Radiaxial fibrous calcite: a replacement after acicular carbonate

Radiaxial fibrous calcite, a common cavity fill in ancient limestones, is characterized by curved twin lamellae, optic axes that converge away from the substrate and subcrystals which diverge in this same direction. The optic axes radiate about three or four axes located in positions between adjacent crystals and orientated parallel with the crystal elongation. The crystals are commonly turbid with inclusions, which may be concentrated along twin lamellae and subcrystal and inter-crystalline boundaries, or form zones parallel to the substrate. Some inclusion patterns reveal the position of former crystal faces. From a consideration of the occurrences, gross morphological characters, the fabrics of the crystals and the inclusion patterns, radiaxial fibrous calcite is interpreted as a replacement of an early diagenetic acicular cement, composed of interfering bundles of radiating crystals. It is suggested that replacement takes place by a solution-precipitation process and the migration of a fluid film through the acicular host, with replacement occurring most rapidly between bundles of acicular carbonate. The optic axis pattern of the fibrous calcite is considered to be inherited from the c-axis orientations of the host acicular crystals. Fibrous calcite intercrystalline boundaries form as fractures after replacement. Some inclusion patterns record the characters of the replaced acicular cement; others, formed of impurities reorganized during the replacement, reveal the form of the replacement front.     

贵州紫云上石炭统叶状藻礁灰岩胶结物特征

贵州紫云县猴场镇扁平村的上石炭统叶状藻礁及其周边灰岩中广泛发育大量的各类胶结物。通过对胶结物的形态、结构和阴极发光特征以及胶结物间的接触关系的研究,可以确定成岩作用的先后并识别成岩环境。浅海海底同生成岩阶段大的孔隙中形成等厚环边针状胶结物、葡萄状胶结物,小的孔隙里形成微晶胶结物。早成岩阶段形成微亮晶和斑块状亮晶方解石胶结物和放射纤维扇状胶结物,表生成岩阶段的溶蚀作用和胶结作用强烈,胶结物类型有斑块状或等粒的方解石胶结物和等厚环壁柱状胶结物,等厚环壁柱状胶结物在所有胶结物中体积是较大的。早期胶结作用使叶状藻礁灰岩孔隙度大为降低。中、晚成岩阶段,孔隙被等厚环壁刃状胶结物和晶簇或斑块状亮晶方解石所充填,有些先成的胶结物被热液改造。后生作用阶段发生的主要是构造破裂作用,其中少数裂隙被红褐色含Fe2O3微晶层和晶体粉砂及渗流豆粒充填。叶状藻礁灰岩的孔隙在晚成岩阶段前或中被胶结而之后没有创造出大且连通的孔隙,是它没能成为油气储集层的原因之一。     

Early diagenesis in Pleistocene coral reefs, southern Sinai, Egypt: response to tectonics, sea-level and climate

The uplifted Pleistocene terraces along the coast of southern Sinai exhibit a well developed reef system formed during isotope stage 9, and a younger one formed during isotope stage 5. An intermediate reef corresponding to isotope stage 7 occurs only as an erosional relic in the study area. The sediments comprise reefal framestones, peri-reefal facies, coral rubble, and siliciclastic-dominated beach and aeolian facies. The compositional and textural complexity of the sediments leads to a highly variable spatial distribution of diagenetic features. However, the geometric relationships and elemental analyses allow a reconstruction of the general diagenetic evolution: during the major eustatic sea-level highstand of isotope stage 9, the Older Reef was constructed and cemented with aragonite and high-Mg calcite. Climate was probably semiarid with some rainy periods which permitted the installation of ephemeral freshwater lenses, especially during the minor sea-level lowstand within isotope stage 9. In these lenses, and during the subsequent major sea-level lowstand, some freshwater dissolution occurred. The highstand during isotope stage 7 led to the construction of the Intermediate Reef. In the Older Reef, some high-Mg calcite precipitated at that time. Dolomite cement formed either in marine interstitial waters modified by some freshwater input, or in a hypersaline context. Phreatic-meteoric low-Mg calcite cement covers, and partly replaces, previous marine cements and dolomite, but is still attributed to the major highstand of isotope stage 7 when freshwater lenses could develop during minor sea-level lowstands. The subsequent major sea-level lowstand was dominated by an arid climate, and only a little freshwater corrosion occurred. The Younger Reef formed during the major highstand of isotope stage 5. Aragonite and high-Mg calcite cements, as well as some dolomite, are common within the reef, whereas freshwater cements are limited to beach and aeolian facies. Due to tectonic uplift, only the lower part of the Older Reef was reflooded during isotope stage 5, and only some aragonite crystals precipitated on top of dolomite or low-Mg calcite. The interrelationships between tectonics, sea-level variations of different orders, and climatic changes thus had a profound impact on the diagenetic history of these reef systems.     

Influence of lysozyme on the precipitation of calcium carbonate: a kinetic and morphologic study

Several mechanisms have been proposed to explain the interactions between proteins and mineral surfaces, among them a combination of electrostatic, stereochemical interactions and molecular recognition between the protein and the crystal surface. To identify the mechanisms of interaction in the lysozyme-calcium carbonate model system, the effect of this protein on the precipitation kinetics and morphology of calcite crystals was examined. The solution chemistry and morphology of the solid were monitored over time in a set of time-series free-drift experiments in which CaCO₃ was precipitated from solution in a closed system at 25°C and 1 atm total pressure, in the presence and absence of lysozyme. The precipitation of calcite was preceded by the precipitation of a metastable phase that later dissolved and gave rise to calcite as the sole phase. With increasing lysozyme concentration, the nucleation of both the metastable phase and calcite occurred at lower Ω_calcite, indicating that lysozyme favored the nucleation of both phases. Calcite growth rate was not affected by the presence of lysozyme, at least at protein concentrations ranging from 0 mg/mL to 10 mg/mL.Lysozyme modified the habit of calcite crystals. The degree of habit modification changed with protein concentration. At lower concentrations of lysozyme, the typical rhombohedral habit of calcite crystals was modified by the expression of {110} faces, which resulted from the preferential adsorption of protein on these faces. With increasing lysozyme concentration, the growth of {110}, {100}, and finally {001} faces was sequentially inhibited. This adsorption sequence may be explained by an electrostatic interaction between lysozyme and calcite, in which the inhibition of the growth of {110}, {100}, and {001} faces could be explained by a combined effect of the density of carbonate groups in the calcite face and the specific orientation (perpendicular) of these carbonate groups with respect to the calcite surface. Overgrowth of calcite in the presence of lysozyme demonstrated that the protein favored and controlled the nucleation on the calcite substrate. Overgrowth crystals nucleated epitaxially in lines which run diagonal to rhombohedral {104} faces.     

贵州紫云上石炭统叶状藻礁灰岩的成岩作用

贵州紫云县猴场镇扁平村的上石炭统中的叶状藻礁及其周边灰岩中发育强烈的成岩作用和胶结物,这些胶结物在猴场研究区内是显著的和有代表性的。通过观察、分析野外露头、光片、薄片、薄片的阴极发光和染色,来研究礁体岩石的成岩作用,确定了成岩作用序列、成岩环境、成岩阶段。成岩作用类型主要有泥晶化、溶蚀、胶结、新生变形、机械压实、剪切或...     

Holocene carbonate sedimentation in Lake Manitoba, Canada

The carbonate mineral suite of the modern offshore bottom sediment of the South Basin of Lake Manitoba consists mainly of high magnesian calcite and dolomite with minor amounts of low-Mg calcite and aragonite. The high-Mg calcite is derived from inorganic precipitation within the water column in response to supersaturation brought about by high levels of organic productivity in the basin. Both dolomite and pure calcite are detrital in origin, derived from erosion of the surrounding carbonate-rich glacial deposits. Aragonite, present only in trace amounts in the offshore sediments, is bioclastic in origin. The upward increase in the amount of magnesian calcite in the post-glacial sediment record is attributed to increasing photosynthetic utilization of CO₂ in the lake. Stratigraphic variation in the amount of magnesium incorporated into the calcite lattice is interpreted as reflecting a variable magnesium input to the lake from ground water and surface runoff, and possibly variable calcium removal in the precipitating lake water. The effects of long-term chemical weathering at the source and size segregation explain the changes in dolomite content throughout the section.     

Molar tooth structures of the Neoarchean Monteville Formation, Transvaal Supergroup, South Africa. I: Constraints on microcrystalline CaCO3 precipitation

Molar tooth (MT) structures are enigmatic, contorted millimetre‐ to decimetre‐long veins and spheroids of microcrystalline calcite that formed during very early diagenesis in Precambrian sediments. MT structures in the ca 2·6 Ga Monteville Formation are 600–800 Myr older than previously reported occurrences and establish that conditions necessary for MT genesis were met locally throughout much of the Precambrian. In the Monteville Formation, MT structures were formed shallow subtidally, extending to depths near storm wave base, in shale host sediments intercalated with storm‐generated carbonate sand lenses. They are filled with microcrystalline calcite and rare pyrite. Microcrystalline calcite identical to that in MT structures fills other pore space, including porosity between grains in carbonate sand lenses, moldic porosity in sand grains, sheet cracks in columnar stromatolites, and shallow cracks on sandy bedding planes. Relationships in the Monteville Formation demonstrate that microcrystalline CaCO₃ precipitated in fluid‐filled cracks and pores; microcrystalline calcite characteristics, as well as the paucity of carbonate mud in host rocks, are inconsistent with injection of lime mud as the origin of MT structures. Locally, MT cracks were filled by detrital sediment before or during precipitation. Precipitation occurred in stages, and MT CaCO₃ evolved from granular cores to a rigid mass of cores with overgrowths – allowing both plastic and brittle deformation of MT structures, as well as reworking of eroded MT structures as rigid clasts and lime mud. Crystal size distributions and morphology suggest that cores precipitated through nucleation, Ostwald ripening and size‐dependent crystal growth, whereas overgrowths formed during size‐independent crystal growth.     

Low-Mg calcite marine cement in Cretaceous turbidites: origin, spatial distribution and relationship to seawater chemistry

Lower Cretaceous (Hauterivian) bioclastic sandstone turbidites in the Scapa Member (North Sea Basin) were extensively cemented by low-Mg calcite spars, initially as rim cements and subsequently as concretions. Five petrographically distinct cement stages form a consistent paragenetic sequence across the Scapa Field. The dominant and pervasive second cement stage accounts for the majority of concretions, and is the focus of this study. Stable-isotope characterization of the cement is hampered by the presence of calcitic bioclasts and of later cements in sponge spicule moulds throughout the concretions. Nevertheless, trends from whole-rock data, augmented by cement separates from synlithification fractures, indicate an early calcite δ¹⁸O value of+0·5 to -1·5‰ PDB. As such, the calcite probably precipitated from marine pore fluids shortly after turbidite deposition. Carbon isotopes (δ¹³C=0 to -2‰ PDB) and petrographic data indicate that calcite formed as a consequence of bioclastic aragonite dissolution. Textural integrity of calcitic nannoplankton in the sandstones demonstrates that pore fluids remained at or above calcite saturation, as expected for a mineral-controlled transformation. Electron probe microanalyses demonstrate that early calcite cement contains <2 mol% MgCO₃, despite its marine parentage. Production of this cement is ascribed to a combination of an elevated aragonite saturation depth and a lowered marine Mg²⁺/Ca²⁺ ratio in early Cretaceous ‘calcite seas’, relative to modern oceans. Scapa cement compositions concur with published models in suggesting that Hauterivian ocean water had a Mg²⁺/Ca²⁺ ratio of ≤1. This is also supported by consideration of the spatial distribution of early calcite cement in terms of concretion growth kinetics. In contrast to the dominant early cement, late-stage ferroan, ¹⁸O-depleted calcites were sourced outwith the Scapa Member and precipitated after 1–2 km of burial. Our results emphasize that bioclast dissolution and low-Mg calcite cementation in sandstone reservoirs should not automatically be regarded as evidence for uplift and meteoric diagenesis.     

Structure, chemistry and origins of gypsum crusts in southern Tunisia and the central Namib Desert

Gypsum crusts are broadly defined as accumulations at or within about 10 m of the land surface from 0.10m to 5.0 m thick containing more than 15% by weight gypsum (CaSO₄·2H₂O) and at least 5.0% by weight more gypsum than the underlying bedrock. The deposits are often, but not invariably, consolidated owing to cementation by gypsum. The crusts are found in many of the world's deserts where mean monthly potential evaporation exceeds mean monthly precipitation throughout the year. Using structural, fabric and textural criteria, three main types of crust may be distinguished:(1) bedded crusts, found either at or beneath the land surface, which are made up of discrete horizontal strata up to 0.10 m thick, each showing a gradation in gypsum crystal size from less than 50 μm at the top to more than 0.50 mm at the base; (2) subsurface crusts, of which there are two forms, one made up of large, lenticular crystals (up to 0.50 m in diameter)—the desert rose crusts—and the other, a mesocrystalline form, with gypsum crystals up to about 1.0 mm in diameter; and (3) surface crusts, which are subdivided into columnar, powdery and cobble forms, all of which are made up of predominantly alabastrine gypsum (crystallites less than 50 μm in diameter). In southern Tunisia and the central Namib Desert, bedded crusts are found around ephemeral lakes and lagoons. They are characterized by size-graded beds, gypsum contents of 50–80% by weight and comparatively high concentrations of sodium, potassium, magnesium and iron. They are interpreted as shallow-water evaporites which accumulate when saline pools evaporate to dryness. Desert rose crusts or croûtes de nappe generally contain 50–70% by weight gypsum, and have higher sodium concentrations than the second subsurface form. Texturally they are characterized by poikilitic inclusion of clastic material within large lenticular crystals. They are interpreted as hydromorphic accretions, which precipitate in host sediments at near-surface water tables through the evaporation of groundwater. The second form of subsurface crust—the mesocrystalline—often occurs in close association with the various surface forms. Unlike the hydromorphic crusts, they are not restricted to low-lying terrain. They are characterized by gypsum contents reaching 90% by weight, and have a close chemical and textural similarity to columnar surface crusts. This mesocrystalline form represents an illuvial accumulation; the surface forms—excluding the bedded crusts—are exhumed examples at various stages of solutional degradation. Subsurface precipitation of gypsum from meteoric waters containing salts leached from the surface, results in displacive gypsum accumulation in the soil zone. In southern Tunisia, the gypsum is derived from sand and dust deflated from evaporitic basins; in the central Namib, salts dissolved in fog water are the most likely source. Where other salts are present, differential leaching may form two-tiered crusts, calcrete—gypsum or gypsum—halite, if rainfall is sufficient to mobilize the less soluble salt yet insufficient to flush the more soluble. Gypsum crust genesis is restricted to arid environments, and if their susceptibility to post-depositional alteration is acknowledged, they can provide valuable palaeoclimatic indicators.     

Diagenesis of Pennsylvanian phylloid algal mounds from the southern Cantabrian Zone (Spain)

The Pennsylvanian phylloid algal mounds exposed in the Cervatina Limestone of the Cantabrian Zone (NW Spain) developed during the highstands of high-frequency shallowing-upward cycles and lack evidence of subaerial exposure at their tops. Mound core facies are composed of massive bafflestones with variable amounts of calcite cements and anchicodiacean phylloid algae with cyathiform thalli preserved in growth position. Through standard petrographic, isotopic (δ¹⁸O and δ¹³C), major and trace element (Ca, Mg, Fe, Mn, Sr) and cathodoluminescence analyses, five calcite cement phases (cement 1 (C1)–cement 5 (C5)) have been identified filling primary and secondary pores. Early marine diagenesis is represented by micritization and non-luminescent to mottled-dull luminescent high-Mg calcite fibrous marine cement (C1). A dissolution phase then occurred and created vuggy and moldic pores. Based on the absence of field or petrographical or geochemical evidence of exposure, it is inferred that dissolution occurred in near-surface undersaturated marine waters with respect to aragonite related to progressive organic matter oxidation. Secondary porosity was subsequently filled by dull-bright-dull bladed high-Mg calcite (C2), which precipitated in the early shallow burial from marine-derived pore waters. Remaining porosity was occluded by shallow-burial precipitates consisting of non-luminescent scalenohedral low-Mg calcite (C3) followed by non-ferroan dull luminescent calcite spar (C4). Latter phases of calcite spar exhibiting non- and dull luminescence (C5) are associated with burial calcite veins. Low δ¹⁸O values (around ?8‰), moderately depleted δ¹³C values (around 0.5‰) and the homogeneity of trace element contents of carbonate matrix, cements and vein-filling calcites suggest burial isotopic re-equilibration and recrystallization, probably in Early Permian times during post-thrusting orocline formation.     

海南岛全新世海滩岩的胶结作用与成岩环境的关系

我国海南岛及南海诸岛沿岸,广泛发育海滩岩。1980年我队赴海南岛考察现代沉积时,对海滩岩的分布、岩性特征及其与周围环境的关系进行了观察和采样。样品采自崖县鹿回头三亚湾水尾岭海蚀崖、西洲岛、小东海、东瑁岛、西瑁岛、天涯海角,乐东县莺歌海,文昌县渔业等地(图1)。有关的地质、地貌及岩性特征等,已有许多描述,对海滩岩的岩石学及成岩作用也有许多研究。本文侧重探讨海滩岩的胶结作用及与成岩环境的关系。     

川东北下侏罗统大安寨段陆相页岩方解石成因

为分析陆相页岩中方解石的成因及其对储层的影响,以四川盆地下侏罗统大安寨段的介壳泥岩与灰岩夹层为主要研究对象,利用X-射线衍射、普通薄片、岩芯观察、阴极发光及电子探针测试手段,识别出文石转化方解石、胶结物方解石和重结晶作用形成的方解石。在同生期和成岩早期,生物介壳中的文石转化为泥晶无铁方解石,阴极发光为橙黄色。成岩早期,生物介壳边缘可形成纤维状第一世代无铁方解石胶结物。在成岩晚期,岩石孔隙中形成颗粒状铁方解石胶结物,阴极发光为暗色。同时,部分介壳中的泥晶方解石新生变形为斑块状细晶方解石或柱状方解石。根据方解石的存在形式可知,方解石在成岩演化过程中,经历了转化、压实、溶解、胶结和重结晶作用。其中,溶解作用改善储层的物性。压实、胶结和重结晶作用破坏储集空间。统计裂缝密度发现,元坝地区大安寨段层理缝最为发育,涪陵地区大安寨段以层理缝和溶蚀缝为主。结果表明,方解石介壳有利于大安寨段内岩石层理缝和溶蚀缝的产生。     

鄂尔多斯盆地渭北地区上三叠统延长组长7油层组碳酸盐结核中自生碳酸盐矿物的特征

早期形成的碳酸盐结核在埋藏期间会经历多种碳酸盐矿物相沉淀的复杂胶结作用,岩石学研究是探究结核成因的关键。通过野外剖面观察、岩石学观察和阴极发光技术,分析了鄂尔多斯盆地渭北地区上三叠统延长组长7油层组泥页岩中各种形状的方解石和白云石结核中自生碳酸盐矿物的特征。这些结核为成岩早期的产物,构成结核的自生碳酸盐矿物特征显著:(1)球粒方解石结核中,方解石呈纤维状或刃片状,球粒间充填晶粒方解石或因压实呈贴面结合,纤维状方解石发桔红色和暗红色2种光,刃片状方解石发暗红色光;(2)粉晶方解石结核中,方解石呈他形粒状,含有机质包裹体或纤维状晶形残余,晶间含沥青和纤维状方解石残余,主要发暗红色光;(3)白云石结核有泥晶和粉晶2种晶体类型,粉晶白云石结核含较多泥质,泥质条带或有机质条带处常见纤柱状白云石;(4)沿裂缝充填的方解石和白云石常呈纤维状或纤柱状结构,发暗红色光或不发光。研究区长7油层组碳酸盐结核中的方解石和白云石具有不同的成因类型和复杂的胶结作用:球粒方解石和泥晶白云石代表了结核开始形成时的胶结作用,可以准确地反映结核的成因;粉晶方解石、粉晶白云石反映了交代成因;裂缝中纤维状、纤柱状方解石和白云石集合体则为结核经历了较强压实作用之后充填裂缝而成。     

Diagenetic alteration of early marine cements of Upper Silurian stromatactis

Stromatactis is a spar network whose elements in cross section have flat to undulose lower surfaces and digitate upper surfaces. The network is composed principally of isopachous crusts of centripetal cement and commonly occurs embedded in finely crystalline limestone. It is the cement filling of interconnected cavities. Stromatactis of Upper Silurian red stromatactis limestone from Gaspé Peninsula, Québec Appalachians, exhibits two types of cements: (1) an isopachous cement that lined the walls of the conduits and is interpreted as early marine; and (2) a later blocky cement that occupies the centres of cavities. The first cement is composed exclusively of non-ferroan calcite, whereas the second cement is mixed non-ferroan and ferroan calcite. The early isopachous cement is white on polished slabs and has a turbid aspect under transmitted light. In a few samples, the relative homogeneity of this early cement is broken by the presence of distinctive grey clear calcite. Under cathodoluminscence, the grey clear calcite is non-luminescent and exhibits well defined bladed crystal shapes, whereas the white turbid cement has a dull orange luminescence and indistinct crystal shapes. The relationships between the two cements indicate that the dull luminescent cement is a secondary form of the non-luminescent cement, and it is concluded that the dull cement is the product of alteration of the non-luminescent cement by burial or meteoric fluids. The later blocky cement has the same dull luminescence as the white turbid cement and is thought to have been precipitated from the same fluids as those responsible for the alteration of the early marine cements. Oxygen isotopic values of the dull cement of the early isopachous crusts (mean δ¹⁸O= -6.8%_o are intermediate between those of the non-luminescent early marine cement (mean δ¹⁸O= -5.3%_o) and the dull luminescent blocky cement (mean δ¹⁸O= -11.8%_o), while carbon isotopic values do not differ significantly (δ¹³C=+2.9, +2.4 and +2.6%_o, respectively). The alteration also has affected the distribution of some trace elements, particularly Mg. Both unaltered and altered cements contain less than 1% microdolomite inclusions, but the Mg content of the background calcite of unaltered cement is three times that of altered cement (14171 vs. 5502 ppm). Precursor early marine cement is thought to have been low-Mg calcite. The mean δ¹⁸O value (− 5.3%_o) of unaltered early marine cement is higher than values for the oxygen isotopic signature of Silurian oceans provided by brachiopod shells.     

Composition of carbonate overgrowths produced on Iceland spar calcite crystals buried in bahamian carbonate-rich sediments

High-magnesium calcite overgrowths were precipitated on Iceland spar calcite crystals buried in Bahamian sediments. Their composition was within the range of carbonate cements in this area. The precipitation rate of the overgrowths was slower and the magnesium content higher than predicted from laboratory experiments, possibly due to adsorption of organic compounds.     

Sandstone pseudomorphs of aragonite fossils in an Ordovician vadose zone

Moulds after aragonite fossils from two Upper Ordovician limestones in the Oslo Region are filled with well sorted clastic fine sand. The fossil moulds are thought to have been formed by selective dissolution of aragonite shell material by fresh water in the vadose zone. Internal sedimentation post-dates precipitation of a thin veneer of iron poor drusy calcite cement, but predates precipitation of ferroan blocky calcite cement. These age relationships and the texture of the fine sand suggests sedimentation in semiconsolidated sediment in the vadose zone of an island during early emergence.     

Sequence of mineral formation in clastic ores of the Saf’yanovka volcanic-hosted copper massive sulfide deposit,the Central Urals

The bedded clastic ore widespread on the slopes and flanks of the deeply eroded sulfide mound at the Saf’yanovka volcanic-hosted copper massive sulfide deposit consists of products of destruction of the Paleozoic black smoker along with diverse newly formed sulfides. The size of ore clasts gradually decreases with distance from the massive ore mound, from more than tens of centimeters to a few millimeters. The clastic sediments are characterized by good preservation of sulfide material composed of hydrothermal sedimentary colloform pyrite, chalcopyrite with lamellae of relict isocubanite, and concentrically zoned sphalerite. Numerous pyrite framboids, nodules, and euhedral crystals; chalcopyrite segregations; and twinned sphalerite are typical of sulfide-bearing black shale. Enargite, tennantite, and galena were formed after pyrite, filling interstices between nodules or partially replacing and corroding the previously formed minerals. The interrelations between minerals show that the fine-clastic sulfide-bearing black shale underwent diagenesis in the presence of organic matter.     

Growth patterns and implications of complex dendrites in calcite travertines from Lýsuhóll, Snæfellsnes, Iceland

Calcite dendrite crystals are important but poorly understood components of calcite travertine that forms around many hot springs. The Lýsuhóll hot-spring deposits, located in western Iceland, are formed primarily of siliceous sinters that were precipitated around numerous springs that are now inactive. Calcite travertine formed around the vent and on the discharge apron of one of the springs at the northern edge of the area. The travertine is formed largely of two types (I and II) of complex calcite dendrite crystals, up to 1 cm high, that grew through the gradual addition of trilete sub-crystals. The morphology of the dendrite crystals was controlled by flow direction and the competition for growth space with neighbouring crystals. Densely crowded dendrites with limited branching characterize the rimstone dams whereas widely spaced dendrites with open branching are found in the pools. Many dendrite bushes in the pools nucleated around plant stems. Growth of the dendrite crystals was seasonal and incremental. Calcite precipitation was driven by rapid CO₂ degassing of CO₂-rich spring waters during the spring and summer. During winter, when snow covered the ground and temperatures were low, opal-A precipitated on the exposed surfaces of the dendrites. Segmentation of dendrite branches by discontinuities coated with opal-A and overgrowth development around sub-crystals resulted from this seasonal growth cycle. The calcite dendrite crystals in the Lýsuhóll travertine differ in morphology from those at other hot springs, such as those at Lake Bogoria, Kenya, and Waikite in New Zealand. Comparison with the calcite dendrite crystals found at those sites shows that dendrite morphology is site-specific and probably controlled by carbonate saturation levels that, in turn, are controlled by the rate of CO₂ degassing and location in the spring outflow system.     

Evinosponges in the Triassic Esino Limestone (Southern Alps): documentation of early lithification and late diagenetic overprint

A carbonate buildup of Middle Triassic age, the Esino Limestone, outcrops in the Southern Calcareous Alps of Lombardy (N Italy). Along its margin and within the open subtidal facies, the Esino Limestone contains calcite cement-filled cavities of cm to m size. These features, known as evinosponges, may form pervasive networks within the host rock. The filling consists of concentric, isopachous layers of fibrous low-Mg calcite crystals characterized by strong undulose extinction and bent cleavages. The cement crusts are non-luminescent under cathodoluminescence, but both cements and host rock are cross-cut by micro-fractures filled with bright-luminescent calcite, related to late void-filling sparite. Mixing of different carbonates is reflected in stable isotope data. On the hand specimen scale, the oxygen and carbon isotope compositions of cements and host rock show little variation. When compared on a regional scale, the values cover a broad range from δ¹⁸O(PDB)=?5‰ to ?12‰ and from δ¹³O =0‰ to +3‰. The linear covariant trends defined by the oxygen and carbon isotope data for different sampling regions reflect the admixture of late, isotopically depleted calcite with an isotopically enriched non-luminescent calcite of early diagenetic origin. The Esino Limestone fibrous cements, which were probably precipitated in the marine or marine-meteoric phreatic environment, were affected by late diagenetic processes that caused mineral deformation and isotopic depletion through recrystallization and the admixture of a later calcite. These later calcites precipitated from penetrative fluids possibly related to Late Triassic volcanic activity and/or to the Late Cretaceous/Early Palaeogene alpine orogeny.