COSAD: A computer aided system for automatization of deformation measurements

The COSAD measurement system detects deformations in structures, rock faces and extended earth-surface areas. The instrument is semi-automatic with electronic data-acquisition parts. In this paper, the theory and the accuracy, the measurement method and examples of applications are given. Results from structural deformation and a computer simulation of deformation in large extended areas are also included.     

Anaerobic diagenesis within Recent, Pleistocene, and Eocene marine carbonate frameworks

Porewaters from a variety of Recent, Pleistocene, and Eocene lithified marine carbonate frameworks displayed similar chemical characteristics: highly depleted concentrations of dissolved oxygen (>20 μM), elevated levels of dissolved methane (25-5000 nM), and near-seawater sulphate levels. These porewaters also had low pH values (7·5-7·9), and contained elevated concentrations of sulphide (4–10 μM), dissolved inorganic carbon (2·05–2·46 mM), and inorganic nutrients. Hydrocarbon composition data indicate that the methane is biogenic, whereas the methane δ¹³C values (–47·4 ± 2·7%0) suggest that it has been subject to oxidation. The porewater dissolved inorganic carbon δ¹³C values varied from –0·6 to –39%0, suggesting input of carbon dioxide from organic matter oxidation. We conclude that anaerobic diagenesis involving bacterial degradation of organic matter is a common process in lithified marine carbonates and hypothesize that it may be an important factor controlling their carbonate geochemistry.     

Epithermal environments and styles of mineralization: Variations and their causes, and guidelines for exploration

Epithermal precious- and base-metal deposits are diverse, reflecting the different tectonic, igneous and structural settings in which they occur, the complexities of their local setting, and the many processes involved in their formation. Most epithermal deposits form at shallow crustal levels where abrupt changes in physical and chemical conditions result in metal deposition and attendant hydrothermal alteration. The principal factors that influence the conditions prevailing in the epithermal environment, and which ultimately determine the sites and character of mineralization, include: geology (structure, stratigraphy, intrusions and rock type, which affect the style and degree of permeability and the reactivity of the host); pressure and temperature (which in the epithermal environment are related on the boiling point with depth curve); hydrology (the relationship between permeability and topography which governs fluid flow, and discharge/recharge characteristics, as well as access of steam-heated waters); chemistry of the mineralizing fluid (which determines the metal-carrying capacity, as well as the associated vein and alteration assemblage); and syn-hydrothermal development of permeability and/or changes in hydraulic gradients.Many attempts have been made to classify epithermal deposits based on mineralogy and alteration, the host rocks, deposit form, genetic models, and standard deposits. All have their strengths and weaknesses. We prefer a simple approach using the fundamental fluid chemistry (high or low sulfidation, reflecting relatively oxidized or reduced conditions, respectively) as readily inferred from vein and alteration mineralogy and zoning, together with the form of the deposit, and using comparative examples to clarify the character of the deposit.Guidelines for exploration vary according to the scale at which work is conducted, and are commonly constrained by a variety of local conditions. On a regional scale the tectonic, igneous and structural settings can be used, together with assessment of the depth of erosion, to select areas for project area scale exploration. At project area scale, direct (i.e. geochemical) or indirect guidelines may be used. Indirect methods involve locating and interpreting hydrothermal alteration as a guide to ore, with the topographic and hydrologic reconstruction of the system being of high priority. These pursuits may involve mineralogic, structural, geophysical or remote sensing methods. On a prospect scale, both direct and indirect methods may be used; however, they can only be effective in the framework of a sound conceptual understanding of the processes that occur in the epithermal environment, and the signatures they leave.     

Lithogeochemistry of hypogene, supergene and leached cap samples, berg porphyry copper deposit, British Columbia

In this paper we examine the influence of the development of supergene oxide and sulphide zones on the original hypogene geochemical patterns at the Berg deposit, British Columbia.The deposit, in the alpine zone of the Tahtsa Range, was logged (GEOLOG) and sampled in fourteen diamond drill holes along a N—S section and from outcrop where possible. Anomalous populations of major and trace elements were defined using log probability graphs and a sequential extraction (10% hydrochloric acid— ammonium oxalate — potassium chlorate/hydrochloric acid — nitric/perchloric acids) was used to study the distribution of elements between carbonate, oxide, sulphide and silicate phases.Core logs and assays show that primary ore minerals (chalcopyrite—molybdenite) extend from the outer part of the porphyry intrusion into the surrounding hornfels where the best grades of copper are found close to the intrusive contact. Maximum copper grades, however, result from development of a supergene enrichment blanket. Within the hypogene zone, principal lithogeochemical patterns reflect the differences in composition of the hornfels, originally intermediate to basic volcanics, and the intrusion, as well as the introduction of F and trace metals (Cu, Mo, Pb, Zn and Ag). Distribution of Ag is broadly comparable to that of Cu and Mo whereas anomalous Pb and Zn are present as peripheral haloes around the potential ore zones.Emergence of strongly acidic ground water and precipitation of iron oxides, indicate that leaching processes are active. Furthermore, although primary sulphides, associated with both their oxidation products and secondary sulphides, can still be found in surface samples, sequential extractions on drill core clearly indicate vertical redistribution of copper between oxide, carbonate and sulphide phases. Using ratios of metal concentrations to TiO₂, the surface concentrations of trace metals can be compared with those at depth and the relative amount of enrichment or depletion can be quantified. In highly leached sites the absolute concentrations of Cu, Mn and Zn are low which is reflected in TiO₂ ratios of <1. However, Mo, Pb and Ag are enriched at the same sites (TiO₂ ratios >1). In areas where physical erosion exceeds leaching (topographic lows) primary sulphides co-exist with secondary sulphide and oxide minerals. Here Cu, Mo, Pb, Zn, Mn and Ag are enriched. Fluorine is relatively unaffected by the leaching process. It would appear signature for a cale alkaline Cu and Mo porphyry deposit in an area where outcrop was intensely leached.     

The response of subaqueous dunes to floods in sand and gravel bed reaches of the Dutch Rhine

Abstract The branches of the River Rhine in the Netherlands, characterized by a sand–gravel bed in the upstream part and a sand bed in the downstream part of the river system, show migrating dunes, especially during floods. In the last 20 years, these dunes have been studied extensively. High-resolution echo-sounding measurements of these dunes, made with single and multibeam equipment, were analysed for three different sections of the Rhine river system during several floods. This analysis was done to quantify the growth, decay and migration rates of the dunes during floods. In addition, the migrating dunes were used to calculate bedload transport rates with dune tracking. The results of dune growth and decay and migration rate are shown to be very different for the various sections during the various floods, and these differences are related to differences in grain size of the bed and to differences in the distribution of discharge over the main channel and the floodplain. The relations are used to show that the growth and migration rate of dunes, and the calculated bedload transport rates during the rising stage of a flood wave can be predicted from the mobility of the bed material with simple power relations.     

From source terrains of the Eastern Alps to the Molasse Basin: Detrital record of non-steady-state exhumation

Fission-track cooling ages of detrital apatite (AFT) in the East Alpine Molasse Basin display age groups corresponding to geodynamic events in the orogen since Jurassic times. These age groups are typical of certain thermotectonic units, which formed a patchwork in the Swiss and Eastern Alps. By a combination of petrographic and thermochronologic data, progressive erosion of source terrains is monitored in different catchments since the Oligocene. The AFT cooling ages show a decrease in lag time until when rapidly cooled debris derived from tectonically exhumed core complexes became exposed. After termination of tectonic exhumation, lag times of debris derived from the core complexes increased. Neither on the scale of the entire Eastern Alps, or on the scale of individual catchments, steady-state exhumation is observed, due to the highly dynamic changes of exhumation rates since Late Eocene collision.     

Sediment Phosphorus Chemistry and Microbial Biomass along a Lowland New Zealand Stream

An evaluation of the distribution of P concentrations in streamflow, P fractions andthe microbial biomass P pool was made of bed and bank sediments along a lowlandstream in New Zealand. Agricultural intensification increased downstream. However,most P fractions decreased downstream (total P decreased from c. 400 to 250 mg kg^-1) in bed sediments, while P in streamflow remained relatively constant (generally < 0.005 mg l^-1) and sediment microbial P increased from 2 to 8 mg kg^-1. An investigation of P release from dried and rewetted sediments showed that solution P (CaCl2-P) increased, on average > 300%, and proportional to the size of the microbial biomass P pool before drying, except in sediments with much organic carbon (OC). When supplied with a P source (1 mg l^-1) and then simultaneously with a C source (glucose, 100 mg l^-1), all sediment behaved similarly and biotic sorption accounted for, on average, 27 and 34% of the total sediment uptake, respectively (maximum of 58%). The quantity of P taken up was related to the initial size of the microbial biomass P pool, and the availability of P as influenced by organic P complexes and OC. The sediment microbial biomass represents a transient, but small store of P could be useful to indicate bioavailable P inputs.