Infrared spectroscopy of Triassic conodonts: a new tool for assessing conodont diagenesis

The Fourier transform infrared spectra of individual conodonts with various CAI values indicate definite changes in conodont francolite during diagenesis. Steady decarbonation can be observed in the increasing intensity of the band with the wavenumber 2340 an^-1, which is assigned to trapped molecular CO₂. Carbon dioxide originates from decomposing CO^2-₃-ions occupying the B-site in francolite. Furthermore, the intensity of the water-deformation band at 1644 cm^-1 decreases with higher CAI values. These changes of intensity can be quantified by calculating the maximum extinction (E_max) for the corresponding absorption maxima and correlated with the CAI. Unaltered conodonts have a relative variable water 'content' and very little CO₂. Up to a CAI value of 4 conodont francolite continuously expells water and carbon dioxide is trapped. Conodonts with CAI = 5 have similar water 'contents' to CAI = 4 conodonts, but decarbonation continues to take place during this stage of diagenesis.     

Towards a better understanding of magnesium-isotope ratios from marine skeletal carbonates

This study presents magnesium stable-isotope compositions of various biogenic carbonates of several marine calcifying organisms and an algae species, seawater samples collected from the western Dutch Wadden Sea, and reference materials. The aim of this study is to explore the influence of mineralogy, taxonomy and environmental factors (e.g., seawater isotopic composition, temperature, salinity) on magnesium-isotopic (δ²⁶Mg) ratios of skeletal carbonates. Using high-precision multi-collector inductively coupled plasma mass spectrometry, we observed that the magnesium-isotopic composition of seawater from the semi-enclosed Dutch Wadden Sea is identical to that of open marine seawater. We further found that a considerable component of the observed variability in δ²⁶Mg values of marine skeletal carbonates can be attributed to differences in mineralogy. Furthermore, magnesium-isotope fractionation is species-dependent, with all skeletal carbonates being isotopically lighter than seawater. While δ²⁶Mg values of skeletal aragonite and high-magnesium calcite of coralline red algae indicate the absence or negligibility of metabolic influences, the δ²⁶Mg values of echinoids, brachiopods and bivalves likely result from a taxon-specific level of control on Mg-isotope incorporation during biocalcification. Moreover, no resolvable salinity and temperature effect were observed for coralline red algae and echinoids. In contrast, Mg-isotope data of bivalves yield ambiguous results, which require further validation. The data presented here, point to a limited use of Mg isotopes as temperature proxy, but highlight the method’s potential as tracer of seawater chemistry through Earth’s history.     

The cubic-tetragonal phase transition in the system majorite (Mg4Si4O12) – pyrope (Mg3Al2Si3O12), and garnet symmetry in the Earth's transition zone

 Garnets along the join Mg₄Si₄O₁₂ (majorite end member) – Mg₃Al₂Si₃O₁₂ (pyrope) synthesized at 2000 °C, 19 GPa are, after quench, tetragonal in the compositional range up to 20 mol% pyrope, but cubic at higher Al contents. Lattice constants a _tet and a _tet in the tetragonal compositional range converge with increasing pyrope contents towards the lattice constant of the cubic garnets. The elastic strain and the intensity of the (222) reflection as a function of composition indicate a second-order phase transition near 20 mol% pyrope. From the wedge-like shape of pseudomerohedral twins and their interaction near 90° twin-boundary corners, as well as from the absence of growth-induced dislocations, it is concluded that the Al-poor garnets are also cubic at synthesis conditions but invert by (Mg,Si) ordering on the octahedral sites into tetragonal phases of space group I4₁/a upon quench. This implies that the cubic-to-tetragonal phase transition in Mg₄Si₄O₁₂ garnet occurs below 2000 °C at 19 GPa and at even lower temperatures in more aluminous compositions. A composition-dependent Landau model is consistent with a direct transformation from Ia3d to I4₁/a. Comparison of the T-X stability field of majorite-pyrope garnets with the chemistry of majorite-rich garnets expected to occur in the Earth's transition zone shows that the latter will be cubic under all conditions. Softening of elastic constants, which commonly accompanies ferroelastic phase transitions, may affect the seismic velocities of garnets in the deeper transition zone where majorite contents are highest. Received July 5, 1996 / Revised, accepted September 24, 1996     

North Sea near-surface wind climate and its relation to the large-scale circulation patterns

The North Sea 10-m wind speed (WS10) climate is compared and related to circulation patterns based on the sea level pressure (SLP) extracted from three reanalysis and one high-resolution model dataset. The mean magnitude and the trends of WS10 depend considerably on the selected reanalysis. The variability of WS10 among the three reanalysis datasets is highly correlated in the recent period (1980–2000) but less so in the past period (1960–1980). The WS10 over the North Sea is well represented by the relatively low reanalysis resolution when compared to the high-resolution WS10 model data partially owing to the high spatial correlation of WS10. Exceptions are observed only at the coastal areas. The dominant mode of WS10 explains coherent variability of WS10 over the North Sea and is related to a SLP pattern similar to the North Atlantic oscillation (NAO). The increase of the magnitude of the dominant WS10 pattern is related to the increase of the magnitude of the NAO-like SLP pattern from 1960s to mid-1990s. The second dominant WS10 pattern—a dipole in WS10 to the north and south of Great Britain—is related to the differences in SLP between Scandinavia and Iceland. The relation between the second WS10 and SLP patterns is more prominent in the recent period. The extreme WS10 in the German Bight is related to the low SLP over Scandinavia. The extreme WS10 is strongly increasing from the early 1980s to the beginning of 1990s, which is not observed in the corresponding SLP time series over Scandinavia.     

Zur Anwendung der Kathodolumineszenz in der Karbonatpetrographie

Mn-activated cathodoluminescence can be used in several fields of carbonate petrography. It may, for instance, be possible to recognize

1. cement sequences and their correlation (Tab. 1, Figs. 1, 2, 4; Tab. 2, Fig. 1)
2. growth fabrics of skeletons (Tab. 2, Figs. 2, 3, 4; Tab. 3, Figs. 1, 2)
3. dolomitisation processes and problems (Tab. 1, Figs. 1, 2; Tab. 4, Fig. 2)
4. transformation paths from Mg-calcite to calcite and from aragonite to calcite (Tab. 2, Fig. 1; Tab. 3, Figs. 3, 4; Tab. 4, Fig. 1)
5. growth structures in certain types of ooids (Tab. 1, Fig. 4; Tab. 3, Fig. 3; Tab. 4, Fig. 1)
6. reworked skeletal particles (Tab. 3, Fig. 4)
7. phantom grains and fossil-outlines in a micro- or macrocrystalline groundmass (Tab. 4, Figs. 2, 3)
8. healed fissures crossing micro- or macrocrystalline carbonate rocks (Tab. 4, Fig. 4).

These are, however, no general luminescence criteria indicating the depositional environment. Luminescence of calcite and dolomite requires 20–40 ppm Mn, with the equipments used in this study. Aragonite is not yet investigated systematically. Zonal luminescence in carbonate cements may indicate changes of the chemical composition of the aquifer and may be used for “cement stratigraphy”. In skeletons it rather indicates physiological changes. While aragonitic skeletons lose their luminescence Zonation during replacement by calcite, Mg-calcite skeletons may keep parts of it, because their replacement preserves the original crystal fabric. Blotchy luminescence developes in Mg-calcitic particles during their adjustment to lower Mg-calcites by dissolution-precipitation processes in solutions with changing Mn/Fe-ratios.