Sandra Siljeström
SP Technical Research Institute of Sweden
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Featured researches published by Sandra Siljeström.
The Astrophysical Journal | 2016
Martin Hilchenbach; J. Kissel; Yves Langevin; Christelle Briois; H. von Hoerner; Andreas Koch; R. Schulz; Johan Silen; Kathrin Altwegg; L. Colangeli; H. Cottin; C. Engrand; Henning Fischer; Albrecht Glasmachers; E. Grün; Gerhard Haerendel; H. Henkel; H. Höfner; Klaus Hornung; Elmar K. Jessberger; Harry J. Lehto; Kirsi Lehto; F. Raulin; L. Le Roy; Jouni Rynö; W. Steiger; Thomas G. Stephan; Laurent Thirkell; R. Thomas; K. Torkar
The COmetary Secondary Ion Mass Analyser instrument on board ESAs Rosetta mission has collected dust particles in the coma of comet 67P/Churyumov-Gerasimenko. During the early-orbit phase of the Rosetta mission, particles and particle agglomerates have been imaged and analyzed in the inner coma at distances between 100 km and 10 km off the cometary nucleus and at more than 3 AU from the Sun. We identified 585 particles of more than 14 μm in size. The particles are collected at low impact speeds and constitute a sample of the dust particles in the inner coma impacting and fragmenting on the targets. The sizes of the particles range from 14 μm up to sub-millimeter sizes and the differential dust flux size distribution is fitted with a power law exponent of -3.1. After impact, the larger particles tend to stick together, spread out or consist of single or a group of clumps, and the flocculent morphology of the fragmented particles is revealed. The elemental composition of the dust particles is heterogeneous and the particles could contain typical silicates like olivine and pyroxenes, as well as iron sulfides. The sodium to iron elemental ratio is enriched with regard to abundances in CI carbonaceous chondrites by a factor from ˜1.5 to ˜15. No clear evidence for organic matter has been identified. The composition and morphology of the collected dust particles appear to be similar to that of interplanetary dust particles.
Nature | 2016
Nicolas Fray; Anais Bardyn; H. Cottin; Kathrin Altwegg; Donia Baklouti; Christelle Briois; L. Colangeli; C. Engrand; Henning Fischer; Albrecht Glasmachers; E. Grün; Gerhard Haerendel; Hartmut Henkel; H. Höfner; Klaus Hornung; Elmar K. Jessberger; Andreas Koch; Harald Krüger; Yves Langevin; Harry J. Lehto; Kirsi Lehto; Léna Le Roy; S. Merouane; Paola Modica; F.-R. Orthous-Daunay; John Paquette; F. Raulin; Jouni Rynö; R. Schulz; Johan Silen
The presence of solid carbonaceous matter in cometary dust was established by the detection of elements such as carbon, hydrogen, oxygen and nitrogen in particles from comet 1P/Halley. Such matter is generally thought to have originated in the interstellar medium, but it might have formed in the solar nebula—the cloud of gas and dust that was left over after the Sun formed. This solid carbonaceous material cannot be observed from Earth, so it has eluded unambiguous characterization. Many gaseous organic molecules, however, have been observed; they come mostly from the sublimation of ices at the surface or in the subsurface of cometary nuclei. These ices could have been formed from material inherited from the interstellar medium that suffered little processing in the solar nebula. Here we report the in situ detection of solid organic matter in the dust particles emitted by comet 67P/Churyumov–Gerasimenko; the carbon in this organic material is bound in very large macromolecular compounds, analogous to the insoluble organic matter found in the carbonaceous chondrite meteorites. The organic matter in meteorites might have formed in the interstellar medium and/or the solar nebula, but was almost certainly modified in the meteorites’ parent bodies. We conclude that the observed cometary carbonaceous solid matter could have the same origin as the meteoritic insoluble organic matter, but suffered less modification before and/or after being incorporated into the comet.
Nature Communications | 2015
Henrik Drake; Mats E. Åström; Christine Heim; Curt Broman; Jan Åström; Martin J. Whitehouse; Magnus Ivarsson; Sandra Siljeström; Peter Sjövall
Precipitation of exceptionally 13C-depleted authigenic carbonate is a result of, and thus a tracer for, sulphate-dependent anaerobic methane oxidation, particularly in marine sediments. Although these carbonates typically are less depleted in 13C than in the source methane, because of incorporation of C also from other sources, they are far more depleted in 13C (δ13C as light as −69‰ V-PDB) than in carbonates formed where no methane is involved. Here we show that oxidation of biogenic methane in carbon-poor deep groundwater in fractured granitoid rocks has resulted in fracture-wall precipitation of the most extremely 13C-depleted carbonates ever reported, δ13C down to −125‰ V-PDB. A microbial consortium of sulphate reducers and methane oxidizers has been involved, as revealed by biomarker signatures in the carbonates and S-isotope compositions of co-genetic sulphide. Methane formed at shallow depths has been oxidized at several hundred metres depth at the transition to a deep-seated sulphate-rich saline water. This process is so far an unrecognized terrestrial sink of methane.
Rapid Communications in Mass Spectrometry | 2013
Tim Leefmann; Christine Heim; Sandra Siljeström; Martin Blumenberg; Peter Sjövall; Volker Thiel
RATIONALE Over the last decade, the high lateral resolution and imaging capabilities of time-of-flight secondary ion mass spectrometry (ToF-SIMS) have increasingly stimulated interest in studying organic molecules in complex environmental materials. However, unlike with the established mass spectrometric techniques, the use of ToF-SIMS in the biogeosciences is still hampered by a lack of reference spectra of the relevant biomarker compounds. Here we present and interpret ToF-SIMS reference spectra of ten different cyclic lipids that are frequently used as biological tracers in ecological, organic geochemical and geobiological studies. METHODS Standard compounds of α,β,β-(20R,24S)-24-methylcholestane, (22E)-ergosta-5,7,22-trien-3β-ol, 17α(H),21β-(H)-30-norhopane, hope-17(21)-ene, hop-22(29)-ene, 17β(H),21β(H)-bacteriohopane-32,33,34,35-tetrol, 17β(H),21β(H)-35-aminobacteriohopane-32,33,34-triol, α-tocopherol, β,β-carotene, chlorophyll a, and cryosections of microbial mats and a fungus were analyzed using a ToF-SIMS instrument equipped with a Bi(3)(+) cluster ion source. RESULTS The spectra obtained from the standard compounds showed peaks in the molecular weight range (molecular ions, protonated and deprotonated molecules, adduct ions) and diagnostic fragment ion peaks in both, positive and negative ion modes. For the cyclic hydrocarbons, however, the positive ion mode spectra typically showed more and stronger characteristic peaks than the negative ion mode spectra. Using real world samples the capability of ToF-SIMS to detect and image selected compounds in complex organic matrices was tested. 17β(H),21β(H)-35-Aminobacteriohopane-32,33,34-triol, carotene and chlorophyll a were successfully identified in cryosections of microbial mats, and the distribution of ergosterol was mapped at µm resolution in a cryosection of a fungus (Tuber uncinatum). CONCLUSIONS This study further highlights the utility of ToF-SIMS for the identification and localization of lipids within environmental samples and as a technique for biomarker-related research in organic geochemistry and geobiology.
Geobiology | 2010
Sandra Siljeström; Jukka Lausmaa; Peter Sjövall; Curt Broman; Volker Thiel; Tomas Hode
Steranes and hopanes are organic biomarkers used as indicators for the first appearance of eukaryotes and cyanobacteria on Earth. Oil-bearing fluid inclusions may provide a contamination-free source of Precambrian biomarkers, as the oil has been secluded from the environment since the formation of the inclusion. However, analysis of biomarkers in single oil-bearing fluid inclusions, which is often necessary due to the presence of different generations of inclusions, has not been possible due to the small size of most inclusions. Here, we have used time-of-flight secondary ion mass spectrometry (ToF-SIMS) to monitor in real time the opening of individual inclusions trapped in hydrothermal veins of fluorite and calcite and containing oil from Ordovician source rocks. Opening of the inclusions was performed by using a focused C(60)(+) ion beam and the in situ content was precisely analysed for C(27)-C(29) steranes and C(29)-C(32) hopanes using Bi(3)(+) as primary ions. The capacity to unambiguously detect these biomarkers in the picoliter amount of crude oil from a single, normal-sized (15-30 mum in diameter) inclusion makes the approach promising in the search of organic biomarkers for lifes early evolution on Earth.
Planetary and Space Science | 2015
Harald Krüger; Thomas G. Stephan; C. Engrand; Christelle Briois; Sandra Siljeström; S. Merouane; Donia Baklouti; Henning Fischer; Nicolas Fray; Klaus Hornung; Harry J. Lehto; F.-R. Orthous-Daunay; Jouni Rynö; R. Schulz; Johan Silen; Laurent Thirkell; Mario Trieloff; Martin Hilchenbach
COSIMA (COmetary Secondary Ion Mass Analyser) is a time-of-flight secondary ion mass spectrometer (TOF-SIMS) on board the Rosetta space mission. COSIMA has been designed to measure the composition of cometary dust grains. It has a mass resolution m/{\Delta}m of 1400 at mass 100 u, thus enabling the discrimination of inorganic mass peaks from organic ones in the mass spectra. We have evaluated the identification capabilities of the reference model of COSIMA for inorganic compounds using a suite of terrestrial minerals that are relevant for cometary science. Ground calibration demonstrated that the performances of the flight model were similar to that of the reference model. The list of minerals used in this study was chosen based on the mineralogy of meteorites, interplanetary dust particles and Stardust samples. It contains anhydrous and hydrous ferromagnesian silicates, refractory silicates and oxides (present in meteoritic Ca-Al-rich inclusions), carbonates, and Fe-Ni sulfides. From the analyses of these minerals, we have calculated relative sensitivity factors for a suite of major and minor elements in order to provide a basis for element quantification for the possible identification of major mineral classes present in the cometary grains.
eLife | 2016
Lara Maldanis; Murilo Carvalho; Mariana R. Almeida; Francisco I. Freitas; José A. Andrade; Rafael Silva Nunes; Carlos Eduardo Rochitte; Ronei J. Poppi; Raul Oliveira Freitas; Fabio Rodrigues; Sandra Siljeström; Frederico A. Lima; Douglas Galante; Ismar de Souza Carvalho; Carlos A. Pérez; Marcelo R. de Carvalho; Jefferson Bettini; Vincent Fernandez; José Xavier-Neto
Elucidating cardiac evolution has been frustrated by lack of fossils. One celebrated enigma in cardiac evolution involves the transition from a cardiac outflow tract dominated by a multi-valved conus arteriosus in basal actinopterygians, to an outflow tract commanded by the non-valved, elastic, bulbus arteriosus in higher actinopterygians. We demonstrate that cardiac preservation is possible in the extinct fish Rhacolepis buccalis from the Brazilian Cretaceous. Using X-ray synchrotron microtomography, we show that Rhacolepis fossils display hearts with a conus arteriosus containing at least five valve rows. This represents a transitional morphology between the primitive, multivalvar, conal condition and the derived, monovalvar, bulbar state of the outflow tract in modern actinopterygians. Our data rescue a long-lost cardiac phenotype (119-113 Ma) and suggest that outflow tract simplification in actinopterygians is compatible with a gradual, rather than a drastic saltation event. Overall, our results demonstrate the feasibility of studying cardiac evolution in fossils. DOI: http://dx.doi.org/10.7554/eLife.14698.001
International Journal of Astrobiology | 2016
W. Goetz; William B. Brinckerhoff; Ricardo Arevalo; Caroline Freissinet; Stephanie A. Getty; D. P. Glavin; Sandra Siljeström; Arnaud Buch; Fabien Stalport; A. Grubisic; Xiang Li; V. Pinnick; Ryan M. Danell; F. H. W. Van Amerom; Fred Goesmann; Harald Steininger; Noël Grand; F. Raulin; Cyril Szopa; Uwe J. Meierhenrich; John Robert Brucato
This paper describes strategies to search for, detect, and identify organic material on the surface and subsurface of Mars. The strategies described include those applied by landed missions in the past and those that will be applied in the future. The value and role of ESAs ExoMars rover and of her key science instrument Mars Organic Molecule Analyzer (MOMA) are critically assessed.
Philosophical Transactions of the Royal Society A | 2017
Martin Hilchenbach; Henning Fischer; Yves Langevin; S. Merouane; John Paquette; Jouni Rynö; Oliver Stenzel; Christelle Briois; J. Kissel; Andreas Koch; R. Schulz; Johan Silen; Nicolas Altobelli; Donia Baklouti; Anais Bardyn; H. Cottin; C. Engrand; Nicolas Fray; Gerhard Haerendel; Hartmut Henkel; H. Höfner; Klaus Hornung; Harry J. Lehto; Eva Maria Mellado; Paola Modica; Léna Le Roy; Sandra Siljeström; W. Steiger; Laurent Thirkell; Roger Thomas
The in situ cometary dust particle instrument COSIMA (COmetary Secondary Ion Mass Analyser) onboard ESAs Rosetta mission has collected about 31 000 dust particles in the inner coma of comet 67P/Churyumov–Gerasimenko since August 2014. The particles are identified by optical microscope imaging and analysed by time-of-flight secondary ion mass spectrometry. After dust particle collection by low speed impact on metal targets, the collected particle morphology points towards four families of cometary dust particles. COSIMA is an in situ laboratory that operates remotely controlled next to the comet nucleus. The particles can be further manipulated within the instrument by mechanical and electrostatic means after their collection by impact. The particles are stored above 0°C in the instrument and the experiments are carried out on the refractory, ice-free matter of the captured cometary dust particles. An interesting particle morphology class, the compact particles, is not fragmented on impact. One of these particles was mechanically pressed and thereby crushed into large fragments. The particles are good electrical insulators and transform into rubble pile agglomerates by the application of an energetic indium ion beam during the secondary ion mass spectrometry analysis. This article is part of the themed issue ‘Cometary science after Rosetta’.
Astrobiology | 2014
Sandra Siljeström; Caroline Freissinet; Fred Goesmann; Harald Steininger; W. Goetz; Andrew Steele; Hans Erik Foss Amundsen
The characterization of any organic molecules on Mars is a top-priority objective for the ExoMars European Space Agency-Russian Federal Space Agency joint mission. The main instrument for organic analysis on the ExoMars rover is the Mars Organic Molecule Analyzer (MOMA). In preparation for the upcoming mission in 2018, different Mars analog samples are studied with MOMA and include samples collected during the Arctic Mars Analog Svalbard Expedition (AMASE) to Svalbard, Norway. In this paper, we present results obtained from two different Mars analog sites visited during AMASE11, Colletthøgda and Botniahalvøya. Measurements were performed on the samples during AMASE11 with a MOMA gas chromatograph (GC) prototype connected to a commercial mass spectrometer (MS) and later in home institutions with commercial pyrolysis-GCMS instruments. In addition, derivatization experiments were performed on the samples during AMASE11 and in the laboratory. Three different samples were studied from the Colletthøgda that included one evaporite and two carbonate-bearing samples. Only a single sample was studied from the Botniahalvøya site, a weathered basalt covered by a shiny surface consisting of manganese and iron oxides. Organic molecules were detected in all four samples and included aromatics, long-chained hydrocarbons, amino acids, nucleobases, sugars, and carboxylic acids. Both pyrolysis and derivatization indicated the presence of extinct biota by the detection of carboxylic acids in the samples from Colletthøgda, while the presence of amino acids, nucleobases, carboxylic acids, and sugars indicated an active biota in the sample from Botniahalvøya. The results obtained with the prototype flight model in the field coupled with repeat measurements with commercial instruments within the laboratory were reassuringly similar. This demonstrates the performance of the MOMA instrument and validates that the instrument will aid researchers in their efforts to answer fundamental questions regarding the speciation and possible source of organic content on Mars.