PMSE observations at three different frequencies in northern Europe during summer 1994

Simultaneous observations of polar mesosphere summer echoes (PMSE) have been carried out during summer 1994 in northern Norway using three radars on different frequencies: the ALOMAR SOUSY radar at Andenes on 53.5 MHz, the EISCAT VHP radar at Tromsø on 224 MHz and the MF radar at Tromsø on 2.78 MHz. During the common measuring period in July/August 1994, PMSE could be detected at 224 and 53.5 MHz, and there are strong hints that PMSE also occur at 2.78 MHz. Reliable correlations between hourly backscattered power values indicate that the PMSE structures have zonal extensions of more than 130 km and can be detected at very different scales (half wavelength) between 0.67 (EISCAT VHP radar) and 54 m (MF radar). Using the wind values derived by the MF radar it can be shown that the mesospheric wind field influences the structure of PMSE. The diurnal variation of PMSE is strongly connected with tidal-wind components, whereas spatial differences of PMSE can partly be explained by the mean wind field.     

Carbon and Strontium Isotopes of Late Palaeozoic Marine Carbonates in the Upper Yangtze Platform,Southwest China

238 marine carbonate samples were collected from seven sedimentary sections ofthe entire late Palaeozoic (Permian, Carboniferous and Devonian) in the Upper Yangtze Plat-form, southwest China. Based on the absence of cathodoluminescence and very low Mn (gener-ally<50 ppm) contents of the samples, it is thought that they contain information on the orig-inal sea water geochemistry. The results of isotopic analyses of these samples are presented interms of δ~(13)C and ~(87)Sr/~(86)Sr ratios versus geological time. The strontium data, consistent withother similar data based on samples from North America, Europe, Africa and other areas inAsia, support the notion of a global consistency in strontium isotope composition of marinecarbonates. The strontium data exhibit three intervals of relatively low ~(87)Sr/~(86)Sr ratios in thelate Middle Devonian to early Late Devonian, Early Carboniferous and Early Permian, corre-sponding to global eustatic high sea level stands. The lowest ~(87)Sr/~(86)Sr ratio recorded in theLate Permian was probably caused by substantial basalt eruptions in the Upper Yangtze Plat-form at the time. Three corresponding periods of relatively high δ~(13)C values at roughly the samethe intervals were caused by a relatively high rate of accumulation of organic carbon duringsea level rises at these times. The deposition of coal was probably responsible for the increaseof sea water δ~(13)C at other times. The δ~(13)C values drop dramatically near theDevonian/Carboniferous, Carboniferous/Permian and Permian/Triassic boundaries, con-sistent with other similar data, which further support the notion that geological time boundariesare associated with mass extinction and subsequent rejuvenation.     

Post-collisional potassic granitoids from the southern and northwestern parts of the Late Neoproterozoic East African Orogen: a review

Potassic metaluminous granitoids with enrichments of HFS elements constitute part of widespread post-collisional magmatism related to the Late Neoproterozoic Pan-African orogeny in northeastern Africa (Sudan, Ethiopia, Somalia) and Madagascar. The plutons were emplaced between 580 and 470 Ma and comprise both subsolvus and hypersolvus biotite–granite, biotite–hornblende–granite, quartz–monzonite and quartz–syenite. Pyroxene-bearing granitoids are subordinate. Basic dikes and enclaves of monzodioritic composition are locally associated with the granitoid plutons. Granitoids emplaced in pre-Neoproterozoic crust have Sr_i-ratios between 0.7060 and 0.7236 and _Nd(t) values between −15.8 and −5.6 while those emplaced in, or close to the contact with, juvenile Neoproterozoic crust have lower Sr_i-ratios (0.7036–0.7075) and positive _Nd(t) values (4.6). However, it is unlikely that the potassic granitoids represent products of crustal melting alone. The association with basic magmas derived from subduction-modified enriched mantle sources strongly suggests that the granitoids represent hybrid magmas produced by interaction and mixing of mantle and crust derived melts in the lower crust. The most intense period of this potassic granitoid magmatism occurred between 585 and 540 Ma, largely coeval with HT granulite facies metamorphism in Madagascar and with amphibolite facies retrogression in northeastern Africa (Somalia, Sudan). Granitoid magmatism and high-grade metamorphism are probably both related to post-collisional lithospheric thinning, magmatic underplating and crustal relaxation. However, the emplacement of potassic granites continued until about 470 Ma and implies several magmatic pulses associated with different phases of crustal uplift and cooling. The potassic metaluminous granites are temporally and spatially associated with post-collisional high-K calc-alkaline granites with which they share many petrographical, geochemical and isotopical similarities, except the incompatible element enrichments. The resemblance indicates a strongly related petrogenesis of both granite associations.     

Rare-metal pegmatites of Wamba,central Nigeria - their formation in relationship to late Pan-African granites

he Sn-(Nb, Ta) mineralization of the Wamba field (central Nigeria) occurs in muscovite-quartz-microcline pegmatites, which are related to the late-orogenic Pan-African (f 550 Ma) "Older Granites". The emplacement of granites and pegmatites was controlled by late Pan-African shear tectonics. The granitoid magmatism was multiphase and has produced peraluminous biotite granite, biotite-muscovite granite, and muscovite granite plutons. Sodic metasomatism has altered highly evolved granite cupolas and many of the pegmatite dikes. The pegmatitic mineralization of predominantly cassiterite is closely associated with albitization. Chemical data of granites and granitic and pegmatitic muscovites show that Rb, Cs, Sn, Nb, and Ta are enriched during both magmatic and postmagmatic evolution, with highest contents of these elements in early muscovites of the albitized and mineralized pegmatites. Trace-element chemistry of the pegmatitic muscovites reveals a chemical zonation of the pegmatite field related to the late-orogenic shear system.     

Origin and composition of organic matter in tidal flat sediments from the German Wadden Sea

Two sediment cores of up to 550 cm length from an intertidal flat of the German Wadden Sea near the island of Spiekeroog were investigated for the quantity and composition of fossil organic matter (OM). The lowermost parts of the cores are dominated by grey mud of a salt marsh facies containing mainly terrestrial OM estimated to account for 60–75% of the total OM, based on δ¹³C values and the ratio of short to long chain n-alkanols. The terrigenous origin of the dominant fraction is indicated, among others, by high proportions of C₂₉ sterols and long chain n-alkanes typical of plant waxes. Coarse shell beds overlying the grey mud at 2–2.5 m depth represent a flooding and erosion event possibly related to heavy storm floods in the Middle Ages. Within the intertidal sand-dominated sediments in the upper parts of the cores total organic carbon (TOC) contents are generally low, ranging from 0.1% to 0.5%, and correlate well with the amount of mud fraction (r² 0.90). At the surface, marine OM has not undergone intense diagenetic alteration and so is the dominant fraction. Eroded peat particles are common throughout most of the sequence and values of the Phragmites peat indicator (PPI) > 5 indicate an origin from reed peat due to a high relative abundance of the n-C₂₄ alkane. Changes in the composition of microbial communities over the depth interval investigated are documented by varying compositions of unsaturated fatty acids with 16 and 18 carbons. Eicosapentaenoic acid (EPA) was detected along the entire cores and indicates the presence of EPA-producing bacterial strains.     

Redox sensitivity of P cycling during marine black shale formation: Dynamics of sulfidic and anoxic, non-sulfidic bottom waters

A high-resolution geochemical record of a 120 cm black shale interval deposited during the Coniacian-Santonian Oceanic Anoxic Event 3 (ODP Leg 207, Site 1261, Demerara Rise) has been constructed to provide detailed insight into rapid changes in deep ocean and sediment paleo-redox conditions. High contents of organic matter, sulfur and redox-sensitive trace metals (Cd, Mo, V, Zn), as well as continuous lamination, point to deposition under consistently oxygen-free and largely sulfidic bottom water conditions. However, rapid and cyclic changes in deep ocean redox are documented by short-term (∼15-20 ka) intervals with decreased total organic carbon (TOC), S and redox-sensitive trace metal contents, and in particular pronounced phosphorus peaks (up to 2.5 wt% P) associated with elevated Fe oxide contents. Sequential iron and phosphate extractions confirm that P is dominantly bound to iron oxides and incorporated into authigenic apatite. Preservation of this Fe-P coupling in an otherwise sulfidic depositional environment (as indicated by Fe speciation and high amounts of sulfurized organic matter) may be unexpected, and provides evidence for temporarily non-sulfidic bottom waters. However, there is no evidence for deposition under oxic conditions. Instead, sulfidic conditions were punctuated by periods of anoxic, non-sulfidic bottom waters. During these periods, phosphate was effectively scavenged during precipitation of iron (oxyhydr)oxides in the upper water column, and was subsequently deposited and largely preserved at the sea floor. After ∼15-25 ka, sulfidic bottom water conditions were re-established, leading to the initial precipitation of CdS, ZnS and pyrite. Subsequently, increasing concentrations of H₂S in the water column led to extensive formation of sulfurized organic matter, which effectively scavenged particle-reactive Mo complexes (thiomolybdates). At Site 1261, sulfidic bottom waters lasted for ∼90-100 ka, followed by another period of anoxic, non-sulfidic conditions lasting for ∼15-20 ka. The observed cyclicity at the lower end of the redox scale may have been triggered by repeated incursions of more oxygenated surface- to mid-waters from the South Atlantic resulting in a lowering of the oxic-anoxic chemocline in the water column. Alternatively, sea water sulfate might have been stripped by long-lasting high rates of sulfate reduction, removing the ultimate source for HS⁻ production.     

Glaukonit aus der Regensburger Oberkreideformation

Some of the upper cretaceous sedimentary rocks near Regensburg, Germany, are rich in glauconite pellets of 63–200µ diameter. The clay fractions < 2µ of the same rocks are rich in glauconite-mica too.X-ray analysis, chemical analysis and petrographical tests show that, the glauconite pellets must be excrements of marine animals which took up glauconite-mica from sea-bottom.The glauconite materials from these rocks are 1M-micapolymorphs. A comparison of this glauconite with 1M-glauconites cited in literature by other authors shows close aggreement in K₂O/MgO- and K₂O/Fe₂O₃ ratios. Within the range of analytical errors the structure formulae of all these 1M-glauconites differ from one another only by the oxidation ratio of iron and — corresponding to this ratio — by the aluminum contents of the octahedral lattice layer. The differences of the 1M-glauconites in octahedral layer populations may due to different redox potentials during glauconite formation or to oxidation during rock diagenesis or rock weathering later on.In a similar manner 1Md-polymorphs of glauconite-mica may have developed from 1M-glauconite by oxidation of iron and corresponding removement of K⁺ and (H₃O)⁺ ions from interlayer lattice positions.     

Contrasting responses of dimictic and polymictic lakes to environmental change: a spatial and temporal study

Although comparative analyses between dimictic and polymictic lakes have noted the key role of mixing regime in governing water quality, limnologists have historically focused on dimictic lakes, leaving polymictic lakes relatively understudied. In this study, we investigated whether the effects of agricultural development on water quality differed between dimictic and polymictic lakes in a naturally nutrient-rich region of Alberta, Canada. Through a spatial limnological analysis of 36 sites, we found that the relationship between surface water total phosphorus concentration and the percent of agriculture (% Agr) in the catchments differed between dimictic and polymictic lakes, where the proportion of variance explained was much more pronounced in the dimictic (79% explained) than in the polymictic systems (7% explained). Paleolimnological analyses of subfossil chironomids in surface sediment samples (0–1 cm) from 18 of the 36 study lakes, and in sediment core profiles from the dimictic and polymictic basins of a eutrophic lake, showed that water quality differed between mixis groups. We found that the surface sediment chironomid assemblages differed significantly between polymictic and dimictic lakes. Detailed analyses of the sediment cores demonstrated that the two basin types differed in their responses to land-use change through time, as only the dimictic basin showed a parallel increase in anoxia with increasing agricultural development. We suggest that in naturally-fertile landscapes, external nutrient loading exerts a more notable effect on dimictic lakes, whereas internal nutrient loading is more important in polymictic systems.