Clinoform geometry,geomorphology, facies character and stratigraphic architecture of a sand‐rich subaqueous delta: Jurassic Sognefjord Formation,offshore Norway

The integration of core sedimentology, seismic stratigraphy and seismic geomorphology has enabled interpretation of delta‐scale (i.e. tens of metres high) subaqueous clinoforms in the upper Jurassic Sognefjord Formation of the Troll Field. Mud‐prone subaqueous deltas characterized by a compound clinoform morphology and sandy delta‐scale subaqueous clinoforms are common in recent tide‐influenced, wave‐influenced and current‐influenced settings, but ancient examples are virtually unknown. The data presented help to fully comprehend the criteria for the recognition of other ancient delta‐scale subaqueous clinoforms, as well as refining the depositional model of the reservoir in the super‐giant Troll hydrocarbon field. Two 10 to 60 m thick, overall coarsening‐upward packages are distinguished in the lower Sognefjord Formation. Progressively higher energy, wave‐dominated or current‐dominated facies occur from the base to the top of each package. Each package corresponds to a set of seismically resolved, westerly dipping clinoforms, the bounding surfaces of which form the seismic ‘envelope’ of a clinoform set and the major marine flooding surfaces recognized in cores. The packages thicken westwards, until they reach a maximum where the clinoform ‘envelope’ rolls over to define a topset–foreset–toeset geometry. All clinoforms are consistently oriented sub‐parallel to the edge of the Horda Platform (N005–N030). In the eastern half of the field, individual foresets are relatively gently dipping (1° to 6°) and bound thin (10 to 30 m) clinothems. Core data indicate that these proximal clinothems are dominated by fine‐grained, hummocky cross‐stratified sandstones. Towards the west, clinoforms gradually become steeper (5° to 14°) and bound thicker (15 to 60 m) clinothems that comprise medium‐grained, cross‐bedded sandstones. Topsets are consistently well‐developed, except in the westernmost area. No seismic or sedimentological evidence of subaerial exposure is observed. Deposition created fully subaqueous, near‐linear clinoforms that prograded westwards across the Horda Platform. Subaqueous clinoforms were probably fed by a river outlet in the north‐east and sculpted by the action of currents sub‐parallel to the clinoform strike.     

Changes in beach water table elevation during neap and spring tides on a sandy estuarine beach, Delaware Bay, New Jersey

A field investigation of temporal and spatial changes in wind and wave characteristics, runup and beach water table elevation was conducted on the foreshore of an estuarine beach in Delaware Bay during neap (April 9, 1995) and spring (April 16, 1995) tides under low wave-energy conditions. The beach has a relatively steep, sandy foreshore and semi-diurnal tides with a mean range of 1.6 m and a mean spring range of 1.9 m. Data from a pressure transducer placed on the low tide terrace reveal a rate of rise and fall of the water level on April 16 of 0.09 mm s⁻¹ resulting in a steeper tidal curve than the neap tide on April 9. Data from three pressure transducers placed in wells in the intertidal foreshore reveal that the landward slope of the water table during the rising neap tide was lower than the slope during spring tide, and there was a slower rate of fall of the beach water table relative to the fall of the tide. Wave heights were lower on April 9 (significant height from 17.1 min records <0.16 m). The water table elevation was 0.08 m higher than the water in the bay at the time of high water, when maximum runup elevation was 0.29 m above high water and maximum runup width was 2.0 m. The elevation of the water table was 0.13 m higher than the maximum elevation of water level in the bay 74 min after high water, when wave height was 0.12 m and wave period was 2.7 s. The use of mean bay water level at high tide will underpredict the elevation of the water table in the beach, and demarcation of biological sampling stations across the intertidal profile based on mean tide conditions will not accurately reflect the water content of the sandy beach matrix.     

Hydrogeochemistry of the Chhota Shigri glacier meltwater,Chandra basin,Himachal Pradesh,India: solute acquisition processes,dissolved load and chemical weathering rates

The chemical compositions of various ions in meltwater of the Chhota Shigri glacier were analysed during the observation period from May to October 2010. Total 164 samples of meltwater were collected in two times a day at 8.0 a.m and 6.0 p.m. Bicarbonate and calcium were the dominant anion and cation in meltwater of the investigation area. High ratios of (Ca + Mg) versus TZ⁺ and (Ca + Mg) versus (Na + K) demonstrate that hydrogeochemistry of the study area was mainly governed by carbonate type weathering. The average sulphate mass fraction of meltwater was computed to be 0.31 ± 0.12, showing dominancy of bicarbonate over sulphate. This excess bicarbonate would be generated by an alternative proton supply mechanism due to biological activities in the bed rock lithology and sulphide oxidation may be about the same as carbonation as a driver of chemical weathering at Chhota Shigri glacier. In general, major ions and total dissolved solid concentrations showed decreasing trend with increasing discharge from the study area. The average daily mean dissolved load of this glacier was much lower than that of the Gangotri glacier, which may be due to low meltwater runoff and lithology of the investigation area. The cation weathering rates of study area for early, peak and late melt seasons were computed to be 694, 1631 and 481 meq m^?2 a^?1, respectively. The average value of chemical denudation rates of the Chhota Shigri glacier meltwater was found lower than that of the Dokriani glacier.     

Evaluation of geochemical impact of tsunami on Pichavaram mangrove ecosystem,southeast coast of India

The 26 December 2004-tsunami has deposited sediments in the Pichavaram mangrove ecosystem, east coast of India. Ten surface and three core sediment samples were collected within 30 days of the event and analyzed for nutrients. Water samples were also analyzed to see the impact of tsunami on the geochemical behavior of nutrients. An increase in the concentration of various nutrients namely nitrate and phosphate was observed. The geochemistry of the mangrove forest was observed to be influenced by a number of factors like rapid increase of aquaculture farms, agricultural practices and the anthropogenic discharge from the nearby-inhabited areas. Further the sediment column was disturbed due to energetic tsunami waves, which has caused a sheer increase in the dissolved oxygen in water. As a result, the change in the redox potential has resulted in change in the nutrients absorbed/associated with the sediments. In addition, role of retreating water after tsunami on the nutrient geochemistry was also evaluated.     

Resistance of quartz silt to isotopic exchange under burial and intense weathering conditions

Oxygen isotopic compositions of quartz from silty sediments buried to 5400 m depth from two wells in the Gulf of Mexico each showed δ5¹⁸O variations of less than 1.7%. Clay diagenesis has been reported within this depth. The observed variations in the quartz do not appear to be primarly diagenetic effects, but rather are mainly depositional features reflecting variations in the sources of the sediments. Sources may be influenced by the variation of distance from the shore at different depths in a given sampling location and by sediment production by continental glaciations. Stability of the oxygen isotopic composition of quartz in the 10–20 μm size range under long-time humid, temperate weathering conditions was studied by analysis of saprolites formed from Pennsylvanian to Precambrian crystalline rocks. In four of the five cases, the 10–20 μm fraction was found to have only 0.1–0.5%. greater δ¹⁸O than the corresponding 20–50 μm fraction. This increase may be attributable either to a slight oxygen isotopic exchange with ambient ground waters or original differences within the rock since the saprolites were sufficiently coherent to make an influx of extraneous detrital silt unlikely. The amount of oxygen isotopic exchange in silt size quartz over periods of many million years of shallow burial or weathering appears to be small enough to permit the use of the oxygen isotopic ratio of quartz in tracing the origin of eolian and fluvial additions of minerals to continental soils and pelagic sediments.     

Carbon chemistry of Luna 16 and Luna 20 samples

Luna 16 and Luna 20 samples were analyzed for volatilizable species using vacuum pyrolysis to 1400°C. The major gaseous products evolved (ranging from 10–650 μg/g) were H₂O, CO, CO₂, N₂ and CH₄. Minor components (all < 10 μg/g) included NH₃, HCN, NO, SO₂, H₂S, C₂H₂, C₂H₄, C₂H₆, C₃H₆ and higher hydrocarbons, benzene, toluene, and the polymeric contaminants Teflon^® and silicone oil. The total carbon and nitrogen contents (μg/g) for these sieved samples (< 125 μm) were: Luna 16—C 418, N 134 and Luna 20—C 380, N 80.     

Revision of the Carboniferous cystoporate bryozoan Fistulipora incrustans (Phillips, 1836), with remarks on the type species of Fistulipora M'Coy, 1849

The type species of the Palaeozoic cystoporate bryozoan genus Fistulipora M'Coy, 1849 is redescribed. Fistulipora minor M'Coy, 1849 is the type species, and was the first species described under the genus Fistulipora. Quantitative assessment of type and figured specimens of Calamopora incrustans Phillips, 1836 and F. minor has shown them to fall within the range of morphological variation exhibited by abundant comparative material collected at several horizons and they are referable to one morphologically variable taxon. F. minor is the junior subjective synonym of C. incrustans and the form can be quoted as F. minor M'Coy, 1849 = C. incrustans Phillips, 1836 with a valid name of F. incrustans (Phillips, 1836). However, this does not alter the name of the type species, which is F. minor M'Coy, 1849. The type specimen of Berenicea megastoma M'Coy, 1844 has also been examined, and this form is also conspecific with F. minor M'Coy, 1849 = C. incrustans Phillips, 1836. Examination of the type specimen of F. major M'Coy (1849) has shown it to be referable to the tabulate coral genus Chaetetes. A lectotype and paralectotypes are designated for F. minor and the status of the type specimens of F. incrustans is clarified.     

Nutrient chemistry and salinity mapping of the Delhi aquifer,India: source identification perspective

Present study is an effort to distinguish between the contributions of natural weathering and anthropogenic inputs towards high salinity and nutrient concentrations in the groundwater of National Capital Territory (NCT) Delhi, India. Apart from the source identification, the aquifer of entire territory has been characterized and mapped on the basis of salinity in space and water suitability with its depth. Major element chemistry, conventional graphical plots and specific ionic ratio of Na⁺/Cl⁻, SO₄ ²⁻/Cl⁻, Mg²⁺/Ca²⁺ and Ca²⁺/(HCO₃ ⁻ + SO₄ ²⁻) are conjointly used to distinguish different salinization sources. Results suggest that leaching from the various unlined landfill sites and drains is the prime cause of NO₃ ⁻ contamination while study area is highly affected with inland salinity which is geogenic in origin. The seasonal water level fluctuation and rising water level increases nutrients concentration in groundwater. Mixing with old saline sub-surface groundwater and dissolution of surface salts in the salt affected soil areas were identified as the principle processes controlling groundwater salinity through comparison of ionic ratio. Only minor increase of salinity is the result of evaporation effect and pollution inflows. The entire territory has characterized into four groups as fresh, freshening, near freshening and saline with respect to salinity in groundwater. The salinity mapping suggests that in general, for drinking needs, groundwater in the fresh, freshening and near freshening zone is suitable up to a depth of 45, 20 and 12 m, respectively, while the saline zones are unsuitable for any domestic use. In the consideration of increasing demand of drinking water in the area; present study is vital and recommends further isotopic investigations and highlights the need of immediate management action for landfill sites and unlined drains.     

Trace Element Analysis of NIST SRM 614 and 616 Glass Reference Materials by Laser Ablation Microprobe-Inductively Coupled Plasma-Mass Spectrometry

Fifty elements in NIST SRM 614 and 616 glass reference materials were determined by laser ablation microprobe-inductively coupled plasma-mass spectrometry (LAM-ICP-MS). The values determined for NIST SRM 614 agreed well with the NIST-certified and information values (mean relative difference ± 3.6%), except for B, Sc and Sb. The values determined for NIST SRM 616 agreed with the NIST-certified and information values within a mean relative difference of ± 1.5%, except for B, Sc and Ga. In addition, at an 80 μm sampling scale, NIST SRM 614 and 616 glass discs were homogeneous for trace elements within the observed precisions of 5 and 15% (mean), respectively. Detection limits were in the range 0.01 - 0.3 μg g⁻¹ for elements of lower mass numbers (amu < 80) and 1 - 10 ng g⁻¹ for heavy elements (amu > 80). Detection at the sub ng g⁻¹ level is possible for most of the heavy elements by using an ablation pit size larger than 10 0 μm.     

A MEG study of the olivine and spinel forms of Mg2SiO4

In this paper we present a theoretical investigation of the structures and relative stability of the olivine and spinel phases of Mg₂SiO₄. We use both a purely ionic model, based on the Modified Electron Gas (MEG) model of intermolecular forces, and a bond polarization model, developed for low pressure silica phases, to investigate the role of covalency in these compounds. The standard MEG ionic model gives adequate structural results for the two phases but incorrectly predicts the spinel phase to be more stable at zero pressure. This is mainly because the ionic modeling of Mg₂SiO₄ only accounts for 95 percent of the lattice energy. The remainder can be attributed to covalency and many-body effects. An extension of the MEG ionic model using “many-body” pair potentials corrects the phase stability error, but predicts structures which are in poorer agreement with experiment than the standard ionic approach. In addition, calculations using these many-body pair potentials can only account for 10 percent of the missing lattice energy. This model predicts an olivine-spinel phase transition of 8 GPa, below the experimental value of 20 GPa. Therefore, in order to understand more fully the stability of these structures we must consider polarization. A two-shell bond polarization model enhances the stability of both structures, with the olivine structure being stabilized more. This model predicts a phase transition at about 80 GPa, well above the observed value. Also, the olivine and spinel structures calculated with this approach are in poorer agreement with experiment than the ionic model. Therefore, based on our investigations, to properly model covalency in Mg₂SiO₄, a treatment more sophisticated than the two-shell model is needed.