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111.
112.
Postglacial relative sea‐level observations from Ireland and their role in glacial rebound modelling
Anthony J. Brooks Sarah L. Bradley Robin J. Edwards Glenn A. Milne Ben Horton Ian Shennan 《第四纪科学杂志》2008,23(2):175-192
The British Isles have been the focus of a number of recent modelling studies owing to the existence of a high‐quality sea‐level dataset for this region and the suitability of these data for constraining shallow earth viscosity structure, local to regional ice sheet histories and the magnitude/timing of global meltwater signals. Until recently, the paucity of both glaciological and relative sea‐level (RSL) data from Ireland has meant that the majority of these glacial isostatic adjustment (GIA) modelling studies of the British Isles region have tended to concentrate on reconstructing ice cover over Britain. However, the recent development of a sea‐level database for Ireland along with emergence of new glaciological data on the spatial extent, thickness and deglacial chronology of the Irish Ice Sheet means it is now possible to revisit this region of the British Isles. Here, we employ these new data to constrain the evolution of the Irish Ice Sheet. We find that in order to reconcile differences between model predictions and RSL evidence, a thick, spatially extensive ice sheet of ~600–700 m over much of north and central Ireland is required at the LGM with very rapid deglaciation after 21 k cal. yr BP. Copyright © 2007 John Wiley & Sons, Ltd. 相似文献
113.
Performance characteristics of a new electronic snow water equivalent sensor in different climates
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Jerome B. Johnson Arthur B. Gelvin Paul Duvoy Garry L. Schaefer Garry Poole Glenn D. Horton 《水文研究》2015,29(6):1418-1433
The US Army ERDC CRREL and the US Department of Agriculture Natural Resources Conservation Service developed a square electronic snow water equivalent (e‐SWE) sensor as an alternative to using fluid‐filled snow pillows to measure SWE. The sensors consist of a centre panel to measure SWE and eight outer panels to buffer edge stress concentrations. Seven 3 m square e‐SWE sensors were installed in five different climate zones. During the 2011–2012 winter, 1.8 and 1.2 m square e‐SWE sensors were installed and operated in Oregon. With the exception of New York State and Newfoundland, the e‐SWE sensors accurately measured SWE, with R2 values between the sensor and manual SWE measurements of between 0.86 and 0.98. The e‐SWE sensor at Hogg Pass, Oregon, accurately measured SWE during the past 8 years of operations. In the thin, icy snow of New York during midwinter 2008–2009, the e‐SWE sensors overmeasured SWE because of edge stress concentrations associated with strong icy layers and a shallow snow cover. The New York e‐SWE sensors' measurement accuracy improved in spring 2009 and further improved during the 2011–2012 winter with operating experience. At Santiam Junction, measured SWE from the 1.8 and 1.2 m square e‐SWE sensors agreed well with the snow pillow, 3 m square e‐SWE sensor, and manual SWE measurements until February 2013, when dust and gravel blew onto the testing area resulting in anomalous measurements. © 2014 The Authors. Hydrological Processes published by John Wiley & Sons Ltd. 相似文献
114.
Melissa J. Nelson Horton E. Newsom David S. Draper 《Geochimica et cosmochimica acta》2005,69(10):2701-2711
The martian soil is a fine-grained regolith that is chemically basaltic in character with evidence for both gains and losses of volatile and mobile elements compared to martian basalt compositions. These chemical fractionations provide clues to geochemical processes on the surface of Mars. Geochemical processes contributing to the soil proposed in the past include the chemical and mechanical breakdown of rocks under surface conditions, the addition of volcanic aerosols containing S and Cl compounds, and the alteration of basaltic glass to palagonite. Our studies of terrestrial analogs suggest that hydrothermal alteration processes involving impact craters and volcanism could also contribute to the major element trends observed in martian soil. Data from Viking, Pathfinder, and the current MER missions consistently show that relative to basaltic martian meteorite compositions, the major element compositions of the soils are (1) depleted in the fluid-mobile element calcium, (2) generally similar or somewhat enriched in iron oxide and magnesium but MgO depleted compared to Gusev rocks, (3) locally variable in potassium, (4) possibly poorer in aluminum, and (6) very enriched in chlorine and sulfur. The major element trends, aside from the Cl and S enrichment, could be explained by the formation or addition of palagonite according to McSween and Keil (2000), but the missing CaO remains a problem. The chlorine and sulfur are probably derived from other processes such as volcanic aerosols and hydrothermal fluids. McSween and Keil (2000) also argued that hydrothermal alteration of basalts produce alteration trends that are inconsistent with the Mars soil, but this study concludes otherwise. We have used quantitative mass balance mixing models to investigate possible models involving mixtures of basaltic compositions with different types of alteration materials, including palagonite. We show that the Mars soil composition can be matched with a combination of unweathered basaltic martian meteorites with basaltic FeO-rich, CaO-poor alteration products. Palagonite is a possible, but not a necessary component of successful model mixtures. The hydrothermal alteration materials that form successful model mixtures are formed in low temperature, low water/rock ratio environments, and they can reproduce the required geochemical trends because they are poorer in CaO but not in FeO compared to their respective protoliths. These results argue that material altered by hydrothermal processes could be a plausible component of the soil, and that removal of CaO from the soil into some undiscovered reservoir after its formation is not required. The current soil on Mars, therefore, did not have to undergo an episode of in situ aqueous alteration but could represent a sink for materials that experienced aqueous processes in a different setting before erosion to form the soil. The soil can also represent a sink for mobile elements (e.g., S, Cl, and Br) derived from other sources such as volcanic aerosols and hydrothermal fluids. 相似文献
115.
Duane G. Horton 《Contributions to Mineralogy and Petrology》1985,91(2):171-179
Ordered illite/smectite is the most abundant and widespread product of argillic alteration associated with the Oligocene, epithermal, Ag-Pb-Zn-Cu-Au Amethyst vein system, southwest Colorado. Hydrothermal illite/smectites exhibit all Reichweite from 1 to 3 and span the composition range from about 25% to about 3% illite.— The composition and Reichweite of illite/smectite vary smoothly with distance from the Amethyst vein. With increasing distance from the vein, percent illite and the Reichweite decrease. When composition-temperature relationships of illite/smectite from modern geothermal systems are applied to the fossil Amethyst system, isotherms describing the thermal regime at the time of argillization can be estimated. Temperatures near 240° C appear to have existed near the Amethyst vein; these temperatures agree with homogenization temperatures obtained from fluid inclusions in vein minerals. The most distal illite/smectites, sampled about 260 m from the vein, indicate temperatures near 110° C. Estimated thermal gradients are on the order of 0.4 to 1° C per meter. — Although illite/smectite composition and structure vary systematically with distance from the Amethyst vein, there are no systematic trends associated with the numerous, smaller veins and veinlets in the hanging wall of the system. This indicates that temperatures of both wallrock and the fluids in all but the major Amethyst vein were nearly the same during clay formation. Apparently, the hydrothermal system had reached a fairly steady, mature, thermal state at the time of argillization. 相似文献
116.
A depositional model for offshore deposits of the lower Blue Gate Member,Mancos Shale,Uinta Basin,Utah, USA
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Lauren P. Birgenheier Brendan Horton Andrew D. McCauley Cari L. Johnson Angela Kennedy 《Sedimentology》2017,64(5):1402-1438
Depositional models that use heterogeneity in mud‐dominated successions to distinguish and diagnose environments within the offshore realm are still in their infancy, despite significant recent advances in understanding the complex and dynamic processes of mud deposition. Six cored intervals of the main body of the Mancos Shale, the lower Blue Gate Member, Uinta Basin, were examined sedimentologically, stratigraphically and geochemically in order to evaluate facies heterogeneity and depositional mechanisms. Unique sedimentological and geochemical features are used to identify three offshore environments of deposition: the prodelta, the mudbelt and the sediment‐starved shelf. Prodelta deposits consist of interlaminated siltstone and sandstone and exhibit variable and stressed trace fossil assemblages, and indicators of high sedimentation rates. The prodelta was dominated by river‐fed hyperpycnal flow. Mudbelt deposits consist of interlaminated siltstone and sandstone and are characterized by higher bioturbation indices and more diverse trace fossil assemblages. Ripples, scours, truncations and normally graded laminations are abundant in prodelta and mudbelt deposits indicating dynamic current conditions. Mudbelt sediment dispersal was achieved by both combined flow above storm wave base and current‐enhanced and wave‐enhanced sediment gravity flows below storm wave base. Sediment‐starved shelf deposits are dominantly siltstone to claystone with the highest calcite and organic content. Bioturbation is limited to absent. Sediment‐starved shelf deposits were the result of a combination of shelfal currents and hypopycnal settling of sediment. Despite representing the smallest volume, sediment‐starved shelf deposits are the most prospective for shale hydrocarbon resource development, due to elevated organic and carbonate content. Sediment‐starved shelf deposits are found in either retrogradational to aggradational parasequence sets or early distal aggradational to progradational parasequence sets, bounding the maximum flooding surface. An improved framework classification of offshore mudstone depositional processes based on diagnostic sedimentary criteria advances our predictive ability in complex and dynamic mud‐dominated environments and informs resource prospectivity. 相似文献