Chemical and structural relations of epitaxial xenotime and zircon substratum in sedimentary and hydrothermal environments: a TEM study

Xenotime overgrowths on detrital zircon in siliciclastic sediments have been reported in numerous studies. However, in natural samples, solid solution of zircon and xenotime is limited to near-end-member compositions. In order to characterize the interface region between both minerals and to draw inferences on the growth mechanisms of authigenic xenotime, we studied xenotime overgrowths on detrital zircon grains from two Phanerozoic sandstone samples with contrasting post-depositional histories. In one sample, the small (≤10 μm), pyramidal xenotime overgrowths are of diagenetic origin and grew without major discontinuity on the detrital zircon grain. The second sample shows up to >50-μm-wide, porous and inclusion-rich, hydrothermal xenotime overgrowths on detrital zircon, whereas the transition zone between both minerals is accompanied by large pore volume. Chemical compositions of the xenotime precipitates from the two samples differ particularly in Y, REE, Th and Sc concentrations, whereas high MREE availability in the diagenetic sample and the presence of Sc in the hydrothermal sample, respectively, appear to have promoted xenotime growth. Transmission electron microscopy on electron-transparent foils cut from the interface region shows that both the diagenetic xenotime and the hydrothermal xenotime are crystalline and grew in optical and crystallographic continuity to their detrital zircon substrata. Only a narrow transition zone (≤90 nm—diagenetic sample, 200–300 nm—hydrothermal sample) between zircon and xenotime is in part made up of nanometre-scale crystalline domains that are slightly distorted and may have formed from dissolution–re-precipitation processes at the zircon rim along with precipitation from the respective fluid.     

Some life history aspects of the seaboard goby (gobiosoma ginsburgi) in Rhode Island

This paper represents the first report of adultG. ginsburgi from Rhode Island waters since 1938. Gobies were collected only from subtidal shell communities in high salinity waters. Seaboard gobies eat a variety of benthic invertebrates but feed most heavily on harpacticoid copepods. Gravid females collected in July contained one size class of ova indicating a single spawning per season. Egg counts ranged from 1268 to 1977 per female. Larval densities indicate that peak spawning occurs in July and suggest thatG. ginsburgi is more abundant in the Sakonnet River and nearby Narragansett Bay than previously reported.     

Petrology of palagonite tuffs of Koko Craters,Oahu, Hawaii

Tuff deposits of the Koko Crater group consist largely of alkali basalt glass, either fresh or palagonitized. Most of the deposits are progressively palagonitized at depth, and topographic relations of palagonite on Koko Crater indicate that the palagonite was formed after the cone had been deeply eroded.The principal authigenic minerals in the palagonite tuffs were deposited in following sequence: phillipsite, chabazite, analcime, montmorillonite together with opal, and calcite. The amount of authigenic minerals in a given sample is generally proportional to the amount of palagonite, indicating that the authigenic minerals are produced in palagonitization of glass.Chemical analyses of sideromelane and associated palagonite by the electron microprobe show that about a quarter of the SiO₂, half of the Al₂O₃ and MgO, and three quarters or more of the CaO, Na₂O, and K₂O are lost in converting sideromelane to an equal volume of palagonite. A substantial proportion of these components lost from the sideromelane are precipitated nearby in zeolites, montmorillonite, opal, and calcite.Reaction of sideromelane with percolating ground water at low temperatures accounts for the vertical zoning from relatively fresh tuffs down into palagonite tuffs. The pH and ionic strength of percolating water probably increased with depth by solution and hydrolysis of glass, and where the pH and ionic strength became sufficiently high, the glass reacted to form palagonite and zeolites. Palagonite was formed by a microsolution-precipitation mechanism rather than by hydration or devitrification.     

Geochemical Characterization of Bolivian Formative Earthen Architecture by Wavelength‐Dispersive X‐ray Fluorescence

In this study, we employ wavelength‐dispersive X‐ray fluorescence (WDXRF) to characterize construction materials from Formative civic architecture (1000 B.C.E.–C.E. 400), ethnographic mudbricks, and off‐site controls from the Taraco Peninsula, Bolivia. The preparation of earthen construction materials for civic buildings can shed light on aspects of community development such as labor organization, resource management, and architectural technologies. We apply geochemical results to reconstructing how public buildings were made as communities moved toward socio‐political complexity in this region. However, there are few geochemical studies in the Andes, and little prior scientific analysis of earthen architecture. We therefore tested the efficacy of WDXRF for this region, and developed control materials. Our archaeological samples were selected from two Formative villages, Chiripa and Kala Uyuni. In this study, we performed WDXRF analyses on 63 archaeological and control samples including archaeological floors, walling, plasters, and mortars, as well as contemporary ethnographic walling and topsoils. Elemental signatures for 28 elements clearly distinguished the archaeological flooring, walling, plaster, and mortars from ethnographic and off‐site controls. More subtle variations were detected that distinguish study sites and the different material types. Laboratory‐calibrated multi‐element XRF effectively supports efforts to reconstruct the pathways to social complexity in the Titicaca Basin.     

Determination of Selenium in Thirty-Two Geochemical Reference Materials by Continuous - Flow Hydride Generation Atomic Absorption Spectrophotometry

A continuous-flow hydride atomic absorption spectrophotometric method has been applied to 32 geochemical reference materials for the determination of selenium. The sample is decomposed with a mixture of nitric, perchloric and hydrofluoric acids. Selenium values obtained in this study are in general agreement with literature values and provide additional certification for these reference materials. The precision of the method is generally better than 5% relative standard deviation. The lower limit of determination of selenium in the sample is 12 ppb.     

pp′-DDT adsorption to suspended particulate matter in sea water

A procedure was devised to study pp′-DDT [2,2-bis($\text{p-}\text{chlorophenyl}$)-1,1,1-trichloroethane] adsorption and desorption to suspended particulates in aqueous solutions. DDT adsorption to a marine sediment, sediment fractions, clay and humic acid suspended in sea water was investigated and the humic fraction was found to have a greater adsorbing capacity than the clay or sediment. Removal of the humic fraction from sediment reduced the adsorption capacity to less than 60 per cent of the original sediment sample. It was concluded that suspended humic particulates may be important agents for transporting chlorinated hydrocarbons through the water column and for concentrating them in sediments and in detritus-feeding organisms.     

Distribution coefficients of Eu and Sr for plagioclase-liquid and clinopyroxene-liquid equilibria in oceanic ridge basalt: an experimental study

The distribution coefficients of Eu and Sr for plagioclase-liquid and clinopyroxene-liquid pairs as a function of temperature and oxygen fugacity were experimentally investigated using an oceanic ridge basalt enriched with Eu and Sr as the starting material. Experiments were conducted between 1190° and 1140°C over a range of oxygen fugacities between 10^?8 and 10^?14 atm.The molar distribution coefficients are given by the equations: log^PL_Sr = 7320/T ? 4.62logK^CPX_Sr = 18020/T ? 13.10. Similarly, the weight fraction distribution coefficients are given by the equations: logD^PL_Sr = 6570/T ? 4.30logD^CPX_Sr = 18434/T ? 13.62.Although the mole fraction distribution coefficients have a smaller dependence on bulk composition than do the weight fraction distribution coefficients, they are not independent of bulk composition, thereby restricting the application of these experimental results to rocks similar to oceanic ridge basalts in bulk composition.Because the Sr distribution coefficients are independent of oxygen fugacity, they may be used as geothermometers. If the temperature can be determined independently — for example, with the Sr distribution coefficients, the Eu distribution coefficients may be used as oxygen geobarometers. Throughout the range of oxygen fugacities ascribed to terrestrial and lunar basalts, plagioclase concentrates Eu but clinopyroxene rejects Eu.     

Geochemical characteristics of Cocos Plate seamount lavas

A wide compositional continuum of basalts has been erupted from near-ridge seamounts constructed on the Cocos Plate between the Clipperton and Orozco Francture Zones. They range from highly evolved to moderately primitive (3.0–7.8% MgO), LREE-enriched alkali basalts, to moderately evolved to near-primary (5.2–9.5% MgO) tholeiites indistinguishable from N-type MORB. The data set of 159 quench glass analyses exhibits a remarkably consistent variation in both major and trace element composition that is keyed to variations in (La/Sm). Modeling of potential liquid lines of descent at pressures ranging from 1 bar to 8 kbar shows that this covariation is partially due to systematic differences in liquid lines of descent, where the alkaline lavas have undergone substantially more high pressure clinopyroxene fractionation and substantially less low pressure plagioclase fractionation than the tholeiites. In addition, systematic variation in the composition of the more primitive glasses indicates that they were derived from mixing of discrete enriched and depleted melts in the heterogenous seamount mantle source at pressures of 8–10 kbar and greater, and that clinopyroxene may be a residual phase during partial melting. These results show that porous media flow in the seamount mantle source is minor and that melt transport is accomplished primarily through cracking and diking. This study supports suggestions that the general homogeneity of basalt along the EPR is due to mixing in sub-axial magma chambers and mush zones, with additional mixing during partial mantle melting and melt segregation.