleration by significantly improving microbial biomass and activities. Sequence analysis and phylogentic classification of soil bacterial and fungal community structure after 42 days treatment identified the dominancy of indigenous bacterial families Pseudomonadaceae, Sphingobacteriaceae and Xanthomonadaceae, and fungal family Trichocomaceae, which were responsible for PCP biodegradation and stimulated by vermicomposting. Further investigation revealed the dominant roles of sterile compost during PCP biodegradation as the formation of humus-PCP in soil rather than neutralizing soil pH and increasing PCP availability. The mechanisms of vermicomposting include humus-PCP complex degradation, humus consumption and soil pH neutralization. This study provides a comprehensive understanding of the synergetic effect of vermicomposting on microbial community functions and PCP degradation enhancement in soils

Ice-core evidence of the thickness and character of clear-facies basal ice:Glacier de Tsanfleuron, Switzerland

Five ice cores have been retrieved from a transect close to the terminus of Glacier de Tsanfleuron, Switzerland. The cores extend from the ice surface to the glacier bed, and are 3.5-44.8 m long. Stratigraphic logging based on bubble size and density reveals the presence of a highly metamorphosed basal ice layer, about 10 m thick, from which all traces of bubble-rich ice have been removed. This bubble-poor ice, which corresponds closely with clear-facies ice observed in cavities beneath numerous temperate-based glaciers, contrasts with the overlying bubble-rich or bubble-foliated englacial ice and the underlying debris-rich and bubble-free dispersed-facies basal ice. Down-core patterns in major-ion composition, stable-isotope composition and total gas content and composition are generally consistent with formation of clear-facies ice by deformation-related metamorphism of bubbly, englacial ice. In addition, isotopic data suggest that storage of downward-percolating meltwaters occurs close to the upper surface of the clear-facies ice layer, perhaps reflecting a local variation in ice permeability across the transition from englacial to clear-facies ice. Enrichment in crustally derived ionic species is noted in the lowermost decimetres of the debris-free, clear-facies ice that immediately overlies debris-rich dispersed-facies basal ice. This ionic enrichment in debris-free ice is interpreted in terms of active inter-granular meltwater flow within some decimetres of the glacier bed.info:eu-repo/semantics/publishe

Marine derived 87Sr/86Sr in coal, a new key to geochronology and palaeoenvironment: Elucidation of the India-Eurasia and China-Indochina collisions in Yunnan, China

Coal has formed in terrestrial and coastal-marine environments from sub-polar to equatorial regions since the Devonian. It contains detailed long-term records of contemporaneous environment, climate, and subsequent modifications. However, in general, direct chronological information in coal has been sparse. The coal investigated in the present study is from the Mile intermontane basin, Yunnan Province, China, north of an arm of the Mesozoic Tethys Ocean. The coal contains marine geochemical signatures and syngenetic gypsum, common in coastal-marine sediments. The gypsum contains marine-derived Sr and, hence, has geochronological potential. The 87Sr/86Sr record (0.708350-0.708591) in the Mile coal agrees with time-calibrated 87Sr/86Sr records of marine planktonic foraminifera obtained from core DSDP 588C, 22.25-18.27 Ma (Early Miocene). The peat of the Mile coal was deposited over 4.6 Ma., which possibly is the longest deposition of a coal bed in the world to have been found today, although this duration should include the period of non-peat deposition or erosion if present during the time of the 4.6-Ma.During this period, the regional geological structures were determined by the India-Eurasia collision, which resulted in transform faults with extensive rift structures, including the Mile rhomb-shaped graben. This structural setting enabled the flow of seawater from the South China Sea to reach inland graben structures, including that of the Mile Basin, where peat was deposited. Subsequent deformation caused by the South China-Indochina collision changed the regional structural and geographical-hydrological patterns. This affected the hydrology of the Mile Basin and resulted in its uplift to its present-day elevation of 1350 m.This study is, to our knowledge, the first to use the marine-derived 87Sr/86Sr indicator and chronometer in coal. At present, marine-influenced peats generated in coastal salt marshes extend from the Arctic Ocean (Alaska and Siberia) in the north, to Patagonia and New Zealand in the south, while mangrove forests abound in equatorial and low-latitude coastal areas. The 87Sr/86Sr record of marine-influenced coal in this study area, provides a key for the determination of age-duration-rate of geological processes in the inland basin, associated with the closure of the Tethys Ocean. Results indicate that this method has potential for providing a temporal framework for geological events and processes in other areas. These may be found near marine shore lines across the globe dating back to the Devonian. Moreover, the 87Sr/86Sr signal in marine-influenced coal can be used for correlation with the well-established 87Sr/86Sr chronology of marine planktonic foraminifera. In turn, the 87Sr/86Sr signal provides a basis for correlating terrestrial records of climate and environment contained in this type of coal and associated sediments, with those of marine sediments, such as those based on ?18O in planktonic foraminifera

Time, hydrologic landscape and the long‐term storage of peatland carbon in sedimentary basins

Peatland carbon may enter long‐term storage in sedimentary basins preserved as either coal or lignite. The time required to account for the carbon in 1 – 10 m thick coal seams must represent 105 to 106 years, an order of magnitude more than previously assumed. To understand the process by which this happens requires extrapolation of our understanding of peatland carbon accumulation over timescales that greatly exceed those of Holocene peat. We analyse the consequences of extrapolating peat growth to periods of 106 years. We deduce that that key to sustained peat growth are hydrologic landscapes that can maintain a saturated peat body above the level of clastic deposition. Contrary to current stratigraphic frameworks we conclude that the generation of accommodation space at low rates of 0.1 to 0.2 mm/yr can adequately accommodate thick peat accumulation over periods >105 yrs. However, generation of accommodation space at rates >0.5 mm/yr cannot. The low rates that permit accommodation of thick peat are typical of the rates of subsidence in specific tectonic settings, particularly foreland basins, and this has implications for our understanding of the links between terrestrial carbon burial, tectonics and the carbon cycle. The long‐term stability of extensive peatland required to form coal also requires sediment bypass, modifying basin wide sediment transport and deposition. Limits to peatland growth under very low accommodation rates must exist but the relative importance of the limiting process is not understood. Finally, we discuss the consequences of these factors for predicting the future of the peatland carbon reservoir

Deducing the source and composition of rare earth mineralising fluids in carbonatites: insights from isotopic (C, O, 87Sr/86Sr) data from Kangankunde, Malawi

This is the final version of the article. Available from Springer Verlag via the DOI in this record.Carbonatites host some of the largest and highest grade rare earth element (REE) deposits but the composition and source of their REE-mineralising fluids remains enigmatic. Using C, O and 87Sr/86Sr isotope data together with major and trace element compositions for the REE-rich Kangankunde carbonatite (Malawi), we show that the commonly observed, dark brown, Fe-rich carbonatite that hosts REE minerals in many carbonatites is decoupled from the REE mineral assemblage. REE-rich ferroan dolomite carbonatites, containing 8–15 wt% REE2O3, comprise assemblages of monazite-(Ce), strontianite and baryte forming hexagonal pseudomorphs after probable burbankite. The 87Sr/86Sr values (0.70302–0.70307) affirm a carbonatitic origin for these pseudomorph-forming fluids. Carbon and oxygen isotope ratios of strontianite, representing the REE mineral assemblage, indicate equilibrium between these assemblages and a carbonatite-derived, deuteric fluid between 250 and 400 °C (δ18O + 3 to + 5‰VSMOW and δ13C − 3.5 to − 3.2‰VPDB). In contrast, dolomite in the same samples has similar δ13C values but much higher δ18O, corresponding to increasing degrees of exchange with low-temperature fluids (< 125 °C), causing exsolution of Fe oxides resulting in the dark colour of these rocks. REE-rich quartz rocks, which occur outside of the intrusion, have similar δ18O and 87Sr/86Sr to those of the main complex, indicating both are carbonatite-derived and, locally, REE mineralisation can extend up to 1.5 km away from the intrusion. Early, REE-poor apatite-bearing dolomite carbonatite (beforsite: δ18O + 7.7 to + 10.3‰ and δ13C −5.2 to −6.0‰; 87Sr/86Sr 0.70296–0.70298) is not directly linked with the REE mineralisation.This project was funded by the UK Natural Environment Research Council (NERC) SoS RARE project (NE/M011429/1) and by NIGL (NERC Isotope Geoscience Laboratory) Project number 20135

Sources of acidity and metals in a stream draining acid sulphate soil, till and peat, western Finland, revealed by a hydrochemical and sulphur isotope study

The main aim of this study was to determine, during extreme hydrological conditions, the source(s) of acids, sulphate and metals (alkali and alkaline earths) in the Munsala stream (western Finland) draining mainly acid sulphate soil, peat and till. Samples were collected at 6 sites along the main stem on 3 high-flow and 3 low-flow events, and were analysed for the required chemical and isotopic variables. The acid sulphate soils (located under farmland) had a large impact on the stream as indicated by pH values occasionally down to 4.0, moderately to strongly increased concentrations of inorganic solutes, and a high acid SO4 2- load characterised by negative d34S(sulphate) values. In addition, the forested areas underlain mainly with till and peat released low SO4 2- but low pH waters (down to at least 4.6) during high flows, indicating the importance of humic acids in controlling the pH. These humic acids flocculated abundantly in the middle/ lower reaches as a result of interaction with acid sulphate water. Therefore, not only the farmland acid sulphate soils but also the organic-rich soils/horizons in the forested areas contribute to water-quality deterioration.vo

Sulphur sources for epithermal and mesothermal veins in Cretaceous-Tertiary magmatic-arc rocks, Livingston Island, South Shetland Islands

Epithermal veins in early Triassic turbidites on Hurd Peninsula are isotopically homogeneous over an area of 13 km × 2 km (mean δ34S = +2.2‰, 1σ= 1.7, n = 65) suggesting derivation from a deep circulating, neutral-chloride hydrothermal plume containing magmatic sulphur. The sense of fractionation (pyrite = +3.5, arsenopyrite = +3.2, sphalerite = +2.9, chalcopyrite = +2.5, galena = +0.9‰) and isotopic temperatures between 250 and 345°C suggest partial isotopic equilibration. Sulphides in massive dark carbonate/peperitic dyke breccias, with abundant magnetite, hematite and titanite and traces of barite, garnet, zircon and monazite are isotopically heavy (+7 to +14.9‰, n = 12) due either to dyke intrusion into the hydrothermal system resulting in degassing of H2S, or to a second, isotopically heavy and sulphate-bearing solution in fault zones along which dykes were subsequently intruded. Vein sulphides in nearby Cretaceous volcanic rocks are similar to the epithermal system (mean = + 1.8‰, 1σ = 0.9, n = 6, pyrite = +2.0, chalcopyrite = +1.5), suggesting sulphur-derivation by degassing of sub-volcanic magma, or remobilization of disseminated sulphides during plutonism. Sulphide in an Eocene tonalite pluton is slightly 32S-enriched (mean = 0‰, 1σ = 1.9, n =7, molybdenite = +0.7, pyrite = +1.5, chalcopyrite = –2.6) and was exsolved directly from the cooling tonalitic magma