Fred’s Flow (Canada) and Murphy Well (Australia): thick komatiitic lava flows with contrasting compositions,emplacement mechanisms and water contents

Two Archaean komatiitic flows, Fred’s Flow in Canada and the Murphy Well Flow in Australia, have similar thicknesses (120 and 160 m) but very different compositions and internal structures. Their contrasting differentiation profiles are keys to determine the cooling and crystallization mechanisms that operated during the eruption of Archaean ultramafic lavas. Fred’s Flow is the type example of a thick komatiitic basalt flow. It is strongly differentiated and consists of a succession of layers with contrasting textures and compositions. The layering is readily explained by the accumulation of olivine and pyroxene in a lower cumulate layer and by evolution of the liquid composition during downward growth of spinifex-textured rocks within the upper crust. The magmas that erupted to form Fred’s Flow had variable compositions, ranging from 12 to 20 wt% MgO, and phenocryst contents from 0 to 20 vol%. The flow was emplaced by two pulses. A first ~20-m-thick pulse was followed by another more voluminous but less magnesian pulse that inflated the flow to its present 120 m thickness. Following the second pulse, the flow crystallized in a closed system and differentiated into cumulates containing 30–38 wt% MgO and a residual gabbroic layer with only 6 wt% MgO. The Murphy Well Flow, in contrast, has a remarkably uniform composition throughout. It comprises a 20-m-thick upper layer of fine-grained dendritic olivine and 2–5 vol% amygdales, a 110–120 m intermediate layer of olivine porphyry and a 20–30 m basal layer of olivine orthocumulate. Throughout the flow, MgO contents vary little, from only 30 to 33 wt%, except for the slightly more magnesian basal layer (38–40 wt%). The uniform composition of the flow and dendritic olivine habits in the upper 20 m point to rapid cooling of a highly magnesian liquid with a composition like that of the bulk of the flow. Under equilibrium conditions, this liquid should have crystallized olivine with the composition Fo94.9, but the most magnesian composition measured by electron microprobe in samples from the flow is Fo92.9. To explain these features, we propose that the parental liquid contained around 32 wt% MgO and 3 wt% H₂O. This liquid degassed during the eruption, creating a supercooled liquid that solidified quickly and crystallized olivine with non-equilibrium textures and compositions.     

Distribution,abundance and growth of New Zealand sea lion Phocarctos hookeri pups on Campbell Island

Nine weeks field work was completed during two trips in January/February and March/ April 2003 to investigate the distribution and abundance of New Zealand sea lion Phocarctos hookeri pups at Campbell Island. A total of 161 pups were tagged and a further 138 dead pups were found. A closed mark‐recapture model was used to estimate the total number of live pups (e.g., tagged plus untagged pups) at Campbell Island in April as 247 (SE = 28, 95% CI 198–308). Pup production at Campbell Island is estimated at 385, which comprises 13% of the total pup production for the species in the 2003 season. This is the first robust estimate of pup production for New Zealand sea lions at Campbell Island. The figure of 385 pups is considerably higher than any of the previous estimates reported from Campbell Island. The high level of pup mortality (36%) at Campbell Island for approximately the first 2 months after birth is higher than the 17% reported for the Auckland Islands for approximately the same period in 2003, but is similar to unusually high levels of mortality (20–30%) reported at the Auckland Islands in recent years. It was not possible to determine the cause of death of the 138 dead pups owing to scavenging and decomposition. Pups were found over the whole Island, with the exception of its northern end. Male pups were significantly heavier and faster growing than female pups over the same period.     

Tracing the metasomatic and magmatic evolution of continental mantle roots with Sr, Nd, Hf and and Pb isotopes: A case study of Middle Atlas (Morocco) peridotite xenoliths

We studied clinopyroxenes from spinel-facies peridotite xenoliths sampled by the Quaternary intra-plate volcanism of the Middle Atlas (Morocco) and present new trace element and Sr-Nd-Hf isotope data. However, we focus in particular on Pb isotope data and ²³⁸U/²⁰⁴Pb and ²³²Th/²⁰⁴Pb ratios of these clinopyroxenes. This data allows us to investigate: (a) the timing of metasomatic events, (b) the prevalence and persistence of elevated ²³⁸U/²⁰⁴Pb, ²³²Th/²³⁸U and ²³²Th/²⁰⁴Pb in continental mantle roots and (c) the ²³⁸U/²⁰⁴Pb and ²³²Th/²⁰⁴Pb composition of putative basaltic melts generated from such metasomatised sub-continental lithospheric mantle (SCLM).Incompatible trace element concentrations in these clinopyroxenes are elevated, marked by high-field strength element depletion and fractionated elemental ratios (e.g., U/Nb, Zr/Hf) most consistent with enrichment due to carbonatitic liquids. Sr, Nd and Hf isotopes have an affinity to HIMU.U, Th and Pb abundances in the clinopyroxenes generally exceed estimates of primitive mantle clinopyroxene. Pb isotope compositions of these clinopyroxenes are radiogenic and vary between ²⁰⁶Pb/²⁰⁴Pb = 19.93-20.25, ²⁰⁷Pb/²⁰⁴Pb = 15.63-15.66 and ²⁰⁸Pb/²⁰⁴Pb = 39.72-40.23. These Pb isotope systematics result in generally negative Δ7/4 but positive Δ8/4; setting these samples distinctly apart from typical HIMU. These Pb isotope compositions are also distinct from the associated host volcanic rocks. ²³⁸U/²⁰⁴Pb and ²³²Th/²⁰⁴Pb of these clinopyroxenes, which range from 26 to 81 and 136 to 399, respectively, are elevated and more extreme than estimates of MORB- and HIMU-source mantle.The Pb isotope evolution of the clinopyroxenes suggests that the metasomatic enrichment is younger than 200 Ma, which discounts the volcanic activity due to the opening of the Atlantic and the onset of the collision of the African and Eurasian plates as processes generating the lithophile element and isotope composition of this continental mantle root. Instead, the enrichment is thought to be associated with the Quaternary intra-plate volcanism in the Middle Atlas. However, the erupted mafic melts have unradiogenic Pb isotopes and lower ²³⁸U/²⁰⁴Pb, ²³²Th/²⁰⁴Pb and ²³²Th/²³⁸U relative to the clinopyroxene and do not seem to have equilibrated with the clinopyroxenes. The high Th abundances and the high ²³²Th/²³⁸U also suggest that the metasomatism was due to carbonatitic liquids.When literature data for Pb isotopes in mantle minerals are considered, the Pb isotope range of Archean, Proterozoic and Phanerozoic continental mantle roots is remarkable in that they are similar to the convecting mantle. This observation does not support the existence of sub-continental lithospheric mantle with high ²³⁸U/²⁰⁴Pb and ²³²Th/²⁰⁴Pb for long periods of time. Consequently, the narrow range of Pb isotopes in SCLM worldwide suggests that only the youngest metasomatic events are recorded by incompatible elements such as U, Th and Pb. Numerical modelling of putative magmas generated from Middle Atlas SCLM by fractional, non-modal melting calculations yield extremely high ²³⁸U/²⁰⁴Pb and ²³²Th/²⁰⁴Pb ratios. For example, pure SCLM magmas generated from 0.5% to 10% melting are anticipated to have ²³²Th/²⁰⁴Pb ratios exceeding those known from terrestrial basalts.     

Comparison of numerical methods for simulating strongly nonlinear and heterogeneous reactive transport problems—the MoMaS benchmark case

Although multicomponent reactive transport modeling is gaining wider application in various geoscience fields, it continues to present significant mathematical and computational challenges. There is a need to solve and compare the solutions to complex benchmark problems, using a variety of codes, because such intercomparisons can reveal promising numerical solution approaches and increase confidence in the application of reactive transport codes. In this contribution, the results and performance of five current reactive transport codes are compared for the 1D and 2D subproblems of the so-called easy test case of the MoMaS benchmark (Carrayrou et al., Comput Geosci, 2009, this issue). This benchmark presents a simple fictitious reactive transport problem that highlights the main numerical difficulties encountered in real reactive transport problems. As a group, the codes include iterative and noniterative operator splitting and global implicit solution approaches. The 1D easy advective and 1D easy diffusive scenarios were solved using all codes, and, in general, there was a good agreement, with solution discrepancies limited to regions with rapid concentration changes. Computational demands were typically consistent with what was expected for the various solution approaches. The differences between solutions given by the three codes solving the 2D problem are more important. The very high computing effort required by the 2D problem illustrates the importance of parallel computations. The most important outcome of the benchmark exercise is that all codes are able to generate comparable results for problems of significant complexity and computational difficulty.     

Die Glaukophangesteine,ihre stofflichen Äquivalente und Uniwandlungsprodukte in Nordcalabrien (Süditalien)

In the southern Apennin (= northern part of the region dealt with) and the Coasta Chain (= southern part) there are metabasalts wich are classified in the northern part as:

1. Glaucophane rocks of the albite-lawsonite-glaucophane-subfacies with the assemblage glaucophane + pumpellyite + lawsonite ±albite ±aragonite ±muscovite (7 rock analyses, 8 mineral analyses). These rocks are conceived as relics of an older burial metamorphism.
2. Rocks with pumpellyite and chlorite or also chlorite alone, that are interpreted as reaction rims between the metastable glaucophane rocks and the country rock (phyllites, quartzites). The assemblages pumpellyite + chlorite and chlorite alone are to be found (2 rock analyses and 2 mineral analyses).
3. Rocks with lawsonite and/or epidote belong to the same mineral facies as the country rock: a facies similar to the greenschist facies (called “lawsonite-albite-chlorite-subfacies”) which is characterized by the assemblages lawsonite + albite + chlorite ±calcite and also epidote ±lawsonite + albite + chlorite ± muscovite. These types are attributed to a younger dynamo-metamorphism (2 rock analyses).

In the southern part, the metabasalts can be found only as rocks with epidote and/or lawsonite, a metamorphism with more than one event cannot be proved petrologically (3 rock analyses). Equations of the observed mineral reactions are given. The transitions of one facies into another are represented in the pseudo-quaternary system Al₂O₃-CaO-Na₂O · Al₂O₃-2 Fe₂O₃ + FeO + MnO + MgO-(H₂O). The pressure-temperature conditions are estimated on the basis of published experimental data (300° C and 6–7 kb for the glaucophane rocks; 400° C and about 6 kb for the rocks with lawsonite and/or epidote) and are compared with geologic facts.     

北京东郊722土壤垂向剖面重金属污染的磁学响应及其统计意义

对北京城东附近某苗圃内典型的土壤污染剖面进行了环境磁学和地球化学分析,发现某些重金属(Pb、Zn、Sr、Ba、Cu)和磁性参数呈现相同的垂向变化趋势,都在37cm以上显示高值区,磁化率均值达到192.02×10-8m3/kg,如Pb含量达到67.62mg/kg,而在37cm以下,明显属低值区,磁化率均值只有18.38×10-8m3/kg,Pb含量也只有23.43mg/kg.借助于指标聚类分析和主成分分析方法,揭示出各种指标之间的内在联系,表明磁参数与Pb、Zn、Sr、Ba、Cu等元素显著相关,彼此的相关系数都达到0.90以上,属于同一类别的隶属度在80%以上,说明磁指标可以作为这些重金属污染的一种代用指标.利用模糊C均值聚类分析分辨出了土壤上部污染物堆积层和下部未污染土壤背景2种不同的特征段.     

Mineralogy and the release of trace elements from slag from the Hegeler Zinc smelter,Illinois (USA)

Slag from the former Hegeler Zn-smelting facility in Illinois (USA) is mainly composed of spinifex Ca-rich plagioclase, fine-grained dendritic or coarse-grained subhedral to anhedral clinopyroxenes, euhedral to subhedral spinels, spherical blebs of Fe sulfides, silicate glass, and less commonly fayalitic olivine. Mullite and quartz were also identified in one sample as representing remnants of the furnace lining. Secondary phases such as goethite, hematite and gypsum are significant in some samples and reflect surficial weathering of the dump piles or represent byproducts of roasting. A relatively rare Zn-rich material contains anhedral willemite, subhedral gahnite, massive zincite, hardystonite and a Zn sulfate (brianyoungite), among other phases, and likely represents the molten content of the smelting furnace before Zn extraction. The bulk major-element chemistry of most slag samples is dominated by SiO₂, Al₂O₃, Fe₂O₃ and CaO. The bulk composition of the slag suggests a high viscosity of the melt and the mineralogy suggests a high silica content of the melt. Bulk slag trace-element chemistry shows that the dominant metal is Zn with >28.4 wt.% in the Zn-rich material and between 212 and 14,900 mg/kg in the other slags. The concentrations of other trace elements reach the following: 45 mg/kg As, 1170 mg/kg Ba, 191 mg/kg Cd, 242 mg/kg Co, 103 mg/kg Cr, 6360 mg/kg Cu, 107 mg/kg Ni, and 711 mg/kg Pb.     

The Las Chacras-Potrerillos batholith (Pampean Ranges,Argentina): structural evidences,emplacement and timing of the intrusion

Within the southern part of the Sierra Pampeanas (the Sierra de San Luis, Argentina), a series of extensive intrusive bodies are regarded to post-date the Famatinian cycle but were emplaced during the Achalian, a period of heterogeneous deformation along crustal scale fault zones. The largest of those is the Las Chacras-Potrerillos batholith that is situated at the northern end of the transpressive, sinistral Guzmán shear zone. This composite pluton exhibits three sub-domains that comprise two granitoid sub-units each: The southern Potrerillos stock (muscovite-bearing red granite and biotite-bearing red granite) and the central (biotite porphyritic granite and giant porphyritic granite) and northern domain (equigranular granite and porphyritic granite) of the Las Chacras stock. The crystallisation ages of the biotite porphyritic granite is around 381 Ma (U/Pb on zircons and Pb/Pb on sphene), while the host rock was already cooled below 350 °C at 420 Ma. Thermal modelling approaches favour a pulsed intrusion with a duration of 1.5 Ma. The emplacement was followed by rapid cooling below the muscovite cooling temperature. Biotite cooling ages in different sub-units reflect either a long-lasting cooling history of approximately 30 Ma (which is supported by the modelling) or a reheating effect at around 350 Ma. Devonian-age determinations on the fault rocks and granitoids point to a syn-tectonic emplacement of the batholith. The pluton is interpreted to be positioned at the crossover of sinistral shear zones. The origin of this NNE directed extensional setting in a transpressive regime seems to be related to the transfer of displacement along a secondary set of NNW-trending sinistral faults. The final emplacement is due to a subsequent ballooning of the batholith following the direction of space creation. This model is based on the relative timing of the emplacement sequence and macroscopically visible planar fabrics in the field as well as magnetic fabric data. Our results indicate that the emplacement is syn-kinematic with respect to the Achalian deformation event.     

Mollusc and brachiopod skeletal hard parts: Intricate archives of their marine environment

The biogenic carbonate hard parts of fossil bivalves, cephalopods and brachiopods are among the most widely exploited marine archives of Phanerozoic environmental and climate dynamics research. The advent of novel analytical tools has led many workers to explore non‐traditional geochemical and petrographic proxies, and work performed in neighbouring disciplines sheds light on the complex biomineralization strategies applied by these organisms. These considerations form a strong motivation to review the potential and problems related to the compilation and interpretation of proxy data from bivalve, cephalopod and brachiopod hard parts from the viewpoint of the sedimentologist and palaeoceanographer. Specific focus is on the complex biomineralization pathways of a given dissolved ion or food particle from its aquatic environment via the digestion and biomineralization apparatus in molluscs and brachiopods and its incorporation into a biomineral. Given that molluscs and brachiopods do not secrete their hard parts from seawater but rather from their mantle and periostracum, this paper evaluates differences and similarities of seawater versus that of body fluids. Cephalopods, bivalves and brachiopods exert a strong biological control on biomineralization that, to some degree, may buffer their shell geochemistry against secular changes in seawater chemistry. Disordered (amorphous) calcium carbonate precursor phases, later transformed to crystalline biominerals, may be significant in carbonate archive research due to expected geochemical offset relative to the direct precipitation of stable phases. A reasonable level of understanding of the related mechanisms is thus crucial for those who use these skeletal hard parts as archives of the palaeo‐environment. The impact of what is commonly referred to as ‘biological factors’ on the geochemistry of mollusc and brachiopod hard parts is explored for conventional isotope systems such as carbon, oxygen, strontium and traditionally used element to calcium ratios. In particular, the often used δ¹³C_carb or the Mg/Ca and Sr/Ca elemental proxies are fraught with problems. An interesting new research field represents the analysis, calibration and application of non‐traditional proxies to mollusc and brachiopod hard parts. Examples include the carbonate clumped isotope (Δ₄₇) approach and the analysis of the isotopes of Ca, Mg, N, Li, S or element to Ca ratios such as Li/Ca or B/Ca and rare earth elements. Based on considerations discussed here, a series of “do's and don'ts” in mollusc and brachiopod archive research are proposed and suggestions for future work are presented. In essence, the suggestions proposed here include experimental work (also field experiments) making use of recent archive organisms or, where possible, a reasonable recent analogue in the case of extinct groups. Moreover, the detailed understanding of the architecture of mollusc and brachiopod hard parts and their ultra‐structures must guide sampling strategies for geochemical analyses. Where feasible, a detailed understanding of the diagenetic pathways and the application of multi‐proxy and multi‐archive approaches should form the foundation of fossil carbonate archive research. The uncritical compilation of large data sets from various carbonate‐shelled organisms collected at different locations is not encouraged.