The lost world of the olenid trilobites

Trilobites of the Family Olenidae (Upper Cambrian to Upper Ordovidan) were closely tied to an oxygen-poor environment. They show a remarkable range of adaptations, testifying to a singular evolutionary plasticity.     

THE INFLUENCE OF PERMEABILITY ON COMPRESSIONAL WAVE VELOCITY IN MARINE SEDIMENTS*

To investigate the effect of permeability on the propagation of seismo-acoustic waves through marine sediments, a theoretical model based on Biot's equations is established which relates the compressional wave velocity measured at a fixed frequency to computed velocities at zero and infinite frequencies in terms of sediment porosity and permeability. The model is examined experimentally in a standard soil mechanics consolidation test (itself dependent, among other things, on sediment porosity and permeability) which has been modified to include measurements of compressional wave velocity at 1 MHz and shear-wave velocity at 5 kHz. This test allows the elastic modulus of the sediment frame to be assessed under different load conditions simultaneous with the velocity determinations. From a number of tests on different samples, five samples are chosen to typify the range of sediment sizes. The results show that the difference between the measured velocity at 1 MHz and the model-derived velocity at zero frequency increases with increasing particle size (from clays to fine sand), with decreasing porosity, and with increasing permeability. For sediments coarser than fine sand the simple model breaks down, possibly because of the dominance of scattering/diffraction effects at the high frequency of the experiment. Within this limitation the model seems satisfactory to offer a capability of predicting the permeability of a sea floor sediment to an order of magnitude by the in situ measurement of seismic velocities over a wide range of frequencies; the prediction process requires a good in situ determination of sediment porosity such as that offered by electrical formation factor measurements.     

Effect of Silica Activity on OH- IR Spectra of Olivine: Implications for Low-aSiO2 Mantle Metasomatism

Hydrogen solubility and hydroxyl substitution mechanism in olivineat upper-mantle conditions are not only a function of pressure,temperature, water fugacity and hydrogen fugacity, but are alsoinfluenced by silica activity. Olivine synthesized in equilibriumwith magnesiowüstite displays hydroxyl stretching bandsin the wavenumber range from 3640 to 3430 cm^–1. In contrast,olivine in equilibrium with orthopyroxene shows absorption bandsin a narrower wavenumber range from 3380 to 3285 cm^–1.The two fundamentally different spectra are assigned to hydroxylin tetrahedral and octahedral sublattices, respectively. Olivinein equilibrium with orthopyroxene is also less capable of incorporatinghydroxyl, relative to olivines in equilibrium with magnesiowüstite,by about a factor of ten. A comparison of spectra obtained aspart of this study with hydroxyl spectra of natural mantle olivinesshows that the latter display hydroxyl stretching patterns reminiscentof equilibrium with magnesiowüstite, although undoubtedlyolivine in the Earth’s mantle coexists with orthopyroxene.This may be attributed to a metasomatic overprint by a low-silicafluid and/or melt that was in reaction relationship with orthopyroxene.A likely metasomatic agent is a carbonatitic melt. When carbonatiticmelts decompose to oxides and CO₂, they may temporarily imposea low-aSiO₂ environment inherited by the olivine structure.If this suggestion proves true, Fourier transform IR spectroscopymay be used to fingerprint metasomatic episodes in the lithosphericmantle. KEY WORDS: FTIR spectrometry; olivine; mantle; metasomatism; water     

AN UNUSUAL CARBONATE BAND IN THE EAST PENNINE COALFIELD (ENGLAND)

A combined petrographical and geochemical study has been made on a per- sistent carbonate horizon from the Mansfield Marine Band, an important marker horizon in the Westphalian Coal Measures of the east Pennines. The composition of this carbonate is unusual for it normally consists of ankerite, but in some localities the carbonate is siderite and not ankerite. The position of the carbonate in the sedimentary cycle is discussed and the conclusion drawn that physicochemical conditions were suitable for the precipitation of CaC03 to occur. Furthermore the detrital material in the carbonate band continued to accumulate at a similar rate to the shales above and below the carbonate. The alteration of the CaC03 is thought to have been a diagenetic effect and the result of a change in the physicochemical environment. Variations in the concentration of dissolved sulphur species and their effect on the solubilities of iron and manganese provide an adequate mechanism to explain how CaC03 may alter to siderite on the one hand or ankerite on the other.     

Martian basalt (shergottite) Queen Alexandra Range 94201 and lunar basalt 15555: A tale of two pyroxenes

Abstract— We present here ion microprobe analyses of rare earth and other selected trace and minor elements in pyroxenes of shergottite Queen Alexandra Range 94201 and lunar basalt 15555. Pyroxene zonation patterns record the crystallization histories of these two basaltic samples from Mars and the Moon, respectively, and allow a comparison of mafic melt evolution on these two planetary bodies. Elemental abundances and trends in pyroxenes of these two rocks indicate that their minerals formed by continuous, closed system fractional crystallization of their respective parent melts. This further supports the idea that QUE 94201 closely represents the composition of a true Martian basaltic melt (McSween et al., 1996). The main differences in pyroxene elemental zonation patterns in these two objects are attributed to earlier crystallization of whitlockite in QUE 94201 (i.e., before the Fe-rich pyroxenes) than in 15555 (after the Fe-rich pyroxenes). The size of Eu anomalies in pyroxenes of QUE 94201 is intermediate between that in pyroxenes of 15555 and the other shergottites and may imply that fO₂ conditions during crystallization of this Martian basalt were significantly more reducing than for other shergottites, although not quite as reducing as for lunar basalts. Cerium anomalies appear to be less prevalent in pyroxenes of QUE 94201 than other Antarctic shergottites and could be indicative of lesser degree of weathering in the Antarctic.     

Quantitative Simulation of the Hydrothermal Systems of Crystallizing Magmas on the Basis of Transport Theory and Oxygen Isotope Data: An analysis of the Skaergaard Intrusion

Application of the principles of transport theory to studiesof magma-hydrothermal systems permits quantitative predictionsto be made of the consequences of magma intruding into permeablerocks. Transport processes which redistribute energy, mass,and momentum in these environments can be represented by a setof partial differential equations involving the rate of changeof extensive properties in the system. Numerical approximationand computer evaluation of the transport equations effectivelysimulates the crystallization of magma, cooling of the igneousrocks, advection of chemical components, and chemical and isotopicmass transfer between minerals and aqueous solution. Numerical modeling of the deep portions of the Skaergaard magma-hydrothermalsystem has produced detailed maps of the temperature, pressure,fluid velocity, integrated fluid flux, ¹⁸O-values in rock andfluid, and extent of nonequilibrium exchange reactions betweenfluid and rock as a function of time for a two-dimensional cross-sectionthrough the pluton. An excellent match was made between calculated¹⁸O-values and the measured ¹⁸O-values in the three principalrock units, basalt, gabbro, and gneiss, as well as in xenolithsof roof rocks that are now embedded in Layered Series; the latterwere evidently depleted in ¹⁸O early in the system's coolinghistory, prior to falling to the bottom of the magma chamber.The best match was realized for a system in which the bulk rockpermeabilities were 10^–13 cm² for the intrusion, 10^–11cm² for basalt, and 10^–16 cm² for gneiss; reaction domainsizes were 0.2 cm in the intrusion and gneiss and 0.01 cm inthe basalts, and activation energy for the isotope exchangereaction between fluid and plagioclase was 30 kcal/mole. The calculated thermal history of the Skaergaard system wascharacterized by extensive fluid circulation that was largelyrestricted to the permeable basalts and to regions of the plutonstratigraphically above the basalt-gneiss unconformity. Althoughfluids circulated all around the crystallizing magma, fluidflow paths were deflected around the magma sheet during theinitial 130,000 years. At that time, crystallization of thefinal sheet of magma and fracture of the rock shifted the circulationsystem toward the center of the intrusion, thereby minimizingthe extent of isotope exchange between rocks near the marginof the intrusion at this level. For comparison, similar calculationswere also made for pure conductive cooling; it was found thatthe rate of crystallization of the magma body was not changed.The solidified pluton cooled by a factor of about 2 faster inthe presence of a hydrothermal system. Transport rates of thermal energy out of the intrusion and oflow-¹⁸O fluids into the intrusion controlled the overall isotopeexchange process. During the initial 150,000 years, temperatureswere high and reaction rates were fast; thus, fluids flowinginto the intrusion quickly equilibrated with plagioclase. However,the temperature decreased between 120,000 and 175,000 yearsand caused a decrease in reaction rates and an increase in theequilibrium fractionation factor between plagioclase and fluid.Consequently, during this time period fluids in the intrusiontended to be out of equilibrium with plagioclase. After 175,000years temperatures had decreased sufficiently that reactionrates became insignificant, but convection rates were largeenough to redistribute fluid and enlarge the regions where fluidand plagioclase were out of equilibrium. By 400,000 years, thepluton had cooled to approximately ambient temperatures, andthe final ¹⁸O values were ‘frozen in’. Reactionsbetween hydrothermal fluid and the intrusion occurred over abroad range in temperature, 1000-200 °C, but 75 per centof the fluid circulated through the intrusion while its averagetemperature was >480 °C. This relatively high temperatureis consistent with the observation that only minor amounts ofhydrothermal alteration products were formed in the naturalsystem, even where several per mil shifts in ¹⁸O were detected. The relative quantities of fluid to rock integrated over theentire cooling history were 0.52 for the upper part of intrusion,0.88 for the basalt, 0.003 for the gneiss, and 0.41 for theentire domain. Almost all of the fluid flowed into the intrusionfrom the basalt host rocks that occur adjacent to the side contactsof the intrusion. Convection transferred about 20 per cent ofthe total heat contained in the gabbro upward into the overlyingbasalts; the remaining 80 per cent of the heat was transferredby conduction.     

Intrusion and differentiation of granitic magma at a high level in the crust: the Puscao pluton, Lima Province, Peru

Regression surface techniques have been used on partial whole-rockchemical analyses from the Puscao pluton to establish the three-dimensionalnature of the chemical variations within this body, which wasemplaced at a depth of between 4 km and 8 km within the crust.Block diagrams produced by the computer program are consistentwith the hypothesis that during the period preceding the totalconsolidation of the magma, the pluton has undergone in situdifferentiation to give a layered structure. Statistical analysis confirms that there is a large scale variationwithin the pluton and that local variation, such as might beexpected to result from the contamination of the Puscao magmaby assimilated volcanic material, did not contribute significantlyto the overall variation. Evidence is presented which suggests that the layering withinthe Puscao pluton was disturbed as a result of the emplacementof the much later Cañhas pluton, and that this disturbancehas the form of a simple doming centred upon the site of thepresent Cañas intrusion.     

Comparisons of the four Miller Range nakhlites,MIL 03346, 090030, 090032 and 090136: Textural and compositional observations of primary and secondary mineral assemblages

Abstract– Petrological and geochemical analyses of Miller Range (MIL) 03346 indicate that this meteorite originated from the same augitic cumulate layer(s) as the nakhlite Martian meteorites, but underwent rapid cooling prior to complete crystallization. As with the other nakhlites, MIL 03346 contains a secondary alteration assemblage, in this case consisting of iddingsite‐like alteration veins in olivine phenocrysts, Fe‐oxide alteration veins associated with the mesostasis, and Ca‐ and K,Fe‐sulfate veins. We compared the textural and mineralogical compositions of MIL 090030, 090032, and 090136 with MIL 03346, focusing on the composition and Raman spectra of the alteration assemblages. These observations indicate that the meteorites are paired, and that the preterrestrial olivine‐bound alteration assemblages were produced by weakly acidic brine. Although these alteration assemblages resemble similar assemblages in Nakhla, the absence of siderite and halite in the Miller Range nakhlites indicates that the parental alteration brine was comparatively HCO₃^? depleted, and less concentrated, than that which altered Nakhla. This indicates that the Miller Range nakhlite alteration brine experienced a separate evolutionary pathway to that which altered Nakhla, and therefore represents a separate branch of the Lafayette‐Nakhla evaporation sequence. Thin‐sections cut from the internal portions of these meteorites (away from any fusion crust or terrestrially exposed edge), contain little Ca‐sulfate (identified as gypsum), and no jarosite, whereas thin‐sections with terrestrially exposed edges have much higher sulfate abundances. These observations suggest that at least the majority of sulfate within the Miller Range nakhlites is terrestrially derived.     

Tomography: A window on the role of sulfur in the structure of micrometeorites

Abstract– To determine the role played by sulfides in the formation of vesicles and FeNi metal beads, we mapped the locations and tabulated the numbers of sulfides, metal beads, and vesicles in 1583 sectioned micrometeorites (MMs) using conventional microscopy and in 190 whole MMs using synchrotron computed microtomography (SCMT). Both the section and the SCMT images show that sulfides melt, coalesce, and migrate to the MMs surface. The decomposition of sulfides may occur during all these stages. Given the sulfide morphologies and compositions that we see in section, we think the breakdown of Ni sulfides produces the FeNi beads. The SCMT images show that metal beads are common in melted MMs, >50% have them. Vesicles in porphyritic and scoriaceous MMs are also probably formed as sulfides decompose. Not only do sulfides abut the vesicles but also the temperatures at which sulfides decompose overlap those at which MM surfaces first melt and temporarily seal, suggesting that S gases could produce most of these vesicles. As the vesicle shapes and patterns of distribution differ among MM classes, tomography can be used to nondestructively screen for specific types of MMs. Tomography is a powerful tool for visualizing the three‐dimensional distribution of metal beads, sulfides, mean densities, and vesicles in MMs.     

The lunar rock and mineral characterization consortium: Deconstruction and integrated mineralogical,petrologic, and spectroscopic analyses of mare basalts

The lunar rock and mineral characterization consortium (LRMCC) has conducted coordinated mineralogy/petrography/spectroscopy analyses of a suite of pristine lunar basalts. Four basalt slabs (two low‐Ti, two high‐Ti) and paired thin sections were analyzed. Thin sections were analyzed for mineralogy/petrography, while the slabs were used to prepare particulate separates of major mineral phases and bulk samples. Mineral separates and particulate bulk samples were crushed to controlled grain sizes and their reflectance spectra measured in the NASA RELAB at Brown University. The resulting data set provides an essential foundation for spectral mixing models, offers valuable endmember constraints for space weathering analyses, and represents critical new ground truth results for lunar science and exploration efforts.