Non-tropical carbonate deposits on the modern New Zealand shelf

Extensive (ca. 50,000 km²) shallow-marine platforms (< 250 m) off northern (34°S) and southern (48°S) New Zealand, and more local areas of shelf between, are blanketed by skeletal carbonate sediments > 70% CaCO₃), despite proximity to a tectonically active plate margin. In these regions the terrigenous sediment supply is presently low, and growth of epibenthos is fostered by firm substrates (rock, gravels, shells, seaweeds) and the generally energetic nature and high nutrient levels of open-shelf waters. Rapid transition into adjacent terrigenous-dominated facies is characteristic. Irrespective of water depth, the carbonates are coarse-grained and fragmental; carbonate mud is rare. Calcite dominates over aragonite. High-Mg calcite, widespread off northern New Zealand, is rare in the south. Skeletal material is dominated by bryozoans and bivalve molluscs, with significant local contributions from foraminifers, barnacles, calcareous red algae and echinoderms. The name bryomol is suggested for this distinctive temperate-region skeletal carbonate facies, which can be usefully subdivided based on dominant zoarial growth forms of the bryozoan component, known to be habitat-related. Bioerosion is an important mechanism of skeletal fragmentation and degradation. Many grains, especially aragontic bivalves, are infested by endolithic borers and have low preservation potential. Ages of skeletal material in the surficial deposits range from more than 20,000 years B.P. to modern, which is consistent with both low rates of carbonate production and sediment accumulation, and the wide range in preservation state of grains. Some data suggest that the skeletal carbonates are dispersed and mixed mainly during infrequent movement of sand ribbons, sand waves and sand sheets driven by storm-assisted tidal flows. Tracts of modern, palimpsest and relict carbonates can occur in juxtaposition.

The facies characteristics of the New Zealand shelf carbonate deposits contrast significantly with those of the classical Bahaman-type carbonate model. However, they are similar to those reported from many other mid- to high-latitude carbonate shelves, and afford good analogues for most onland occurrences of New Zealand Cenozoic limestones.     

A skeletal assemblage classification system for non-tropical carbonate deposits based on New Zealand Cenozoic limestones

Cenozoic limestones in New Zealand are mainly skeletal grainstones and packstones formed under non-tropical climatic conditions in open marine shelf or ramp environments. Following petrographic analysis of the nature and abundance of the skeletal components in nearly 500 samples of these limestones, a complete linkage cluster analysis identified seven major skeletal assemblages that may be regarded as subdivisions of the single foramol skeletal association defined by Lees and Buller (1972) for temperate-region carbonate deposits. The seven assemblages are given contracted names, as follows: (a) BARNAMOL = barnacle/bivalve-dominated; (b) BIMOL = bivalve-dominated; (c) BRYOMOL = bryozoan/bivalve-dominated; (d) ECHINOFOR = echinoderm/benthic foraminiferal-dominated; (e) NANNOFOR = nannofossil/planktonic foraminiferal-dominated; (f) RHODALGAL = calcareous red algal-dominated; and (g) RHODECHFOR = calcareous red algal/echinoderm/benthic foraminiferal-dominated. A composite triangular classification diagram has been devised for naming the skeletal assemblage of an unknown sample on the basis of its three main skeletal components. The diagram successfully characterises more than 85% of the New Zealand Cenozoic limestone samples and also appears to be applicable for the skeletal assemblage designation of many overseas examples of non-tropical carbonate deposits. Limitations relate mainly to locally common skeletal types (e.g. serpulids, brachiopods) that are presently not incorporated into the New Zealand-based scheme. The general ecological preferences of the main skeletal contributors in each of the seven skeletal assemblages form a basis for relating the assemblages to broad shelf habitats. Consequently, as well as the benefits of providing a more consistent skeletal assemblage terminology for comparative studies between different workers, the scheme can assist with the paleoenvironmental interpretation of non-tropical skeletal carbonate facies.     

Cenozoic stratigraphy of the northern Sakhalin shelf

The analysis of diatom, palynofloral, and benthic foraminiferal assemblages made it possible to substantiate the age of Cenozoic sections recovered by wells on the northern and northeastern Sakhalin shelf. Biostratigraphic materials, lithological properties of stratigraphic units, and standard logs served as the basis for developing the first stratigraphic correlation scale of Cenozoic sequences on the Sakhalin shelf.     

Grain-size parameters of insoluble residues in mixed terrigenous-skeletal carbonate sediments and sedimentary rocks: some New Zealand examples

Grain-size parameters derived from the mechanical analysis of acid-insoluble residues from mixed terrigenous-shell beach sediments from Auckland, New Zealand, are more effective for interpreting the depositional processes, and for characterizing the beach environment on textural scatter plots, than are parameters based on the analysis of the total beach samples. This results mainly from the wide variations in size of hydraulically equivalent skeletal carbonate grains in the sediment, especially in the coarser size grades, but may also be accentuated by the local origin and susceptibility to alteration of the shell material. Compared with the total sediment grain-size distribution, the insoluble residues from the beach deposits are characteristically finer-grained, better sorted, and more consistently coarse-skewed and leptokurtic. The grain-size distribution characteristics of insoluble residues from several stratigraphic units in a sequence of Oligocene mixed terrigenous-skeletal shelf sediments in the South Auckland region distinguish depositional mechanisms and environmental energy levels for each unit that are consistent with interpretations made on the basis of carbonate petrography and palaeontology. With regard to the bulk content of terrigenous mud in the insoluble residues, the grain-size distribution of the fraction coarser than 4φ is alone diagnostic of the energy-time trends in these sediments. The grain-size parameters of the acid-insoluble residues in modern and ancient mixed terrigenous-skeletal carbonate sediments may provide more reliable criteria for distinguishing and characterizing the depositional environment of these deposits than do the parameters obtained from the size distribution of the total grain population.     

Methylmercury cycling in sediments on the continental shelf of southern New England

Exposure of humans to monomethylmercury (MMHg) occurs primarily through consumption of marine fish, yet there is limited understanding concerning the bioaccumulation and biogeochemistry of MMHg in the biologically productive coastal ocean. We examined the cycling of MMHg in sediments at three locations on the continental shelf of southern New England in September 2003. MMHg in surface sediments is related positively to inorganic Hg (Hg(II) = total Hg − MMHg), the geographical distribution of which is influenced by organic material. Organic matter also largely controls the sediment-water partitioning of Hg species and governs the availability of dissolved Hg(II) for methylation. Potential gross rates of MMHg production, assayed by experimental addition of ²⁰⁰Hg to intact sediment cores, are correlated inversely with the distribution coefficient (K_D) of Hg(II) and positively with the concentration of Hg(II), most probably as HgS⁰, in 0.2-μm filtered pore water of these low-sulfide deposits. Moreover, the efflux of dissolved MMHg to overlying water (i.e., net production at steady state) is correlated with the gross potential rate of MMHg production in surface sediments. These results suggest that the production and efflux of MMHg from coastal marine sediments is limited by Hg(II), loadings of which presumably are principally from atmospheric deposition to this region of the continental shelf. The estimated diffusive flux of MMHg from the shelf sediments averages 9 pmol m⁻² d⁻¹. This flux is comparable to that required to sustain the current rate of MMHg accumulation by marine fish, and may be enhanced by the efflux of MMHg from near-shore deposits contaminated more substantially with anthropogenic Hg. Hence, production and subsequent mobilization of MMHg from sediments in the coastal zone may be a major source of MMHg to the ocean and marine biota, including fishes consumed by humans.     

Temperate carbonate sediments of Northern Spencer Gulf, South Australia: a high salinity 'foramol' province

Cool-water skeletal carbonate sediments are forming in Spencer Gulf, South Australia, an area of high salinity and moderate tidal range. Four environments can be distinguished: deeper marine areas (10–20 m); shallow subtidal platforms and banks (2–10 m); intertidal and supratidal zones; and coastal springs and lakes fed by saline continental groundwaters. The sediments are predominately bioclastic carbonate sands; muddy sediments occur in protected intertidal environments. The most common grain types are gastropods, bivalves, foraminifera, coralline algae and quartz. Indurated non-skeletal carbonate grains have not been seen. Composition of the sediment varies little between environments, but considerable textural variation results from variation in the stability of the substrate, hydrodynamic conditions, depth of water, period of tidal inundation, supply of terrigenous grains, temperature, and salinity. The Spencer Gulf data suggests that temperature, and particularly minimum temperature, controls the distribution of skeletal and non-skeletal grain associations in high-salinity environments. The textures of the sedimentary facies of Spencer Gulf closely parallel those of equivalent environments in warm-water carbonate provinces.     

长江三角洲晚新生代沉积物有机碳、总氮和碳酸盐组成及古环境意义

长江三角洲地区埋深达320m的PD钻孔揭示了上新世以来河湖相、滨海相和三角洲相的沉积环境特征。钻孔沉积物中有机碳、总氮和碳酸盐组成变化较大,但具有一定的规律性。上新世东部地区气候较暖湿,古湖泊发育,化学风化强烈,有机质保存率较低;早更新世气候波动较大,相对温湿气候下高等植被发育;中、晚更新世长江流域气候逐渐变冷干,晚第四纪气候变化较显著,流域植被类型发生明显变化;全新世气候转暖,有机质保存率高。有机碳、总氮和碳酸盐组成揭示的古气候变化与孢粉、沉积地层等资料相当吻合,与相邻内陆地区的第四纪古环境研究认识也具有明显的可比性。本研究也揭示,运用有机碳、总氮和碳酸盐组成重建我国东部地区第四纪古环境和季风演化史具有相当的难度,必须充分考虑沉积地层不连续性、粒度、有机质来源、埋藏成岩环境以及陆海相互作用等多因素的复杂影响,同时需要结合有机碳同位素等分析来深化古环境研究。     

Cenozoic temperate and sub‐tropical carbonate sedimentation on an oceanic volcano – Chatham Islands,New Zealand

The Chatham Islands, at the eastern end of the Chatham Rise in the South‐west Pacific, are the emergent part of a Late Cretaceous to Cenozoic stratovolcano complex that is variably covered with limestones and fossiliferous tuffs. Most of these deposits accumulated in relatively shallow, high‐energy, tide‐influenced palaeoenvironments with deposition punctuated by periods of deeper‐water pelagic accumulation. Carbonate components in these neritic deposits are biogenic and dominated by molluscs and bryozoans – a heterozoan assemblage. The widespread Middle to Late Eocene Matanginui Limestone contains local photozoan elements such as large benthonic foraminifera (especially Asterocyclina) and calcareous green algae, reflecting the general Palaeogene sub‐tropical oceanographic setting. More localized Late Eocene to Oligocene deposits (Te One Limestone) as well as Pliocene carbonates (Onoua Limestone) are, however, wholly heterozoan and confirm a generally cooler‐water oceanographic setting, similar to today. Early sea floor diagenesis is interpreted to have removed most aragonite components (infaunal bivalves and epifaunal gastropods). Lack of aragonite resulted in the absence of intergranular calcite cementation during subaerial exposure, such that most carbonates are friable or unlithified. Cementation is, however, present at nodular hardground–firmground caps to metre‐scale cycles. Such cements are microcrystalline or micrometre‐thick isopachous circumgranular rinds with insufficient definitive attributes to pinpoint their environment of formation. The overall palaeoenvironment of deposition is interpreted as mesotrophic, resulting in part from upwelling about the Chatham volcanic massif and in part from nutrient element delivery from the adjacent volcanic terrane and coeval volcanism. Biotic diversity in tuffs is two to three times that in limestones, supporting the notion of especially high nutrient availability during periods of volcanism. These mid‐latitude deposits are strikingly different from their low‐latitude, tropical, photozoan counterparts in the volcanic island–coral reef ecosystem. Ground water seepage and fluvial runoff attenuate coral growth and promote microbial carbonate precipitation in these warm‐water settings. In contrast, nutrients from the same sources feed the system in the Chatham Islands cool‐water setting, promoting active heterozoan carbonate sedimentation.     

碳酸盐沉积物的成岩作用

化学沉淀碳酸盐矿物在沉积后很容易受到各种作用的影响,其中最重要的是其在成岩阶段所经历的成岩作用.碳酸盐沉积物在成岩过程中主要受大气降水、海水和埋藏过程中孔隙流体的控制,经历一系列压实、溶解、矿物的多相转变、重结晶、胶结等成岩作用,逐渐转变为固结的岩石.在成岩过程中,由于孔隙流体与沉积流体之间的异同以及温度的变化,碳酸盐沉积物的原始矿物成分、地球化学特征可能会很好的保存下来,但在许多情况下,也可能会改变,从而使我们无法准确反演碳酸盐沉积物在沉积时水体的特征.因此,我们在应用碳酸盐岩重建相关古环境和古气候变化的时候,必须要通过有效的方法来对碳酸盐岩是否受到成岩作用的影响进行鉴定.     

Marine cements in mid-Tertiary cool-water shelf limestones of New Zealand and southern Australia

Large areas of southern Australia and New Zealand are covered by mid‐Tertiary limestones formed in cool‐water, shelf environments. The generally destructive character of sea‐floor diagenesis in such settings precludes ubiquitous inorganic precipitation of carbonates, yet these limestones include occasional units with marine cements: (1) within rare in situ biomounds; (2) within some stacked, cross‐bedded sand bodies; (3) at the top of metre‐scale, subtidal, carbonate cycles; and (4) most commonly, associated with certain unconformities. The marine cements are dominated by isopachous rinds of fibrous to bladed spar, interstitial homogeneous micrite and interstitial micropeloidal micrite, often precipitated sequentially in that order. Internal sedimentation of microbioclastic micrite may occur at any stage. The paradox of marine‐cemented limestone units in an overall destructive cool‐water diagenetic regime may be explained by the precipitation of cement as intermediate Mg‐calcite from marine waters undersaturated with respect to aragonite. In some of the marine‐cemented limestones, aragonite biomoulds may include marine cement/sediment internally, suggesting that dissolution of aragonite can at times be wholly marine and not always involve meteoric influences. We suggest that marine cementation occurred preferentially, but not exclusively, during periods of relatively lowered sea level, probably glacio‐eustatically driven in the mid‐Tertiary. At times of reduced sea level, there was a relative increase in both the temperature and the carbonate saturation state of the shelf waters, and the locus of carbonate sedimentation shifted towards formerly deeper shelf sites, which now experienced increased swell wave and/or tidal energy levels, fostering sediment abrasion and reworking, reduced sedimentation rates and freer exchange of sediment pore‐waters. Energy levels were probably also enhanced by increased upwelling of cold, deep waters onto the Southern Ocean margins of the Australasian carbonate platforms, where water‐mass mixing, warming and loss of CO₂ locally maintained critical levels of carbonate saturation for sea‐floor cement precipitation and promoted the phosphate‐glauconite mineralization associated with some of the marine‐cemented limestone units.     

Recycling and chemical weathering in tectonically controlled Mesozoic–Cenozoic basins of New Zealand

Sedimentation in molasse basins is controlled by tectonics, however, recycling and chemical weathering play a critical role in the compositional evolution of a sedimentary succession. The Cretaceous to Pliocene molasse deposits of Central Otago, New Zealand are excellent examples of tectonically related deposits that were governed by the effects of chemical weathering and recycling. Preserved in fault-controlled basins floored by flysch deposits of the Otago Schist, the clastic successions contain ubiquitous unconformities and lithofacies consistent with alluvial, fluvial and lacustrine depositional settings. Textural analysis of Central Otago sandstones establishes a general quartz enrichment and increased mixing of angular and well-rounded quartz varieties up-section, consistent with a history of sediment recycling. Rare earth element (REE) patterns, which reflect upper crustal compositions, are similar for the flysch-type Otago Schist (Permian–Early Cretaceous), a palaeo-weathering profile, and the overlying molasse deposits. The development of quartz arenites is also consistent with high degrees of chemical weathering, and erosion of the schist basement, which contains numerous quartz veins. Although recycling has occurred, SiO₂ and TiO₂ do not consistently show a negative correlation over time. This reflects erosion of previously deposited quartz-rich sediment and the Otago weathering profile, which produced an inverse stratigraphy. CIA values range from 52 for lithic-rich, coarse-grained sandstones and polymictic conglomerate matrices, to 93 for coarse-grained to pebble-rich quartz arenites. Individual samples were split into finer- and coarser-grained pairs (<2·5φ and 2·5 to −1φ) and were analysed separately. The results show that finer-grained samples contain higher REE abundances and less SiO₂, but the coarser-grained Miocene–Pliocene samples have higher CIA values than their finer-grained counterparts. These coarse-grained deposits are quartz-rich and plot erratically on tectonic discrimination diagrams, implying that using SiO₂-poor samples is more reliable for geochemical analysis. Overall, the petrographic and geochemical results indicate that the main factors controlling the composition of the Central Otago molasse deposits were source composition, chemical weathering and recycling. Studies of this nature can be conducted in Archaean tectonically controlled molasse basins that are affected by similar allocyclic factors.     

Acid leached analyses of stormdrain and harbor sediments, New Zealand

 Sediments from stormdrain catchments in Wellington city and sediment traps from Wellington Harbor were sampled for trace metal content. Samples were analyzed for acid leached metal content by extraction with 0.11 mol acetic acid l^–1 and using ICP-MS. Cu and Zn levels in harbor sediment traps increased towards the periphery of the harbor, while Pb levels adjacent to a road almost doubled. In general, areas of light industry in the Inner City stormdrain catchments exhibited higher acid leached metal concentrations. However, large-scale renovation work probably contributed to point sources of high metal levels. The proximity of stormdrain outlets to recreational activities, such as wharf fishing and shellfish gathering, should be of prime concern to local authorities. Some positive correlations are found between acid leached and total metal levels. These may prove useful for assessing the biological impact of significant increases in total metal concentrations in the vicinity of Wellington Harbor. Significant savings in the time and costs of analyses may be achieved. Received: 27 February 1998 · Accepted: 27 April 1998     

A model of the Cenozoic evolution of northern New Zealand and adjacent areas of the southwest Pacific

New information from the southwest Pacific indicates that earlier attempts at formulating the evolution of the area assuming a single Upper Cenozoic magmatic arc are untenable. It now appears that there were two arcs during the Miocene and Pliocene, a western Northland/Three Kings Rise arc, and an eastern Tonga-Lau/Kermadec-Colville arc. Both appear to have developed above west-dipping subduction zones. It is suggested that the Norfolk- and Reinga basins formed as back-arc basins to the western arc, and that eastern North Island lay adjacent to Northland and formed the accretionary prism to that arc. Upper Cenozoic evolution of the region involved the simultaneous opening of the Norfolk/Reinga basins, consumption of the western portion of the Oligocene South Fiji Basin by subduction beneath the western arc, and eastwards movement of New Zealand/Three Kings Rise towards the Tonga/Kermadec arc. When the Kermadec and Hikurangi trenches came into line late in the Pliocene, the Tonga/Kermadec arc was able to propagate rapidly southwards into North Island; simultaneously the western arc became extinct, and the tectonic tempo and strike-slip faulting accelerated markedly throughout New Zealand. Eastern North Island was moved dextrally an uncertain distance relative to the western North Island, and rotated 25°–30° clockwise. This accounts for the paradox of a 22-m.y. old accretionary margin lying adjacent to a 2-m.y. old arc (Taupo Volcanic Zone) at the present day.     

Origin of friable sediments of the Barents Sea shelf

The origin of friable sediments blanketing the Barents Sea shelf is considered. It is shown that their characteristic seismoacoustic record patterns reflect low degree of diagenetic transformations and indicates continuous sedimentation. According to traditional views, this single sedimentary complex also includes diamicton, and the section is interpreted as a three-unit structure: diamicton, which is considered a till; the overlying friable sediments accumulated under different conditions of deglaciation in glaciomarine settings; and the postglacial marine sediments. It is demonstrated that such views are inconsistent with geomorphologic features (datings by physical methods included) indicating a prolonged hiatus that separates epochs of the diamicton accumulation and formation of friable sediments. The analysis revealed that the composition, vertical succession, and lateral distribution of different lithological types of friable sediments are related to the regular spatiotemporal replacements of different facies settings in the transgressing Arctic sea rather than by the glacial process. This inference is confirmed by the composition of foraminiferal assemblages.     

Bitumen formation in sediments of carbonate facies

This paper cites evidence to show that the Organic content of Recent carbonate facies is as readily preserved by entombment as it is in the torrigenous facies and that there is little difference in composition or proportion of organic constituents in terrigenous and some types of carbonate facies. The variations in organic content with grain size follow those for terrigenous facies. Organic constituents in Recent limey sediments are at least as reduced as they are in terrigenous facies. The tendency toward reduction of organic constituents to petroleum bitumens and petroleum is just as obvious and as rapid as in terrigenous. Thus it is quite possible for syngenetic petroleum to be entombed in appropriate carbonate facies.—B. N. Cooper     

Particulate calcium carbonate in New England shelf waters: result of shell degradation and resuspension*

Aragonite and calcite needles, 30–500 μm long, were found to be prominent visual components throughout the water column in some areas of the New England (northeastern U.S.A.) continental shelf during winter months. Further investigation showed these‘needles’to be laths derived from the degradation of mollusc shells which were resuspended from bottom sediments during winter storms. Such degradation and subsequent transport/dissolution of carbonate particles may help explain why the terrigenous 'starved’shelf sediments off New England contain such small amounts of calcium carbonate.     

Glauconitic bryozoan shells in shelf sediments of Western Kamchatka

Glauconite segregations in Oligocene–Miocene shelf sediments of Western Kamchatka (Kakert and Gakkha horizons) are studied. Glauconite occurs in the studied samples as morphologically different grains, finely dispersed cement, and pseudomorphoses after organogenic structures (siliceous sponge spicules, diatom algae frustules, and others). In addition, samples of the clasts of bryozoans, volcanic glass, and terrigenous grains revealed for the first time traces of the boring algae similar to recent species of genus Hyella and, possibly, Dalmatella, whose tubules are sometimes filled with the finely dispersed glauconite. Our data based on the detailed petrographic studies and SEM investigations confirm and supplement the opinion of several researchers about an important role of microbiota on the glauconite formation. The paper discusses different stages of the glauconite formation in sediments of the Kakert and Gakkha horizons and the possible setting of glauconite infilling in the algal borer trails and holes.     

Geological structure of Cenozoic sedimentary basin in the Northwestern margin of the Barents Sea shelf

There are two stages in Cenozoic development of the West Barents continental margin: rifting and passive margins. The main thickness of the Pliocene-Eocene complex is typical of the Serverstsnaget Basin, Vestbakken Volcanic Province, and Hornsund fault zone formed under conditions of strike-slip tectonics (“pull-apart” conditions). However, the thickness of the Oligocene-Pliocene sediments reaches its maximum on the eastern slope of the North Atlantic ocean basin. Paleogene and Neogene sediments consist mostly of claystones and siltstones but there are also sandy intervals formed because of gravity flows. The sandy layers can form lithological hydrocarbon traps.     

Diagenesis in carbonate sediments: A review

Reading the old textbooks of more than twenty-five years ago reveals the enormous progress made in our understanding since those days. Advances have been made along several related paths, particularly through the study of texture and structure with the microscope, the examination of Recent marine sediments and the application of the principles of solution chemistry. As a result we can now relate many diagenetic products with distinctive textures or structures to one of, say, four main types of aqueous solution. Sea water yields characteristic growths of aragonite and Mg-calcite whose fossilized calcitic remains we can yet recognise in the ancient. Fresh water gives rise to other individual calcite textures whose imprint also we can distinguish in the old rocks. Solution extruded at depth from compacting clays produce even other calcite textures which we are now beginning to understand. Certain mixtures of sea water with fresh water provide not only beach rocks with aragonite and Mg-calcite cements but dolomites through the Dorag process. Clearly influential in the control of marine precipitation we find organic compounds such as the humic acids.Superimposed on these products are the results of pressure solution. Clues to the action of processes in the distant past remain in the form of traces of magnesium, strontium or uranium and of relic isotopic ratios of oxygen and carbon, indicators of the composition of long vanished solutions. We think more clearly that before about rates of processes, duration of exposure to diagenetic environments, the balance between relatively closed and open chemical systems, the movements and mixing of ground waters and their chemical changes. In these and other ways carbonate diagenesis has come of age.

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Zusammenfassung Liest man alte Lehrbücher, die vor mehr als 25 Jahren erschienen sind, so erkennt man, welcher Fortschritt auf dem Gebiet der Karbonatdiagenese seither zu verzeichnen ist. Diese Fortschritte sind auf verschiedenen benachbarten Wegen erreicht worden, speziell durch Gefügeuntersuchungen mit dem Mikroskop, durch das Studium rezenter mariner Sedimente und durch die Anwendung der Prinzipien der Elementreaktionen in Lösungen. Als Ergebnis können wir heute viele diagenetische Stadien mit bestimmten Gefügemerkmalen und in erster Annäherung mit 4 Lösungsmilieus in Verbindung bringen. Meereswasser bewirkt typisches Wachstum von Aragonit und Hoch-Mg-Calcit, die wir in den fossilen calcitischen Gefügen wiedererkennen können. Süßwasser bewirkt auf der anderen Seite ein typisches Calcitwachstum, das wir ebenfalls in alten Gesteinen wiederfinden können. Lösungen, die aus kompaktierenden tonhaltigen Sedimenten aufsteigen, erzeugen calcitische Zementationsgefüge, die wir heute zu verstehen gelernt haben. Eine Mischung von Meereswasser und Süßwasser ist nicht nur für die beach-rock Zementation mit Aragonit und Hoch-Mg-Calcit verantwortlich, sie bewirkt auch Dolomitisierung nach dem Dorag-Modell.Organische Komponenten wie etwa Huminsäuren haben einen deutlichen Einfluß auf die Diageneseprozesse unter marinen Bedingungen. Den Diageneseprodukten werden schließlich die Einwirkungen der Drucklösung überlagert. Als Schlüssel zum Ablauf der Diagenese vergangener Zeiten verbleiben Spurenelemente wie Magnesium, Strontium und Uran sowie das reliktische Isotopenverhältnis von Sauerstoff und Kohlenstoff erhalten; sie markieren die Zusammensetzung längst vergangener Lösungen. Wir können heute besser die Anteile verschiedener Diageneseprozesse, die Dauer der Wirkung bestimmter Prozesse, den Ausgleich zwischen geschlossenen und offenen chemischen Systemen, die Bewegungen und Mischungen sowie chemischen Veränderungen des Grundwassers abschätzen.

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Résumé Parmi les vieux manuels agés de vingt-cinq ans ou davantage, on est frappé d'un coup d'il du progrès réalisé, surtout par l'étude des textures et des structures au microscope, par l'examen des sédiments marins actuels et par l'application de la chimie aqeuse. Conséquement on peut aujourd'hui lier les produits diagénétiques avec quatre solutions principaux. L'eau de mer donne les accroissements typiques en aragonite et en calcite-hautement magnésienne, reconnaisables aux calcaires anciens. L'eau douce fait surgir des textures individuelles en calcite. Aux profondeurs plus grands, les solutions exprimées des argiles y peuvent encore provoquer d'autres textures en calcite. L'eau de mer et l'eau douce, melées ensembles, y donnent naissance aux beach-rocks et aux dolomies. Franchement influents, aux précipitations marines, sont les composés organiques. Tout peut Être subi de la pression-solution. Données de la diagenèse ancienne restent telles que les traces du magnésium, du strontium et de l'uranium et des niveaux en ¹⁸O et ¹³C, témoins des compositions des solutions depuis longtemps disparues. On pense plus clairement qu'autrefois des taux des processus, des durées d'exposition aux milieux diagénétiques, du bilan entre les systèmes relativement fermés ou ouverts, des mouvements et des mélanges des eaux sousterraines et de leures changements chimiques. Dans telles mesures, l'étude de la diagenèse carbonatée a atteint sa majorité.

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