The distribution and production of the hard clam,Mercenaria mercenaria,in Wassaw Sound,Georgia

Estuaries and Coasts - Hard clams,Mercenaria mercenaria, occurred in four intertidal habitats in the outer, high salinity (18‰) region of Wassaw Sound, Georgia: small feeder creeks $$(\bar x...     

Explosive magma-water interactions: Thermodynamics,explosion mechanisms,and field studies

Physical analysis of explosive, magma-water interaction is complicated by several important controls: (1) the initial geometry and location of the contact between magma and water; (2) the process by which thermal energy is transferred from the magma to the water; (3) the degree to and manner by which the magma and water become intermingled prior to eruption; (4) the thermodynamic equation of state for mixtures of magma fragments and water; (5) the dynamic metastability of superheated water; and (6) the propagation of shock waves through the system. All of these controls can be analyzed while addressing aspects of tephra emplacement from the eruptive column by fallout, surge, and flow processes. An ideal thermodynamic treatment, in which the magma and external water are allowed to come to thermal equilibrium before explosive expansion, shows that the maximum system pressure and entropy are determined by the mass ratio of water and magma interacting. Explosive (thermodynamic) efficiency, measured by the ratio of maximum work potential to thermal energy of the magma, depends upon heat transfer from the pyroclasts to the vapor during the expansion stage. The adiabatic case, in which steam immediately separates from the tephra during ejection, produces lower efficiencies than does the isothermal case, in which heat is continually transferred from tephra to steam as it expands. Mechanisms by which thermal equilibrium between water and magma can be obtained require intimate mixing of the two. Interface instabilities of the Landau and Taylor type have been documented by experiments to cause fine-scale mixing prior to vapor explosion. In these cases, water is heated rapidly to a metastable state of superheat where vapor explosion occurs by spontaneous nucleation when a temperature limit is exceeded. Mixing may also be promoted by shock wave propagation. If the shock is of sufficient strength to break the magma into small pieces, thermal equilibrium and vapor production in its wake may drive the shock as a thermal detonation. Because these mechanisms of magma fragmentation allow calculation of grain size, vapor temperature and pressure, and pressure rise times, detailed emplacement models can be developed by critical field and laboratory analysis of the resulting tephra deposits. Deposits left by dense flows of tephra and wet steam as opposed to those left by dilute flows of dry steam and tephra show contrasts in median grain size, dispersal area, grain shape, grain surface chemistry, and bed form.     

Surface study of HF- and HFH2SO4-treated feldspar using Auger electron spectroscopy

Auger electron spectroscopy has been used to study K-feldspar that has been reacted with both aqueous 10% HF and a 50% mixture of a 10% HF/0.1 N H₂SO₄ solution. In the feldspar/HF system, the resulting feldspar surface was shown to have been fluorinated; depth profiling, using argon ion sputtering, showed the fluorination to have occurred substantially into the mineral bulk. In the feldspar/ $\text{HF}\text{H}{}_2\text{SO}{}_4$ system, the resulting surface contained both fluorine and sulfur. The fluorination had again penetrated into the bulk, but the sulfur could be removed with mild argon ion sputtering. The $\text{Al}\text{F}$ signal ratio was much lower on the feldspar surface treated with the 10% HF/0.1 N H₂SO₄ solution than the feldspar surface treated with the weaker 10% HF acid solution.     

The monosaccharide spectra of natural waters

Monosaccharides were determined in waters and sediment pore waters from a wide variety of environments and locations. Desalting was performed by electrodialysis and concentrated extracts were analyzed by two forms of liquid chromatography. At least 12 sugars were identified. Glucose and fructose were the dominant monosaccharides in nearly all samples examined. Analyses of over 150 seawater and sediment pore water samples showed that fructose is highly significantly correlated (>0.99) with glucose concentrations. Laboratory kinetic experiments on the epimerization reaction, glucose ? fructose, in sterilized natural seawater in the dark, yielded a forward rate constant, k₁, of 1.2 × 10^?5 h^?1 at 25°C and 1.6 × 10^?7 h^?1 at 2°C. The approximate time required to attain equilibrium at 25°C was 1.1 y and at 2°C, 15.4 y; the measured equilibrium constant was in the range 0.3–0.4. The actual ratio of fructose to glucose in natural water samples was usually in the range 1.0–1.4/l, independent of the total monosaccharide concentrations, which varied in the samples by a factor of ～100. Several possible explanations for the apparent discrepancy in the determined and found ratios are discussed: the presence of universal, as yet, undiscovered major biological sources for fructose in marine environments; preferential utilization of glucose; preferential incorporation of fructose into or onto inorganic colloids; and preferential formation of fructose-transition metal ion associations.     

Surface and subsurface sedimentary structures produced by salt crusts

The growth and subsequent dissolution of salts on or within sediment may alter sedimentary structures and textures to such an extent that it is difficult to identify the depositional origin of that sediment and, as a result, the sediment may be misinterpreted. To help to overcome such problems with investigating ancient successions, results are presented from a comprehensive study of the morphology and fabrics of three large areas of modern salt flats in SE Arabia: the Sabkhat Matti inland region and the At Taf coastal region, both in the Emirate of Abu Dhabi, and the Umm as Samim region in Oman. These salt flats are affected by tidal‐marine, alluvial and aeolian depositional processes and include both clastic‐ and carbonate‐dominated surficial sediments. The efflorescent and precipitated salt crusts in these areas can be grouped into two main types: thick crusts, with high relief (>10 cm) and a polygonal or blocky morphology; or thin crusts, with low relief (<10 cm) and a polygonal or blister‐like appearance. The thin crusts may assume the surface morphology of underlying features, such as ripples or biogenic mats. A variety of small‐scale textures were observed: pustular growths, hair‐like spikes and irregular wrinkles. Evolution of these crusts over time results in a variety of distinctive sedimentary fabrics produced by salt‐growth sediment deformation, salt‐solution sediment collapse, sediment aggradation and compound mixtures of these processes. Salt‐crust processes produce features that may be confused with aeolian adhesion structures. An example from the Lower Triassic Ormskirk Sandstone Formation of the Irish Sea Basin demonstrates how this knowledge of modern environments improves the interpretation of the rock record. A distinctive wavy‐laminated facies in this formation had previously been interpreted as the product of fluvial sheetfloods modified by soft‐sediment deformation and bioturbation. Close inspection of laminations seen in core reveals many of the same sedimentary fabrics seen in SE Arabia associated with salt crusts. This facies is the product of salt growth on aeolian sediment and is not of fluvial origin.     

A loess-paleosol record of climate and glacial history over the past two glacial-interglacial cycles (~ 150 ka), southern Jackson Hole, Wyoming

Loess accumulated on a Bull Lake outwash terrace of Marine Oxygen Isotope Stage 6 (MIS 6) age in southern Jackson Hole, Wyoming. The 9 m section displays eight intervals of loess deposition (Loess 1 to Loess 8, oldest), each followed by soil development. Our age-depth model is constrained by thermoluminescence, meteoric ¹⁰Be accumulation in soils, and cosmogenic ¹⁰Be surface exposure ages. We use particle size, geochemical, mineral-magnetic, and clay mineralogical data to interpret loess sources and pedogenesis. Deposition of MIS 6 loess was followed by a tripartite soil/thin loess complex (Soils 8, 7, and 6) apparently reflecting the large climatic oscillations of MIS 5. Soil 8 (MIS 5e) shows the strongest development. Loess 5 accumulated during a glacial interval (~ 76-69 ka; MIS 4) followed by soil development under conditions wetter and probably colder than present. Deposition of thick Loess 3 (~ 43-51 ka, MIS 3) was followed by soil development comparable with that observed in Soil 1. Loess 1 (MIS 2) accumulated during the Pinedale glaciation and was followed by development of Soil 1 under a semiarid climate. This record of alternating loess deposition and soil development is compatible with the history of Yellowstone vegetation and the glacial flour record from the Sierra Nevada.     

New insights into the origin of perylene in geological samples

The origin of the polycyclic aromatic hydrocarbon (PAH) perylene in sediments and petroleum has been a matter of continued debate. Reported to occur in Phanerozoic organic matter (OM), fossil crinoids and tropical termite mounds, its mechanism of formation remains unclear. While a combustion source can be excluded, structural similarities to perylene quinone-like components present in e.g. fungi, plants, crinoids and insects, potentially suggest a product-precursor relationship. Here, we report perylene concentrations, ¹³C/¹²C, and D/H ratios from a Holocene sediment profile from the Qingpu trench, Yangtze Delta region, China. Perylene concentrations differ from those of pyrogenic PAHs, and rise to prominence in a stratigraphic interval that was dominated by woody vegetation as determined by palynology including fungal spores. In this zone, perylene concentrations exhibit an inverse relationship to the lignin marker guaiacol, D/H ratios between −284‰ and −317‰, similar to the methoxy groups in lignin, as well as co-variation with spores from wood-degrading fungi. ¹³C/¹²C of perylene differs from that of land plant wax alkanes and falls in the fractionation range expected for saprophytic fungi that utilise lignin, which is isotopically lighter than cellulose and whole wood. During progressive lignin degradation, the relative carbon isotopic ratio of the perylene decreases. We therefore hypothesise a relationship of perylene to the activity of wood-degrading fungi. To support our hypothesis, we analysed a wide range of Phanerozoic sediments and oils, and found perylene to generally be present in subordinate amounts before the evolutionary rise of vascular plants, and to be generally absent from marine-sourced oils, few exceptions being attributed perhaps to a contribution of marine and/or terrestrial-derived fungi, anoxia (especially under marine conditions) and/or contamination of core material by fungi. A series of low-molecular-weight aromatic quinones bearing the perylene-backbone were detected in Devonian and Cretaceous sediments, potentially representing precursor components to perylene.     

Quantitative analysis of variations in depositional sequence thickness from submarine channel levees

Abstract Thickness variations across‐levee and downchannel in acoustically defined depositional sequences from six submarine channel‐levee systems show consistent and quantifiable patterns. The thickness of depositional sequences perpendicular to the channel trend, i.e. across the levee, decreases exponentially, as characterized by a spatial decay constant, k. Similarly, the thickness of sediment at the levee crest decreases exponentially down the upper reaches of submarine channels and can be characterized by a second spatial decay constant, λ. The inverse of these decay constants has units of length and defines depositional length scales such that k^?1 is a measure of levee width and λ^?1 is a measure of levee length. Quantification of levee architecture in this way allowed investigation of relationships between levee architecture and channel dimensions. It was found that these measures of levee e‐folding width and levee e‐folding length are directly related to channel width and relief. The dimensions of channels and levees are thus intimately related, thereby limiting the range of potential channel‐levee morphologies, regardless of allocyclic forcing. A simple sediment budget model relates the product of the levee e‐folding width and e‐folding length to through‐channel volume discharge. A classification system based on the quantitative downchannel behaviour of levee architecture allows identification of a ‘mid‐channel’ reach, where sediment is passively transferred from the through‐channel flow to the levees as an overspilling flow. Downstream from this reach, the channel gradually looses its control on guiding turbidity currents, and the resulting flow can be considered as an unconfined or spreading flow.