Beitrag zur Kenntnis der planktisch lebenden Ruderfusskrebse (Crustacea Copepoda) des Engstlensees (Berner Oberland)

Zusammenfassung Eine am 22. September 1969 im 1850 m hoch gelegenen Engstlensee gesammelte Planktonprobe enthielt zwei verschiedene Copepodenarten. Der Diaptomide ist ein Gield der GattungArctodiaptomus. Bereits 1885 ist er aus diesem Gew?sser als neue Artalpinus erw?hnt worden. Sp?tere Forscher haben ihn dann aber—wie alle ?hnlichen Populationen hochgelegener Alpenseen—mit der Speziesbacillifer Koelbel identifiziert. Nach den Ergebnissen vergleichender Untersuchungen des Verfassers istalpinus indessen doch als selbst?ndige Art zu bewerten, die hier zum erstenmal ausführlich beschrieben wird. DerCyclops des Engstlensees wird alsCyclops abyssorum tatricus (Kozminski, 1927) gekennzeichnet.

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Résumé Le 22 septembre 1969, l’auteur a effectué une récolte de faune pélagique dans l’Engstlensee. L’étude de cette récolte a permis de déterminer les deux Copépodes suivants:Arctodiaptomus alpinus (Imhof) etCyclops abyssorum tatricus (Kozminski). Tous les deux sont des Crustacés caractéristiques pour la faune pélagique de beaucoup de lacs élevés des Alpes. Jusqu’à présent, l’Arctodiaptomus alpinus a été nommébacillifer. Mais au cours d’une revision du ?groupebacillifer? du genreArctodiaptomus, l’auteur a constaté que ?bacillifer Koelbel? et ?alpinus Imhof? sont en réalité deux espèces différentes. Les résultats complets de cette revision seront publiés par un autre journal d’hydrobiologie.

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Herrn Prof. OttJaag zum 70. Geburtstag     

Vibrational and thermodynamic properties of Ni<Subscript>3</Subscript>S<Subscript>2</Subscript> polymorphs from first-principles calculations

We have calculated the compressional, vibrational, and thermodynamic properties of Ni₃S₂ heazlewoodite and the high-pressure orthorhombic phase (with Cmcm symmetry) using the generalized gradient approximation to the density functional theory in conjunction with the quasi-harmonic approximation. The predicted Raman frequencies of heazlewoodite are in good agreement with room-temperature measurements. The calculated thermodynamic properties of heazlewoodite at room conditions agree very well with experiments, but at high temperatures (especially above 500 K) the heat capacity data from experiments are significantly larger than the quasi-harmonic results, indicating that heazlewoodite is anharmonic. On the other hand, the obtained vibrational density of states of the orthorhombic phase at 20 GPa reveals a group of low-frequency vibrational modes which are absent in heazlewoodite. These low-frequency modes contribute substantially to thermal expansivity, heat capacity, entropy, and Grüneisen parameter of the orthorhombic phase. The calculated phase boundary between heazlewoodite and the orthorhombic phase is consistent with high-pressure experiments; the predicted transition pressure is 17.9 GPa at 300 K with a negative Clapeyron slope of −8.5 MPa/K.     

Geochronology and sedimentology of the lower Passaic River,New Jersey

In an attempt to characterize localized rates of sediment accretion, 10 sediment cores were collected from the lower reach of the Passaic River, a major tributary of Newark Bay, New Jersey. Sediments were assayed for ²¹⁰Pb activity at predetermined depths and the rate of sediment accretion (cm yr^?1) was estimated from the least squares regression of the log of unsupported activity versus depth. Sediment accretion rates, derived from ²¹⁰Pb measurements (R_Pb) were used to predict the depth interval within the core containing sediments deposited around 1954; subsequent ¹³⁷Cs analyses were focused on this depth interval. Sediment accretion rates derived from ¹³⁷Cs measurements (R_Cs) were extrapolated from the depth of the 1954 horizon. Lead-210 derived sediment accretion rates in cores collected from a sediment bench extending along the inside bend on the southern shore of a meander in the river, ranged from 4.1 cm yr^?1 to 10.2 cm yr^?1 and averaged 6.8 cm yr^?1. The R_Cs estimates for cores from this area ranged from 3.8 cm yr^?1 to 8.9 cm yr^?1 and averaged 6.6 cm yr^?1. The R_Cs for cores collected in a more hydrologically dynamic reach of the river upstream of the sediment bench, were only 0.41 cm yr^?1 and 0.66 cm yr^?1. The results of this investigation indicate that this reach of the lower Passaic River is an area of high sediment accumulation, retaining much of the sediment load deposited from upstream and downstream sources. The rates of sediment accretion in the lower Passaic River are among the highest reported anywhere in the Newark Bay estuary.     

Transmission electron microscopic study of antiphase domains in CaAl2Ge2O8-Feldspar

Transmission electron microscopic study of synthetic CaAl₂Ge₂O₈-feldspar revealed two types of antiphase domains: type “b”-antiphase domains with the displacement vector 1/2 [110] and type “c”-antiphase domains with the displacement vector 1/2 [111]. The “b”-domains were on the order of 0.1 μm in size, while the “c”-domains displayed wall to wall distances mostly between 0.1 and 1 μm. The formation of the two types of antiphase domains is due to reductions in translational symmetry associated with the phase transitions \(C\bar 1 \to I\bar 1 \to P\bar 1\) . The antiphase domain textures of CaAl₂Ge₂O₈-feldspar are very similar to the textures found in natural and synthetic anorthite, CaAl₂Si₂O₈.     

Refractory- and metallurgical-type chromite ores,Zambales ophiolite,Luzon, Philippines

The Zambales ophiolite is the major source of chromite ore in the Philippines. The chromitites are concordant cumulates and are associated with distinct chromitite-bearing sequences within the mantle peridotites. Refractory and metallurgical chromite deposits are spatially separated and related to different lithologic associations, which crystallized from different parental magmas. — Refractory chromite ores (30–44 wt% Cr₂O₃; 20–30 wt% Al₂O₃) are linked with the peridotite-troctolite-olivine gabbro lineage. Two main types were found: (1) Al-rich refractory ores associated with harzburgites and feldspathic periodotites and (2) more Cr-rich varieties associated with lherzolites. — Metallurgical chromite ores (45–53 wt% Cr₂O₃; 12–18 wt% Al₂O₃) are linked with the peridotite-pyroxenite-norite lineage. Two main types were also found: (1) Cr-rich metallurgical ores associated with orthopyroxenites and (2) more Al-rich varieties related to clinopyroxenites. — The chemical composition of chromite within the deposits varies depending on the chromite/silicate ratios of the ore types and grades continuously into accessory chrome spinels in the wall-rock peridotites. — The geochemistry of accessory chrome spinels in various peridotites and mafic cumulates depends on the mineralogical composition and the stratigraphic position of their host rocks.New address: BEB Erdgas und Erdöl GmbH, Riethorst 12, D-3000 Hannover 51The terms chrome-spinels and chromite are used as follows: 1. Chrome-spinel is only used for those occuring as accessory minerals in various ultramafic and mafic rocks (= accessory chrome-spinels). Their chemical composition has been determined only by microprobe analysis. — 2. Chromite is used for ore and ore deposits (=chromitites); the chemical composition has been determined by wet chemistry (AAS) or by microprobe analysis     

Redistribution of HFSE elements during rutile replacement by titanite

Titanite growth at the expense of rutile during retrograde hydration of eclogite into amphibolite is a common phenomenon. We investigated an amphibolite sample from the Tromsø eclogite facies terrain in Northern Norway to gain insight into the trace element distribution between rutile and titanite during incomplete resorption of the rutile by titanite. Patchy compositional zoning of Al, Ti, and F in titanite relates to the presence of a fluid with variable Ti/Al and/or F during its growth. Laser ablation ICP–MS and electron microprobe data for high field strength elements (HFSE: Nb, Zr, Ta, and Hf) of rutile resorbed by titanite indicate a pronounced enrichment of these elements in the rim of a large single rutile crystal (~8 mm) and a systematic decrease towards uniform HFSE contents in the large core. HFSE contents of smaller rutile grains (~0.5 mm) and rutile inclusions (<100 μm) in the titanite overgrowth are similar or higher than in the rims of large rutile crystals. Element profiles from the rim inward demonstrate that HFSE enrichment in rutile is controlled by diffusion. HFSE ratios in diffusion-altered rutile show systematic variations compared with the uniform core composition of the large rutile. Modelling of Zr and Nb diffusion in rutile indicates that diffusion coefficients in rutile in fluid-dominated natural systems must be considerably higher than those determined experimentally at 1 bar in dry systems. Variations of HFSE contents in the newly formed titanite show no systematic spatial distribution. HFSE ratios in titanite and the rims of rutile are different, indicating different solid/fluid distribution coefficients in these minerals. Element fractionation by diffusion into the relict rutile and during fluid-mediated growth of new titanite could substantially change the HFSE budget of these minerals and could affect their use for geochemical tracing and other applications, such as Zr-based geothermobarometry.     

Geology, geochemistry and petrogenesis of intrusive rocks of the Wallagga area, western Ethiopia

Crystalline rocks from the western Ethiopian Precambrian terrain comprise two major rock groups: (1) the often migmatised eastern and western high-grade gneisses; and (2) the central low-grade metavolcanosedimentary rocks. Granitoid bodies of different ages and compositions intrude these rocks. Field observations, petrographic investigations, and geochemical features support a two-fold classification of the granitoid rocks. The volcanic arc granitoids (VAG) are most common and include the Ujjukka granite and granodiorite, and the Dhagaa Booqa and Guttin K-feldspar megacrystic granites. The second and geographically more restricted group represents within-plate or anorogenic (A-type) granitoids, typified by the Tullu Kapii syenite. Geochemically, the Tullu Kapii syenite is characterised by moderate to high contents of SiO₂, total alkalis, Y, Nb, Ta, Hf, Zn, Zr, Ga, ΣREE, higher ratios of Fe₂O_3(total)/MgO, , , and lower contents of CaO, MgO, Sr, and Ba, compared to the other granitoids. The VAG group shows chondrite-normalised REE patterns with slightly enriched LREE and flat HREE patterns without significant Eu anomalies. In contrast, the Tullu Kapii A-type granitoid is characterised by a nearly horizontal REE pattern with variable negative Eu anomalies. The Ujjukka granite and granodiorite; and the Dhagaa Booqa and Guttin K-feldspar megacrystic granites originated in a two-step process, which involves batch equilibrium melting of basaltic or andesitic material producing tonalitic magma, followed by fractional crystallisation. The Tullu Kapii syenite was the product of partial melting of source rocks enriched in high field strength elements.     

Public policy and the changing landscape

The paper illustrates how spatially explicit forecasting of residential development can be undertaken and how it can be made sensitive to policy instruments available to local and state governments. Predicted values in residential use based on a hedonic analysis of residential property prices is found to have a significant effect on the hazard of development in a survival model used to explain the likelihood that a farm or forest will be converted to residential use. Policy instruments are imbedded in both the hedonic model of residential property values and a hazard model of parcel conversion, so as to test how effective changes in policies can be at changing the pattern of land-use change. Some of the statistical and modeling obstacles that impede progress on this spatially explicit modeling are also discussed.     

Diffusion-limited REE uptake by eclogite garnets and its consequences for Lu–Hf and Sm–Nd geochronology

Garnets from the Zermatt-Saas Fee eclogites contain narrow central peaks for Lu + Yb + Tm ± Er and at least one additional small peak towards the rim. The REE Sm + Eu + Gd + Tb ± Dy are depleted in the cores but show one prominent peak close to the rim. These patterns cannot be modeled using Rayleigh fractionation accompanied by mineral breakdown reactions. Instead, the patterns are well explained using a transient matrix diffusion model where REE uptake is limited by diffusion in the matrix surrounding the porphyroblast. Observed profiles are well matched if a roughly linear radius growth rate is used. The secondary peaks in the garnet profiles are interpreted to reflect thermally activated diffusion due to temperature increase during prograde metamorphism. The model predicts anomalously low ¹⁷⁶Lu/¹⁷⁷Hf and ¹⁴⁷Sm/¹⁴⁴Nd ratios in garnets where growth rates are fast compared to diffusion of the REE, and these results have important implications for Lu–Hf and Sm–Nd geochronology using garnet.     

Unusual exsolution phenomena in omphacite and partial replacement of phengite by phlogopite + kyanite in an eclogite from the Erzgebirge

In the Erzgebirge Crystalline Complex, eclogites occur in three different high pressure (HP) units (1, 2 and 3) recording contrasting pressure (P)–temperature (T) conditions. Eclogites from HP-unit 1 experienced peak metamorphic conditions in the coesite stability field at about 33 kbar/850 °C. Commonly, these eclogites from HP-unit 1 are all very similar, with an eclogitic peak assemblage of omphacite–garnet–coesite–K-feldspar, rarely accompanied by kyanite, and omphacites systematically deviating from a stoichiometric composition. In contrast, an eclogite recently found near Blumenau, is mineralogically and geochemically different from the typical eclogites of HP-unit 1. This unusual eclogite reveals the eclogitic equilibrium assemblage omphacite–garnet–coesite–phengite–phlogopite–kyanite, and yields metamorphic peak conditions of 870 °C and >29 kbar. There is clear textural evidence of the formation of phlogopite and kyanite under partial consumption of phengite and garnet. Moreover, the omphacite is stoichiometric and contains abundant exsolution lamellae, the thickest of which were identified as quartz by the electron microprobe. The finer lamellae were studied by transmission electron microscopy (TEM). Oligoclase was identified as an exsolution phase. Other lamellae proved to consist of K-white mica, also interpreted as exsolution. Prior to exsolution, the omphacite composition must have been cation-deficient, as that of the other, common HP-unit 1 eclogites. These non-stoichiometric compositions are ascribed to partial substitution by the Ca-Eskola pyroxene component, which calculates to an average of 8 mol% for omphacite in HP-unit 1 eclogites. According to experiments, this substitution becomes significant at P > 30 kbar. Exsolution of K-white mica may indicate hydroxyl defects in the original omphacite, also favoured by high pressure. Oligoclase and K-white mica exsolution from Ca-Eskola-rich clinopyroxene has not previously been reported. The omphacite has a disordered C2/c structure; and in just one case very small (a few tens of nanometres) antiphase domains, resulting from the C2/c to P2/n transformation, are present. These features may indicate a brief thermal history and rapid tectonic processes. Received: 4 January 1999 / Accepted: 20 April 2000