Distribution of lithium,beryllium, and boron in meteoritic chondrules

Abstract— The distribution of Li, Be, and B was studied by ion microprobe mass spectrometry in 36 chondrules from the Semarkona, Bishunpur, Allende, Clovis #1, and Hedjaz meteorites. Within a single chondrule, Li-Be-B concentrations can vary up to one order of magnitude. For example, in a chondrule from Hedjaz, concentrations range from 0.3 to 2.4 ppm for Li, from <0.001 to 0.17 ppm for Be, and from 0.4 to 5.5 ppm for B. Among chondrules from Semarkona and Bishunpur, clear crystal-mesostasis partitioning was observed in nine chondrules for Li, in nine chondrules for Be, and in three chondrules for B. The heterogeneities in the distribution of Li, Be, and B in chondrules from Semarkona and Bishunpur appear to be primary features that were inherited from the chondrules' precursors and not totally obscured during the chondrules' formation. A redistribution of B was nevertheless observed at the whole-rock scale for Allende (B-Al₂O₃ correlation) and Hedjaz (B–SiO₂ correlation). At the scale of bulk chondrules, a robust correlation is observed for all studied meteorites between the B/Be and the B/Li ratios, which indicates that Li and Be are much less heterogeneously distributed in chondrites than B. Mean Li, Be, and B concentrations of chondrules ([Li] ? 0.83^+0.86 ppm; [Be] ? 0.043^0.027 ppm; [B] ? 0.89^+3.71_-0.72 ppm) are consistent with those of Orgueil ([Li] ? 1.49 ppm; [Be] ? 0.0249 ppm; [B] ? 0.87 ppm), but the mean Li/Be ratio of chondrules (24.5^+6.5_-9.1) is a factor of ～4 depleted relative to Orgueil (Li/Be ratio of ～78). Such a depletion is puzzling because no correlation between Li and Na or B has been found as would be expected to result from volatilization processes during chondrule melting and cooling. As a consequence, the exact abundance of solar system Li remains an open question.     

应用各种示踪剂研究岩溶泉系统的补给边界

应用三种化学示踪剂,对桂林岩溶水文地质试验场“31号泉系统”的补给边界进行了研究。试验在雨期进行,示踪剂分别是降雨后投入落水洞随表层岩溶水带入地下;或在降雨前投入无水的落水洞中,待降雨后由地表产流带入地下。 试验表明,氯化锌、钼酸铵是较理想的示踪剂,地下水速度为4～250米/小时,速度差可能是由于包气带岩溶含水介质渗透性和水力坡度不同所致;泉口历时浓度曲线常呈多峰型,多是由于降雨脉冲影响所致;峰丛区高程不等的洼地多通道补给山边泉,峰丛区含水介质结构具有叠置性,即水平方向多通道,垂直方向多层次,故水均衡计算不可忽视;“31号泉系统”的补给边界,通过圈定有水力连系之洼地的地表分水岭来确定。      

Hydrodynamic time parameters response to meteorological and physical forcings: toward a stagnation risk assessment device in coastal areas

Ocean Dynamics - Identifying zones of stagnation and deposition of terrigenous matter or contaminants induced by human activity is a key issue in coastal areas. In this paper, circulation processes...     

A case study of using Raman lidar measurements in high-accuracy GPS applications

This paper investigates the impact of rapid small-scale water vapor fluctuations on GPS height determination. Water vapor measurements from a Raman lidar are used for documenting the water vapor heterogeneities and correcting GPS signal propagation delays in clear sky conditions. We use data from four short observing sessions (6 h) during the VAPIC experiment (15 May–15 June 2004). The retrieval of wet delays from our Raman lidar is shown to agree well with radiosonde retrievals (bias and standard deviation (SD) were smaller than 1 and 2.8 mm, respectively) and microwave radiometers (from two different instruments, bias was 6.0/−6.6 mm and SD 1.3/3.8 mm). A standard GPS data analysis is shown to fail in accurately reproducing fast zenith wet delay (ZWD) variations. The ZWD estimates could be improved when mean post-fit phase residuals were removed. Several methodologies for integrating zenith lidar observations into the GPS data processing are also presented. The final method consists in using lidar wet delays for correcting a priori the GPS phase observations and estimating a scale factor for the lidar wet delays jointly with the GPS station position. The estimation of this scale factor allows correcting for a mis-calibration in the lidar data and provides in the same way an estimate of the Raman lidar instrument constant. The agreement of this constant with an independent determination using radiosonde data is at the level of 1–4%. The lidar wet delays were derived by ray-tracing from zenith pointing measurements: further improvement in GPS positioning is expected from slant path lidar measurements that would properly account for water vapor anisotropy.     

Intra‐crater sedimentary deposits at the Haughton impact structure,Devon Island,Canadian High Arctic

Abstract— Detailed field mapping has revealed the presence of a series of intra‐crater sedimentary deposits within the interior of the Haughton impact structure, Devon Island, Canadian High Arctic. Coarse‐grained, well‐sorted, pale gray lithic sandstones (reworked impact melt breccias) unconformably overlie pristine impact melt breccias and attest to an episode of erosion, during which time significant quantities of impact melt breccias were removed. The reworked impact melt breccias are, in turn, unconformably overlain by paleolacustrine sediments of the Miocene Haughton Formation. Sediments of the Haughton Formation were clearly derived from pre‐impact lower Paleozoic target rocks of the Allen Bay Formation, which form the crater rim in the northern, western, and southern regions of the Haughton structure. Collectively, these field relationships indicate that the Haughton Formation was deposited up to several million years after the formation of the Haughton crater and that they do not, therefore, represent an immediate, post‐impact crater lake deposit. This is consistent with new isotopic dating of impactites from Haughton that indicate an Eocene age for the impact event (Sherlock et al. 2005). In addition, isolated deposits of post‐Miocene intra‐crater glacigenic and fluvioglacial sediments were found lying unconformably over remnants of the Haughton Formation, impact melt breccias, and other pre‐impact target rock formations. These deposits provide clear evidence for glaciation at the Haughton crater. The wealth and complexity of geological and climatological information preserved as intra‐crater deposits at Haughton suggests that craters on Mars with intra‐crater sedimentary records might present us with similar opportunities, but also possibly significant challenges.     

Chlorine isotopic composition in seafloor serpentinites and high-pressure metaperidotites. Insights into oceanic serpentinization and subduction processes

Bulk-rock chlorine content and isotopic composition (δ³⁷Cl) were determined in oceanic serpentinites, high-pressure metaperidotites and metasediments in order to gain constraints on the global chlorine cycle associated with hydrothermal alteration and subduction of oceanic lithosphere. The distribution of insoluble chlorine in oceanic serpentinites was also investigated by electron microprobe. The hydrothermally-altered ultramafic samples were dredged along the South West Indian Ridge and the Mid-Atlantic Ridge. The high-pressure metamorphic samples were collected in the Western Alps: metaperidotites in the Erro-Tobbio unit and metasediments in the Schistes Lustrés nappe.Oceanic serpentinites show relatively large variations of bulk-rock Cl contents and δ³⁷Cl values with mean values of 1105 ± 596 ppm and −0.7 ± 0.4‰, respectively (n = 8; 1σ). Serpentines formed after olivine (meshes) show lower Cl content than those formed after orthopyroxene (bastites). In bastites of two different samples, Cl is positively correlated with Al₂O₃ and negatively correlated with SiO₂. These relationships are interpreted as reflecting preferential Cl-incorporation into the bastite structure distorted by Al (substituted for Si) rather than different alteration conditions between olivine and orthopyroxene minerals. High-pressure metaperidotites display relatively homogeneous Cl contents and δ³⁷Cl values with mean values of 467 ± 88 ppm and −1.4 ± 0.1‰, respectively (n = 7; 1σ). A macroscopic high-pressure olivine-bearing vein, formed from partial devolatilization of serpentinites at ∼2.5 GPa and 500-600 °C, shows a Cl content and a δ³⁷Cl value of 603 ppm and −1.6‰, respectively. Metasediments (n = 2) show low whole-rock Cl contents (<15 ppm Cl) that did not allow Cl isotope analyses to be obtained.The range of negative δ³⁷Cl values observed in oceanic serpentinites is likely to result from water-rock interaction with fluids that have negative δ³⁷Cl values. The homogeneity of δ³⁷Cl values from the high-pressure olivine-bearing vein and the metaperidotite samples implies that progressive loss of Cl inherited from oceanic alteration throughout subduction did not significantly fractionate Cl isotopes. Chlorine recycled in subduction zones via metaperidotites should thus show a range of δ³⁷Cl values similar to the range found in oceanic serpentinized peridotites.     

Crowdsourcing a cyclist perspective on suggested recreational paths in real-world networks

ABSTRACT

Routing and navigation services for leisure activities are conditioned by special needs and trade-offs. The advent of online communities and large crowdsourced datasets offers opportunities to improve the adoption of a user’s perspective in these suggested paths. This paper focuses on achieving two goals. First, the presented methodology analyses a dataset of 190,610 historical GPS traces to gain insights into the appreciation or attractiveness of each edge in a real-world network for a specific leisure activity (i.e. road cycling). Second, as literature on these leisure activities is still sparse, we want to create a thorough understanding of the activities at hand for future work. An appreciation model is proposed and the spread of this score is analyzed in shortest-path alternatives of popular routing engines for this activity. This analysis successfully discriminates these shortest paths based on the scoring value and three morphological parameters of the path. However, the robustness of the model should be improved to ensure the viability of the proposed approach in future work. More specifically, further research on the local optimality of the route choices will be imperative.     

Why Is the Climate Forcing of Sulfate Aerosols So Uncertain?

l. IntroductionAlthough the aerosol has been recognized as an important factor which has innuence onthe past, present and future climate for a long time, it still has much uncertainty in assessingits climate forcing. The direct radiative forcing of sulfate aerosols has been estimated rangingfrom --0.3 W/ m2 to --0.9 W/ m2 in recent publications (Charlson et al., l992, Kiehl andBriegleb l993; Taylor and Penner 1994, Boucher and Anderson l995, Kieh1 and Rodhe l995;Chuang et al., l997, Penne…     

Analytical Procedures for the Measurement of Boron Isotope Compositions by Ion Microprobe in Meteorites and Mantle Rocks

An analytical procedure has been developed to measure in situ the ¹¹ B/¹⁰ B ratio in terrestrial basaltic rocks and meteoritic chondrules having B concentration of less than 1 μg g^?1 using a small radius ims3f ion microprobe. The central difficulties for these measurements are (i) the removal of the trace amount of B contamination introduced in the sample during polishing, (ii) the precise calibration of instrumental mass fractionation of B isotopes and (iii) the low count rates of ¹⁰ B and ¹¹ B. Contamination experiments conducted with isotopically labelled B enriched in ¹⁰ B showed that ultrasonic cleaning in bi-distilled water (< 1 ng g^?1 B) and pre-sputtering of the analysed area decrease B contamination to the level of 0.01 μg g^?1. Analyses of isotope standards spanning a range of ¹¹ B/¹⁰ B between 3.93 and 4.20 showed that instrumental mass fractionation was constant within? during one session of analyses. Repeated analyses of a standard glass showed a reproducibility of instrumental mass fractionation between February 1991 and October 1996 of 1.3. Taking into account all sources of error, boron isotope measurements are accurate to within 5 for meteoritic samples having B contents in the range 0.1 to 1 μg g^?1. A slightly better accuracy of 1.5 can be achieved for basaltic glasses which can be sputtered with very intense primary beams.