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1.
The importance of the discovery of jarosite at the Meridiani Planum region of Mars is discussed. Terrestrial studies demonstrate that jarosite requires a unique environment for its formation, crystallizing from highly acidic (pH < 4) S-rich brines under highly oxidizing conditions. A likely scenario for jarosite formation on Mars is that degassing of shallow magmas likely released SO2 that reacted with aqueous solutions in shallow aquifers or on the martian surface. This interaction forms both H2SO4 and H2S. A martian oxidant must be identified to both oxidize H2S to produce the required acidity of the fluid, and to oxidize Fe2+ to Fe3+. We suggest that reactions involving both sulfur and the reduction of CO2 to CO may provide part of the answer. The jarosite crystal structure is truly remarkable in terms of its tolerance for the substitution of a large number of different cations with different ionic radii and charges. The structure accommodates hydrogen, oxygen, and sulfur, the stable isotope systematics of which are strong recorders of low-temperature fluid-rock-atmosphere interactions. Jarosite has been proven to be a robust chronometer for Ar-Ar and K-Ar dating techniques, and there is every reason to believe that U-Pb, Rb-Sr, and Nd-Sm techniques for older jarosite from Mars will also be robust. Although the discovery of jarosite on Mars alone, with no other analytical measurements on the phase, has given us insights to martian surficial processes, the true power of jarosite can not be exploited until jarosite is sampled and returned from Mars. Mars sample return is a long way off but, until then, we should be vigilant about examining martian meteorites for alteration assemblages that contain jarosite. A suite of jarosite samples representing a significant time span on Mars may hold the key to reading the record of martian atmospheric evolution. 相似文献
2.
Christopher D.K Herd Lars E BorgJohn H Jones James J Papike 《Geochimica et cosmochimica acta》2002,66(11):2025-2036
The oxygen fugacity of the Dar al Gani 476 martian basalt is determined to be quartz-fayalite-magnetite (QFM) −2.3 ± 0.4 through analysis of olivine, low-Ca pyroxene, and Cr-spinel and is in good agreement with revised results from Fe-Ti oxides that yield QFM −2.5 ± 0.7. This estimate falls within the range of oxygen fugacity for the other martian basalts, QFM −3 to QFM −1. Oxygen fugacity in martian basalts correlates with 87Sr/86Sr, 143Nd/144Nd, and La/Yb ratios, indicating that the mantle source of the basalts is reduced and that assimilation of crust-like material controls the oxygen fugacity. This allows constraints to be placed on the oxidation state of the martian mantle and on the nature of assimilated crustal material. The assimilated material may be the product of early and extensive hydrothermal alteration of the martian crust, or it may be amphibole- or phlogopite-bearing basaltic rock within the crust. In either case, water may play a significant role in the oxidation of basaltic magmas on Mars, although it may be secondary to assimilation of ferric iron-rich material. 相似文献
3.
Coral mortality may result in macroalgal proliferation or a phase shift into an alga-dominated state. Subtidal, high-latitude western Indian Ocean coral communities at Sodwana Bay on the KwaZulu-Natal coast, South Africa, have experienced some mortality because of warm-water anomalies, storms and other causes, but the response of the macroalgae is unknown. We investigated the abundance and diversity of benthic algae on different hard natural substrata (dead digitate, brain and plate corals and beach rock) on Two-Mile Reef, Sodwana Bay. We also compared algal communities colonising ceramic, marble and pretreated ceramic tiles placed on the reef for six months. We identified 95 algae (14 Chlorophyta, 11 Phaeophyceae, 69 Rhodophyta and one cyanobacterium). Assemblages on natural and artificial substrata were dominated by the brown alga Lobophora variegata (Lamouroux) Womersley ex Oliveira and non-geniculate corallines (Rhodophyta, Corallinaceae). Cluster and ordination analyses revealed that the algae showed no affinity for particular substrata, whether natural or artificial. Algal cover was occasionally higher on rougher tiles and crustose corallines were significantly more abundant on marble than ceramic tiles. Two-Mile Reef had 23.1% dead and 48.4% live scleractinian coral cover, where dead corals were colonised indiscriminately by many small algal species, but there was no evidence of algal proliferation. The results provide a baseline for monitoring this high-latitude reef system. 相似文献
4.
辉钼矿Re-Os同位素定年方法的改进与应用 总被引：13，自引：9，他引：4
公认的Re-Os同位素定年代表物辉钼矿,目前已在金属硫化物矿床年代学研究领域获得了广泛的应用。本研究采用浓HNO3分解辉钼矿样品,大大地简化了Re和Os的化学制备过程,并根据辉钼矿中正常Os含量水平相对放射成因187Os可以忽略的特点,以正常Os标准为稀释剂,实现了仪器测量过程中Os同位素质量分馏的在线校正,改善了分析数据的质量。该方法经辉钼矿国家标准物质进行验证,获得了满意的Re、Os含量及Re-Os年龄数据,并且在南岭地区与连阳复式岩体相关的姓坪夕卡岩型钼矿床成矿年龄研究中获得了成功应用。在实际应用中,为了获得有意义的能反映真实地质事件的年龄数据,辉钼矿样品不仅要有足够的取样量,而且还要保证粒度细、混合均匀。 相似文献
5.
Crystal chemistry of merrillite from Martian meteorites: Mineralogical recorders of magmatic processes and planetary differentiation 
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下载免费PDF全文 C. K. Shearer P. V. Burger J. J. Papike F. M. McCubbin A. S. Bell 《Meteoritics & planetary science》2015,50(4):649-673
Merrillite is a ubiquitous accessory phase in a variety of Martian meteorite lithologies. The Martian merrillites exhibit a positive correlation between Mg# and Na and a negative correlation between Mg# and both Mn and vacancies in the octahedral Na‐site. Their REE patterns are varied and range from LREE‐depleted to LREE‐enriched. The dominant cation substitutions in the Martian merrillites are Fe2+VI Mg‐site?Mg2+VI Mg‐site and Ca2+VI Na‐site + □VI Na‐site?2Na+VI Na‐site. The REE substitution into the 8‐fold coordinated Ca‐site is accommodated by the coupled substitution CaVIII Ca‐site + (Na)VI Na‐site ?(Y3+ + REE3+)VIII Ca‐site + □VI Na‐site. The REE substitution is significantly more prevalent in lunar merrillite and can be used as a “fingerprint” to distinguish lunar from Martian meteorites. The substitution of OH? (whitlockite) and/or F? (bobdownsite) for O2? on one of the phosphate tetrahedrons appears to be rather insignificant. The correlations among Na, Mg#, Mn, and Na‐site vacancies are linked to the premerrillite crystallization history of the melt and the crystal chemical behavior of the Mg‐ and Na‐sites. The former reflects the sequence and extent of plagioclase and pyroxene crystallization. The differences in REE pattern shapes among the merrillites reflect source regions for the Martian basalts and the shapes are not greatly perturbed by the crystallization history. The occurrence of merrillite does not imply low‐volatile component in the Martian magmas. However, the low whitlockite and bobdownsite contents suggest that these samples were not altered by hydrothermal fluids and therefore not reset owing to aqueous fluid interactions. Consequently, the young ages of the shergottites are probably true igneous crystallization ages. 相似文献
6.
N Loiseau JJ Kiszka T Bouveroux MR Heithaus M Soria P Chabanet 《African Journal of Marine Science》2016,38(1):73-79
Bull sharks Carcharhinus leucas are common along the coast of Reunion Island (South-West Indian Ocean) and were suspected to aggregate in the vicinity of an aquaculture farm in Saint-Paul Bay on the west coast. In order to understand the behaviour and interaction of bull sharks near aquaculture cages at Saint-Paul Bay, we deployed an experimental unbaited stationary video camera. From 175 hours of recording during daylight hours from March to April 2012, eight individual female bull sharks (seven adults and one immature) were identified based on their natural markings. These sharks were resighted between 3 and 45 times. Residency analysis revealed site attachment under the aquaculture cages for at least three individuals over the course of the study. Recorded behaviours included intraspecific social interactions such as synchronised swimming. Social interactions and relatively strong paired associations for two pairs of females suggest some level of sociality among bull sharks around Reunion Island. Overall, our results demonstrate the utility of unbaited video systems to monitor the behaviour of adult coastal sharks. 相似文献
7.
豫西沙沟脉状Ag-Pb-Zn矿床地质特征和成矿流体研究 总被引：6，自引：1，他引：5
豫西沙沟薄脉状Ag-Pb-Zn硫化物矿床位于华北陆块南缘熊耳山地区,主要由多金属硫化物-石英-碳酸盐脉型和石英-碳酸盐-绢云母-多金属硫化物蚀变岩型两种矿化类型组成。主要矿脉的矿物共生序列可以分为成矿前的石英-黄铁矿阶段(Ⅰ)、闪锌矿-石英-方铅矿-少量银矿物阶段(Ⅱ1)、方铅矿-石英-闪锌矿-含铁白云石-银矿物阶段(Ⅱ2)和成矿后的方解石-(石英)阶段(Ⅲ)。对不同阶段的成矿流体研究表明,石英-黄铁矿阶段(Ⅰ)中的含氯化钠子晶三相(LVH)包裹体(Ⅰ1)可能是直接从饱和水的结晶岩浆熔体中出溶形成或是由岩浆流体的减压沸腾形成,显示该区很可能存在岩浆流体端元。多金属硫化物阶段(Ⅱ1Ⅱ2)捕获富液相包裹体(LV型)和个别CO2包裹体(C型),这两个阶段流体包裹体反映了主成矿阶段流体的基本特征,结合包裹体气相和液相成分色谱分析以及包裹体初融温度,认为成矿流体应该为中-低温低盐度含CO2的H2O-NaCl体系。其中,阶段(Ⅱ2)的均一温度(145～288℃,平均为194℃)比阶段(Ⅱ1)的均一温度(185～357℃,平均240℃)低46℃;同时,阶段(Ⅱ2)的盐度(1.91%～10.86%,平均6.38%)较阶段(Ⅱ1)盐度(4.65%～10.11%,平均7.77%)略低。对这一温度和盐度的总体下降趋势的合理解释是大气水的逐渐混入。多金属硫化物阶段(Ⅱ1Ⅱ2)之后的方解石-(石英)阶段普遍为富液相包裹体(LV型),该阶段显著降低的温度(129～208℃,平均165℃)和盐度(1.40%～4.03%,平均2.50%),进一步佐证大气水的不断混入。而且,流体混合可能在引起矿石矿物从热液中沉淀方面起到重要作用。 相似文献
8.
A study of the chemical trends displayed by lunar armalcolites has been made in conjunction with single-crystal X-ray structure refinements of lunar and synthetic armalcolite in order to assess the possible importance of Ti3+ in lunar armalcolite and to characterize the effects of cation substitutions on the structure. The apparent cation deficiencies found in lunar armalcolites analyzed with the electron microprobe most likely reflect the presence of Ti3+, although the existence of vacancies cannot be ruled out. Structure refinements of an Apollo 17 armalcolite are consistent with either interpretation. These results support experimental evidence suggesting the presence of Ti3+ in armalcolite and indicate that virtually all lunar armalcolites probably contain ～4–11 mol.% Ti23+Ti4+O5 component in solid solution. The cation distribution in lunar armalcolite is essentially completely ordered. However, synthetic crystals quenched from near 1200°C have been found to retain significant cation disorder. 相似文献
9.
Basalt magmas, derived by the partial melting of planetary interiors, have compositions that reflect the pre-accretionary history of the material from which the planet formed, the planets, subsequent evolutionary history, the chemistry and mineralogy of the source regions, and the intensive thermodynamic parameters operating at the source and emplacement sites. Studies of basalt suites from the Earth, its Moon, and the eucrite parent body reveal compositional differences intrinsic to their source regions which are, in turn, a characteristic of the planet and its formational and evolutionary history.Major interplanetary differences are observed in iron,
, TiO2, Al2O3, Na2O, Cr, Ni, and in volatile element abundances. The most primitive mare basalts have Mg#s 0.6, on the Earth they are 0.70–0.72 for mid-ocean ridge basalts (MORBs) and up to 0.9 for Archean peridotitic komatiites. Eucrites have Mg#s approaching 0.5 (excepting Binda). These differences reflect inherent differences in
of their sources. Striking differences in the TiO2 abundances of the planetary basalts reflect both inter- and intra-planetary variations in source chemistry. Primitive MORBs and primitive oceanic intraplate tholeiites have a factor of 2–3 difference in TiO2 at comparable Mg# (0.7–1.2 vs 2–3 wt.% respectively). Three major titania groups are recognized in the mare suite; high TiO2 (8–13 wt.%), low TiO2 (2–5 wt.%) and very low TiO2 (<1 wt.%). The eucrites have TiO2 contents <1 wt.%.The mare basalts and eucrites have pronounced Na2O depletion relative to all terrestrial basalts. This is a consequence of the preplanetary accretion loss of volatiles from the material that formed the Moon and the eucrite parent bodies.Mare basalts have consistently lower Al2O3 contents than the terrestrial basalts. This may be due either to an inherently lower content of Al2O3 in the mare sources or it may reflect Al2O3 retention in an aluminous phase.The transition metals are fractionated in all three basalt suites. For terrestrial basalts this may reflect core-separation; however, in the case of the Moon and eucrite parent bodies pre-accretionary separation of metal and silicates is a more reasonable explanation. A pronounced Cr anomaly is observed in terrestrial MORBs but not in the mare basalts. This appears to be related to fO2 differences in the respective mantles.Overall rare earth element abundances are comparable between all three objects. Mare basalts have a pronounced negative Eu anomaly which is inherited from their source region and is record of plagioclase removal from crystallizing magma ocean early in lunar history (4.4–4.6 Ga). Early separation of plagioclase on the Earth appears to have been a relatively unimportant process. 相似文献
10.
Christopher D. K. Herd Craig S. Schwandt John H. Jones James J. Papike 《Meteoritics & planetary science》2002,37(7):987-1000
Abstract— A composition approximating the lithology A groundmass of the Elephant Moraine (EET) 79001 martian basalt (Eg; McSween and Jarosewich, 1983) has been used to investigate the petrogenesis of the meteorite and the behavior of Cr and V at different oxygen fugacities. Crystallization experiments were carried out over a range of temperatures, and oxygen fugacities of either iron‐wüstite (IW) or IW + 2 (i.e., 1.5 log units below the quartz‐fayalite‐magnetite (QFM) buffer). Comparison of trace element concentrations (obtained by secondary ion mass spectrometry (SIMS) analysis) in experimental silicates with those of natural silicates supports the Fe‐Ti oxide‐derived oxygen fugacity of QFM ?1.8 ± 0.3 for this basalt (Herd et al., 2001). Experimental distribution coefficients, in conjunction with SIMS analyses of rims from the olivine and pyroxene xenocrysts in lithology A, as well as analyses of lithology A groundmass pigeonite cores, are used to calculate coexisting liquid concentrations of V and Cr. Liquid compositions derived from pigeonite xenocryst rims and groundmass pigeonite cores are similar, suggesting that the rims of orthopyroxene xenocrysts are overgrowths, which have not previously been accounted for when reconstructing the groundmass composition. This implies that the Eg composition requires modification. A similar exercise for the ferroan rims on olivine xenocrysts yields very different liquid compositions, indicating that these rims are not overgrowths but are part of the xenocryst assemblage. These results are shown to be consistent with the petrography of lithology A xenocrysts. 相似文献