64 resultados para ddc: N3983


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In this article the sand-/gravelbodies from Hausberge-Veltheim and Krankenhagen- Möllenbeck in the Wesertal are described and compared considering their depositional and architectural regime. A scenario is developed to explain the genetic sequence of the deposits. The sand-/gravel-body exposed at Krankenhagen-Möllenbeck was deposited first in form of a marginal käme. Subsequently during the Drenthe-stade of the Saale ice age, the sedimentation of the sand- /gravelbody at Hausberge-Veltheim took place under the depositional environment of an end- moraine.

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Biographie und Danksagung an Johann Peter Groetzner

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Am Osthang des Eggegebirges zwischen Horn-Bad-Meinberg und Langeland ist der Lias vom Hettangium bis zum Sinemurium in meist lückenhaften Aufschlüssen erhalten. Aus den Teilprofilen wurde in dieser Arbeit ein Normalprofil zusammengestellt. Die Liasschichten sind ihrer beckenrandnahen Lage entsprechend kalkig, mergelig und tonig mit unterschiedlich hohen Anteilen von terrigenem Detritus ausgebildet. Aufgrund lithologischer Unterschiede wurden verschiedene Gesteinstypen klassifiziert und beschrieben und das Normalprofil in fünf petrographische Abschnitte unterteilt. Die orthostratigraphische Einstufung erfolgte mit Ammoniten.

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This article is a first summary of the heavy-mineral content of moraine and meltwater deposits of the Saalian glaciation in the Münsterland and its northeastern extension (NW Germany). In the beginning the appearance and distribution of both types of sediments are described (E. Speetzen), then the heavy mineral composition of selected outcrops is reported and the results are compared (D. Henningsen). Generally the predominant heavy minerals are garnet, minerals of the epidote group, zircon, and ordinary hornblende. The heavy mineral contents of moraine sediments sometimes are similar to that of meltwater deposits, in other cases they are different. Obviously there exists no relation between the heavy mineral composition and various advances of the Scandinavian ice sheet and their sediments, the content of heavy minerals rather depends on local influences.

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Aus der crenistria-Zone (Subzone des Goniatites crenistria crenistria = cu III alpha3) von Lautenthal (Ober-Harz) werden zwei Arten von ArchegonusJ(Latibole) G.& R.HAHN, 1969 beschrieben und abgebildet: Archegonus (Latibole) laevicauda laevicauda (SARRES, 1857) und Archegonus (Latibole) n.sp.L. Es ist der erste Nachweis dieser Untergattung aus dem Harz. Hinter A. (Latibole) n.sp.L verbirgt sich sehr wahrscheinlich eine neue Art, die aber infolge des z.Zt. noch zu geringen Materials noch nicht ausreichend gekennzeichnet werden kann.

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Digital data from various scientific fields is stored in separate information systems („FIS geology“, „FIS pedology“, etc.) in the Lower Saxony Geo-Information System NIBIS so that it can be processed and interpreted; this is necessary to meet increasing demand for soil-relevant information for decision-making and planning purposes. The necessary work will be considerably accelerated and its quality improved by setting up and actually using such a tool. A detailed account is given of the Lower Saxony Geo-Information System NIBIS, in particular how the data base is set up and how the NIBIS is used in cases where concrete problems occured.

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The vertical distribution pattem of mesofaunal elements is described from clay-marl bedding rhythms from the Frielingen section (Hannover, NW Germany), which exposes latest Hau- terivian sediments (early Cretaceous). Some mesofaunal groups show a correlation with the pale- dark bedding rhythms. The pale, marly beds are chracterised by bryozoans. In addition remnants of crinoids, echinoids, asteroids, ophiuroids and holothuroids are more common in pale layers than in dark ones. Converseley, the relative abundance of serpulids, fish remains, bivalves and gastropods shows no relationship to the bedding rhythms.

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The Gorleben salt dome is actually investigated for its suitability as a repository for radioactive waste. It is crossed by a subglacial drainage channel, formed during the Elsterian glaciation (Gorleben channel). Some units of its filling vary strongly in niveau and thickness. Lowest positions and/or largest thickness are found above the salt dome. This is interpreted as a result of subrosion during the Saalean glaciation. The rate can be calculated from niveau differences of sediments formed during the Holsteinian interglacial. However, their position might have been influenced by other factors also (relief of the channel bottom, glacial tectonics, settlement of underlying clay-rich sediments). Their relevance was estimated applying statistical techniques to niveau and thickness data from 79 drillings in the Gorleben channel. Two classes of drillings with features caused by either Saalean subrosion or sedimentary processes during the filling of the Gorleben channel can be distinguished by means of factor and discriminant analysis. This interpretation is supported by the results of classwise correlation and regression analysis. Effects of glacial tectonics on the position of Holsteinian sediments cannot be misunderstood as subrosional. The influence of the settlement of underlying clay sediments can be estimated quantitatively. Saalean subrosion rates calculated from niveau differences of Holsteinian sediments between both classes differ with respect to the method applied: maximum values are 0,83 or 0,96 mm/a, average values are 0,31 or 0,41 mm/a.

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The Late Glacial and Holocene landscape development in the vicinity of the River Elbe near Neuhaus, Lower Saxony, was studied during geological mapping of the area. The geological and geobotanical methods used in these investigations were chosen to cope with the difficulties which arise during research on Quaternary flood plains in low country. Paleochannel fill and areas of flood-plain sediments were drilled, the lithology examined, and the sediments dated on the basis of their pollen content. No evidence was found for the existence before the Middle Ages of paleo- channels the size of the present River Elbe. Before the first measures were made to regulate the Elbe River, it was an anastomosing river system with numerous small branches. The lower parts of the flood-plain profiles are predominantly sand and the upper parts silty-clayey loam. With the construction of effective levees over the last several centuries, the flow velocity of the Elbe has increased considerably during high water periods and instead of the deposition of meadow loam, sand was deposited as natural levees. The main belt of sand dunes on the east bank of the Elbe overlies Preboreal to Boreal lake mud and is, therefore, of Holocene age.

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3400 pyritized internal moulds of Upper Devonian, Triassic, Jurassic and Lower Cretaceous ammonoids show various soft tissue attachment structures. They are preserved as regularly distributed black patterns on the moulds. All structures can be interpreted as attachment areas of muscles, ligaments and intracameral membranes. Paired structures are developed along the umbilicus and on the flanks of the moulds, unpaired ones appear on the middle of their dorsal and ventral sides. Strong lateral muscles cause paired twin lines on the flanks of the phragmocone and of the body chamber. A ventral muscle is deduced from small rounded or crescent shaped spots in front of each septum on the ventral side. These spots are often connected, forming a band-like structure. Broad dark external bands on the ventral side of the phragmocone, ventral preseptal areas in the posterior part of the living chamber, small twin lines or oval shaped areas on the ventral side of the living chamber represent paired or unpaired attachment areas of the hyponome muscle. A middorsal muscle is documented by small roughened areas in front of each dorsal lobe. Dark spots along the umbilicus, often connected and thus forming a band-like structure (tracking band), are remains of a pair of small dorsolateral muscles at the posterior end of the soft body. Dark bands, lines and rows of small crescent shaped structures behind the tips of sutural lobes are due to spotlike fixation places of the posterior part of the mantle and their translocation before subsequent septal secretion. Devonian goniatites had a paired system of lateral and ventrolateral muscles preserved on the moulds as black or incised lines on the flanks of the living chamber and as dark preseptal areas, ventrally indented. These structures represent the attachment areas of paired lateral cephalic and paired ventral hyponome retractors. Fine black lines on the phragmocone situated parallel to the sutures (pseudosutures) represent a rhythmical secretion of camera! membranes during softbody translocation. Goniatites had a paired system of lateral and ventrolateral muscles, whilst Neoammonoids have a paired lateral and dorsolateral system, and, additionally, an unpaired system on the ventral and on the dorsal side. Mesoammonoids show only a paired lateral and an unpaired dorsal one. Fine black lines situated parallel to the saddles and behind the lobes of the suture line can be interpreted as structures left during softbody translocation and a temporary attachment of rhythmical secreted cameral membranes. Cameral membranes had supported the efficiency of the phragmocone. Only some of the observed structures are also present in recent Nautilus. Differences in the form and position of attachment sites between ammonoids and recent Nautilus indicate different soft body organizations between ammonoids and nautiloids. The attachment structures of goniatites especially of tornoceratids can be compared with those of Nautilus which indicates Richter - Gewebeansatz-Strukturen bei Ammonoideen 3 a comparable mode of life. Differences in the form and position of attachment structures between goniatites and ammonites may indicate an increasing differentiation of the muscular system in the phylogeny of this group. Different soft body organization may depend on shell morphology and on a different mode of life. On the modification or reduction of distinct muscle systems ammonoids can be assigned to different ecotypes. Based on shell morphology and the attachment areas of cephalic and hyponome retractor muscles two groups can be subdivided: - Depressed, evolute morphotypes with longidome body-chambers show only small ventral hyponome retractor muscles. Lateral cephalic retractors are not developed. These morphotypes are adapted to a demersal mode of life. Without strong cephalic retractor muscles no efficient jet propulsion can be produced. These groups represent vertical migrants with efficient phragmocone properties (multilobate sutures, cameral membranes, narrow septal spacing). - Compressed, involute moiphotypes with brevidome body-chambers show strong cephalic and hyponome retractor muscles and represent a group of active swimmers. These morphotypes were able to live at different depths, in the free water column or/and near the seafloor. They are not confined only to one habitat. Most of the examined genera and species belong to this group. Changes of the attachment structures in the course of ontogeny confirm that juveniles of Amaltheus and Quenstedtoceras lived as passive planche drifters in upper and intermediate parts of the free water column after hatching. At the end of the juvenile stage with a shell diameter of 0,3 - 0,5 cm cephalic retractor muscles developed. With the beginning of an active swimming mode of life (neanic stage) the subadult animals left the free water column and moved into shallow water habitats. Fuciniceras showed no marked changes in the attachment structures during ontogeny. This indicates that there occur no differences in the mode of life between juvenile and adult growth stages. Based on attachment structures and shell morphology of Devonian goniatites their relation to the systematic position permits statements about probable phylogenetic relationships between the Cheiloceratidae and Tornoceratidae. In some cases attachment structures of ammonites permit statements about phylogenetic relationships on family and genus level.

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The hydrodynamics and hydrochemistry of salt and fresh water from solid rock aquifer systems in the Pyrmont area are described and interpreted on the basis of recent investigations including geoelectrics, isotope hydrology, soil air analysis. Theories on the source of the springs in this area are developed, which explain the different compositions of the springs and make it possible to protect them. Data from new and re-interpretated drill holes, borehole logs and outcrops suggest a revision of the geological structure of the Pyrmont dome. Bad Pyrmont is situated on a wide dome of Triassic rocks in the southern part of the Lower Saxony uplands. Inversion of the relief has caused the development of an erosional basin surrounded by prominent ridges. Deep faults developed at the crest of the dome as this part of the structure was subjected to the strongest tectonic stress. Subrosion of the Zechstein salts in the western part of the dome has caused the main salt bed to wedge out below the western part of the dome along a N-S striking structure; this structure is refered to as the „Salzhang“ (salt slope). West of the „Salzhang“, where subrosion has removed the salt bed that prevents gas rising from below, carbon dioxide of deep volcanic origin can now rise to the surface. Hydraulic cross sections illustrate the presence of extensive and deep-seated groundwater flow within the entire Pyrmont dome. While groundwater flow is directed vertically downwards in the ridges surrounding the dome, centripetal horizontal flow predominates the intermediate area. In the central part of the dome, groundwater rises to join the River Emmer, which is the main receiving water course in the central part of the eroded basin. The depth of the saltwater/freshwater interface is determinated by the weight of the superimposed freshwater body. Hydrochemical cross sections show the shape and position of the interface and document a certain degree of hydrochemical zonation of the gently mineralized fresh water. Genetic relationships between the two main water types and the hydrochemical zones of the freshwater body are discussed. The knowledge of the hydrogeological relationship in the Bad Pyrmont aquifer systems permits a spatially narrow coexistence of wells withdrawing groundwater for different purposes (medicinal, mineral, drinking and industrial water).

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In this study the conodont multielement apparatus of Late Devonian (Famennian) Icriodus altematus is described which has been reconstructed from clustered group findings and separated elements. This apparatus is markedly different from classical ozarkodinid apparatuses and needs further consideration of its functional morphology. Since bedding plane assemblages of Icriodus altematus are yet unknown, a spatial reconstruction of this apparatus and a feeding mechanism are proposed which are based on the oropharyngal apparatus of recent lampreys. Though the extant representatives of petromyzontoids are not close phylogenetic relatives of extinct conodonts, there exist intriguing analogies concerning the morphology of the tooth types and the presumed spatial distribution within the oral cavity of both taxa.

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The Hainholz quarry in the Osterwald hills of NW-Germany is the most impressive outcrop in the Lower Saxony Basin exposing Late Jurassic (Korallenoolith, Oxfordian) coral buildups. The Korallenoolith deposits in the quarry commence with a oolitic sequence about 20 m thick which is limited by a distinctive hardground at its top. This sequence is overlain by the so called “Obere Korallenbank”-Member about 13 m in thickness which is mainly build up by coral reef complexes. Throughout a lateral extend of about 400 m exposed in the quarry, the Obere Korallenbank Member shows numerous pillar-shaped reefal build ups which are flanked by a reefal debris limestone. The coral fauna of the in situ reefal bioconstructions comprises not less than 37 taxa most of which have been described from the Lower Saxony Basin for the first time. Probably, the pillar-shaped reefs formed a small positive relief of only a few dm against the debris deposits during deposition. The interreef debris limestones in the lower and middle part of the Obere Korallenbank Member show three intercalated biostromal coral layers. In the upper part of the member, the interreef facies is represented by a mikritic peloidal limestone rich in sponge remains and, unusual in such a depositional environment, ammonites (Dichotomo-sphinctes bifurcatoides, D. sp.). Additionaly, at the top of of the peloidal limestone a layer enriched in nerineids and other gastropods limits the reefal constructions of the Obere Korallenbank Member against the overlying “humeralis-Oolith” sequence. On the basis of the facies development of this depositional sequence the reef formation in relation to sealevel changes is discussed.

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An overview is given here on the palaeobiogeography of the Korallenoolith Formation (middle Oxfordian to early Kimmeridgian) in NW Germany (Lower Saxony Basin). Based on microfacies observations, abundant faunal and floral elements of the tropical tethyan realm are recognized in shallow-marine calcareous sediments of the Korallenoolith Formation. Foraminiferal fauna is both highly diverse and abundant and mostly of mediterranean character. Also, there is a small flora recorded, which includes heavily calcified red algae, aragonitic green algae, and cayeuxiid algae. They display restricted diversity when compared to those of shallow-marine tropical tethyan seas. Chaetetids and diceratids are locally abundant. Lithocodium aggregatum and Bacinella irregularis have been observed in Late Jurassic palaeolatitudes north of the Tethys for the first time. Corals are present in numerous genera and species. Their occurrence is restricted to a few horizons of the Korallenoolith Formation where they build patch reefs, coral biostroms and coral meadows. The overall character of the coral-thrombolite-reefs (florigemma-Bank Member) is very similar to those of the Tethys. The presence of these marine tethyan taxa assigned the position of the Lower Saxony Basin during middle Oxfordian to early Kimmeridgian palaeobiogeographically into the submediterranean province and reflects northward migration of tropical tethyan fauna and flora which reach in the Lower Saxony Basin their northern limit. These biota seem to be biogeo-graphically transitional between communities present in England and the Tethys.

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Borings of bryozoan colonies are rare fossils and hitherto unknown from Central America. Four different types of zoaria, belonging to Spathipora sp., Terebripora sp. A, Terebripora cf. falunica and Iramena sp., were recognized. They are developed on shells of Miocene oysters (Saccostrea sp. and Ostrea sp.) from shell - beds of the Venado-Formation (Northern Limon - San Carlos Basin, Costa Rica). The period of colonization and growth by bryozoans and/or a few other benthic invertebrates was probably a short - term event, followed by suffocation from accumlating sediment.