Improved collection of rooftop micrometeorites through optimized extraction methods: The Budel collection

The scientific value of micrometeorites collected from deep-sea sediments or glacial deposits can be limited by poorly constrained accumulation times or severe alteration, coupled with a complex infrastructure of sampling expeditions. Collecting micrometeorites from rooftops has recently become a feasible alternative, but extraction methods have not been optimized or standardized to date. Here, we show that existing methods for the recovery of melted cosmic spherules (CSs) can be strongly improved by using a sequence of mineral separation techniques, including shape separation with an asymmetric vibrator and heavy liquid density separation with overflow centrifuges. We retrieved 1006 micrometeorites from the gutter of a barn in Budel, the Netherlands. Particle diameters are 80–515 μm, with the major mode at 130 μm and a slope exponent of −4.88. Differences in size distributions among various types of CSs indicate a multi-source influx, with CS textures controlled by their parent body's mineralogy and orbital parameters. Repeated sampling of the rooftop after accumulation times of 959 and 333 days allows for a time-integrated global mass flux estimate of 472 t year⁻¹. This estimate is notably higher than previous rooftop-based estimates but is still severely affected by micrometeorite loss from the gutter through drainage. The mass flux peaks at an equivalent particle diameter of ~200 μm. The Budel collection is the first rooftop collection to contain abundant vitreous micrometeorites and include the coarse-grained S-type CS class. Unmelted and I-type micrometeorites remain difficult to extract from rooftop samples. Vitreous micrometeorites display various stages of weathering, showing that severe alteration of glass can progress at a faster rate in populated regions than previously assumed. This study demonstrates that methodological adjustments can drastically increase the scientific potential of rooftop micrometeorite collections.     

The use of low frequencies in a full‐waveform inversion and impedance inversion land seismic case study

Velocity model building and impedance inversion generally suffer from a lack of intermediate wavenumber content in seismic data. Intermediate wavenumbers may be retrieved directly from seismic data sets if enough low frequencies are recorded. Over the past years, improvements in acquisition have allowed us to obtain seismic data with a broader frequency spectrum. To illustrate the benefits of broadband acquisition, notably the recording of low frequencies, we discuss the inversion of land seismic data acquired in Inner Mongolia, China. This data set contains frequencies from 1.5–80 Hz. We show that the velocity estimate based on an acoustic full‐waveform inversion approach is superior to one obtained from reflection traveltime inversion because after full‐waveform inversion the background velocity conforms to geology. We also illustrate the added value of low frequencies in an impedance estimate.     

Long-term relationships between climate oscillation and basin-scale hydrological variability during rainy season in eastern Northeast Brazil

ABSTRACT

The high variability in the hydrological regime of the Eastern Hydrological Region (EHR) of Northeast Brazil often results in floods and droughts, leading to serious socio-economic issues. Therefore, this work aimed to investigate connections between spatiotemporal hydrological variability of the EHR and large-scale climate phenomena. Multivariate statistical techniques were applied to relate climate indices with hydrological variables within two representative river basins in the EHR. The results indicated a multi-annual relationship between the state of the sea surface temperature of the Atlantic and Pacific oceans and anomalous hydrological variability in the basins. In addition, the northern Tropical Atlantic conditions were shown to play an important role in modulating the long-term variability of the hydrological response of the basins, whilst only extreme ENSO anomalies seemed to affect the rainy season. This knowledge is an important step towards long-term prediction of hydrological conditions and contributes to the improvement of water resources planning and management in the EHR.     

Dependence of clinopyroxene composition on cooling rate in basaltic magmas: Implications for thermobarometry

The compositional variation of clinopyroxene and the partitioning of major elements between clinopyroxene and melt are estimated as a function of the cooling rate. Clinopyroxenes were crystallized under variable cooling regimes (15, 9.4, 3, 2.1, and 0.5 °C/min from 1250 down to 1000 °C) and at isothermal conditions of 1000 °C from a basaltic composition at a pressure of 500 MPa under anhydrous and hydrous (H₂O = 1.3 wt.%) conditions. The clinopyroxene chemistry shows that, as the cooling rate increases, crystals are progressively depleted in Ca, Mg, Fe²⁺ and Si and enriched in Na, Fe³⁺, Al (mainly Al^IV), and Ti. Di and Hd versus CaTs and CaFeTs form a continuous binary solid solution characterized by higher amounts of tschermakitic components with increasing cooling rate. Two parameters (DH = Di + Hd and TE = CaTs + CaFeTs + En) are calculated to describe the effect of cooling rate on the clinopyroxene composition. The variation of DH/TE with increasing cooling rate evidences the kinetic process induced by rapid cooling in basic rocks under hydrous and anhydrous conditions.Dynamic crystallization conditions affect the partitioning of major elements between clinopyroxene and melt; with increasing cooling rate, the value of crystal–melt partition coefficient departs from that obtained at the isothermal condition. However, in spite of these variations, the values of ^cpx–meltKd_Fe–Mg remain almost constant. Therefore, the Fe²–Mg exchange between clinopyroxene and melt is not suitable to prove the (dis)equilibrium conditions in basaltic cooling magmas, giving rise to possible mismatches in the application of thermobarometers. The results of our study are consistent with that observed at the margin of dikes or in the exterior portions of lavas, where the cooling rate is maximized and disequilibrium compositions of clinopyroxene have been found.     

Is there a possibility to correct fossil n-alkane data for postsedimentary alteration effects?

The long chain n-alkane composition of plant material can significantly differ between plant groups e.g. trees and grasses. Due to their relative recalcitrance, they have been employed in paleoecological research as molecular proxies for different types of vegetation. Most of those paleoenvironmental studies rely on the assumption that characteristic molecular fingerprints of plant material are preserved in the fossil organic material without significant alteration. However, there exists evidence that n-alkane distributions may change in the course of plant litter degradation. Here, the authors propose and discuss a conceptual approach to the correction of n-alkane patterns in paleosols and terrestrial sediments for postsedimentary alteration effects. This might have potential to improve paleoenvironmental reconstructions derived from these molecular fossils. In soil depth profiles typically a correlation between the OEP (odd over even predominance) and paleoecological valuable long-chain n-alkane ratios (LARs) can be found. Similar relationships have been also obtained from n-alkane records in paleosols. With the OEP serving as a proxy of microbial reworking, the correction procedure applies OEP vs. LAR regression functions to correct fossil LARs for degradation effects. The regression functions have been derived from modern soils. The application of the procedure and its significance for paleoecological interpretations is demonstrated on a case study of a loess-paleosol sequence (∼400–700 ka) in Romania. It is shown that changes in the C27/C31 n-alkane ratio at this site are closely related to degradation effects rather than to changes in the paleovegetation (e.g. tree vs. grass abundance). However, it was found that the C29/C31 ratio is a more suitable paleoenvironmental proxy at the Mircea Voda site. The results indicate that there is a future potential to correct fossil n-alkane ratios via the OEP/LAR relationship, however at the moment a general straight forward application of this approach might be critical due to lack of extended and diverse n-alkane records from modern soils. The need of more systematic n-alkane studies on soil profiles is highlighted to improve knowledge concerning dynamics and actual mechanisms of postsedimentary LAR and OEP changes.     

The Calcium Isotope Composition of Modern Seawater Determined by Thermal Ionisation Mass Spectrometry

The Ca isotopic composition of modern seawater has been determined using a ⁴³Ca-⁴⁸Ca double spike, which was calibrated using a ⁴²Ca/⁴⁴Ca seawater ratio of 0.30587 ± 0.00026. This ratio was determined from a total evaporation experiment in which the ion beam was measured from the beginning to the end of the emission. With integration of the peak intensities, the fractionation effects can be minimised, since total evaporation of the reservoir cancels out the effect of vapour enrichment in the light isotopes. This experiment avoids the gravimetric uncertainty inherent in the double spike calibration. This calibration allows the precise redetermination of the seawater isotopic composition of Ca. A mean ⁴⁰Ca/⁴⁴Ca ratio for two Atlantic water samples of 45.143 (2s_mean= 0.003) was found. The good reproducibility of the Ca isotope ratios in present seawater and the very strong isotopic homogeneity of Ca in the oceans illustrate the advantage of using seawater as the common standard, with the advantage of decreasing interlaboratory bias.