Ein Computer-Programm zur quantitativen Bestimmung der Keimzahl mittels der Most-Probable-Number (MPN)-Methode

There are explained the statistical fundamentals of the estimation of the number of bacteria by means of the most-probable-number method (MPN method) inclusive of the confidence intervals and the probability of the sample results. On this basis, a program in Turbo-Pascal is prepared for the operating systems C/PM or MS-DOS for the computation of both single MPN estimations and complete tables inclusive of probability and confidence limits, their listing being appended.     

Petrochemistry of eclogites from the Koidu Kimberlite Complex,Sierra Leone

Petrography, mineral and bulk chemistry of upper mantle-derived eclogites (garnet and clinopyroxene) from the Koidu Kimberlite Complex, Sierra Leone, are presented in the first comprehensive study of these xenoliths from West Africa. Although peridotite-suite xenoliths are generally more common in kimberlites, the upper mantle sample preserved in Pipe Number 1 at Koidu is exclusively eclogitic, making this the fifth locality in which eclogite is the sole polymineralic xenolith in kimberlite. Over 2000 xenoliths were collected, of which 47 are described in detail that include diamond, graphite, kyanite, corundum, quartz after coesite, and amphibole eclogites. Grossular-pyrope-almandine garnets are chromium-poor (<0.72 wt% Cr₂O₃) and fall into two distinct groups based on magnesium content. High-MgO garnets have an average composition of Pyr₆₇Alm₂₂Gross₁₁, low-MgO garnets are grossular- and almandine-rich with an average composition of Gross₃₄Pyr₃₃Alm₃₃. Clinopyroxenes are omphacitic with a range in jadeite contents from 7.7 to 70.1 mol%. Three eclogites contain zoned and mantled garnets with almandine-rich cores and pyrope-rich rims, and zoned clinopyroxenes with diopside-rich cores and jadeite-rich rims, and are among a very rare group of eclogites reported on a world-wide basis. The bulk compositions of eclogites have ranges comparable to that of basalts. High-MgO eclogites (16–20 wt% MgO) have close chemical affinities to picrites, whereas low-MgO eclogites (6–13 wt% MgO) are similar to alkali basalts. High-MgO eclogites contain high-MgO garnets and jadeiterich clinopyroxenes. Low-MgO eclogites contain low-MgO garnets, diopside and omphacite, and the group of primary accessory phases (diamond, graphite, quartz after coesite, kyanite, and corundum); grospydites are peraluminous. Estimated temperatures and pressures of equilibration of diamond-bearing eclogites, using the diamond-graphite stability curve and the Ellis and Green (1979) geothermometer, are 1031°–1363° C at 45–50 kb.K _D values of Fe-Mg in garnet and clinopyroxene range from 2.3 to 12.2. Diamonds in eclogites are green, yellow, and clear, and range from cube to octahedral morphologies; the entire spectrum in color and morphology is present in a single metasomatized eclogite with zoned garnet and clinopyroxene. Ages estimated from Sm-Nd mineral isochrons range from 92–247 Ma. _Nd values range from +4.05 to 5.23. Values of specific gravity range from 3.06–3.60 g/cc, with calculated seismic Vp of 7.4–8.7 km/s. Petrographie, mineral, and bulk chemical data demonstrate an overall close similarity between the Koidu xenolith suite and upper mantle eclogites from other districts in Africa, Siberia and the United States. At least two origins are implied byP-T, bulk chemistry and mineral compositions: low-MgO eclogites, with diamond and other accessory minerals, are considered to have formed from melts trapped and metamorphically equilibrated in the lithosphere; high-MgO eclogites are picritic and are the products of large degrees of partial melting, with equilibration in the asthenosphere. Fluid or diluted melt metasomatism is pervasive and contributed here and elsewhere to the LIL and refractory silicate incompatible element signature in kimberlites and lamproites, and to secondary diamond growth.     

Geochemical Constraints of the Ediacaran Volcano-Sedimentary Succession of the Sa’al Metamorphic Complex at Wadi Zaghra, South Sinai, Egypt

The volcano-sedimentary succession around Wadi Zaghra in Sinai, at the northernmost segment of the Arabian Nubian Shield, comprises volcanic rocks interbedded with rather immature sediments. The succession is dominated by intermediate to silicic volcanics of medium-to high-K calc-alkaline affinity. It is divided into two units, the lower unit includes intermediate rocks and dacites interbedded with graywackes, semi-pelites and pelites and topped by polymict conglomerates. This unit is subjected to folding and regional metamorphism(up to garnet zone) and is intruded by quartz diorite-granodiorite inducing, locally, low-pressure contact thermal metamorphism. The unmetamorphosed upper unit encompasses acid volcanics intercalated with litharenite, sublitharenite and minor arenite. The rhyolites of this unit pertain to the highly fractionated granites and are characterized by an agpaitic index(NK/A) ranging from 0.87 to 0.96. They may reflect either extensive interaction of subduction-related magmas with the continental crust or a change in the tectonic regime. The present lithological and geochemical characteristics of the studied sediments together with available zircon ages indicate rather distal provenance of their detritus. This detritus comprises fluvial-alluvial sediments accumulated in the intermontane basins, which are half-grabens or tilted fault blocks. The tectonic setting of the depositional basins is active continental margin and continental island arcs. Geochemical patterns of the Zaghra volcano-sedimentary succession indicate their correlation with the Dokhan Volcanics-Hammamat Clastics sequence of the Eastern Desert of Egypt. Also, the Zaghra volcanics display geochemical similarities with those exposed in Sinai, at the Rutig, Ferani and Iqna Shar'a areas. The Zaghra succession is dated as Ediacaran but is not related either to the ensimatic island arc assemblage or to the rift-related assemblage formed during the early stages of the break-up of Rodinia as previously thought.     

Mineralogical and geochemical patterns of urban surface soils, the example of Pforzheim, Germany

This study presents a combined geochemical and mineralogical survey of urban surface soils. Many studies on urban soils are restricted to purely chemical surveys in order to investigate soil pollution caused by anthropogenic activities such as traffic, heating, industrial processing, waste disposal and many more. In environmental studies, chemical elements are often distinguished as lithogenic and anthropogenic elements. As a novel contribution to those studies, the authors combined the analysis of a broad set of chemical elements with the analysis of the main mineralogical phases. The semi-quantification of mineralogical phases supported the assignment of groups of chemical elements to lithogenic or anthropogenic origin. Minerals are important sinks for toxic elements. Thus, knowledge about their distribution in soils is crucial for the assessment of the environmental hazards due to pollution of urban soils. In Pforzheim, surface soils (0–5 cm depth) from various land use types (forest, agriculture, urban green space, settlement areas of various site densities) overlying different geological units (clastic and chemical sediments) were investigated. Urban surface soils of Pforzheim reflect to a considerable degree the mineral and chemical composition of parent rocks. Irrespective of the parent rocks, elevated concentrations of heavy metals (Zn, Cu, Pb, Sn, Ag) were found in soils throughout the whole inner urban settlement area of Pforzheim indicating pollution. These pollutants will tend to accumulate in inner urban surface soils according to the available adsorption capacity, which is normally higher in soils overlying limestone than in soils overlying sandstone. However, inner urban surface soils overlying sandstone show elevated concentrations of carbonates, phyllo-silicates and Fe and elevated pH values compared with forest soils overlying sandstone. Thus, in comparison to forest soils overlying sandstones, inner urban soils overlying sandstone affected by pollution concurrently possess elevated concentrations of mineral phases typically providing relatively high adsorption capacities for heavy metals.     

Dated Paleontological cave sites of Central Europe from Late Middle Pleistocene to early Upper Pleistocene (OIS 5 to OIS 8)

Caves are terrestrial depositories that preserve a large variety of organic and inorganic remains. These may contain important Quaternary climatic and ecological information. Most of the faunal remains, however, cannot be linked to any Interglacial or Glacial period exclusively. Reliable dating of such remains is therefore required. Experience has, however, shown that ESR dating of speleothems or ²³⁰Th/U dating of bones are of disputable value. Only TIMS-²³⁰Th/U dating of speleothems appears to yield reliable ages. Dating the bottom and top of speleothem layers permit assigning Pleistocene faunal remains to the OIS chronology if the deposition of the speleothems and the faunal remains are clearly correlated. Care must be taken to consider the depositional situation of each site before interpreting any age dates. In this paper we present an overview of all numerically dated paleontological cave sites in Central Europe between OIS 5 and OIS 8. A total of 25 strata were dated from 13 sites, most of them deposited during OIS 5; the rest belonging to OIS 6 and 7. Numerically dated paleontological sites older than OIS 8 are not known.     

Geochemistry of modern seawater and brines from salt pans: Main components and bromine distribution

Seawater at different stages of evaporation from the salt works of Seovlje near Portoro (Yugoslavia) was analyzed geochemically. The seawater there passes through 20 stages of concentration until the first halite crystallizes. All important parameters were determined at all stages: concentrations of Cl, SO₄, Na, K, Ca, Mg, and Br, temperature, pH, Eh, oxygen content and titration alkalinity. With increasing evaporation calcium carbonate crystallizes first followed by calcium sulphate as gypsum and after these halite. All three components crystallize from supersaturated solutions. The pH of the initial seawater is 8.32; it falls abruptly to 6.65 when the first calcium carbonate precipitates. Eh in the original seawater is +393 mv; negative values were found in the halite crystallization pans, which contain an anaerobic mud as a reducing agent. The oxygen content of the solution decreases parallel to the drop in Eh. In the pans in which NaCl crystallizes Eh is zero. Apparently the mud also adsorbs K, as can be inferred from a change in the Mg/K ratio.The bromine partition between crystallizing halite and the brine in the salt pans of Seovlje is discussed with regard to some genetic problems of marine salt deposits. In the conditions in the salt pans the bromine partition coefficient at the beginning of NaCl crystallization from seawater—expressed as b=wt.-% Br (mineral)/wt.-% Br (solution)—is 0.12 to 0.14 or—expressed as D=Br/Cl(mineral)/Br/Cl(solution)—0.030 to 0.034 at temperatures between 33° C and 42° C. The conclusion is that a Br content of about 60 to 75 ppm is to be expected for the first halite that crystallizes from evaporating seawater.     

Einige Probleme bei der Anwendung des MPN-Verfahrens zur quantitativen Salmonellenbestimmung

So far, the MPN technique has been the method chosen for detecting pathogenic bacteria in waters, since it allows us to use larger volumes. In the evaluation, however, comparatively frequently (10 … 15%) nontypical codes occur. The validity of the Poisson model is confirmed for pure cultures by extensive laboratory experiments with pure cultures and controlled mixed cultures. In mixed cultures, however, a comparatively large number of atypical codes occur, since obviously a single organism is not sufficient for the formation of a growth-cover on the test tube, so that the true number of germs may be considerably underestimated. Obviously, the accompanying flora has an inhibiting effect on the salmonella detection.     

On the relationship between vegetation and climate in tropical and northern Africa

Vegetation cover is a crucial component of the Earth’s climate system but, still, our understanding of the mechanisms governing the reciprocal influence between atmosphere and vegetation is limited. In this study, we investigate the unilateral atmospheric impact on vegetation cover in tropical and northern Africa, differentiated into regions with different circulation regimes and into detailed land-cover classes. In contrast to former studies, climate predictors from a regional climate model are used as input for a multiple regression model. Climate models provide consistent data without gaps at high spatial resolution, a considerably larger set of available climate variables and the perspective to transfer the statistical relationships to future projections, e.g., in the context of anthropogenic climate change. Indeed, robust climate predictors which drive up to 70 % of observed interannual vegetation variability could be extracted from the climate model. Besides precipitation and temperature, global radiation, and relative humidity play an important role. The statistical transfer functions are plausible in terms of the affected regions and land-cover classes and draw a rather complex picture of the atmosphere–vegetation relation in Africa.     

Monitoring biological effects of pollution in the Baltic Sea: neglected--but still wanted?

In the Baltic Sea, studies regarding biological effects of contaminants are relatively few, partly due to political and economical reasons, specific hydrographic characteristics, and a strong eutrophication-targeted research focus during the past three decades. The development of a monitoring strategy concerning biological effects and its implementation into environmental monitoring programmes in the Baltic Sea is lagging behind the progress currently taking place in most of western and southern Europe. The pan-European project BEEP (Biological Effects of Environmental Pollution on Marine Coastal Ecosystems, 2001-2004) included the Baltic Sea as one of the target areas for the evaluation of a suite of biological effects indicators in European coastal waters. The main aims of the BEEP project are described and how the expected outcome for the Baltic Sea could provide the needed "baseline" information and expertise for a biological effect monitoring and contribute to harmonise environmental monitoring programmes within the EU.