排序方式: 共有24条查询结果,搜索用时 15 毫秒
11.
Sbastien Blanchard Edward J. Matheson Christopher R. Fielding James L. Best Alexander B. Bryk Kalin J. Howell Charles C. Monson Gosia Mahoney Jeffrey Peakall 《Sedimentology》2019,66(1):329-361
Delta fronts are often characterized by high rates of sediment supply that result in unstable slopes and a wide variety of soft‐sediment deformation, including the formation of overpressured and mobile muds that may flow plastically during early burial, potentially forming mud diapirs. The coastal cliffs of County Clare, western Ireland, expose Pennsylvanian (Namurian) delta‐front deposits of the Shannon Basin at large scale and in three dimensions. These deposits include decametre‐scale, internally chaotic mudstone masses that clearly impact the surrounding sedimentary strata. Evidence indicates that these were true mud (unlithified sediment) diapirs that pierced overlying strata. This study documents a well‐exposed ca 20 m tall mud diapir and its impact on the surrounding mouth‐bar deposits of the Tullig Cyclothem. A synsedimentary fault and associated rollover dome, evident from stratal thicknesses and the dip of the beds, define one edge of the diapir. These features are interpreted as recording the reactive rise of the mud diapir in response to extensional faulting along its margin. Above the diapir, heterolithic sandstones and siltstones contain evidence for the creation of localized accommodation, suggesting synsedimentary filling, tilting and erosion of a shallow sag basin accommodated by the progressive collapse of the diapir. Two other diapirs are investigated using three‐dimensional models built from ‘structure from motion’ drone imagery. Both diapirs are interpreted to have grown predominantly through passive rise (downbuilding). Stratal relationships for all three diapirs indicate that they were uncompacted and fluid‐rich mud beds that became mobilized through soft‐sediment deformation during early burial (i.e. <50 m, likely <10 m depth). Each diapir locally controlled the stratigraphic architecture in the shallow subsurface and potentially influenced local palaeocurrents on the delta. The mud diapirs studied herein are distinct from deeper ‘shale diapirs’ that have been inferred from seismic sections worldwide, now largely disputed. 相似文献
12.
13.
Soils at the hyperarid margin: The isotopic composition of soil carbonate from the Atacama Desert, Northern Chile 总被引:1,自引:0,他引:1
Jay Quade Jason A. Rech Julio L. Betancourt Mary T.K. Kalin 《Geochimica et cosmochimica acta》2007,71(15):3772-3795
We evaluate the impact of exceptionally sparse plant cover (0-20%) and rainfall (2-114 mm/yr) on the stable carbon and oxygen composition of soil carbonate along elevation transects in what is among the driest places on the planet, the Atacama Desert in northern Chile. δ13C and δ18O values of carbonates from the Atacama are the highest of any desert in the world. δ13C (VPDB) values from soil carbonate range from −8.2‰ at the wettest sites to +7.9‰ at the driest. We measured plant composition and modeled respiration rates required to form these carbonate isotopic values using a modified version of the soil diffusion model of [Cerling (1984) Earth Planet. Sci. Lett.71, 229-240], in which we assumed an exponential form of the soil CO2 production function, and relatively shallow (20-30 cm) average production depths. Overall, we find that respiration rates are the main predictor of the δ13C value of soil carbonate in the Atacama, whereas the fraction C3 to C4 biomass at individual sites has a subordinate influence. The high average δ13C value (+4.1‰) of carbonate from the driest study sites indicates it formed—perhaps abiotically—in the presence of pure atmospheric CO2.δ18O (VPDB) values from soil carbonate range from −5.9‰ at the wettest sites to +7.3‰ at the driest and show much less regular variation with elevation change than δ13C values. δ18O values for soil carbonate predicted from local temperature and δ18O values of rainfall values suggest that extreme (>80% in some cases) soil dewatering by evaporation occurs at most sites prior to carbonate formation. The effects of evaporation compromise the use of δ18O values from ancient soil carbonate to reconstruct paleoelevation in such arid settings. 相似文献
14.
James Feathers Renato Kipnis Luis Pil Manuel Arroyo‐Kalin David Coblentz 《Geoarchaeology》2010,25(4):395-436
During an excavation in the 1970s, a disarticulated female human skeleton, later nicknamed Luzia, was discovered at 12m depth at Lapa Vermelha rockshelter in central Brazil. Radiocarbon dating of associated charcoal suggested an age of 11.4‐16.4 ka for the skeleton. The scattering of the skeletal parts, some uncertainty about the exact provenience of the skeleton, and evidence of pervasive insect turbation in the archaeological layers have raised doubts about the accuracy of the age. Luminescence dates for the depositional ages of the sediments at Lapa Vermelha are reported here. Single‐grain optically stimulated luminescence (OSL) of quartz along with grain‐size, chemical and micro‐morphological analyses of the sediments were employed to assess stratigraphic integrity, particularly the degree of sediment mixing. These various lines of evidence point to high stratigraphic integrity with little mixing at Lapa Vermelha. Sediments closest to where Luzia was recovered give OSL ages ranging from 12.7 to 16.0 ka, thus not refuting the original dates. © 2010 Wiley Periodicals, Inc. 相似文献
15.
D.?H.?PhillipsEmail author A.?O.?Thomas K.?Forde K.?Dickson S.?Plant G.?Norris B.?Bone R.?M.?Kalin 《Environmental Geology》2007,52(6):1117-1131
Volatile organic compound (VOC) contamination of subsurface geological material and groundwater was discovered on the Nortel
Monkstown industrial site, Belfast, Northern Ireland. The objectives of this study were to (1) investigate the characteristics
of the geological material and its influences on contaminated groundwater flow across the site using borehole logs and hydrological
evaluations, and (2) identify the contaminants and examine their distribution in the subsurface geological material and groundwater
using chemical analysis. This report focuses on the eastern car park (ECP) which was a former storage area associated with
trichloroethene (TCE) degreasing operations. This is where the greatest amount of volatile organic compounds (VOCs), particularly
TCE, were detected. The study site is on a complex deposit of clayey glacial till with discontinuous coarser grained lenses,
mainly silts, sands and gravel, which occur at 0.45–7.82 m below ground level (bgl). The lenses overall form an elongated
formation that acts as a small unconfined shallow aquifer. There is a continuous low permeable stiff clayey till layer beneath
the lenses that performs as an aquitard to the groundwater. Highest concentrations of VOCs, mainly TCE, in the geological
material and groundwater are in these coarser lenses at ∼4.5–7 m bgl. Highest TCE measurements at 390,000 μg L−1 for groundwater and at 39,000 μg kg−1 at 5.7 m for geological material were in borehole GA19 in the coarse lens zone. It is assumed that TCE gained entrance to
the subsurface near this borehole where the clayey till was thin to absent above coarse lenses which provided little retardation
to the vertical migration of this dense non-aqueous phase liquid (DNAPL) into the groundwater. However, TCE is present in
low concentrations in the geological material overlying the coarse lens zone. Additionally, VOCs appear to be associated with
poorly drained layers and in peat <3.0 m bgl in the ECP. Some indication of natural attenuation as VOCs degradation products
vinyl chloride (VC) and dichloromethane (DCM) also occur on the site. 相似文献
16.
This paper describes a natural-gradient field tracer test to characterise solute-transport properties in a sand and gravel
aquifer in the Hebei Province, northern China. Some laboratory-scale column tests on aquifer material and a local-scale field
borehole-dilution test have been conducted previously, but the field test reported herein represents the only large-scale
tracer test in the aquifer, which is the sole water supply to the city of Shi Jiazhuang and which is threatened by urban pollution.
The aim of the study was to quantify the transport behaviour of nonreactive pollutants in this aquifer. Little quantitative
data are available concerning its solute-transport properties; thus, the results of the tracer test are significant and critical
for understanding pollutant transport and fate. The in-situ tracer test was carried out in the aquifer using a slug injection
of the geochemically conservative, radioactive iodine tracer 131I. The longitudinal (α
L
) and transverse (α
T
) hydrodynamic dispersivities for solute transport in the field are 1.72 and 0.0013 m, respectively. The ratio of longitudinal
dispersivity α
L
and the flow length at the field scale is 1:10. The ratio between α
L
and α
T
from the in-situ test (~1,300:1) demonstrates a dominant longitudinal dispersion in this fluvial sand and gravel aquifer.
The tracer test further indicates a relatively short transit time for the aquifer (linear velocities ~13 m/d) under natural-gradient
conditions.
Electronic Publication 相似文献
17.
Siobhan F. Cox John D. McKinley Andrew S. Ferguson Gwen O’Sullivan Robert M. Kalin 《Environmental Earth Sciences》2013,68(7):1935-1944
This study is the first investigation of biodegradation of carbon disulphide (CS2) in soil that provides estimates of degradation rates and identifies intermediate degradation products and carbon isotope signatures of degradation. Microcosm studies were undertaken under anaerobic conditions using soil and groundwater recovered from CS2-contaminated sites. Proposed degradation mechanisms were validated using equilibrium speciation modelling of concentrations and carbon isotope ratios. A first-order degradation rate constant of 1.25 × 10?2 h?1 was obtained for biological degradation with soil. Carbonyl sulphide (COS) and hydrogen sulphide (H2S) were found to be intermediates of degradation, but did not accumulate in vials. A 13C/12C enrichment factor of ?7.5 ± 0.8 ‰ was obtained for degradation within microcosms with both soil and groundwater whereas a 13C/12C enrichment factor of ?23.0 ± 2.1 ‰ was obtained for degradation with site groundwater alone. It can be concluded that biological degradation of both CS2-contaminated soil and groundwater is likely to occur in the field suggesting that natural attenuation may be an appropriate remedial tool at some sites. The presence of biodegradation by-products including COS and H2S indicates that biodegradation of CS2 is occurring and stable carbon isotopes are a promising tool to quantify CS2 degradation. 相似文献
18.
19.
At the global scale, the population density of coastal areas is nearly three times that of inland areas, and consequently, land development represents a threat to coastal ecosystems. It is critical to understand how increasing urbanization affects coastal watersheds. To that end, the objective of this study was to examine the influence of urban development on stream water quality and hydrology in a coastal setting, a scenario that has received less attention than other physiographic regions. Stream hydrologic, physicochemical, and microbial data were collected in watersheds near Apalachicola, Florida with a range of impervious surfaces from 0 to 15%. Watersheds with greater impervious cover exhibited higher pH, specific conductance, and temperature, elevated nutrient concentrations and loads (, and total phosphorus), higher bacterial concentrations (fecal coliform and Escherichia coli), and increased maximum flow and hydrograph flashiness. Different responses to development here compared to other physiographic regions included lower total suspended solid concentrations, higher total dissolved solid concentrations, and a lack of response of base flow to increased urbanization. Additionally, Na+ and Cl? concentrations were elevated to a greater extent than is often the case in non‐coastal areas. In the coming years, urban development is projected to increase substantially in coastal zones and thus there is risk of further stream degradation in coastal watersheds. Copyright © 2011 John Wiley & Sons, Ltd. 相似文献
20.
B.?RottierEmail author H.?Rezeau V.?Casanova K.?Kouzmanov R.?Moritz K.?Schl?glova M.?W?lle L.?Fontboté 《Contributions to Mineralogy and Petrology》2017,172(4):23
Heating of quartz crystals in order to study melt and high-temperature fluid inclusions is a common practice to constrain major physical and chemical parameters of magmatic and hydrothermal processes. Diffusion and modification of trace element content in quartz and its hosted melt inclusions have been investigated through step-heating experiments of both matrix-free quartz crystals and quartz crystals associated with sulfides and other minerals using a Linkam TS1500 stage. Magmatic and hydrothermal quartz were successively analyzed after each heating step for Cu, Al, and Ti using electron probe micro-analyzer. After the last heating step, quartz crystals and their hosted melt inclusions were analyzed by laser ablation inductively coupled plasma mass spectrometry and compared to unheated samples. Heated samples reveal modification of Cu, Li, Na, and B contents in quartz and modification of Cu, Li, Ag, and K concentrations in melt inclusions. Our results show that different mechanisms of Cu, Li, and Na incorporation occur in magmatic and hydrothermal quartz. Heated magmatic quartz records only small, up to a few ppm, enrichment in Cu and Na, mostly substituting for Li. By contrast, heated hydrothermal quartz shows enrichment up to several hundreds of ppm in Cu, Li, and Na, which substitute for originally present H. This study reveals that the composition of both quartz and its hosted melt inclusions may be significantly modified upon heating experiments, leading to erroneous quantification of elemental concentrations. In addition, each quartz crystal also becomes significantly enriched in Cu in the sub-surface layer during heating. We propose that sub-surface Cu enrichment is a direct indication of Cu diffusion in quartz externally sourced from both the surrounding sulfides as well as the copper pins belonging to the heating device. Our study shows that the chemical compositions of both heated quartz and its hosted inclusions must be interpreted with great caution to avoid misleading geological interpretations. 相似文献