An Improved 20-Year Arctic Ocean Altimetric Sea Level Data Record

For ocean and climate research, it is essential to get long-term altimetric sea level data that is as accurate as possible. However, the accuracy of the altimetric data is frequently degraded in the interior of the Arctic Ocean due to the presence of seasonal or permanent sea ice. We have reprocessed ERS-1/2/Envisat satellite altimetry to develop an improved 20-year sea level dataset for the Arctic Ocean. We have developed both an along-track dataset and three-day gridded sea level anomaly (SLA) maps from September 1992 to April 2012. A major improvement in data coverage was gained by tailoring the standard altimetric editing criteria to Arctic conditions. The new reprocessed data has significant increased data coverage with between 4 and 10 times the amount of data in regions such as the Beaufort Gyre region compared with AVISO and RADS datasets. This allows for a more accurate estimation of sea level changes from satellite altimetry in the Arctic Ocean. The reprocessed dataset exhibit a mean sea level trend of 2.1 ± 1.3 mm/year (without Glacial Isostatic Adjustment correction) covering the Arctic Ocean between 66°N and 82°N with significant higher spatial coherency in the ice-covered regions than the RADS and DUACS datasets.     

Coordination chemistry and hydrolysis of Fe(III) in a peat humic acid studied by X-ray absorption spectroscopy

The speciation of iron (Fe) in soils, sediments and surface waters is highly dependent on chemical interactions with natural organic matter (NOM). However, the molecular structure and hydrolysis of the Fe species formed in association with NOM is still poorly described. In this study extended X-ray absorption fine structure (EXAFS) spectroscopy was used to determine the coordination chemistry and hydrolysis of Fe(III) in solution of a peat humic acid (5010-49,200 μg Fe g⁻¹ dry weight, pH 3.0-7.2). Data were analyzed by both conventional EXAFS data fitting and by wavelet transforms in order to facilitate the identification of the nature of backscattering atoms. Our results show that Fe occurs predominantly in the oxidized form as ferric ions and that the speciation varies with pH and Fe concentration. At low Fe concentrations (5010-9920 μg g⁻¹; pH 3.0-7.2) mononuclear Fe(III)-NOM complexes completely dominates the speciation. The determined bond distances for the Fe(III)-NOM complexes are similar to distances obtained for Fe(III) complexed by desferrioxamine B and oxalate indicating the formation of a five-membered chelate ring structure. At higher Fe concentrations (49,200 μg g⁻¹; pH 4.2-6.9) we detect a mixture of mononuclear Fe(III)-NOM complexes and polymeric Fe(III) (hydr)oxides with an increasing amount of Fe(III) (hydr)oxides at higher pH. However, even at pH 6.9 and a Fe concentration of 49,200 μg g⁻¹ our data indicates that a substantial amount of the total Fe (>50%) is in the form of organic complexes. Thus, in environments with significant amounts of organic matter organic Fe complexes will be of great importance for the geochemistry of Fe. Furthermore, the formation of five-membered chelate ring structures is in line with the strong complexation and limited hydrolytic polymerization of Fe(III) in our samples and also agrees with EXAFS derived structures of Fe(III) in organic soils.     

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.     

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.     

Iron isotope variations in Holocene sediments of the Gotland Deep, Baltic Sea

Holocene sediments from the Gotland Deep basin in the Baltic Sea were investigated for their Fe isotopic composition in order to assess the impact of changes in redox conditions and a transition from freshwater to brackish water on the isotope signature of iron. The sediments display variations in δ⁵⁶Fe (differences in the ⁵⁶Fe/⁵⁴Fe ratio relative to the IRMM-14 standard) from −0.27 ± 0.09‰ to +0.21 ± 0.08‰. Samples deposited in a mainly limnic environment with oxygenated bottom water have a mean δ⁵⁶Fe of +0.08 ± 0.13‰, which is identical to the mean Fe isotopic composition of igneous rocks and oxic marine sediments. In contrast, sediments that formed in brackish water under periodically euxinic conditions display significantly lighter Fe isotope signatures with a mean δ⁵⁶Fe of −0.14 ± 0.19‰. Negative correlations of the δ⁵⁶Fe values with the Fe/Al ratio and S content of the samples suggest that the isotopically light Fe in the periodically euxinic samples is associated with reactive Fe enrichments and sulfides. This is supported by analyses of pyrite separates from this unit that have a mean Fe isotopic composition of −1.06 ± 0.20‰ for δ⁵⁶Fe. The supply of additional Fe with a light Fe isotopic signature can be explained with the shelf to basin Fe shuttle model. According to the Fe shuttle model, oxides and benthic ferrous Fe that is derived from dissimilatory iron reduction from shelves is transported and accumulated in euxinic basins. The data furthermore suggest that the euxinic water has a negative dissolved δ⁵⁶Fe value of about −1.4‰ to −0.9‰. If negative Fe isotopic signatures are characteristic for euxinic sediment formation, widespread euxinia in the past might have shifted the Fe isotopic composition of dissolved Fe in the ocean towards more positive δ⁵⁶Fe values.     

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.