Landscape variations in stream water SO4 and δSSO4 in a boreal stream network

Despite reduced anthropogenic deposition during the last decades, deposition sulphate may still play an important role in the biogeochemical cycles of S and many catchments may act as net sources of S that may remain for several decades. The aim of this study is to elucidate the temporal and spatial dynamics of both SO₄²⁻ and δ³⁴S_SO4 in stream water from catchments with varying percentage of wetland and forest coverage and to determine their relative importance for catchment losses of S. Stream water samples were collected from 15 subcatchments ranging in size from 3 to 6780 ha, in a boreal stream network, northern Sweden. In forested catchments (<2% wetland cover) S-SO₄²⁻ concentrations in stream water averaged 1.7 mg L⁻¹ whereas in wetland dominated catchments (>30% wetland cover) the concentrations averaged 0.3 mg L⁻¹. A significant negative relationship was observed between S-SO₄²⁻ and percentage wetland coverage (r² = 0.77, p < 0.001) and the annual export of stream water SO₄²⁻ and wetland coverage (r² = 0.76, p < 0.001). The percentage forest coverage was on the other hand positively related to stream water SO₄²⁻ concentrations and the annual export of stream water SO₄²⁻ (r² = 0.77 and r² = 0.79, respectively). The annual average δ³⁴S_SO4 value in wetland dominated streams was +7.6‰ and in streams of forested catchments +6.7‰. At spring flood the δ³⁴S_SO4 values decreased in all streams by 1‰ to 5‰. The δ³⁴S_SO4 values in all streams were higher than the δ³⁴S_SO4 value of +4.7‰ in precipitation (snow). The export of S ranged from 0.5 kg S ha⁻¹ yr⁻¹ (wetland headwater stream) to 3.8 kg S ha⁻¹ yr⁻¹ (forested headwater stream). With an average S deposition in open field of 1.3 kg S ha⁻¹ yr⁻¹ (2002-2006) the mass balance results in a net export of S from all catchments, except in catchments with >30% wetland. The high temporal and spatial resolution of this study demonstrates that the reducing environments of wetlands play a key role for the biogeochemistry of S in boreal landscapes and are net sinks of S. Forested areas, on the other hand were net sources of S.     

Sediment magnetic properties reveal holocene climate change along the Minnesota prairie-forest ecotone

We propose a model that explains variations in magnetic parameters of lake sediments as a record of Holocene climate change. Our model is based on records from 4 lakes and incorporates the effects of erosion, dust deposition, and the authigenesis and diagenesis of the magnetic component of the sediment. Once checked against high resolution multi proxy climate records, which are currently being established for some of our study sites, it will allow us to use magnetic proxies to establish high-resolution climate reconstructions on a regional scale.Our model utilizes a combination of concentration-dependent parameters (magnetic susceptibility, IRM) and grain-size-dependent parameters (ARM/IRM, hysteresis parameters). Magnetic mineralogy is characterized by a combination of low-temperature measurements and S-ratios, and our magnetic measurements are complemented by XRD, LOI and smearslide analyses.During periods of forest growth within the watershed, deposition of terrigenous material is low and the sediment magnetic properties are characterized by low concentrations of mainly authigenic minerals (low values of IRM, high ratios of ARM/IRM). During the early to mid-Holocene dry period, deposition of terrigenous material increased due to intensified dust deposition and the erosion of lake margins caused by lowered water levels. Concentration of magnetic minerals increases (high IRM, ) and so does the grain-size of the magnetic fraction (low ARM/IRM). During the late-Holocene, sediment magnetic properties depend on the varied position of the site with respect to the prairie–forest ecotone.     

Biotic drivers of river and floodplain geomorphology – New molecular methods for assessing present‐day and past biota

Geomorphology has increasingly considered the role of biotic factors as controls upon geomorphic processes across a wide range of spatial and temporal scales. Where timescales are long (centennial and longer), it has been possible to quantify relationships between geomorphic processes and vegetation using, for example, the pollen record. However, where the biotic agents are fauna, longer term reconstruction of the impacts of biological activity upon geomorphic processes is more challenging. Here, we review the prospect of using environmental DNA as a molecular proxy to decipher the presence and nature of faunal influences on geomorphic processes in both present and ancient deposits. When used appropriately, this method has the potential to improve our understanding of biotic drivers of geomorphic processes, notably fauna, over long timescales and so to reconstruct how such drivers might explain the landscape as we see it today. Copyright © 2017 John Wiley & Sons, Ltd.     

Origin and dynamics of groundwater salinity in the alluvial plains of western Delhi and adjacent territories of Haryana State,India

Groundwater salinity is a widespread problem and a challenge to water resources management. It is an increasing concern in the alluvial plains of Delhi and neighbouring Haryana state as well as a risk for agricultural production water supply and sustainable development. This study aims to identify potential sources of dissolved salts and the driving mechanisms of salinity ingress in the shallow aquifer. It combines a comprehensive review of environmental conditions and the analysis of groundwater samples from 25 sampling points. Major ions are analysed to describe the composition and distribution of saline groundwater and dissolution/precipitation dynamics. Density stratification and local upconing of saline waters were identified by multilevel monitoring and temperature logging. Bromide–chloride ratios hold information on the formation of saline waters, and nitrate is used as an indicator for anthropogenic influences. In addition, stable isotope analysis helps to identify evaporation and to better understand recharge processes and mixing dynamics in the study region. The results lead to the conclusion that surface water and groundwater influx into the poorly drained semiarid basin naturally results in the accumulation of salts in soil, sediments and groundwater. Human‐induced changes of environmental conditions, especially the implementation of traditional canal and modern groundwater irrigation, have augmented evapotranspiration and led to waterlogging in large areas. In addition, water‐level fluctuations and perturbation of the natural hydraulic equilibrium favour the mobilisation of salts from salt stores in the unsaturated zone and deeper aquifer sections. The holistic approach of this study demonstrates the importance of various salinity mechanisms and provides new insights into the interference of natural and anthropogenic influences. Copyright © 2011 John Wiley & Sons, Ltd.     

Numerical simulation of the plasma double layer

A one-dimensional particle-in-cell computer simulation is used to model the formation of an electrostatic double layer. The conditions for the onset of the layer formation are explored and a relation between the length of the layer and the electrostatic potential difference across is found.     

Fluid and source magma evolution of the Questa porphyry Mo deposit,New Mexico,USA

Combined fluid inclusion microthermometry and microanalysis by laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS) are used to constrain the hydrothermal processes forming a typical Climax-type porphyry Mo deposit. Molybdenum mineralisation at Questa occurred in two superimposed hydrothermal stages, a magmatic-hydrothermal breccia and later stockwork veining. In both stages, texturally earliest fluids were single-phase, of low salinity (~7 wt.% NaCl_equiv.) and intermediate-density. Upon decompression to ~300 bar, they boiled off a vapour phase, leaving behind a residual brine (up to 45 wt.% NaCl_equiv) at temperatures of ~420°C. The highest average Mo concentrations in this hot brine were ~500 μg/g, exceeding the Mo content of the intermediate-density input fluid by about an order of magnitude and reflecting pre-concentration of Mo by fluid phase separation prior to MoS₂ deposition from the brine. Molybdenum concentrations in brine inclusions, then, decrease down to 5 μg/g, recording Mo precipitation in response to cooling of the saline liquid to ~360°C. Molybdenite precipitation from a dense, residual and probably sulphide-depleted brine is proposed to explain the tabular shape of the ore body and the absence of Cu-Fe sulphides in contrast to the more common Cu-Mo deposits related to porphyry stocks. Cesium and Rb concentrations in the single-phase fluids of the breccia range from 2 to 8 and from 40 to 65 μg/g, respectively. In the stockwork veins, Cs and Rb concentrations are significantly higher (45–90 and 110–230 μg/g, respectively). Because Cs and Rb are incompatible and hydrothermally non-reactive elements, the systematic increase in their concentration requires two distinct pulses of fluid exsolution from a progressively more fractionated magma. By contrast, major element and ore metal concentrations of these two fluid pulses remain essentially constant. Mass balance calculations using fluid chemical data from LA-ICPMS suggest that at least 25 km³ of melt and 7 Gt of deep input fluid were necessary to provide the amount of Mo contained in the stockwork vein stage alone. While the absolute amounts of fluid and melt are uncertain, the well-constrained element ratios in the fluids together with empirical fluid/melt partition coefficients derived from the inclusion analyses suggest a high water content of the source melt of ~10%. In line with other circumstantial evidence, these results suggest that initial fluid exsolution may have occurred at a confining pressure exceeding 5 kbar. The source of the molybdenum-mineralising fluids probably was a particularly large magma chamber that crystallised and fractionated in the lower crust or at mid-crustal level, well below the shallow intrusions immediately underlying Questa and other porphyry molybdenum deposits. Electronic supplementary material  The online version of this article (doi:) contains supplementary material, which is available to authorized users.     

Magmatic-to-hydrothermal crystallization in the W–Sn mineralized Mole Granite (NSW, Australia): Part I: Crystallization of zircon and REE-phosphates over three million years—a geochemical and U–Pb geochronological study

Zircon, monazite and xenotime crystallized over a temperature interval of several hundred degrees at the magmatic to hydrothermal transition of the Sn and W mineralized Mole Granite. Magmatic zircon and monazite, thought to have crystallized from hydrous silicate melt, were dated by conventional U–Pb techniques at an age of 247.6 ± 0.4 and 247.7 ± 0.5 Ma, respectively. Xenotime occurring in hydrothermal quartz is found to be significantly younger at 246.2 ± 0.5 Ma and is interpreted to represent hydrothermal growth. From associated fluid inclusions it is concluded that it precipitated from a hydrothermal brine ≤ 600 °C, which is below the accepted closure temperature for U–Pb in this mineral. These data are compatible with a two-stage crystallization process: precipitation of zircon and monazite as magmatic liquidus phases in deep crustal magma followed by complete crystallization and intimately associated Sn–W mineralization after intrusion of the shallow, sill-like body of the Mole Granite. Later hydrothermal formation of monazite in a biotite–fluorite–topaz reaction rim around a mineralized vein was dated at 244.4 ± 1.4 Ma, which distinctly postdates the Mole Granite and is possibly related to a younger hidden intrusion and its hydrothermal fluid system.

Obtaining precise age data for magmatic and hydrothermal minerals of the Mole Granite is hampered by uncertainties introduced by different corrections required for multiple highly radiogenic minerals crystallising from evolved hydrous granites, including ²³⁰Th disequilibrium due to Th/U fractionation during monazite and possibly xenotime crystallization, variable Th/U ratios of the fluids from which xenotime was precipitating, elevated contents of common lead, and post-crystallization lead loss in zircon, enhanced by the fluid-saturated environment. The data imply that monazite can also survive as a liquidus phase in protracted magmatic systems over periods of 10⁶ years. The outlined model is in agreement with prominent chemical core-rim variation of the zircon.     

Long-term snow and weather observations at Weissfluhjoch and its relation to other high-altitude observatories in the Alps

Snow and weather observations at Weissfluhjoch were initiated in 1936, when a research team set a snow stake and started digging snow pits on a plateau located at 2,540?m asl above Davos, Switzerland. This was the beginning of what is now the longest series of daily snow depth, new snow height and bi-monthly snow water equivalent measurements from a high-altitude research station. Our investigations reveal that the snow depth at Weissfluhjoch with regard to the evolution and inter-annual variability represents a good proxy for the entire Swiss Alps. In order to set the snow and weather observations from Weissfluhjoch in a broader context, this paper also shows some comparisons with measurements from five other high-altitude observatories in the European Alps. The results show a surprisingly uniform warming of 0.8°C during the last three decades at the six investigated mountain stations. The long-term snow measurements reveal no change in mid-winter, but decreasing trends (especially since the 1980s) for the solid precipitation ratio, snow fall, snow water equivalent and snow depth during the melt season due to a strong temperature increase of 2.5°C in the spring and summer months of the last three decades.     

Crystal-rich mass flow deposits related to the eruption of a sublacustrine silicic cryptodome (Early Permian Collio Basin, Italian Alps)

Sedimentological, granulometric and petrographic data are presented from a detailed study on a crystal-rich mass flow deposit, which is presumably related to the eruption of a sublacustrine cryptodome. The deposit forms a prominent intercalation in the Lower Permian Collio Formation in the Italian Alps north of Brescia. Outcrops of the 10–20-m-thick volcaniclastic deposit (Dasdana I Beds, DB) can be traced over 12 km from east to west. The DB consists of a thick, crystal-rich, sandy–gravelly lower subunit representing a sequence of amalgamated Bouma-a(b) divisions overlain by a thin, well-bedded, sandy–muddy subunit that is rich in outsize porphyritic silicic fragments. Modal and computer-aided image analyses reveal that the crystal-rich lower subunit contains up to 80% of volcanogenic crystals. Some samples contain up to 60% of porphyritic fragments, which have a phenocryst content of about 20%. The wide textural range from cryptocrystalline, poikilomosaic, to rarer medium-grained granophyric groundmass, the irregular to lensoid shapes of the porphyritic fragments, and the presence of basement and sedimentary clasts suggest that the DB originated from a sublacustrine eruption of a partially extrusive cryptodome (ca. 1.6 km³). Two other porphyritic felsic cryptodomes (Dosso dei Lupi, Dosso del Bue), described briefly here, emplaced into the Collio Formation sometime after the DB event, and expose flat bases and tilted sediments at their sides. Textures observed in these domes are comparable to those found in the DB porphyritic fragments.