Structural and Hydrogeological Controls on Hydrocarbon and Brine Migration into Drinking Water Aquifers in Southern New York

Environmental concerns regarding the potential for drinking water contamination in shallow aquifers have accompanied unconventional energy development in the northern Appalachian Basin. These activities have also raised several critical questions about the hydrogeological parameters that control the naturally occurring presence and migration of hydrocarbon gases in shallow aquifers within petroliferous basins. To interrogate these factors, we analyzed the noble gas, dissolved ion, and hydrocarbon gas (molecular and isotopic composition) geochemistry of 98 groundwater samples from south‐central New York. All samples were collected ?1km from unconventional drilling activities and sample locations were intentionally targeted based on their proximity to various types of documented fault systems. In agreement with studies from other petroliferous basins, our results show significant correlations between elevated levels of radiogenic [⁴He], thermogenic [CH₄], and dissolved ions (e.g., Cl, Br, Sr, Ba). In combination, our data suggest that faults have facilitated the transport of exogenous hydrocarbon‐rich brines from Devonian source rocks into overlying Upper Devonian aquifer lithologies over geologic time. These data conflict with previous reports, which conclude that hydrodynamic focusing regulates the occurrence of methane and salt in shallow aquifers and leads to elevated levels of these species in restricted flow zones within valley bottoms. Instead, our data suggest that faults in Paleozoic rocks play a fundamental role in gas and brine transport from depth, regulate the distribution of their occurrence in shallow aquifers, and influence the geochemistry of shallow groundwater in this petroliferous basin.     

The aftermath of the Carnian carbonate platform demise: a basinal perspective (Dolomites, Southern Alps)

In the Dolomites of northernmost Italy the carbonate‐platform growth came to a standstill late in the Early Carnian (Late Triassic). The response to this shutdown of shallow‐water carbonate production in the interplatform basins is largely unknown because erosion has removed most of the soft basinal sediments, giving rise to today's scenic landscape of the Dolomites. Mapping in the central part of the Dolomites and newly available core material has recently revealed a well‐preserved succession of basinal rocks within the Heiligkreuz Hospiz Basin (ital. Ospizio di Santa Croce Basin). In this paper, the regional depositional nature of arrested carbonate platform production is reconstructed by tracing its sedimentological record across the slope and into the basin. The uppermost St. Cassian Formation, the time‐equivalent basinal rocks to the prograding carbonate platforms, is overlain by the Heiligkreuz Formation, whose basal succession was deposited in a restricted and oxygen‐depleted environment immediately post‐dating the platform demise. The succession consists mainly of mudrocks, marlstones, and peloidal packstones, with abundant low‐diversity ostracod and pelecypod fauna and early diagenetic dolomite. C and O isotope values of the basal Heiligkreuz Formation, post‐dating platform demise, average + 2·4 and ? 2·4‰, respectively, and largely overlap the isotopic composition of St. Cassian carbonates. A shift toward slightly lower δ¹³C values in the Heiligkreuz Formation may reflect incorporation of isotopically depleted C released during bacterial sulphate reduction in the Heiligkreuz sediments. Sedimentological, palaeobiological and geochemical indices suggest that near‐normal marine conditions persisted long after the shutdown of shallow water carbonate‐platform growth, although there are clear indications of severely reduced oxygen levels in the restricted Heiligkreuz Hospiz interplatform basin. The Early Carnian platform demise induced a distinct switch in the locus of carbonate production from the shallow‐water platform and slope to the basin floor and a decrease in the availability of dissolved oxygen in the basinal waters. It is inferred that anoxia extended at least temporarily to the top of the carbonate slope, as indicated by the onlap of normal‐marine mounds by dark marlstones of the basal Heiligkreuz Formation.     

The origin of Himalayan anatexis and inverted metamorphism: Models and constraints

The key to comprehending the tectonic evolution of the Himalaya is to understand the relationships between large-scale faulting, anatexis, and inverted metamorphism. The great number and variety of mechanisms that have been proposed to explain some or all of these features reflects the fact that fundamental constraints on such models have been slow in coming. Recent developments, most notably in geophysical imaging and geochronology, have been key to coalescing the results of varied Himalayan investigations into constraints with which to test proposed evolutionary models. These models fall into four general types: (1) the inverted metamorphic sequences within the footwall of the Himalayan thrust and adjacent hanging wall anatexis are spatially and temporally related by thrusting; (2) thrusting results from anatexis; (3) anatexis results from normal faulting; and (4) apparent inverted metamorphism in the footwall of the Himalayan thrust is produced by underplating of right-way-up metamorphic sequences. We review a number of models and find that many are inconsistent with available constraints, most notably the recognition that the exposed crustal melts and inverted metamorphic sequences not temporally related. The generalization that appears to best explain the observed distribution of crustal melts and inverted metamorphic sequences is that, due to specific petrological and tectonic controls, episodic magmatism and out-of-sequence thrusting developed during continuous convergence juxtaposing allochthonous igneous and metamorphic rocks. This coincidental juxtaposition has proven to be something of a red herring, unduly influencing attention toward finding a causal relationship between anatexis and inverted metamorphism.     

Petrogenesis of metatexite and diatexite migmatites determined using zircon U–Pb age,trace element and Hf isotope data,Higo metamorphic terrane,central Kyushu,Japan

Metatexite and diatexite migmatites are widely distributed within the upper amphibolite and granulite facies zones of the Higo low‐P/high‐T metamorphic terrane. Here, we report data from an outcrop in the highest grade part of the granulite facies zone, in which diatexite occurs as a 3 m thick layer between 2 m thick layers of stromatic‐structured metatexite within pelitic gneiss. The migmatites and gneiss contain the same peak mineral assemblage of biotite + plagioclase + quartz + garnet + K‐feldspar with retrograde chlorite ± muscovite and some accessory minerals of ilmenite ± rutile ± titanite + apatite + zircon + monazite ± pyrite ± zinc sulphide ± calcite. Calculated metamorphic P–T conditions are 800–900 °C and 9–12 kbar. Zircon in the diatexite forms elongate euhedral crystals with oscillatory zoning, but no core–rim structure. Zircon from the gneiss and metatexite forms euhedral–subhedral grains comprising inherited cores overgrown by thin rims. The overgrowth rims in the metatexite have lower Th/U ratios than zircon in the diatexite and yield a ²⁰⁶Pb/²³⁸U age of 116.0 ± 1.6 Ma, which is older than the 110.1 ± 0.6 Ma ²⁰⁶Pb/²³⁸U age derived from zircon in the diatexite. Zircon from the diatexite has variable REE contents with convex upward patterns and flat normalized HREE, whereas the overgrowth rims in the metatexite and gneiss have steep HREE‐enriched patterns; however, both types have similar positive Ce and negative Eu anomalies. ¹⁷⁶Hf/¹⁷⁷Hf ratios in the overgrowth rims from the metatexite are more variable and generally lower than values from zircon in the diatexite. Based on U–Pb ages, trace element and Hf isotope data, the zircon rims in the metatexite are interpreted to have crystallized from a locally derived melt, following partial dissolution of inherited protolith zircon during anatexis, whereas the zircon in the diatexite is interpreted to have crystallized from a melt that included an externally derived component. By integrating zircon and petrographic data for the migmatites and pelitic gneiss, the metatexite migmatite is interpreted to have formed by in situ partial melting in which the melt did not migrate from the source, whereas the diatexite migmatite included an externally derived juvenile component. The Cretaceous high‐temperature metamorphism of the Higo metamorphic terrane is interpreted to reflect emplacement of mantle‐derived basalts under a volcanic arc along the eastern margin of the Eurasian continent and advection of heat via hybrid silicic melts from the lower crust. Post‐peak crystallization of anatectic melts in a high‐T region at mid‐crustal depths occurred in the interval c. 116–110 Ma, as indicated by the difference in zircon ages from the metatexite and diatexite migmatites.     

Quantifying different riverbank erosion processes during an extreme flood event

Riverbank erosion is a major contributor to catchment sediment budgets. At large spatial scales data is often restricted to planform channel change, with little information on process distributions and their sediment contribution. This study demonstrates how multi‐temporal LiDAR and high resolution aerial imagery can be used to determine processes and volumes of riverbank erosion at a catchment scale. Remotely sensed data captured before and after an extreme flood event, enabled a digital elevation model of difference (DoD) to be constructed for the channel and floodplain. This meant that: the spatial area that could be assessed was extensive; three‐dimensional forms of bank failures could be mapped at a resolution that enabled process inference; and the volume and rates of different bank erosion processes over time could be assessed. A classification of riverbank mass failures, integrating form and process, identified a total of 437 mass failure polygons throughout the study area. These were interpreted as wet flow mass failures based on the presence of a well defined scarp wall and the absence of failed blocks on the failure floor. The failures appeared to be the result of: bank exfiltration, antecedent moisture conditions preceding the event, and the historic development of the channel. Using one‐dimensional hydraulic modelling to delineate geomorphic features within the main boundary of the macrochannel, an estimated 1 466 322 m² of erosion was interpreted as fluvial entrainment, occurring across catchment areas from 30 to 1668 km². Only 8% of the whole riverbank planform area was occupied by mass failures, whilst fluvial entrainment covered 33%. A third of the volume of material eroded came from mass failures, even though they occupied 19% of the eroded bank area. The availability of repeat LiDAR surveys, combined with high‐resolution aerial photography, was very effective in erosion process determination and quantification at a large spatial scale. Copyright © 2013 John Wiley & Sons, Ltd.     

A new radiocarbon chronology of Baumkirchen,stratotype for the onset of the Upper Würmian in the Alps

The start of the Upper Würmian in the Alps was marked by massive fluvioglacial aggradation prior to the arrival of the Central Alpine glaciers. In 1984, the Subcommission on European Quaternary Stratigraphy defined the clay pit of Baumkirchen (in the foreland of the Inn Valley, Austria) as the stratotype for the Middle to Upper Würmian boundary in the Alps. Key for the selection of this site was its radiocarbon chronology, which still ranks among the most important datasets of this time interval in the Alps. In this study we re‐sampled all available original plant specimens and established an accelerator mass spectrometry chronology which supersedes the published 40‐year‐old chronology. The new data show a much smaller scatter and yielded slightly older conventional radiocarbon dates clustering at ca. 31 ¹⁴C ka BP. When calibrated using INTCAL13 the new data suggest that the sampled interval of 653–681 m in the clay pit was deposited 34–36 cal ka BP. Using two new radiocarbon dates of bone fragments found in the fluvioglacial gravel above the banded clays allows us to constrain the timing of the marked change from lacustrine to fluvioglacial sedimentation to ca. 32–33 cal ka BP, which suggests a possible link to the Heinrich 3 event in the North Atlantic. Copyright © 2013 John Wiley & Sons, Ltd.     

On the use of loss‐on‐ignition techniques to quantify fluvial particulate organic carbon

The fluvial flux of carbon (C) from terrestrial to marine environments represents an important component of the global C‐cycle, which can transfer C from the atmosphere to sedimentary storage. Fluvial fluxes of C are also an essential resource for freshwater ecosystems, critical for habitat heterogeneity and function. As such it is crucial that we are able to quantify this flux accurately. However, at present there are a number of different techniques used to quantify concentrations of fluvial C, and these techniques vary in their accuracy. In this article, we compare particulate organic carbon (POC) measurements derived from two commonly‐used techniques; a simple combustion and loss‐on‐ignition (LOI) technique, and an oxidative–combustion and carbon dioxide (CO₂) detection technique. The techniques were applied to water samples collected from 10 contrasting reference‐condition, temperate river ecosystems. The POC measurements derived from the LOI technique were up to 16 times higher (average four times higher), than those derived from the oxidative–combustion and CO₂ detection technique. This difference was highly variable both across the different river ecosystems and within each river ecosystem over time, suggesting that there is no simple way of converting the mass measured by LOI to estimates of fluvial POC. It is suggested that the difference in POC measured by these two techniques is a consequence of: (1) the loss of inorganic carbon at LOI combustion temperatures of > 425 °C, (2) the potential during the LOI combustion stage to lose hygroscopic and intercrystalline water, not completely driven off by the drying stage at temperatures of < 150 °C, and (3) the variable C content of fluvial organic matter, meaning that the simple application of a fixed correction factor to values obtained from the LOI technique may not be appropriate. These findings suggest that oxidative–combustion and CO₂ detection techniques are preferential for quantifying fluvial POC. Copyright © 2013 John Wiley & Sons, Ltd.