Thorium-234 as a tracer of spatial,temporal and vertical variability in particle flux in the North Pacific

An extensive ²³⁴Th data set was collected at two sites in the North Pacific: ALOHA, an oligotrophic site near Hawaii, and K2, a mesotrophic HNLC site in the NW Pacific as part of the VERTIGO (VERtical Transport In the Global Ocean) study. Total ²³⁴Th:²³⁸U activity ratios near 1.0 indicated low particle fluxes at ALOHA, while ²³⁴Th:²³⁸U ～0.6 in the euphotic zone at K2 indicated higher particle export. However, spatial variability was large at both sites—even greater than seasonal variability as reported in prior studies. This variability in space and time confounds the use of single profiles of ²³⁴Th for sediment trap calibration purposes. At K2, there was a decrease in export flux and increase in ²³⁴Th activities over time associated with the declining phase of a summer diatom bloom, which required the use of non-steady state models for flux predictions. This variability in space and time confounds the use of single profiles of ²³⁴Th for sediment trap calibration purposes. High vertical resolution profiles show narrow layers (20–30 m) of excess ²³⁴Th below the deep chlorophyll maximum at K2 associated with particle remineralization resulting in a decrease in flux at depth that may be missed with standard sampling for ²³⁴Th and/or with sediment traps. Also, the application of ²³⁴Th as POC flux tracer relies on accurate sampling of particulate POC/²³⁴Th ratios and here the ratio is similar on sinking particles and mid-sized particles collected by in-situ filtration (>10–50 μm at ALOHA and >5–350 μm at K2). To further address variability in particle fluxes at K2, a simple model of the drawdown of ²³⁴Th and nutrients is used to demonstrate that while coupled during export, their ratios in the water column will vary with time and depth after export. Overall these ²³⁴Th data provide a detailed view into particle flux and remineralization in the North Pacific over time and space scales that are varying over days to weeks, and 10's–100's km at a resolution that is difficult to obtain with other methods.     

On mass transport in deep water waves

Summary Various formulations of the mass-transport problem are compared for progressive waves in deep water. In order to calculate the mass-transport velocity as a function of depth in the main body of the fluid, it is necessary to include the effect of viscous wave attenuation. It is shown that the usual assumptions of periodicity in distance and attenuation with time or periodicity in time and attenuation with distance, are both physically unsatisfactory. The first does not specify a unique solution, and the second is incompatible with the assumption of zero surface stress. A certain critical constant tangential wind stress will maintain strictly time-periodic deep water waves. The corresponding attenuation with distance is then calculated to order ³. A constant tangential stress greater or less than the critical causes waves, necessarily decaying with distance, to grow or decay with time.     

Use of Carbonatites in the Production of Precipitated Calcium Carbonate: A Case Study from Eppawala,Sri Lanka

The study investigates the possibility of using carbonatite in the production of precipitated calcium carbonate (PCC). We made use of fresh apatite-rich carbonatites found at the phosphate mining sites at Eppawala, Sri Lanka. Analyses of the fresh carbonatite were performed with the aid of optical microscopy, powder X-ray diffraction (XRD), atomic absorption spectrophotometry (AAS), UV/visible spectrophotometry (UVVS), and thermo gravimetric analysis (TGA). Quicklime obtained from calcinations of carbonatites was used in synthesizing PCC via a lime-soda process. The end product was analyzed with XRD, TGA, AAS, and UVVS. Results revealed that the most common CO₃ ^2? phase available in fresh carbonatites is calcite (>65%). The Ca-rich CO₃ ^2? phase can be distinguished easily from other available minerals because its mode of occurrence in carbonatite matrix is different to that of other minerals. The results of TGA show that the decomposition of CO₃ ^2? phase initiates at about 340°C, which leads to lower energy consumption during calcinations. Post-magmatic hydrothermal process may have been the cause of the formation of thermally unstable CO₃ ^2? phases. Hydration of quicklime from the carbonatite yields much higher Ca²⁺ in the solution than from marble under the same experimental conditions. The synthesized PCC particles are in the calcite polymorphic form. The purity of PCC varies from 96 to 98 wt%. The maximum precipitable CaCO₃ from 1 g of quicklime is about 1.1 g. Hence, fresh carbonatites has great economic potential for the production of PCC.     

Petrology,isotope characteristics,and K-Ar ages of the Maranhão,northern Brazil,Mesozoic basalt province

Northern Brazil contains remnants of Mesozoic flood basalts and hypabyssal rocks that were apparently emplaced during tectonism related to opening of the Atlantic Ocean. Analyses and new K-Ar ages reveal that this 700x250 km Maranhão province (5°–8°S) has low-Ti basalts (1.1 wt% TiO₂) in the western part that range about 160 to 190 Ma, and high-Ti basalts (3.4–4.4 wt% TiO₂) in the eastern part about 115–122 Ma. Low-Ti basalt compositions are less evolved and have a smaller range, Mg# 62-56, than the high-Ti basalts, Mg# 44–33. General characteristics of the least evolved members of low- and high-Ti groups include, respectively, Zr 100 and 250 ppm, Sr 225 and 475 ppm, Ba 200 and 500 ppm, Nb 10 and 26 ppm, Y 29 and 36 ppm, La/Yb_(n) 4.2 and 8.8, where La_(n) is 30 and 90. Overall compositions resemble the low- and high-Ti basaltic rocks of the Mesozoic Serra Geral (Paraná) province in southern Brazil. The Maranhão low-Ti basalts have more radiogenic Sr and Pb and higher ¹⁸O than the high-Ti basalts. Respectively, low- vs high-Ti: _Sr26–54 vs 15–18; ²⁰⁶Pb/²⁰⁴Pb=18.25–.78 vs 18.22–.24; and ¹⁸O 8.9–12.6 vs 6.5–8.6. Nd isotopes overlap: _Nd–1.6 to –3.8 vs –2.1 to –3. Ages, compositions, and isotopes indicate that the low- and high-Ti groups had independent parentages from enriched subcontinental mantle. However, both groups can be modeled from one source composition if low-Ti basalt isotopes reflect crustal contamination, and if the parentages for each group were picritic liquids that represent either higher (for low-Ti) or lower (for high-Ti) percentages of melting of that single source. When comparing Pb isotopes of Maranhão and Serra Geral high-Ti basalts (uncontaminated) to evaluate the DUPAL anomaly, Maranhão has Pb 7/4=4.6–11, and Pb 8/4=72–87; Serra Geral has Pb 7/4=10–13, and Pb 8/4=95–125. The small difference is not enough to conform to DUPAL contours, and is inconsistent with large-scale isotopic heterogeneity of mantle beneath Brazil prior to rifting of South America from Africa. Maranhão low-Ti magmas probably relate to the opening of central North Atlantic, and high-Ti magmas to the opening of equatorial Atlantic. The proposed greater percentage of source melting for low-Ti basalts may reflect a Triassic-Jurassic hotspot, while lesser melting for high-Ti magmas may relate to Cretaceous decompressional (rifting) melting.     

Trace elements as indicators of the physicochemical conditions of mineral formation in hydrothermal sulfide systems

The three-mode distribution of trace-element (TE) concentrations is observed in accordance with three main forms of TE occurrence in mineral: structural, surficial, and phase (native TE phases). Minerals of hydrothermally synthesized pyrite–pyrrhotite–magnetite–greenockite assemblage in the presence of Au and Mn are studied. Discrimination of modes is made, using the method of statistical sample of analytical data for single crystals (SSADSC), which is based on the postulate that individual crystals can contain predominantly one of possible forms. This is supported by study of Cd modes of occurrence by element thermorelease atomic-absorption spectrometry. X-ray photoelectron spectroscopy and atomic-force microscopy were used to examine the surficial TE forms. It has been confirmed that the dependence of the TE content on the crystal size in the sample is mainly due to surficial nonautonomous phases absorbing TEs. The effect of correspondence of chemical-component forms on the surfaces of coexisting minerals is also corroborated. This phenomenon is not related to the mutual contamination of phases but is due to the induction of the corresponding states of chemical forms in coexisting nonautonomous phases. It is possible to obtain true coefficients of interface distribution, characterizing structural TE impurities. These coefficients differ strongly from apparent distribution coefficients calculated from the bulk contents of impurities, except for Mn in pyrrhotite and magnetite, where its structural mode is predominant. The results obtained show that TEs can be used as quantitative geochemical indicators, which help to obtain correct information about the parameters of mineral formation and TE contents in the fluid phase.     

The Scale Matcher: a procedure for assessing scale compatibility of spatial data and models

It is becoming easier to combine environmental data and models to provide information for problem-solving by environmental policy analysts, decision-makers, and land managers. However, the scale dependencies of each of these (data, model, and problem) can mean that the resulting information is misleading or even invalid. This paper describes the development of a systematic framework (dubbed the ‘Scale Matcher’) for identifying and matching the scale requirements of a problem with the scale limitations of spatial data and models.

The Scale Matcher framework partitions the complex array of scale issues into more manageable components that can be individually quantified. First, the scale characteristics of data, model, and problem are separated into their scale components of extent, accuracy, and precision, and each is associated with suitable metrics. Second, a comprehensive set of pairwise matches between these components is defined. Third, a procedure is devised to lead the user through a process of systematically comparing or matching each scale component. In some cases, the matches are simple comparisons of the relevant metrics. Others require the combination of data variability and model sensitivity to be investigated by randomly simulating data and model imprecision and inaccuracy. Finally, a conclusion is drawn as to the scale compatibility of the Data–Model–Problem trio based on the overall procedure result. Listing the individual match results as a set of scale assumptions helps to draw attention to them, making users more aware of the limitations of spatial modelling.

Application of the Scale Matcher is briefly illustrated with a case study, in which the scale suitability of two sources of soil map data for identifying areas of vulnerability to groundwater pollution was tested. The Scale Matcher showed that one source of soil map data had unacceptable scale characteristics, and the other was marginal for addressing the problem of nitrate leaching vulnerability. The scale-matching framework successfully partitioned the scale issue into a series of more manageable comparisons and gave the user more confidence in the scale validity of the model output.     

Trace metal concentrations in sediments of the Eastern Mississippi Bight

Sediments collected from 3 onshore-offshore transects (12 stations total) in the Eastern Mississippi Bight at 5 different times during 1987–1988 have been analyzed for total Ag, As, Ba, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Pb, Sb, Se, Sn, Th and Zn. The data show considerable variation both spatially and temporally, largely as a result of natural variability in grain size and mineralogy. Clay-rich samples from deep water were always more metal-rich than sandy samples from shallow areas. Many samples from near the Mississippi River Delta appeared to be enriched in Ba by about a factor of two, probably as a result of contamination from oil well drilling mud, but there were few other indications of pollution influences. Many samples from throughout the area gave Mn/Fe and Cd/Fe ratios a factor of two or more lower than their Mississippi River source material. This shows that biochemical activity in the sediment is capable of solubilizing reducible and adsorbed metals.     

下地壳基性麻粒岩流变强度实验研究

镁铁质基性麻粒岩被认为可能是大陆下地壳的主要组成岩石[1,2],涉及当前地球动力学研究中地壳变形和高原隆升,壳幔边界的力学耦合与拆离,底侵和拆沉作用等一系列地球动力学问题阳[3,4],具有重要的地球动力学意义.大陆下地壳的流变学性质是我们深入认识这些地球深部过程的关键点之一.     

A Mid Cretaceous origin for the Galápagos hotspot: volcanological, petrological and geochemical evidence from Costa Rican oceanic crustal segments

The Quepos, Nicoya and Herradura oceanic igneous terranes in Costa Rica are conspicuous features of a Mid to Late Cretaceous regional magmatic event that encompasses similar terranes in Central America, Colombia, Ecuador and the Caribbean. The Quepos terrane (66?Ma), which consists of ol-cpx phyric, tholeiitic pillow lavas overlain by highly vesicular hyaloclastites, breccias and conglomerates, is interpreted as an uplifted seamount/ocean island complex. The Nicoya (～90?Ma) and Herradura terranes consist of fault-bounded sequences of sediments, tholeiitic volcanics (pillow lavas and massive sheet flows) and plutonic rocks. The volcanic rocks were emplaced at relatively high eruption rates in moderate to deep water, possibly forming part of an oceanic plateau. Major and trace element data from Nicoya/Herradura tholeiites indicate higher melting temperatures than inferred for normal mid-ocean-ridge basalts (MORB) and/or a different source composition. Sr–Nd–Pb isotopic ratios from all three terranes are distinct from MORB but resemble those from the Galápagos hotspot. The volcanological, petrological and geochemical data from Costa Rican volcanic terranes, combined with published age data, paleomagnetic results and plate tectonic reconstructions of this region, provide strong evidence for a Mid Cretaceous (～90Ma) age for the Galápagos hotspot, making it one of the oldest known, active hotspots on Earth. Our results also support an origin of the Caribbean Plate through melting of the head of the Galápagos starting plume.