Some terms of nutation derived from the BIH data

Summary. The z -term of latitude and the w -term of UT, as computed by the BIH, are suitable for investigating imperfections in the representation of the real nutation in space. They have been previously used for deriving only the amplitude of the principal term of nutation (Feissel & Guinot). In this study they are used more generally for deriving the amplitudes of two terms of nutation and searching for a possible nutation in space due to the nearly-diurnal wobble.
Two kinds of data are used for this purpose: the values of z and w from 1962.0 to 1980.0 at 0.05 yr intervals and the values of z from 1967.0 to 1980.0 at 5 day intervals. The first ones have been used previously by Feissel & Guinot (using the values up to 1974.0 and 1976.95 respectively). The second ones have not previously been used for such studies.
The derived amplitudes of the principal and the fortnightly terms of nutation are in good agreement with other values deduced from observations, and with the theoretical ones corresponding to the best models of a non-rigid earth. The values obtained are not yet sufficiently precise to distinguish between these models, but could become so in the near future.
The least-squares fits, performed among the z and w data in order to look for any error in the representation of nutation, show the existence of a retrograde term, of a 434 day period for z and 444 day for w and an amplitude of the order of 0.01 arcsec. It may be due to the nearly-diurnal wobble.     

Intense pyrite formation under low-sulfate conditions in the Achterwasser lagoon, SW Baltic Sea

In comparison to similar low-sulfate coastal environments with anoxic-sulfidic sediments, the Achterwasser lagoon, which is part of the Oder estuary in the SW Baltic Sea, reveals unexpectedly high pyrite concentrations of up to 7.5 wt%. Pyrite occurs mainly as framboidal grains variable in size with diameters between 1 and 20 μm. Pyritization is not uniform down to the investigated sediment depth of 50 cm. The consumption of reactive-Fe is most efficient in the upper 20 cm of the sediment column, leading to degrees of pyritization (DOP) as high as 80 to 95%.Sediment accumulation in the Achterwasser takes place in high productivity waters. The content of organic carbon reaches values of up to 10 wt%, indicating that pyrite formation is not limited by the availability of organic matter. Although dissolved sulfate concentration is relatively low (<2 mmol/L) in the Achterwasser, the presence of H₂S in the pore water suggests that sulfate is unlikely to limit pyrite authigenesis. The lack of free Fe(II) in the pore waters combined with the possibility of a very efficient transformation of Fe-monosulfides to pyrite near the sediment/water interface suggests that pyrite formation is rather controlled by (i) the availability of reactive-Fe, which limits the FeS formation, and by (ii) the availability of an oxidant, which limits the transformation of FeS into pyrite. The ultimate source for reactive-Fe is the river Oder, which provides a high portion of reactive-Fe (∼65% of the total-Fe) in the form of suspended particulate matter. The surficial sediments of the Achterwasser are reduced, but are subject to oxidation from the overlying water by resuspension. Oxidation of the sediments produces sulfur species with oxidation states intermediate between sulfide and sulfate (e.g., thiosulfate and polysulfides), which transform FeS to FeS₂ at a significant rate. This process of FeS-recycling is suggested to be responsible for the formation of pyrite in high concentrations near the sediment surface, with DOP values between 80 and 95% even under low sulfate conditions.A postdepositional sulfidization takes place in the deeper part of the sediment column, at ∼22 cm depth, where the downward diffusion of H₂S is balanced by the upward migration of Fe(II). The vertical fluctuation of the diffusion front intensifies the pyritization of sediments. We suggest that the processes described may occur preferentially in shallow water lagoons with average net-sedimentation rates close to zero. Such environments are prone to surficial sediment resuspension, initiating oxidation of Fe-sulfides near the sediment/water interface. Subsequent FeS₂ formation as well as postdepositional sulfidization leads to a major pyrite spike at depth within the sediment profile.     

Designing Service Architectures for Distributed Geoprocessing: Challenges and Future Directions

In this paper we study the feasibility of using services offered by a Spatial Data Infrastructure as a basis for distributed service oriented geoprocessing. By developing a prototype we demonstrate that a Spatial Data Infrastructure facilitates rapid development of applications that solve typical problems for an existing risk management application. The prototype provides users with a distributed application that enables the assessment of fire damage areas based on land cover data in a given area. The services involved in the application include: Web Feature Services, Web Map Services, a Gazetteer Service, a Catalogue Service, and Geoprocessing Services. We present the architecture of the application and describe details about implementation‐specific issues. We conclude that current OGC specifications provide a sound basis for developing service oriented architectures for geographic applications; however, in particular for geoprocessing applications, we question the feasibility of the use of Web Feature Services as data sources for larger amounts of data and call for further research in this direction.     

Molecular environment of iodine in naturally iodinated humic substances: Insight from X-ray absorption spectroscopy

The molecular environment of iodine in reference inorganic and organic compounds, and in dry humic and fulvic acids (HAs and FAs) extracted from subsurface and deep aquifers was probed by iodine L₃-edge X-ray absorption spectroscopy. The X-ray absorption near-edge structure (XANES) of iodine spectra from HAs and FAs resembled those of organic references and displayed structural features consistent with iodine forming covalent bonds with organic molecules. Simulation of XANES spectra by linear combination of reference spectra suggested the predominance of iodine forming covalent bonds to aromatic rings (aromatic-bound iodine). Comparison of extended X-ray absorption fine structure (EXAFS) spectra of reference and samples further showed that iodine was surrounded by carbon shells at distances comparables to those for references containing aromatic-bound iodine. Quantitative analysis of EXAFS spectra indicated that iodine was bound to about one carbon at a distance d (I-C) of 2.01(4)-2.04(9) Å, which was comparable to the distances observed for aromatic-bound iodine in references (1.99(1)-2.07(6) Å), and significantly shorter than that observed for aliphatic-bound iodine (2.15(2)-2.16(2) Å). These results are in agreement with previous conclusions from X-ray photoelectron spectroscopy and from electrospray ionization mass spectrometry. These results collectively suggest that the aromatic-bound iodine is stable in the various aquifers of this study.     

Foraging by Two Estuarine Fishes, <Emphasis Type="Italic">Fundulus heteroclitus</Emphasis> and <Emphasis Type="Italic">Fundulus majalis</Emphasis>, on Juvenile Asian Shore Crabs (<Emphasis Type="Italic">Hemigrapsus sanguineus</Emphasis>) in Western Long Island Sound

The Asian shore crab, Hemigrapsus sanguineus, is a recent and particularly successful introduction to the east coast of the USA. Little research has been done on the utilization of Asian shore crabs for food by native species, a potential form of biocontrol. Over a 4-year period, we examined the gut contents of cogeners, Fundulus heteroclitus and Fundulus majalis, collected from two embayments in western Long Island Sound for the presence of juvenile H. sanguineus. Frequency (percent) of occurrence of food items in the guts of both species varied over year and study site. Asian shore crabs were consumed more often by F. heteroclitus than by F. majalis, but predation pressure by both species was low. Only 13% of F. heteroclitus and 7.7% of F. majalis found with food in their guts had ingested Asian shore crab remains. Of those, 1/3 had consumed whole crabs; the rest had only autotomized appendages in their guts. The mean carapace width of juvenile Asian shore crabs ingested by F. heteroclitus was 3.59 ± 2.22 mm (N = 33). Results of our study on killifish predation support the hypothesis that H. sanguienus abundance is partly explained by reduced impact of native predators (i.e., the “enemy release hypothesis”). Predation pressure of other potential enemies on both planktonic and benthic stages of the Asian shore crab must be investigated, however, to understand the full impact of predation on H. sanguineus population dynamics.     

The introduction of the Iau 1980 nutation theory in the computation of the Earth Rotation Parameters by the Bureau International de l'Heure

Summary The status of nutation theory in the computation of the Earth Rotation Parameters from the different observational techniques is reviewed. The impact on the combined solution of the Bureau International de l'Heure is evaluated. In view of the improvement brought by the IAU 1980 Nutation Theory, its introduction in the BIH publications, without waiting for the adoption by the astronomical ephemerides (1984 Jan. 1) is decided.     

Temporal variability in the isotopic niches of rocky shore grazers and suspension‐feeders

Carbon and nitrogen stable isotope ratios were measured in rocky inter‐tidal suspension‐feeders (brown mussels and cape reef worms) and grazers (goat's eye limpets and cape sea urchins) to determine the influences of lifestyle and time on the diets of consumers. Niche partitioning between consumer species within the same feeding guild was assessed using isotopic niche area (a proxy for trophic niche). Specimens were collected monthly at a single site in Southeastern South Africa from July 2010 to June 2011. Temporal variations in isotopic signatures were generally greater in the suspension‐feeders compared with the grazers, isotopic niche widths were smaller in the suspension‐feeders and intra‐population variations in isotope signatures were larger in the grazers. No inter‐specific niche overlap (according to standard ellipse areas) was observed within either feeding guild unless standardization calculations were used. Temporal variations in the diets of all the consumers appeared uncoupled from temporal variability in the isotopic signatures of basal resources in the region; as such, shifts in the consumer diets most likely pertained to feeding behaviour and food preferences. Our data provide new insights into how syntopic rocky shore consumers coexist by partitioning their temporally variable food environment.     

Geology,mineralogy and geochemistry of the Kekem dyke swarm (Western Cameroon): Insights into Paleozoic–Mesozoic magmatism and geodynamic implications

The broadly N70°–90°E-trending dykes swarm at Kekem cut across the Paleoproterozoic-to-Achean terranes of West Cameroon remobilized during the Pan-African orogeny. They are picrite basalts and basalts with tholeiitic/transitional affinity, as shown by mineralogical and geochemical data, with variable major and trace element contents, MgO ranges from 7.3 to 12.4 wt.%, Cr from 190 to 411 ppm, Ni from 15 to 234 ppm. All the dykes are light REE enriched with La_N/Yb_N values of 5.3–8.1, suggesting a co-magmatic origin. They originated from a 2.8% partial melting of a spinel-mantle source with no or little crustal input. The geochemical features of Kekem dykes are similar to those of Paleozoic and Mesozoic dykes recorded in North and Central Africa, suggesting multiple reactivations of pre-existing fractures that resulted in the fragmentation of western Gondwana and the opening of Central and South Atlantic Oceans.     

Iron biomineralization by anaerobic neutrophilic iron-oxidizing bacteria

Minerals formed by bio-oxidation of ferrous iron (Fe(II)) at neutral pH, their association with bacterial ultrastructures as well as their impact on the metabolism of iron-oxidizing bacteria remain poorly understood. Here, we investigated iron biomineralization by the anaerobic nitrate-dependent iron-oxidizing bacterium Acidovorax sp. strain BoFeN1 in the presence of dissolved Fe(II) using electron microscopy and Scanning Transmission X-ray Microscopy (STXM). All detected minerals consisted mainly of amorphous iron phosphates, but based on their morphology and localization, three types of precipitates could be discriminated: (1) mineralized filaments at distance from the cells, (2) globules of 100 ± 25 nm in diameter, at the cell surface and (3) a 40-nm thick mineralized layer within the periplasm. All of those phases were shown to be intimately associated with organic molecules. Periplasmic encrustation was accompanied by an accumulation of protein moieties. In the same way, exopolysaccharides were associated with the extracellular mineralized filaments. The evolution of cell encrustation was followed by TEM over the time course of a culture: cell encrustation proceeded progressively, with rapid precipitation in the periplasm (in a few tens of minutes), followed by the formation of surface-bound globules. Moreover, we frequently observed an asymmetric mineral thickening at the cell poles. In parallel, the evolution of iron oxidation was quantified by STXM: iron both contained in the bacteria and in the extracellular precipitates reached complete oxidation within 6 days. While a progressive oxidation of Fe in the bacteria and in the medium could be observed, spatial redox (oxido-reduction state) heterogeneities were detected at the cell poles and in the extracellular precipitates after 1 day. All these findings provide new information to further the understanding of molecular processes involved in iron biomineralization by anaerobic iron-oxidizing bacteria and offer potential signatures of those metabolisms that can be looked for in the geological record.     

Crystal fractionation,magma step ascent,and syn-eruptive mingling: the Averno 2 eruption (Phlegraean Fields,Italy)

The 3.7 ka year-old Averno 2 eruption is one of the rare eruptions to have occurred in the northwest sector of the Phlegraean Fields caldera (PFc) over the past 5 ka. We focus here on the fallout deposits of the pyroclastic succession emplaced during this eruption. We present major and trace element data on the bulk pumices, along with major and volatile element data on clinopyroxene-hosted melt inclusions, in order to assess the conditions of storage, ascent, and eruption of the feeding trachytic magma. Crystal fractionation accounts for the evolution from trachyte to alkali-trachyte magmas; these were intimately mingled (at the micrometer scale) during the climactic phase of the eruption. The Averno 2 alkali trachyte represents one of the most evolved magmas erupted within the Phlegraean Fields area and belongs to the series of differentiated trachytic magmas erupted at different locations 5 ka ago. Melt inclusions record significant variations in H₂O (from 0.4 to 5 wt%), S (from 0.01 to 0.06 wt%), Cl (from 0.75 up to 1 wt%), and F (from 0.20 to >0.50 wt%) during both magma crystallization and degassing. Unlike the eruptions occurring in the central part of the PFc, deep-derived input(s) of gas and/or magma are not required to explain the composition of melt inclusions and the mineralogy of Averno 2 pumices. Compositional data on bulk pumices, glassy matrices, and melt inclusions suggest that the Averno 2 eruption mainly resulted from successive extrusions of independent magma batches probably emplaced at depths of 2–4 km along regional fractures bordering the Neapolitan Yellow Tuff caldera.