Volcanic ash clouds affecting Northern Europe: the long view

The volcanic ash or ‘tephra’ cloud resulting from the relatively small (volume and VEI) eruption of the Icelandic volcano Eyjafjallajökull in 2010 caused major air travel disruption, at substantial global economic cost. On several occasions in the past few centuries, Icelandic eruptions have created ash and/or sulphur dioxide clouds which were detected over Europe (e.g. Hekla in 1947, Askja in 1875, and Laki in 1783). However, these historical observations do not represent a complete record of events serious enough to disrupt aviation in Europe. The only feasible evidence for this is within the geological tephra record. Ash layers are preserved in bogs and lakes where tephra deposited from the atmosphere is incorporated in the peat/mud. In this article we: 1, introduce the analysis of the Northern European sedimentary tephra record; 2, discuss our findings and modelling results; 3, highlight how these were misinterpreted by the popular media; and 4, use this experience to outline several existing problems with current tephra studies and suggest agendas for future research.     

A signature of the donor star in the extra-galactic X-ray binary LMC X−2

Two nights of phase-resolved medium-resolution Very Large Telescope spectroscopy of the extra-galactic low-mass X-ray binary LMC X−2 have revealed a 0.32 ± 0.02 d spectroscopic period in the radial velocity curve of the He  ii λ4686 emission line that we interpret as the orbital period. However, similar to previous findings, this radial velocity curve shows a longer term variation that is most likely due to the presence of a precessing accretion disc in LMC X−2. This is strengthened by He  ii λ4686 Doppler maps that show a bright spot that is moving from night to night. Furthermore, we detect narrow emission lines in the Bowen region of LMC X−2, with a velocity of   K _em= 351 ± 28 km s⁻¹  , that we tentatively interpret as coming from the irradiated side of the donor star. Since K _em must be smaller than K ₂, this leads to the first upper limit on the mass function of LMC X−2 of   f ( M ₁) ≥ 0.86  M_⊙  (95 per cent confidence), and the first constraints on its system parameters.     

Alteration of five organic compounds by glow discharge plasma and UV light under simulated Mars conditions

The Viking missions to Mars failed to detect any organic material in regolith samples. Since then, several removal mechanisms of organic material have been proposed. Two of these proposed methods are removal due to exposure to plasmas created in dust devils and exposure to UV irradiation. The experiments presented here were performed to identify similarities between the two potential removal mechanisms and to identify any compounds produced from these mechanisms that would have been difficult for the Viking instruments to detect. Five organic compounds, phenanthrene, octadecane, octadecanoic acid, decanophenone and benzoic acid, were exposed to a glow discharge plasma created in simulated martian atmospheres as might be present in dust devils, and to UV irradiation similar to that found at the surface of Mars. Glow discharge exposure was carried out in a chamber with 6.9 mbar pressure of a Mars like gas composed mostly of carbon dioxide. The plasma was characterized using emission spectroscopy and found to contain cations and excited neutral species including carbon dioxide, carbon monoxide, and nitrogen. UV irradiation experiments were performed in a Mars chamber which simulates the temperature, pressure, atmospheric composition, and UV fluence rates of equatorial Mars. The non-volatile residues left after each exposure were characterized by mass loss, infrared spectroscopy and high resolution mass spectrometry. Oxidized, higher molecular weight versions of the parent compounds containing carbonyl, hydroxyl and alkenyl functional groups were identified. The presence of these oxidized compounds suggests that searches for organic material in soils on Mars use instrumentation suitable for detection of compounds which contain the above functional groups. Discussions of possible reaction mechanisms are given.     

Evaluating techniques for sampling stream crayfish (Paranephrops planifrons)

We evaluated several capture and analysis techniques for estimating abundance and size structure of freshwater crayfish (Paranephrops planifrons) (koura) from a forested North Island, New Zealand stream to provide a methodological basis for future population studies. Direct observation at night and collecting with baited traps were not considered useful. A quadrat sampler was highly biased toward collecting small individuals. Handnetting at night and estimating abundances using the depletion method were not as efficient as handnetting on different dates and analysing by a mark‐recapture technique. Electrofishing was effective in collecting koura from different habitats and resulted in the highest abundance estimates, and mark‐recapture estimates appeared to be more precise than depletion estimates, especially if multiple recaptures were made. Handnetting captured more large crayfish relative to electrofishing or the quadrat sampler.     

Gemini-N mid-IR observations of the dust properties of the ejecta excavated from Comet 9P/Tempel 1 during Deep Impact

We present mid-infrared spectra and images from the Gemini-N (+MICHELLE) observational campaign of Comet 9P/Tempel 1 before, during, and after its encounter with Deep Impact. We use our thermal grain model to probe the 10 μm properties of the dust grains in the coma of the comet. Before impact (3 July 2005 UT), and more than 24 h after impact (5, 16, and 28 July 2005 UT), the comet dust grains were composed mostly of amorphous olivine, and were relatively large (peak of the grain size distribution ). For the night of impact, we extract spectra by centering on the nucleus, and offset 1″ from the nucleus in the direction of the impact ejecta plume. We find small dust grains (∼0.2 μm) of a diverse mineralogy (amorphous olivine, amorphous pyroxene, amorphous carbon, and crystalline olivine) populating the ejecta. The submicron sized dust grains move faster than the other, larger grains (?0.7 μm), with amorphous olivine and amorphous carbon traveling together, and amorphous pyroxene and crystalline olivine dispersing at a similar rate. Deriving a velocity law from a time-of-flight analysis, we find that the material traveled with a velocity law scaled by and with a power of p=0.5. This velocity power-law requires a sustained release of grains for the duration of 45-60 min after impact. Since the mineral species are traveling at different speeds, and there was a sustained release of grains due to a possible “gas-plume,” we conclude that the different minerals did not originate from grain aggregates destroyed by the impact, but instead arise from an inhomogeneous nucleus.     

Molecular H2O in armenite, BaCa2Al6Si9O30·2H2O, and epididymite, Na2Be2Si6O15·H2O: Heat capacity, entropy and local-bonding behavior of confined H2O in microporous silicates

Armenite, ideal formula BaCa₂Al₆Si₉O₃₀·2H₂O, and its dehydrated analog BaCa₂Al₆Si₉O₃₀ and epididymite, ideal formula Na₂Be₂Si₆O₁₅·H₂O, and its dehydrated analog Na₂Be₂Si₆O₁₅ were studied by low-temperature relaxation calorimetry between 5 and 300 K to determine the heat capacity, C_p, behavior of their confined H₂O. Differential thermal analysis and thermogravimetry measurements, FTIR spectroscopy, electron microprobe analysis and powder Rietveld refinements were undertaken to characterize the phases and the local environment around the H₂O molecule.The determined structural formula for armenite is Ba_0.88(0.01)Ca_1.99(0.02)Na_0.04(0.01)Al_5.89(0.03)Si_9.12(0.02)O₃₀·2H₂O and for epididymite Na_1.88(0.03)K_0.05(0.004)Na_0.01(0.004)Be_2.02(0.008)Si_6.00(0.01)O₁₅·H₂O. The infrared (IR) spectra give information on the nature of the H₂O molecules in the natural phases via their H₂O stretching and bending vibrations, which in the case of epididymite only could be assigned. The powder X-ray diffraction data show that armenite and its dehydrated analog have similar structures, whereas in the case of epididymite there are structural differences between the natural and dehydrated phases. This is also reflected in the lattice IR mode behavior, as observed for the natural phases and the H₂O-free phases. The standard entropy at 298 K for armenite is S° = 795.7 ± 6.2 J/mol K and its dehydrated analog is S° = 737.0 ± 6.2 J/mol K. For epididymite S° = 425.7 ± 4.1 J/mol K was obtained and its dehydrated analog has S° = 372.5 ± 5.0 J/mol K. The heat capacity and entropy of dehydration at 298 K are Δ = 3.4 J/mol K and ΔS^rxn = 319.1 J/mol K and Δ = −14.3 J/mol K and ΔS^rxn = 135.7 J/mol K for armenite and epididymite, respectively. The H₂O molecules in both phases appear to be ordered. They are held in place via an ion-dipole interaction between the H₂O molecule and a Ca cation in the case of armenite and a Na cation in epididymite and through hydrogen-bonding between the H₂O molecule and oxygen atoms of the respective silicate frameworks. Of the three different H₂O phases ice, liquid water and steam, the C_p behavior of confined H₂O in both armenite and epididymite is most similar to that of ice, but there are differences between the two silicates and from the C_p behavior of ice. Hydrogen-bonding behavior and its relation to the entropy of confined H₂O at 298 K is analyzed for various microporous silicates.The entropy of confined H₂O at 298 K in various silicates increases approximately linearly with increasing average wavenumber of the OH-stretching vibrations. The interpretation is that decreased hydrogen-bonding strength between a H₂O molecule and the silicate framework, as well as weak ion-dipole interactions, results in increased entropy of H₂O. This results in increased amplitudes of external H₂O vibrations, especially translations of the molecule, and they contribute strongly to the entropy of confined H₂O at T < 298 K.     

Periglacial climate at the 2.5 Ma onset of Northern Hemisphere glaciation inferred from the Whippoorwill Formation, northern Missouri, USA

The Whippoorwill Formation is a gleyed diamicton that is present locally within bedrock depressions beneath the oldest glacial till in northern Missouri, USA. Stratigraphy, paleomagnetism, and cosmogenic-nuclide burial ages show that it was deposited between the Matuyama-Gauss magnetostratigraphic boundary at 2.58 Ma and the first advance of the Laurentide ice sheet into Missouri at 2.47 ± 0.19 Ma. High cosmogenic-nuclide concentrations also show that the constituents of the Whippoorwill Formation experienced long exposure at a stable landscape surface with erosion rates of 1-2 m/Ma. However, cosmogenic-nuclide concentrations are invariant with depth below the Whippoorwill Formation surface, indicating active mixing of the soil profile shortly before burial by till. The Whippoorwill Formation retains numerous features indicative of cryoturbation. Therefore, we interpret it as a buried Gelisol, a soil formed under periglacial conditions in the presence of permafrost. At the onset of Northern Hemisphere glaciation, climate cooling established permafrost conditions and accelerated erosion by inducing landscape instability. Thus, weathered regolith materials were mobilized and redeposited by gelifluction shortly before the ice sheet overrode the landscape.