Relationship between hydrocarbons and bacterial activity in mediterranean sediments: Part 2—hydrocarbon degrading activity of bacteria from sediments

In marine sediments from the Mediterranean coast polluted by oil spills (Etang de Berre) high bacterial activity is responsible for self-purification, samples collected from these areas showing a bacterial density several orders of magnitude higher than samples from non-polluted areas (Isle des Embiez). Between 60 and 80 % of the heterotrophic bacteria in the polluted areas are hydrocarbon-degrading, compared with 0.01 % in the non-polluted area.Several strains of hydrocarbon utilisers were isolated, a mixture of strains from each biotope was taken to represent a ‘biotope population’ and their activity towards different types of hydrocarbons (n-alkanes, iso-alkanes, cycloalkanes, aromatics) was determined.With ammonia as the nitrogen source the ‘biotope population’ from the polluted area degraded hydrocarbons much more readily than the ‘biotope population’ from the non-polluted area. With nitrate as the nitrogen source the degradation was much reduced, and, for some hydrocarbons, ceased in both ‘populations’.Individual hydrocarbons encouraged the growth of individual strains in the ‘biotope population’. In natural mixtures of hydrocarbons all strains grew well and degraded aliphatics. There was a good correlation between the respiratory activity of the ‘biotope population’ and the ability of the ‘population’ to utilise hydrocarbons for growth.     

An integrated lake-catchment approach for determining sediment source changes at Aqualate Mere,Central England

This paper raises fundamental questions about the sole use of paleolimnological techniques to identify sediment sources and develop catchment management plans. The concept of an integrated lake: catchment framework was established 30 years ago, yet paleolimnologists occasionally fail to appreciate the dynamics of the contributing catchment. This is especially critical when the predominant source of sediment accumulating in a lake is allochthonous. In this paper we argue that a detailed appraisal of catchment sources and investigation of historical documentary evidence is needed to identify and evaluate the relative significance of sediment sources. We used such an approach at Aqualate Mere, Shropshire, UK. Mineral magnetic and radionculide signatures of potential catchment sources and accumulating lake sediments were compared in an attempt to match the sources to sediments deposited in the Mere. Dated lake sediments indicate there has been an increase in sedimentation rate and the relative amount of minerogenic material delivered to the Mere over the last 200 years. In contrast to a previous study at the same site, there is no evidence to attribute this increase to an overspill from a nearby canal. Other catchment disturbances include landscaping in parkland surrounding the Mere in the early nineteenth century and drainage systems installed to improve catchment agriculture over the last ca. 150 years. Both activities may explain the change in sedimentation rates and types, independent of the hypothesized canal origin. Although our results exclude the canal as a major sediment source, identifying the contribution of other potential catchment sources remains problematic. ¹³⁷Cs inventories for the lake are similar to those recorded at a local reference site, suggesting little influx of ¹³⁷Cs-bearing topsoil, yet ¹³⁷Cs activities remain high in the upper 20–30 cm of the lake sediment profile, indicating a topsoil origin. Combined radionuclide and mineral magnetic signatures proved to be relatively poor discriminators of potential sources, and the high atmospheric pollution load from the West Midland conurbation has probably altered recent lake sediment signatures. Although further research is required to identify the origins of recent (last ca. 200 years) minerogenic sediment inputs to the Mere, we suggest that the combined lake: catchment approach offers a more rigorous method for understanding the impact of catchment disturbance than analysis of the paleolimnological record alone.     

Wind erosion from military training lands in the Mojave Desert, California, U.S.A.

Military training activities reduce vegetation cover, disturb crusts, and degrade soil aggregates, making the land more vulnerable to wind erosion. The objective of this study was to quantify wind erosion rates for typical conditions at the Marine Corps Air Ground Combat Center, Twentynine Palms, CA, U.S.A. Five Big Spring Number Eight (BSNE) sampler stations were installed at each of five sites. Each BSNE station consisted of five BSNE samplers with the lowest sampler at 0·05 m and the highest sampler at 1·0 m above the soil surface. Once a month, sediment was collected from the samplers for analysis. Occurrence of saltating soil aggregates was recorded every hour using Sensits, one at each site. The site with the most erosion had a sediment discharge of 311 kg m⁻¹ over a period of 17 months. Other sites eroded much less because of significant rock cover or the presence of a crust. Hourly sediment discharge was estimated combining hourly Sensit count and monthly sediment discharge measured using BSNE samplers. More simultaneously measured data are needed to better characterize the relationship between these two and reconstruct a detailed time-series of wind erosion. This measured time-series can then be used for comparison with simulation results from process-based wind erosion models such as the Wind Erosion Prediction System (WEPS), once it has been adapted to the unique aspects of military lands.     

Sulfide evolution in high-temperature to ultrahigh-temperature metamorphic rocks from Lützow–Holm Complex, East Antarctica

The high-temperature (HT) to ultrahigh-temperature (UHT) metamorphic rocks from Lützow–Holm Complex, East Antarctica show a systematic difference between sulfide assemblages in the rock matrix and those found as inclusions in the silicates stable in high-temperatures. Matrix sulfides are commonly pyrite with or without pentlandite and chalcopyrite. On the other hand, inclusion sulfides are pyrrhotite with or without pentlandite and chalcopyrite lamellae. When recalculated into integrated single-phase sulfide compositions, inclusion sulfides from the UHT region showed a wider range of solid–solution composition than the inclusion sulfides from the HT region. The host minerals of the sulfides with extreme solid–solution compositions are those stable at the peak of metamorphism such as orthopyroxene and garnet. One of the most extreme ones is included in orthopyroxene coexisting with sillimanite ± quartz, which is the diagnostic mineral assemblage of UHT metamorphism. These observations suggest that sulfide inclusions preserve their peak metamorphic compositions. Pyrrhotite did not revert to pyrite because of the closed system behavior of sulfur in inclusion sulfides. On the other hand, in the rock matrix where the open system behavior of sulfur is permitted, original sulfides were partly to completely altered by the later fluid activity.     

The origin of reaction textures in mantle peridotite xenoliths from Sal Island, Cape Verde: the case for “metasomatism” by the host lava

Reaction zones around minerals in mantle xenoliths have been reported from many localities worldwide. Interpretations of the origins of these textures fall into two groups: mantle metasomatic reaction or reaction during transport of the xenoliths to the surface. A suite of harzburgitic mantle xenoliths from Sal, Cape Verde show clear evidence of reaction during transport. The reactions resulted in the formation of olivine–clinopyroxene and Si- and alkali-rich glass reaction zones around orthopyroxene and sieve-textured clinopyroxene and sieve textured spinel, both of which are associated with a Si- and alkali-rich glass similar to that in the orthopyroxene reaction zones. Reaction occurred at pressures less than the mantle equilibration pressure and at temperatures close to the liquidus temperature of the host magma. In addition, there is a clear spatial relation of reaction with the host lava: reaction is most intense near the lava/xenolith contact. The residence time of the xenoliths in the host magma, determined from Fe–Mg interdiffusion profiles in olivine, was approximately 4 years. Our results cannot be reconciled with a recent model for the evolution of the mantle below the Cape Verde Archipelago involving mantle metasomatism by kimberlitic melt. We contend that alkali-rich glasses in the Sal xenoliths are not remnants of a kimberlitic melt, but rather they are the result of reaction between the host lava or a similar magma and xenolith minerals, in particular orthopyroxene. The formation of a Si- and alkali-rich glass by host magma–orthopyroxene reaction appears to be a necessary precursor to formation of sieve textured spinel and clinopyroxene.     

Vertical distribution and water solubility of phosphorus and heavy metals in sediments of the St. Lucie Estuary, South Florida, USA

Accumulation and distribution of heavy metals and phosphorus in sediments impact water quality. There has been an increasing concern regarding fish health in the St. Lucie Estuary, which is related to increased inputs of nutrients and metals in recent decades. To investigate vertical changes of contaminants (P, Cd, Cr, Co, Cu, Ni, Pb, Zn, and Mn) in sediments of the St. Lucie Estuary in South Florida, 117 layer samples from six of the 210 to 420 cm depth cores were analyzed for their total and water-soluble P and heavy metals, clay, total Fe, Al, K, Ca, Mg, Na, and pH. Principal component analysis (PCA) was used in two sets of analytical data (total and water-soluble contaminant concentrations) to document changes of contaminants in each core of sediments. The PCA of total contaminants and minerals resulted in two factors (principal components). The first and second factors accounted for 61.7 and 17.2 % of the total variation in all variables, and contrast indicators associated with contaminants of P, Cd, Co, Cr, Ni, Pb, Zn, and Mn and accumulation of Fe and Al oxides, respectively. The first factor could be used for overall assessment of P and heavy metal contamination, and was higher in the upper 45–90 cm than the lower depths of each core. The concentrations of P and heavy metals in the surface layers of sediments significantly increased, as compared with those in the sediments deeper than 45–90 cm. The PCA of water-soluble contaminants developed two factors. The second factor (Cu–P) was higher in the upper than the lower depths of the sediment, whereas the highest score of the first factor (Cd–Co–Cr–Ni–Pb–Zn–Mn) occurred below 100 cm. The water-soluble Cu and P concentrations were mainly dependent on their total concentrations in the sediments, whereas the water-soluble Cd, Co, Cr, Ni, Pb, Zn, and Mn concentrations were mainly controlled by pH.     

Lithospheric petrology of the eastern Arabian Plate: Constraints from Al-Ashkhara (Oman) xenoliths

Mafic granulite and spinel lherzolite xenoliths from Cenozoic alkaline basalts near Al-Ashkhara, eastern Oman, have been selected for a systematic mineralogical, geochemical and Sr–Nd–Pb isotopic study. This is the only place in E Arabia where samples of both lower crust and upper mantle can be examined. Lower crustal xenoliths consist of two mineralogically and chemically distinct groups: gabbronorite (subequal abundances of ortho- and clino-pyroxene and plagioclase) and plagioclase pyroxenite (dominant pyroxene and subordinate plagioclase). Temperature estimates for lower crustal xenoliths using the two pyroxene geothermometer (T-Wells) yield 810–865 °C. The mineral assemblage (spinel–pyroxene–plagioclase) and Al content in pyroxene indicate that plagioclase-bearing xenoliths equilibrated at 5–8 kbar (13 and 30 km depth) in the lower crust. εNd and ⁸⁷Sr/⁸⁶Sr calculated at 700 Ma for Al-Ashkhara lower crustal xenoliths (+ 6.4 to + 6.6; ⁸⁷Sr/⁸⁶Sr = 0.7028 to 0.7039) are consistent with the interpretation that juvenile, mafic melts were added to the lower crust during Neoproterozoic time and that there was no discernible contribution from pre-Neoproterozoic crust. Upper mantle xenoliths consist of both dry and hydrous (phlogopite-bearing) lherzolites. These peridotites are more Fe-rich than expected for primitive mantle or melt residues and probably formed by pervasive circulation of melts that have refertilized pre-existing mantle peridotites. Mineral equilibration temperatures range from 990 to 1070 °C. Isotopic compositions calculated at 700 Ma are εNd = + 6.8 to + 7.8 and ⁸⁷Sr/⁸⁶Sr = 0.7016 to 0.7025, indicating depleted upper mantle. Pb isotopic compositions indicate that the metasomatism was relatively recent, perhaps related to Paleogene tectonics and basanite igneous activity. Nd model ages for the spinel peridotite xenoliths range between 0.59 and 0.65 Ga. The xenolith data suggest that eastern Arabian lower crust is of hotspot origin, in contrast to western Arabian lower crust, which mostly formed at a convergent plate margin. Geochemical and isotopic differences between lower crust and upper mantle indicate that these are unrelated, possibly because delamination replaced the E Arabian mantle root in Neoproterozoic time.     

The use of variable body forces to control the depth of towed submersibles

The relationship between the depth and trail attained by a towed submerged vehicle and the magnitude and direction of the forces on it has been examined theoretically, for cases involving faired cables.It is shown that when the body force is varied the body in equilibrium moves on an almost circular path as if the cable were straight, and that depth changes depend primarily upon the change in the component of the body force that acts at right angles to the line joining the top and bottom of the cable.Examples are given which demonstrate that for bodies towed at large depression angles the use of water brakes is more effective in changing depth than the use of lifting wings.The data is presented so that a rapid preliminary assessment can be made of any proposed system to obtain the best combination of speed and scope for achieving a given depth with a body having known lift and drag coefficients.