Investigating the ancient Martian magnetic field using microwaves

The new microwave palaeointensity technique has been used to investigate samples from the Martian meteorite Nakhla. This technique is a promising new way to obtain absolute palaeointensity information regarding the ancient Martian magnetic field as recorded by the Martian meteorites. Assuming that a part of the magnetic remanence is of thermal origin and originating on Mars the two samples studied yield estimates of 4 μT for the Martian magnetic field at 1.35 Ga.     

Ar–Ar age and thermal history of martian dunite NWA 2737

We report an ³⁹Ar–⁴⁰Ar age determination of a whole rock sample of the olivine-rich, martian meteorite Northwest Africa (NWA) 2737. Those extractions releasing 0–48% of the ³⁹Ar define an ³⁹Ar–⁴⁰Ar isochron age of 160–190 Ma, when evaluated in various ways. Higher temperature extractions show increasing ages that eventually exceed the reported Sm–Nd age of 1.42 Ga. At least part of this excess ⁴⁰Ar may have been shock implanted from the martian atmosphere. We considered two possible interpretations of the Ar–Ar isochron age, utilizing the measured Ar diffusion characteristics of NWA 2737 and a thermal model, which relates Ar diffusion to the size of a cooling object after shock heating. One interpretation, that ⁴⁰Ar was only partially degassed by an impact event ~ 11 Ma ago (the CRE age), appears possible only if NWA 2737 was shock-heated to temperatures > 600 °C and was ejected from Mars as an object a few 10 s of cm in diameter. The second interpretation, which we prefer, is that NWA experienced an earlier, more intense shock event, which left it residing in a warm ejecta layer, and a less intense event ~ 11 Ma ago, which ejected it into space. Our evaluation would require NWA 2737 to have been heated by this first event to a temperature of ~ 300–500 °C and buried in ejecta to a depth of ~ 1–20 m. These conclusions are compared to model constraints on meteorite ejection from Mars reported in the literature. The second, Mars-ejection impact ~ 11 Ma ago probably heated NWA 2737 to no more than ~ 400 °C. NWA 2737 demonstrates that some martian meteorites probably experienced shock heating in events that did not eject them into space.     

Space weathering processes on airless bodies: Fe isotope fractionation in the lunar regolith

Nanophase Fe metal grains (np-Fe°) are a product of space weathering, formed by processes related to meteorite impacts, and solar-wind sputtering on airless planetary bodies, such as the Moon. Iron isotopes of lunar soils are fractionated during these processes, and the np-Fe° in the finest (<10 μm), mature, size fractions of the soil become enriched in heavier isotopes by ∼0.3‰ in ⁵⁶Fe/⁵⁴Fe in comparison to the bulk rocks (0.03±0.05‰), from which the soil was formed. A positive correlation of δ⁵⁶Fe values with the soil maturity index, I_S/FeO, suggests that the high δ⁵⁶Fe values reflect production of nanophase Fe metal that is produced by space weathering that occurs on airless planetary bodies. Furthermore, the enrichment of δ⁵⁶Fe in the smallest size fraction of lunar soils supports a model for creation of np-Fe° through vapor deposition induced by micrometeorites, as well as that by solar-wind sputtering.     

Cosmic-ray exposure age of Martian meteorite GRV 99027

We have determined the concentrations of 10Be and 26Al in GRV 99027 recovered by the 16th Chinese Antarctic expedition team, which are 14.1 ± 0.6 dpm/kg and 67.5 ± 3.4 dpm/kg, respectively. From the concentration of 10Be, we calculate a cosmic-ray exposure age of 4.4 ± 0.6 Ma for GRV 99027. The concentration of 26Al is too high compared to the 10Be exposure age, indicating extra production from solar ray. The exposure ages, petrologic and geochemical characteristics of mantle-derived Martian meteorites GRV 99027, LEW 88516, Y-793605, NWA 1950 and ALHA77005 are very similar, suggesting that these meteorites most probably were ejected from Mars in the same impact event.     

Low-temperature hydrothermal alteration of intra-caldera tuffs,Miocene Tejeda caldera,Gran Canaria,Canary Islands

The Miocene Tejeda caldera on Gran Canaria erupted ~ 20 rhyolite–trachyte ignimbrites (Mogán Group 14–13.3 Ma), followed by ~ 20 phonolitic lava flows and ignimbrites (Fataga Group 13–8.5 Ma). Upper-Mogán tuffs have been severely altered immediately within the caldera margin, whereas extra-caldera Mogán ignimbrites, and overlying Fataga units, are apparently unaltered. The altered intra-caldera samples contain minerals characteristic of secondary fluid–rock interaction (clays, zeolites, adularia), and relics of the primary mineral assemblage identified in unaltered ignimbrites (K-feldspar, plagioclase, pyroxene, amphibole, and groundmass quartz). Major and trace-element data indicate that Si, Na, K, Pb, Sr, and Rb, were strongly mobilized during fluid–rock interaction, whereas Ti, Zr, and Nb behaved in a more refractory manner, experiencing only minor mobilization. The δ¹⁸O values of the altered intra-caldera tuffs are significantly higher than in unaltered extra-caldera ignimbrites, consistent with an overall low-temperature alteration environment. Unaltered extra-caldera ignimbrites have δD values between − 110‰ and − 173‰, which may reflect Rayleigh-type magma degassing and/or post-depositional vapour release. The δD values of the altered intra-caldera tuffs range from − 52‰ to − 131‰, with ambient meteoric water at the alteration site estimated at ca. − 15‰. Interaction and equilibration of the intra-caldera tuffs with ambient meteoric water at low temperature can only account for whole-rock δD values of around − 45‰, given that ?D_clay–water is ca. − 30‰ at 100 °C, and decreases in magnitude at higher temperatures. All altered tuff samples have δD values that are substantially lower than − 45‰, indicating interaction with a meteoric water source with a δD value more negative than − 15‰, which may have been produced in low-temperature steam fumaroles. Supported by numerical modeling, our Gran Canaria data reflect the near-surface, epithermal part of a larger, fault-controlled hydrothermal system associated with the emplacement of the high-level Fataga magma chamber system. In this near-surface environment, fluid temperatures probably did not exceed 200–250 °C.     

Nitrogen isotope ratios of nitrate as a clue to the origin of nitrogen on the Pacific coast of Japan

To clarify the sources and transformation of NO₃⁻ on the Pacific coast of Japan, observations over the continental shelf were conducted during the summer in 2005 and 2006 when the Kuroshio flowed close to and away from the coastal area, respectively. Below the halocline, there are two prominent salinity peaks that originated in two different waters. In the subsurface layer, the salinity maximum (S_max) was indicative of the Kuroshio Water (KW), while the salinity minimum (S_min) in the middle layer at ∼400 m depth was indicative of the North Pacific Intermediate Water (NPIW). δ¹⁵N_NO3 ranged from 4.1‰ to 5.1‰ with a mean of 4.8±0.4‰ in the deeper water around S_min. Below 50 m depth over the shelf break, δ¹⁵N_NO3 values (3.1±0.8‰ in 2005 and 4.6±0.3‰ in 2006) clearly increased as contribution of NPIW increased in 2006. On the contrary, subsurface δ¹⁵N of NO₃⁻ values (−1.1±0.1‰) remained unchanged in both years, although the contribution of the KW to the subsurface water changed significantly. This suggests that the source of NO₃⁻ has little effect on the δ¹⁵N of NO₃⁻ in this layer. The negative δ¹⁵N values also coincided with the base of the chlorophyll maximum layer suggesting that these isotopic signals must be evidence of active nitrification in the upper layer.     

Nitrogen cycling in the German Bight (SE North Sea) — Clues from modelling stable nitrogen isotopes

Nitrogen isotope values (δ¹⁵N) of surface sediments in the German Bight of the North Sea exhibit a significant gradient from values of 5–6‰ of the open shelf sea to values above 11‰ in the German Bight. This signal has been attributed to high reactive N (N_r) loading enriched in ¹⁵N from rivers and the atmosphere. To better understand the processes that determine the intensity and spatial distribution of δ¹⁵N anomalies in surface sediments, and to explore their usefulness for reconstructions of pristine N-input from rivers, we modeled the cycling of the stable isotopes ¹⁴N and ¹⁵N in reactive nitrogen through the ecosystem of the central and southern North Sea (50.9–57.3°N, 3.4°W−9.2°E) for the year 1995. The 3D-ecosystem model ECOHAM amended with an isotope-tracking module was validated by δ¹⁵N data of surface sediments within the model domain. A typical marine value (δ¹⁵N_nitrate=5‰) was prescribed for nitrate advected into the model domain at the seaside boundaries, whereas δ¹⁵N_nitrate of river inputs were those measured bi-monthly over 1 year; δ¹⁵N values of atmospheric deposition were set to 6‰ and 7‰ for NO_x and NH_y, respectively. The simulated δ¹⁵N values of different nitrogen compounds in the German Bight strongly depend on the mass transfers in the ecosystem. These fluxes, summarized in a nitrogen budget for 1995, give an estimate of the impacts of hydrodynamical and hydrological boundary conditions, and internal biogeochemical transformations on the nitrogen budget of the bight.     

Lithium and lithium isotope profiles through the upper oceanic crust: a study of seawater-basalt exchange at ODP Sites 504B and 896A

Ocean Drilling Program (ODP) Hole 504B near the Costa Rica Rift is the deepest hole drilled in the ocean crust, penetrating a volcanic section, a transition zone and a sheeted dike complex. The distribution of Li and its isotopes through this 1.8-km section of oceanic crust reflects the varying conditions of seawater alteration with depth. The upper volcanic rocks, altered at low temperatures, are enriched in Li (5.6-27.3 ppm) and have heavier isotopic compositions (δ⁷Li=6.6-20.8‰) relative to fresh mid-ocean ridge basalt (MORB) due to uptake of seawater Li into alteration clays. The Li content and isotopic compositions of the deeper volcanic rocks are similar to MORB, reflecting restricted seawater circulation in this section. The transition zone is a region of mixing of seawater with upwelling hydrothermal fluids and sulfide mineralization. Li enrichment in this zone is accompanied by relatively light isotopic compositions (−0.8-2.1‰) which signify influence of basalt-derived Li during mineralization and alteration. Li decreases with depth to 0.6 ppm in the sheeted dike complex as a result of increasing hydrothermal extraction in the high-temperature reaction zone. Rocks in the dike complex have variable isotopic values that range from −1.7 to 7.9‰, depending on the extent of hydrothermal recrystallization and off-axis low-temperature alteration. Hydrothermally altered rocks are isotopically light because ⁶Li is preferentially retained in greenschist and amphibolite facies minerals. The δ⁷Li values of the highly altered rocks of the dike complex are complementary to those of high-temperature mid-ocean ridge vent fluids and compatible to equilibrium control by the alteration mineral assemblage. The inventory of Li in basement rocks permits a reevaluation of the role of oceanic crust in the budget of Li in the ocean. On balance, the upper 1.8 km of oceanic crusts remains a sink for oceanic Li. The observations at 504B and an estimated flux from the underlying 0.5 km of gabbro suggest that the global hydrothermal flux is at most 8×10⁹ mol/yr, compatible with geophysical thermal models. This work defines the distribution of Li and its isotopes in the upper ocean crust and provides a basis to interpret the contribution of subducted lithosphere to arc magmas and cycling of crustal material in the deep mantle.     

Methane in shallow cold seeps at Mocha Island off central Chile

We studied for the first time the intertidal and subtidal gas seepage system in Mocha Island off Central Chile. Four main seepage sites were investigated (of which one site included about 150 bubbling points) that release from 150 to 240 tonnes CH₄ into the atmosphere per year. The total amount of methane emitted into the atmosphere is estimated in the order of 800 tonnes per year. The gases emanated from the seeps contain 70% methane, and the stable carbon isotopic composition of methane, δ¹³C-CH₄ averaged −44.4±1.4‰ which indicates a major contribution of thermogenic gas. Adjacent to one of the subtidal seeps, rocky substrates support a diverse community of microbial filaments, macroalgae, and benthic organisms. While stable carbon isotopic compositions of marine benthic organisms indicate a dominant photosynthesis-based food web, those of some hard-substrate invertebrates were in the range −48.8‰ to −36.8‰, suggesting assimilation of methane-derived carbon by some selected taxa. This work highlights the potential subsidy of the trophic web by CH₄-C, and that its emission to the atmosphere justifies the need of evaluating the use of methane to support the energy requirements of the local community.     

The present-day atmosphere of Mars: Where does it come from?

Recent observations and missions to Mars have provided us with new insight into the past habitability of Mars and its history. At the same time they have raised many questions on the planet evolution. We show that even with the few data available we can propose a scenario for the evolution of the Martian atmosphere in the last three billion years. Our model is obtained with a back integration of the Martian atmosphere, and takes into account the effects of volcanic degassing, which constitutes an input of volatiles, and atmospheric escape into space. We focus on CO₂, the predominant Martian atmospheric gas.Volcanic CO₂ degassing rates are obtained for different models of numerical model crust production rates [Breuer, D., Spohn, T. 2003. Early plate tectonics versus single-plate tectonics on Mars: Evidence from magnetic field history and crust evolution. J. Geophys. Res. - Planets, 108, E7, 5072, Breuer, D., Spohn, T., 2006. Viscosity of the Martian mantle and its initial temperature: Constraints from crust formation history and the evolution of the magnetic field. Planet. Space Sci. 54 (2006) 153–169; Manga, M., Wenzel, M., Zaranek, S.E., 2006. Mantle Plumes and Long-lived Volcanism on Mars as Result of a Layered Mantle. American Geophysical Union Fall Meeting 2006, Abstract #P31C-0149.] and constrained on observation. By estimating the volatile contents of the lavas, the amount of volatiles released in the atmosphere is estimated for different scenarios. Both non-thermal processes (related to the solar activity) and thermal processes are studied and non-thermal processes are incorporated in our modelling of the escape [Chassefière, E., Leblanc, F., Langlais, B., 2006, The combined effects of escape and magnetic field history at Mars. Planet. Space Sci. Volume 55, Issue 3, Pages 343–357.]. We used measurements from ASPERA and Mars Express and these models to estimate the amount of lost atmosphere.An evolution of the CO₂ pressure consistent with its present state is then obtained. A crustal production rate of at least 0.01 km³/year is needed for the atmosphere to be at steady state. Moreover, we show that for most of the scenarios a rapid loss of the primary (and primordial) atmosphere due to atmospheric escape is required in the first 2 Gyr in order to obtain the present-day atmosphere. When CO₂ concentration in the mantle is high enough (i.e. more than 800 ppm), our results imply that present-day atmosphere would have a volcanic origin and would have been created between 1 Gyr and 2 Gyr ago even for models with low volcanic activity. If the volcanic activity and the degassing are intense enough, then the atmosphere can even be entirely secondary and as young as 1 Gyr. However, with low activity and low CO₂ concentration (less than 600 ppm), the present-day atmosphere is likely to be for the major part primordial.     

Iron isotope fractionation during planetary differentiation

The Fe isotope composition of samples from the Moon, Mars (SNC meteorites), HED parent body (eucrites), pallasites (metal and silicate) and the Earth's mantle were measured using high mass resolution MC-ICP-MS. These high precision measurements (δ⁵⁶Fe ≈ ± 0.04‰, 2 S.D.) place tight constraints on Fe isotope fractionation during planetary differentiation.Fractionation during planetary core formation is confined to < 0.1‰ for δ⁵⁶Fe by the indistinguishable Fe isotope composition of pallasite bulk metal (including sulfides and phosphides) and olivine separates. However, large isotopic variations (≈ 0.5‰) were observed among pallasite metal separates, varying systematically with the amounts of troilite, schreibersite, kamacite and taenite. Troilite generally has the lightest (δ⁵⁶Fe ≈ − 0.25‰) and schreibersite the heaviest (δ⁵⁶Fe ≈ + 0.2‰) Fe isotope composition. Taenite is heavier then kamacite. Therefore, these variations probably reflect Fe isotope fractionation during the late stage evolution and differentiation of the S- and P-rich metal melts, and during low-temperature kamacite exsolution, rather than fractionation during silicate-metal separation.Differentiation of the silicate portion of planets also seems to fractionate Fe isotopes. Notably, magmatic rocks (partial melts) are systematically isotopically heavier than their mantle protoliths. This is indicated by the mean of 11 terrestrial peridotite samples from different tectonic settings (δ⁵⁶Fe = + 0.015 ± 0.018‰), which is significantly lighter than the mean of terrestrial basalts (δ⁵⁶Fe = + 0.076 ± 0.029‰). We consider the peridotite mean to be the best estimate for the Fe isotope composition of the bulk silicate Earth, and probably also of bulk Earth. The terrestrial basaltic mean is in good agreement with the mean of the lunar samples (δ⁵⁶Fe = + 0.073 ± 0.019‰), excluding the high-Ti basalts. The high-Ti basalts display the heaviest Fe isotope composition of all rocks measured here (δ⁵⁶Fe ≈ + 0.2‰). This is interpreted as a fingerprint of the lunar magma ocean, which produced a very heterogeneous mantle, including the ilmenite-rich source regions of these basalts.Within uncertainties, samples from Mars (SNC meteorites), HED (eucrites) and the pallasites (average olivine + metal) have the same Fe isotope compositions as the Earth's mantle. This indicates that the solar system is very homogeneous in Fe isotopes. Its average δ⁵⁶Fe is very close to that of the IRMM-014 standard.     

Biological and environmental changes in Lake Baikal during the late Quaternary inferred from carbon, nitrogen and sulfur isotopes

An 8-m continuous sediment core, approximately 250-ky-old at the bottom, from Academician Ridge in Lake Baikal, has been analyzed for the stable isotopes of carbon, nitrogen and sulfur, in order to study the paleoclimatic and paleobiological changes that occurred in the Eurasian continental interior. These isotopic changes are closely related to changes in vertical lake-water circulation between glacial and interglacial periods. Sedimentary organic carbon in cool periods is more enriched in ¹³C (−23.8‰ on average) than that in warm periods (−27.0‰ on average). The ¹³C-enrichment of organic carbon suggests a decrease of land-derived organic matter influx to the lake, less precipitation, and loss of terrestrial vegetation around Lake Baikal in cool periods. Pyrite in high total sulfur/total organic carbon (TS/TOC) layers shows strong depletion in ³⁴S (−20.8‰ to −32.4‰) during climate transitions from glacial to interglacial periods at the beginning of oxygen isotope stages (OIS) 1, 5 and 7. The ³⁴S-depleted pyrite indicates augmentation of dissimilatory sulfate reduction by sulfate reducing bacteria (SRB) at the sediment-water interface. Enhancement of aqueous sulfate concentrations and limitation of oxygen circulation to the surface sediments might also occur in the climate transition periods. The δ¹⁵N values of total nitrogen increase abruptly by ∼2‰ just after the δ³⁴S negative peaks, which may result from low nutrient concentrations in the euphotic zone associated with water circulation changes in Lake Baikal.     

Later Pleistocene/Holocene climate conditions of Qinghai-Xizhang Plateau (Tibet) based on carbon and oxygen stable isotopes of Zabuye Lake sediments

We present a time series of carbon and oxygen stable isotope records of the last 30?000 ¹⁴C years throughout the last glacial-postglacial cycle from western Qinghai-Xizhang (Tibet) Plateau. A 20-m core drilled in the south basin of Zabuye Salt Lake was analyzed for inorganic and organic carbon and total sulfur contents, δ¹³C and δ¹⁸O values of carbonates. Our results indicate that climatic changes have led to a drastic negative shift of stable isotope ratios at the transition between the Last Full Glacial and the postglacial phase during Later Pleistocene times (∼16.2 kyr BP), and a rapid positive shift at the transition from Pleistocene to Holocene (∼10.6 kyr BP). The first shift is marked by the drop of δ¹⁸O_carb values of about 10‰ (from +2 to −8‰) and δ¹³C_carb values of about 3‰ (from 5 to 2‰). The second shift which occurred at the transition from Pleistocene to Holocene was of similar magnitude but in the opposite direction. Isotope data, combined with total organic and inorganic carbon contents and the lithological composition of the core, suggest this lake was an alluvial pre-lake environment prior to ca. 28 ¹⁴C kyr BP. During ca. 28-16.2 ¹⁴C kyr BP, Zabuye Lake was likely a moderately deep lake with limited outflow. The cool and arid glacial climate led the lake level to drop drastically. Extended residence time overwhelmed the lower temperature and caused a steady increase of δ¹³C_carb and δ¹⁸O_carb values and total inorganic carbon content in the sediments. During ca. 16.2-10.6 ¹⁴C kyr BP, this lake probably overflowed and received abundant recharge from melting glaciers when the deglaciation was in its full speed. A spike of markedly enhanced δ¹³C_carb and δ¹⁸O_carb is seen at ∼11.5 kyr BP, probably due to the isotopic effects left behind by the short but severe Younger Dryas (YD) event. After ca. 10.6 ¹⁴C kyr BP, Zabuye Lake probably closed its surface outflow, due to strong desiccation and drastic climate warming. The Early and Middle Holocene were characterized by unstable climatic conditions with alternating warmer/cooler episodes as indicated by the severe fluctuations of total organic carbon, δ¹³C and δ¹⁸O values. A hypersaline salt lake environment was finally formed at Zabuye after ∼5 ¹⁴C kyr BP when the mirabilite and halite concentrations steadily increased and became the dominant minerals in the sediments. Severe imbalance of inflow/outflow resulted in the drastic increase of total sulfur, δ¹³C_carb and δ¹⁸O_carb values and dominance of halite in the lake since ca. 3.8 kyr BP to present.     

Thermoluminescence studies of the Allende meteorite

The Allende meteorite has been examined with a view to applying thermoluminescence (TL) to the study of a meteorite's passage through the atmosphere. At least three kinds of TL-bearing minerals are present. A strong peak at 140°C is due to forsterite, and one at 200°C is probably caused by cordierite. By far the most intense TL comes from an alteration product associated with gehlenite.In the 4-cm diameter meteorite examined the 200°C TL varied in intensity across the stone, showing it to be produced by fragmentation. Temperature gradients induced by atmospheric heating can also be derived, and indicate the orientation of the meteorite. Together with fusion crust measurements these results enable the final phase of the meteorite's passage through the atmosphere to be delineated.     

A 3.5 Ga record of water-limited, acidic weathering conditions on Mars

The secondary mineral budget on Earth is dominated by clay minerals, Al-hydroxides, and Fe-oxides, which are formed under the moderate pH, high water-to-rock ratio conditions typical of Earth's near-surface environment. In contrast, geochemical analyses of rocks and soils from landed missions to Mars indicate that secondary mineralogy is dominated by Mg (± Fe, Ca)-sulfates and Fe-oxides. This discrepancy can be explained as resulting from differences in the chemical weathering environment of Earth and Mars. We suggest that chemical weathering processes on Mars are dominated by: (1) a low-pH, sulfuric acid-rich environment in which the stoichiometric dissolution of labile mineral phases such as olivine and apatite (± Fe–Ti oxides) is promoted; and (2) relatively low water-to-rock ratio, such that other silicate phases with slower dissolution rates (e.g., plagioclase, pyroxene) do not contribute substantially to the secondary mineral budget at the Martian surface. Under these conditions, Al-mobilization is limited, and the formation of significant Al-bearing secondary phases (e.g., clays, Al-hydroxides, Al-sulfates) is inhibited. The antiquity of rock samples analyzed in-situ on Mars suggest that water-limited acidic weathering conditions have more than likely been the defining characteristic of the Martian aqueous environment for billions of years.     

δO of carbonate, quartz and phosphate from belemnite guards: implications for the isotopic record of old fossils and the isotopic composition of ancient seawater

Belemnite guards of Cretaceous and Jurassic age were found to contain varying amounts of quartz deposited both on the external surface and inside the rostrum. The oxygen isotopic composition of coexisting carbonate, quartz and phosphate from the same rostrum was measured according to well-established techniques. None of these compounds showed isotopic values in equilibrium with one another. Assuming δ¹⁸O values of the diagenetic water within the range of meteoric waters, the δ¹⁸O(SiO₂) yield temperatures in agreement with the apparent secondary origin of this phase. The δ¹⁸O(CO₃²⁻) range, with a certain continuity, between −10.8 and +0.97 PDB-1 with most of the intermediate values being within the range of the carbonate isotopic values of Mesozoic fossils. The most positive isotopic results obtained from phosphate are close to +23/+24‰ (V-SMOW). They can hardly be related to a secondary origin of the phosphate, or to the presence of diagenetic effects, since these results are among the most positive ever measured on phosphate. As far as we know there is no widespread diagenetic process determining an ¹⁸O enrichment of phosphate. The very low concentration of phosphate did not allow the determination of its mineralogical composition. All the available δ¹⁸O(PO₄³⁻) values from belemnite and non-belemnite fossils of marine origin of Tertiary and Mesozoic age are reported along with the newly measured belemnites. The following conclusions may be drawn from the data reported: (1) the pristine oxygen isotope composition of fossil marine organisms (either carbonate or phosphate) may easily undergo fairly large changes because of oxygen isotope exchange processes with diagenetic water; this process is apparent even in the case of geologically recent fossils; (2) the δ¹⁸O(PO₄³⁻) of belemnite rostra seems to be, at least in the case of the most positive results, in isotopic equilibrium with environmental water because of the similarity between the results from Cretaceous belemnites and the results from Cretaceous and Lower Tertiary pelecypods and fish teeth; 3) if so, the only feasible interpretation that can be suggested for the ¹⁸O enriched data is the possibility of a relatively large variation of the oxygen isotopic composition of ocean paleowater from Jurassic to recent time.     

Magnetic properties of Antarctic shergottite meteorites EETA 79001 and ALHA 77005: possible relevance to a Martian magnetic field

The possibility that the parent body of the SNC meteorites is Mars implies that the magnetic properties of these meteorites may provide evidence concerning ancient Martian magnetic fields. EETA 79001 possesses a weak, very stable primary magnetization, the properties of which are consistent with its acquisition in an ambient magnetic field either during the meteorite's formation or during the severe shock event later in its history. The samples of ALHA 77005 studied possessed no measurable primary magnetization: the observed remanence appears to be a viscous magnetization acquired in local laboratory fields. The magnetic carriers in the meteorites are fine-grained magnetite and a lower Curie point mineral, probably titanomagnetite or pyrrhotite, present to the extent of less than 0.1% by weight. Estimates of the strength of the magnetizing field for EETA 79001 are in the range 1–10 μT.     

Spectral and petrologic analyses of basaltic sands in Ka'u Desert (Hawaii) – implications for the dark dunes on Mars

Dark aeolian deposits on Mars are thought to consist of volcanic materials due to their mineral assemblages, which are common to basalts. However, the sediment source is still debated. Basaltic dunes on Earth are promising analogs for providing further insights into the assumed basaltic sand dunes on Mars. In our study we characterize basaltic dunes from the Ka'u Desert in Hawaii using optical microscopes, electron microprobe, and spectral analyses. We compare the spectra of terrestrial and Martian dune sands to determine possible origins of the Martian dark sediments. Our results show that the terrestrial sands consist primarily of medium to coarse sand‐sized volcanic glass and rock fragments as well as olivine, pyroxene, and plagioclase minerals. Grain shapes range from angular to subrounded. The sample composition indicates that the material was derived from phreatomagmatic eruptions partially with additional proportions of rock fragments from local lava flows. Grain shape and size indicate the materials were transported by aeolian processes rather than by fluvial processes. Spectral analyses reveal an initial hydration of all terrestrial samples. A spectral mineralogical correlation between the terrestrial and Martian aeolian sands shows a similarity consistent with an origin from volcanic ash and lava. We suggest that the Martian deposits may contain similar abundances of volcanic glass, which has not yet been distinguished in Martian spectral data. Copyright © 2011 John Wiley & Sons, Ltd.     

Chemical divides and evaporite assemblages on Mars

Assemblages of evaporite minerals record detailed physical and chemical characteristics of ancient surficial environments. Accordingly, newly discovered regions of saline minerals on Mars are high priority targets for exploration. The chemical divide concept of evaporite mineral formation is used successfully to predict evaporite mineralogy and brine evolution on Earth. However, basaltic weathering largely controls fluid compositions on Mars and the robust predictive capabilities of terrestrial chemical divides cannot be used to interpret Martian evaporites. Here we present a new chemical divide system that predicts evaporite assemblages identified in SNC-type meteorites, ancient evaporites discovered on Meridiani Planum by the Opportunity rover, and Mars Express OMEGA data. We suggest that a common fluid type that has been buffered to different pH levels by basaltic weathering controls the variability among Martian evaporite assemblages and that evaporite mineralogy and brine evolution is essentially established by the initial composition of the dilute evaporating fluid.     

Oxygen isotopic ratios of some evaporites from Precambrian to Recent ages

The δ¹⁸O values of eighteen marine evaporites of Precambrian to Recent ages were found to vary from +8 to 25‰ relative to SMOW, while the δ³⁴S values previously measured by Thode and Monster [2] vary from +10 to +38‰ relative to meteoritic sulfur. The results strongly suggest that the δ¹⁸O value of ocean sulfate varied with geologic age with a minimum at the Permian age.