Seasonality of materials transport through a coastal freshwater marsh: Riverine versus tidal forcing

Transports of nitrate and suspended solids were measured six times from January 1984 until January 1985 in a small freshwater tidal bayou in south-central Louisiana. The bayou and adjacent marshes are influenced by Atchafalaya River discharges, tides, and coastal weather patterns. Large net ebb-directed water transports occurred in winter, spring, and summer, coincident with high river discharges, indicating riverine dominance. A very small net flood-directed water transport occurred in fall, indicating tidally dominated hydrology. Nitrate and suspended solids transports were net ebb-directed in all seasons, but were two orders of magnitude higher during high river flow. Exports changed as hydrology switched from river dominated to tidally dominated, and as concentrations of materials changed. Comparison of suspended solids and nitrate concentrations in the river and bayou shows that these materials were usually lower in the bayou, indicating retention by the marsh/aquatic system.     

Seismic interaction at separation joints of an instrumented concrete bridge

A multi-span, curved, concrete box-girder bridge has been extensively instrumented by the California Strong Motion Instrumentation Program (CSMIP) in cooperation with the California Department of Transportation (Caltrans). On 28 June 1992, the bridge was shaken by the magnitude 7–5 Landers and magnitude 6–6 Big Bear earthquakes in southern California. The epicentres of these earthquakes were 50 and 29 miles (81 and 46 km) from the bridge, respectively. All 34 strong-motion sensors installed on the bridge recorded the response to these earthquakes and provided an insightful set of data. A striking aspect of the response is the presence of intermittent sharp spikes in nearly all of the acceleration records from sensors at the deck of the bridge. Among these the highest spike was 0.8g for the Landers and 1.0g for the Big Bear earthquake. The peak ground acceleration at the bridge site was only about 0.1g for both these earthquakes. With the aid of visual examination and simple analysis it is deduced that (1) the spikes were caused by forces generated at separation joints by impacts and stretching of the cable restrainers between adjacent bridge segments; (2) the forces of impacts and cable stretching are directly proportional to the size of the spikes and can be estimated by the use of a simple formula; and (3) the spikes travelled from their source to other locations on the bridge with the velocity of a compression wave propagating through concrete.     

Environmental oxidation rate of manganese(II): bacterial catalysis

A simple mass balance for dissolved manganese(II) in waters containing low levels of oxygen in Saanich Inlet indicates that the residence time for Mn(II) removal to the solid phase is on the order of a few days. The average oxidation state of Mn in particulate material sampled from the region of Mn removal was 2.3–2.7, and electron micrographs revealed structures characteristic of bacterially formed Mn precipitates. Radiotracer experiments utilizing ⁵⁴Mn(II) indicated that removal of Mn from solution in the region of active uptake was substantially blocked by a poison mixture, demonstrating that Mn(II) binding to particulates is catalyzed by bacteria in this environment.     

Sulphur uptake by salt grasses,mangroves, and seagrasses in anaerobic sediments

Stable sulfur isotope analyses show that rooted estuarine plants growing in anoxic sediments incorporate substantial amounts of ³⁴S-depleted sulfides, or oxidation products thereof. In roots, this incorporation predominates over sulfate uptake from interstitial porewater. Either the plants incorporate normally toxic sulfides, or they are creating and using a specialized nutrient pool of oxidized sulfides at the root-sediment interface.     

Solubility of rhodochrosite (MnCO3) in water and seawater

The solubility product of rhodochrosite (MnCO₃) was measured in seawater, deionized water and dilute NaCl solutions. The solubility product extrapolated to infinite dilution at 25.0 C was (2.60 ± 0.07)× 10^?11. The stoichiometric solubility product measured in seawater of 34.27%. salinity was (3.24 ± 0.23) × 10^?9 at 25.0 C and (2.28 ± 0.24) × 10^?9 at 3.3 C. The stoichiometric solubility product is in good agreement with the value calculated from an ion association model. The enthalpy of the reaction is in fair agreement with the estimated value.     

Geochemistry and Rb-sr geochronology of associated proterozoic peralkaline and subalkaline anorogenic granites from Labrador

Anorogenic granites of middle to late Proterozoic age in the Davis Inlet — Flowers Bay area of Labrador are subdivided on the basis of petrology and geochemistry into three coeval suites. Two of these are high-temperature anhydrous hypersolvus granites: a peralkaline aegirine-sodic-calcic to sodic amphibole-bearing suite and a non-alkaline fayalite-pyroxene-bearing suite. The third is a group of non-alkaline subsolvus hornblende-biotite-bearing granites. Associated with the hypersolvus peralkaline suite is a group of genetically related syenites and quartz syenites. The granites cut ca. 3,000 Ma old Archaean gneisses as well as Elsonian layered basic intrusions of the Nain Complex. One of these, a crudely layered mass which ranges in composition from gabbro to diorite and monzonite, appears to be related to the syenites. The peralkaline granites and some of the syenites are extremely enriched in the high field-strength elements such as Y, Zr, Nd, as well as Rb, Ga and Zn, and have low abundances of Ba, Sr and most of the transition elements. In contrast, the non-alkaline hypersolvus and subsolvus granites do not show the same degree of enrichment. Concentration of the highly charged cations in the peralkaline suite is believed to be the result of halogen-rich fluid activity during fractionation of the magma. The sodic evolution trend in the peralkaline suite is reflected mineralogically by the development of aegirine and aegirine-hedenbergite solid solutions, and by a spectacular amphibole compositional range from katophorite through winchite, richterite, riebeckite to arfvedsonite and ferro eckermannite. Accessory phases which are ubiquitous in these rocks include aenigmatite, astrophyllite, fluorite, monazite and zircon. The non-alkaline hypersolvus granites typically contain iron-rich phases such as fayalite, eulite, ferrosilite-hedenbergite, and annite rich biotite. In the subsolvus granites, amphiboles range in composition from edenite through common hornblende to actinolite and also coexist with annite-rich biotite.Whole-rock and mineral isotopic data for the different suites yield isochrons that are within error of ca. 1,260 Ma, but they have variable initial ⁸⁷Sr/⁸⁶Sr ratios. The initial ⁸⁷Sr/⁸⁶Sr of the syenites and peralkaline granites (0.7076±11) is significantly lower than the initial ⁸⁷Sr/⁸⁶Sr of the subsolvus granites (0.7138±22). These isotopic data provide further confirmation of the importance of a late Elsonian alkaline event in Labrador which can be correlated with Gardar igneous activity in south Greenland. The petrogenesis of the peralkaline suite is interpreted to reflect the effects of fractionation of anhydrous phases from mantle derived basic magma which was contaminated during ascent by radiogenic partial melts of crustal derivation. The non-alkaline hypersolvus and subsolvus granites are interpreted as crustal melts which formed under conditions of variable in response to the same thermal event, and which subsequently experienced feldspar fractionation during crystallization.     

X-Ray Fluorescence Determination of Trace Elements in 6 B.C.S. and 5 P.R.E. Reference Materials

The concentrations of 20 trace elements in 6 British Chemical Standards (BCS) reference materials and 5 European Federation of Refractories Producers (PRE) reference materials have been determined by X-ray fluorescence spectrometry.     

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.     

Regional Energy Demand Responses To Climate Change: Methodology And Application To The Commonwealth Of Massachusetts

Climate is a major determinant of energy demand. Changes in climate may alter energy demand as well as energy demand patterns. This study investigates the implications of climate change for energy demand under the hypothesis that impacts are scale dependent due to region-specific climatic variables, infrastructure, socioeconomic, and energy use profiles. In this analysis we explore regional energy demand responses to climate change by assessing temperature-sensitive energy demand in the Commonwealth of Massachusetts. The study employs a two-step estimation and modeling procedure. The first step evaluates the historic temperature sensitivity of residential and commercial demand for electricity and heating fuels, using a degree-day methodology. We find that when controlling for socioeconomic factors, degree-day variables have significant explanatory power in describing historic changes in residential and commercial energy demands. In the second step, we assess potential future energy demand responses to scenarios of climate change. Model results are based on alternative climate scenarios that were specifically derived for the region on the basis of local climatological data, coupled with regional information from available global climate models. We find notable changes with respect to overall energy consumption by, and energy mix of the residential and commercial sectors in the region. On the basis of our findings, we identify several methodological issues relevant to the development of climate change impact assessments of energy demand.     

Towards evaluating cloud response to climate change using clustering technique identification of cloud regimes

Most of the discrepancies in the climate sensitivity of general circulation models (GCMs) are believed to be due to differences in cloud radiative feedback. Analysis of cloud response to climate change in different ‘regimes’ may offer a more detailed understanding of how the cloud response differs between GCMs. In which case, evaluation of simulated cloud regimes against observations in terms of both their cloud properties and frequency of occurrence will assist in assessing confidence in the cloud response to climate change in a particular GCM. In this study, we use a clustering technique on International Satellite Cloud Climatology Project (ISCCP) data and on ISCCP-like diagnostics from two versions of the Hadley Centre GCM to identify cloud regimes over four different geographical regions. The two versions of the model are evaluated against observational data and their cloud response to climate change compared within the cloud regime framework. It is found that cloud clusters produced by the more recent GCM, HadSM4, compare more favourably with observations than HadSM3. In response to climate change, although the net cloud response over particular regions is often different in the two models, in several instances the same basic processes may be seen to be operating. Overall, both changes in the frequency of occurrence of cloud regimes and changes in the properties (optical depth and cloud top height) of the cloud regimes contribute to the cloud response to climate change.