Bed-material transport estimated from channel surveys: Vedder River,British Columbia

This study investigates the possibility to estimate bed-material transfer in gravel-bed rivers by analysis of morphological changes along Vedder River, British Columbia. Data from repeated cross-section surveys are used to estimate volume changes along the length of an 8 km reach. Gravel budgets are based on a continuity approach. An error analysis is performed to evaluate the uncertainty in the best estimate of transport rates. The mean annual gravel transport into the reach over a 9 year period was estimated to be 36600 ± 5600 m³ yr^?1. The sediment transport regime along the length of the river is evaluated and examined in relation to peak flood flows. Significant spatial and temporal variability in transport rates is demonstrated, making dubious the generalization of transport estimates from hydraulic calculations, or from sample measurements at a single cross-section. The assumptions, procedures and limitations of the ‘morphological approach’ to sediment transport analysis are discussed. It is concluded that this approach provides information of quality comparable or superior to that of direct measurements of transport, yet requires less field effort. It also provides additional information about river morphological changes, making it a preferred method for geomorphlogical investigations and for many river management concerns.     

Quick clay—A case study of chemical perspective in Southwest Sweden

Quick clay, a soil that changes from normal firm ground to a liquid mass when it is disturbed, has been involved in most of the large and serious clay slides in Sweden, Norway and Canada. The location, time of occurrence and size of quick clay slides are difficult to predict and large slides may cause great devastation. Some geochemical studies of Swedish quick clay were done in the 1960s and early 1970s, but no systematic studies of the interrelationships of pore water chemistry, mineralogy, geotechnical properties and other parameters on quick clays in Sweden have been published. Such studies are of national and general interest because of the many combinations of rock flour source areas and sedimentation conditions that occurred across central Sweden and into the Baltic Sea area during deglaciation. In this study, geotechnical properties related to the in situ chemistry at one quick clay site were extensively studied, and spot sampling was conducted at two other locations in Southwest Sweden. In this area the clay minerals mainly are non-expanding phyllosilicate minerals (illite) and primary minerals (quartz, feldspar), which is consistent with previous studies of quick clay mineralogy. Extensive leaching has occurred at all three locations. At the extensively studied site, Surte, the lowest salinity was found at the greatest depth, inferring that the leaching by fresh water was accomplished by water movement upward and laterally through the sediment from the underlying bedrock. This is consistent with the local setting where bedrock hills rise sharply to over 100 m above the marine sediment surface. An artesian pressure would also be anticipated at this location. There is a correlation (negative) between sensitivity and salinity but there is an indication that the maximum salinity or electrical conductivity consistent with the quick clay behaviour is higher than reported elsewhere. However, for high sensitivities the salinity is about the same as reported elsewhere. In the deepest part of the borehole, there is a higher content of Fe and Al in the pore water, indicating reduced state. Further work is needed to confirm the difference in salinity and to investigate the possible interplay of salinity and potential dispersing agents such as the role of anoxic conditions, in this region. Further work is especially needed in the locations where the sediment accumulation occurred under lower salinity conditions. At all three locations, high remoulded shear strength and low sensitivity have been seen near the surface together with a decrease in pore water cation concentrations.     

The reaction of carbonates in contact with laser-generated,superheated silicate melts: Constraining impact metamorphism of carbonate-bearing target rocks

We simulated entrainment of carbonates (calcite, dolomite) in silicate impact melts by 1-bar laser melting of silicate–carbonate composite targets, using sandstone, basalt, calcite marble, limestone, dolomite marble, and iron meteorite as starting materials. We demonstrate that carbonate assimilation by silicate melts of variable composition is extremely fast (seconds to minutes), resulting in contamination of silicate melts with carbonate-derived CaO and MgO and release of CO₂ at the silicate melt–carbonate interface. We identify several processes, i.e., (1) decomposition of carbonates releases CO₂ and produces residual oxides (CaO, MgO); (2) incorporation of residual oxides from proximally dissociating carbonates into silicate melts; (3) rapid back-reactions between residual CaO and CO₂ produce idiomorphic calcite crystallites and porous carbonate quench products; (4) high-temperature reactions between Ca-contaminated silicate melts and carbonates yield typical skarn minerals and residual oxide melts; (5) mixing and mingling between Ca- or Ca,Mg-contaminated and Ca- or Ca,Mg-normal silicate melts; (6) precipitation of Ca- or Ca,Mg-rich silicates from contaminated silicate melts upon quenching. Our experiments reproduce many textural and compositional features of typical impact melts originating from silicate–carbonate targets. They reinforce hypotheses that thermal decomposition of carbonates, rapid back-reactions between decomposition products, and incorporation of residual oxides into silicate impact melts are prevailing processes during impact melting of mixed silicate–carbonate targets. However, by comparing our results with previous studies and thermodynamic considerations on the phase diagrams of calcite and quartz, we envisage that carbonate impact melts are readily produced during adiabatic decompression from high shock pressure, but subsequently decompose due to heat influx from coexisting silicate impact melts or hot breccia components. Under certain circumstances, postshock conditions may favor production and conservation of carbonate impact melts. We conclude that the response of mixed carbonate–silicate targets to impact might involve melting and decomposition of carbonates, the dominant response being governed by a complex variety of factors.     

Silicate liquid immiscibility in impact melts

We have investigated silicate emulsions in impact glasses and impact melt rocks from the Wabar (Saudi Arabia), Kamil (Egypt), Barringer (USA), and Tenoumer (Mauritania) impact structures, and in experimentally generated impact glasses and laser-generated glasses (MEMIN research unit) by scanning electron microscopy, electron microprobe analysis, and transmission electron microscopy. Textural evidence of silicate liquid immiscibility includes droplets of one glass disseminated in a chemically distinct glassy matrix; sharp phase boundaries (menisci) between the two glasses; deformation and coalescence of droplets; and occurrence of secondary, nanometer-sized quench droplets in Si-rich glasses. The compositions of the conjugate immiscible liquids (Si-rich and Fe-rich) are consistent with phase separation in two-liquid fields in the general system Fe₂SiO₄–KAlSi₃O₈–SiO₂–CaO–MgO–TiO₂–P₂O₅. Major-element partition coefficients are well correlated with the degree of polymerization (NBO/T) of the Si-rich melt: Fe, Ca, Mg, and Ti are concentrated in the poorly polymerized, Fe-rich melt, whereas K, Na, and Si prefer the highly polymerized, Si-rich melt. Partitioning of Al is less pronounced and depends on bulk melt composition. Thus, major element partitioning between the conjugate liquids closely follows trends known from tholeiitic basalts, lunar basalts, and experimental analogs. The characteristics of impact melt inhomogeneity produced by melt unmixing in a miscibility gap are then compared to impact melt inhomogeneity caused by incomplete homogenization of different (miscible or immiscible) impact melts that result from shock melting of different target lithologies from the crater's melt zone, which do not fully homogenize and equilibrate due to rapid quenching. By taking previous reports on silicate emulsions in impact glasses into account, it follows that silicate impact melts of variable composition, cooling rate, and crystallization history might readily unmix during cooling, thereby rendering silicate liquid immiscibility a much more common process in the evolution of impact melts than previously recognized.     

First evidence for the Cenomanian–Turonian oceanic anoxic event (OAE2, ‘Bonarelli’ event) from the Ionian Zone,western continental Greece

Integrated biostratigraphic (planktonic foraminifera, calcareous nannofossils), chemostratigraphic (bulk C and O isotopes) and compound-specific organic geochemical studies of a mid-Cretaceous pelagic carbonate—black shale succession of the Ionian Zone (western Greece), provide the first evidence for the Cenomanian–Turonian oceanic anoxic event (OAE2, ‘Bonarelli’ event) in mainland Greece. The event is manifested by the occurrence of a relatively thin (35 cm), yet exceptionally organic carbon-rich (44.5 wt% TOC), carbonate-free black shale, near the Cenomanian–Turonian boundary within the Vigla limestone formation (Berriasian–Turonian). Compared to the ‘Bonarelli’ black-shale interval from the type locality of OAE2 in Marche–Umbria, Italy, this black shale exhibits greatly reduced stratigraphic thickness, coupled with a considerable relative enrichment in TOC. Isotopically, enriched δ¹³C values for both bulk organic matter (−22.2‰) and specific organic compounds are up to 5‰ higher than those of underlying organic-rich strata of the Aptian-lower Albian Vigla Shale member, and thus compare very well with similar values of Cenomanian–Turonian black shale occurrences elsewhere. The relative predominance of bacterial hopanoids in the saturated, apolar lipid fraction of the OAE2 black shale of the Ionian Zone supports recent findings suggesting the abundance of N₂-fixing cyanobacteria in Cretaceous oceans during the Cenomanian–Turonian and early Aptian oceanic anoxic events.     

Eocene cool-water carbonate and biosiliceous sedimentation dynamics, St Vincent Basin, South Australia

Middle and Upper Eocene biogenic sediments in the Willunga Embayment along the eastern margin of the St Vincent Basin are a series of warm‐temperate limestones, marls and spiculites. The Middle Eocene Tortachilla Limestone is a thin, coarse grained, quartzose, biofragmental, bryozoan–mollusc calcarenite of stacked metre‐scale depositional cycles with hardground caps. Lithification, aragonite dissolution and the filling of moulds by sediment and cement characterize early marine‐meteoric diagenesis. Further meteoric diagenesis at the end of Tortachilla deposition resulted in dissolution, Fe‐oxide precipitation and calcite cementation. The Upper Eocene Blanche Point Formation is composed of coccolith and spiculite marl and spiculite, all locally rich in glauconite, turritellid gastropods and sponges. Decimetre‐scale units, locally capped by firmgrounds, have fossiliferous lower parts and relatively barren upper parts. Carbonate diagenesis is minor, with much aragonite still present, but early silicification is extensive, except in the spiculite, which is still opal‐A. All depositional environments are interpreted as relatively shallow water: high energy during the Middle Eocene and low energy during the Upper Eocene, reflecting the variable importance of a basin‐entrance archipelago of carbonate highs. Marls and spiculites are interpreted to have formed under an overall estuarine circulation system in a humid climate. Basinal waters, although well mixed, were turbid and rich in land‐derived nutrients, yet subphotic near the sea floor. These low‐energy, inner‐shelf biosiliceous sediments occur in coeval environments across other parts of Australia and elsewhere in the rock record, suggesting that they are a recurring element of the cool‐water, carbonate shelf depositional system. Thus, spiculites and spiculitic carbonates in the rock record need be neither deep basinal nor polar in origin. The paradox of a shallow‐water carbonate–spiculite association may be more common in geological history than generally realized and may reflect a characteristic mid‐latitude, humid climate, temperate water, palaeoenvironmental association.     

A three-invariant smooth cap model with mixed hardening

A cap model is presented that uses a multiplicative formulation to define a smooth (continuous derivative) failure surface that includes the third stress invariant. This formulation offers several advantages over previous cap model formulations: elimination of ‘corner’ coding, resulting in a numerical algorithm suitable for vectorization; a three stress invariant implementation that is easily specialized to classical failure surfaces or generalized to represent observed material response; and a framework for easily implementing additional model features such as kinematic hardening as demonstrated.