Pb/Pb geochronology, petrography and chemistry of Zr-rich accessory minerals (zirconolite, tranquillityite and baddeleyite) in mare basalt 10047

In situ U-Pb isotopic measurements were carried out by ion microprobe on the Zr-rich accessory minerals zirconolite [CaZrTi₂O₇], tranquillityite [Fe₈²⁺(ZrY)₂Ti₃Si₃O₂₄] and baddeleyite [ZrO₂] in low-K, high-Ti mare basalt 10047 collected during the Apollo 11 mission. The analysed minerals are concentrated in pockets of late-stage mesostasis that comprises an intergrowth of silica, barian K-feldspar and Si-Al-K glass, from a phaneritic, subophitic, basalt comprising mainly pyroxene, plagioclase, ilmenite, cristobalite and troilite. Most Zr-rich minerals are unaltered, however, some tranquillityite is replaced by a complex intergrowth of zirconolite, baddeleyite, ilmenite and fayalite, suggesting that the mineral became unstable during crystallization. Several baddeleyite crystals have also undergone alteration to secondary zircon. Zirconolite was analysed in thin section 10047,11 and tranquillityite and baddeleyite in 10047,227, using a ∼6 μm primary ion beam. Both zirconolite and tranquillityite have significant U and low initial Pb contents, and are highly suitable for Pb/Pb dating. Fifteen analyses of zirconolite give a ²⁰⁷Pb/²⁰⁶Pb age of 3708 ± 7 Ma (²⁰⁷Pb/²⁰⁶Pb:²⁰⁴Pb/²⁰⁶Pb isochron; 95% confidence, including renormalisation of ratios) and twenty-five analyses of tranquillityite give 3710 ± 6 Ma. The ²⁰⁷Pb/²⁰⁶Pb dates are consistent with each other and refine results from an earlier study. Baddeleyite data were less precise, mainly due to lower secondary ionisation efficiency. Our results show that zirconolite and tranquillityite can provide precise isotopic dates and, given their presence in other samples, they represent important U-Pb chronometers for refining lunar geology.     

High energy coastal sedimentary deposits; an evaluation of depositional processes in Southwest England

Sediments left by coastal flooding have been observed worldwide and have been variously ascribed to the action of storm surges and tsunami waves. To date, no study has attempted to unequivocally establish on stratigraphical, sedimentological, and palaeoecological grounds the means by which these two different processes might be distinguished in coastal sedimentary sequences. This paper examines the evidence for historical storm surges and tsunamis and shows that both high magnitude events have been documented over the past 250 years in southwest England. Sand layers of varying thickness are present within Holocene lagoonal and peat sequences of several shallow lakes of the Scilly Isles. Detailed analysis of Big Pool, St Agnes, indicates that the basal peats date from around 1000 BP. Within the basal peats are numerous thin sand layers. Above the basal peat is an extensive sand layer 15 to 40 cm thick. The base of this latter layer probably dates from the early to mid 18th century. Particle size, grain surface morphology, diatom, and mineral magnetic studies are used to try and determine the most likely mode of deposition. The results of all analyses are inconclusive, but the weight of evidence suggests that the increasing frequency of thin sand layers in the upper part of the basal peat may be related to the increasing frequency and intensity of Atlantic storms during the Little Ice Age superimposed upon a rising sea level. The thick sand layer may have been deposited by the tsunami wave generated by the Lisbon earthquake of November 1,1755. Due to the difficulties in distinguishing depositional processes in coastal environments known to have been affected by storm surges and tsunami waves, it is suggested that generally accepted sedimentological techniques are inadequate for discriminating depositional processes in coastal environments.     

Empowering learning through design: a comparative analysis of ICM course development for web-based and classroom delivery

This article reviews the development of two courses focussed on meeting Integrated Coastal Management capacity building needs: an undergraduate degree course, and a web-based distance learning course. Influential factors in the development of each course are identified and compared. Important considerations are found to be methods of quality assurance, course content, the temporal and spatial context of teaching and learning, level of learner empowerment, and the role of the teacher. It is concluded that in order to understand the role of such courses in capacity building, coastal educators need to share experiences and encourage reflection on the effectiveness of capacity building efforts.     

The meridional phosphine distribution in Saturn's upper troposphere from Cassini/CIRS observations

The Cassini Composite Infrared Spectrometer (CIRS) has been used to derive the vertical and meridional variation of temperature and phosphine (PH₃) abundance in Saturn's upper troposphere. PH₃ has a significant effect on the measured radiances in the thermal infrared and between May 2004 and September 2005 CIRS recorded thousands of spectra in both the far (10-600 cm⁻¹) and mid (600-1400 cm⁻¹) infrared, at a variety of latitudes covering the southern hemisphere. Low spectral resolution (15 cm⁻¹) data has been used to constrain the temperature structure of the troposphere between 100 and 500 mbar. The vertical distributions of phosphine and ammonia were retrieved from far-infrared spectra at the highest spectral resolution (0.5 cm⁻¹), and lower resolution (2.5 cm⁻¹) mid-infrared data were used to map the meridional variation in the abundance of phosphine in the 250-500 mbar range. Temperature variations at the 250 mbar level are shown to occur on the same scale as the prograde and retrograde jets in Saturn's atmosphere [Porco, C.C., and 34 colleagues, 2005. Science 307, 1243-1247]. The PH₃ abundance at 250 mbar is found to be enhanced at the equator when compared with mid-latitudes. At mid latitudes we see anti-correlation between temperature and PH₃ abundance at 250 mbar, phosphine being enhanced at 45° S and depleted at 25 and 55° S. The vertical distribution is markedly different polewards of 60-65° S, with depleted PH₃ at 500 mbar but a slower decline in abundance with altitude when compared with the mid-latitudes. This variation is similar to the variations of cloud and aerosol parameters observed in the visible and near infrared, and may indicate the subsidence of tropospheric air at polar latitudes, coupled with a diminished sunlight penetration depth reducing the rate of PH₃ photolysis in the polar region.     

Analysis of Titan's neutral upper atmosphere from Cassini Ion Neutral Mass Spectrometer measurements

In this paper we present an in-depth study of the distributions of various neutral species in Titan's upper atmosphere, between 950 and 1500 km for abundant species (N₂, CH₄, H₂) and between 950 and 1200 km for other minor species. Our analysis is based on a large sample of Cassini/INMS (Ion Neutral Mass Spectrometer) measurements in the CSN (Closed Source Neutral) mode, obtained during 15 close flybys of Titan. To untangle the overlapping cracking patterns, we adopt Singular Value Decomposition (SVD) to determine simultaneously the densities of different species. Except for N₂, CH₄, H₂ and ⁴⁰Ar (as well as their isotopes), all species present density enhancements measured during the outbound legs. This can be interpreted as a result of wall effects, which could be either adsorption/desorption of these molecules or heterogeneous surface chemistry of the associated radicals on the chamber walls. In this paper, we provide both direct inbound measurements assuming ram pressure enhancement only and abundances corrected for wall adsorption/desorption based on a simple model to reproduce the observed time behavior. Among all minor species of photochemical interest, we have firm detections of C₂H₂, C₂H₄, C₂H₆, CH₃C₂H, C₄H₂, C₆H₆, CH₃CN, HC₃N, C₂N₂ and NH₃ in Titan's upper atmosphere. Upper limits are given for other minor species.The globally averaged distributions of N₂, CH₄ and H₂ are each modeled with the diffusion approximation. The N₂ profile suggests an average thermospheric temperature of 151 K. The CH₄ and H₂ profiles constrain their fluxes to be and , referred to Titan's surface. Both fluxes are significantly higher than the Jeans escape values. The INMS data also suggest horizontal/diurnal variations of temperature and neutral gas distribution in Titan's thermosphere. The equatorial region, the ramside, as well as the nightside hemisphere of Titan appear to be warmer and present some evidence for the depletion of light species such as CH₄. Meridional variations of some heavy species are also observed, with a trend of depletion toward the north pole. Though some of the above variations might be interpreted by either the solar-driven models or auroral-driven models, a physical scenario that reconciles all the observed horizontal/diurnal variations in a consistent way is still missing. With a careful evaluation of the effect of restricted sampling, some of the features shown in the INMS data are more likely to be observational biases.     

Meridional distribution of CH3C2H and C4H2 in Saturn’s stratosphere from CIRS/Cassini limb and nadir observations

Limb and nadir spectra acquired by Cassini/CIRS (Composite InfraRed Spectrometer) are analyzed in order to derive, for the first time, the meridional variations of diacetylene (C₄H₂) and methylacetylene (CH₃C₂H) mixing ratios in Saturn’s stratosphere, from 5 hPa up to 0.05 hPa and 80°S to 45°N. We find that the C₄H₂ and CH₃C₂H meridional distributions mimic that of acetylene (C₂H₂), exhibiting small-scale variations that are not present in photochemical model predictions. The most striking feature of the meridional distribution of both molecules is an asymmetry between mid-southern and mid-northern latitudes. The mid-southern latitudes are found depleted in hydrocarbons relative to their northern counterparts. In contrast, photochemical models predict similar abundances at north and south mid-latitudes. We favor a dynamical explanation for this asymmetry, with upwelling in the south and downwelling in the north, the latter coinciding with the region undergoing ring shadowing. The depletion in hydrocarbons at mid-southern latitudes could also result from chemical reactions with oxygen-bearing molecules.Poleward of 60°S, at 0.1 and 0.05 hPa, we find that the CH₃C₂H and C₄H₂ abundances increase dramatically. This behavior is in sharp contradiction with photochemical model predictions, which exhibit a strong decrease towards the south pole. Several processes could explain our observations, such as subsidence, a large vertical eddy diffusion coefficient at high altitudes, auroral chemistry that enhances CH₃C₂H and C₄H₂ production, or shielding from photolysis by aerosols or molecules produced from auroral chemistry. However, problems remain with all these hypotheses, including the lack of similar behavior at lower altitudes.Our derived mean mixing ratios at 0.5 hPa of (2.4 ± 0.3) × 10⁻¹⁰ for C₄H₂ and of (1.1 ± 0.3) × 10⁻⁹ for CH₃C₂H are compatible with the analysis of global-average ISO observations performed by Moses et al. (Moses, J.I., Bézard, B., Lellouch, E., Gladstone, G.R., Feuchtgruber, H., Allen, M. [2000a]. Icarus 143, 244-298). Finally, we provide values for the ratios [CH₃C₂H]/[C₂H₂] and [C₄H₂]/[C₂H₂] that can constrain the coupled chemistry of these hydrocarbons.