Depth-related ecological zonation of a carboniferous carbonate ramp: Upper Viséan of Béchar Basin,Western Algeria

Summary Following the demise of the stromatoporoid-coral reef community in Late Frasnian time, Lower Carboniferous carbonate shelf profiles possessed a ramp geometry, with major organic buildups represented by mud-rich mounds. Microfacies petrography of the exceptionally well-preserved Upper Viséan (Lower Carboniferous) carbonate ramp of the Béchar Basin, Algerian Sahara, may well contribute significantly to our understanding of the paleoecological zonation of Carboniferous non-rimmed platforms, and of the still enigmatic mounds commonly referred to as Waulsortian banks or mounds. Facies are grouped into two broad groups: (a) a mound facies group which comprises sponge wackestone-bafflestone, sponge-fenestellid bafflestone-wackestone, crinoid wackestone-packstone, and bedded flanks of intraclastic wackestone-packstone, all four facies composing the actual mud-rich mounds, and (b) a supramound facies group composed of coral-microbial framestone, crinoid packstone-grainstone, algal-foraminiferal grainstone and oolite grainstone. Calcareous algae are important bathymetric indicators and are used to delineate three bathymetric zones based on light penetration: the aphotic zone, which contains no calcareous algae; the dysphotic zone, where there is little ambient light, and which is characterized by the presence of red algae (Fasciella, Ungdarella, Stacheia, Epistacheoides) and absence of green algae; and the euphotic zone, which receives the full spectrum of sunlight, and is characterized by the occurrence of both green algae (Koninckopora, Kamaenella, Kamaena, Palaeoberesella, Calcisphaera, Anthracoporellopsis, Issinella, Exvotarisella) and red algae. Integration of algal zonation, distribution of the other biota, and recurrence of distinct assemblages, enable recognition of seven depth-related benthic assemblages. Together with the physical properties of the facies, the benthic assemblages were used to define seven bathymetric zones, from upper to lower ramp: (1) algal assemblage (upper ramp); (2) crinoid-ramose bryozoan assemblage (mid-ramp); and (3) productid brachiopod assemblage, (4) colonial rugose coral-microbial encruster assemblage, (5) crinoid-fenestellid assemblage, (6) sponge-fenestellid, and (7) sponge assemblage (lower ramp). The vertical zonation of the mud-rich mounds and associated facies differ from that reported from the classical Upper Tournaisian-Lower Viséan Waulsortian mound-bearing successions.     

An unusual trochiform gastropod from the upper Ordovician of Sweden

An unusual trochiform gastropod, Semizona bella gen. et sp. nov., is described from the Boda Limestone carbonate mounds (upper Ordovician, Ashgill) of central Sweden. A second species, S. glindmeyeri (Rohr, 1996), is recognised from the Ordovician (Whiterockian) of Nevada. The shell shape and the strongly prosocline tangential aperture of Semizona suggest that balancing of the shell on the head-foot mass was accomplished by tilting of the axis of coiling of the shell to about 65 degrees with 10–30 degrees of regulatory detorsion. The rounded aperture allowed straight contraction of the retractor muscles, suggesting clamping behaviour often associated with a sedate, grazing snail. This agrees with the environmental setting, which suggests a hard substrate with rich microbial growth. Besides clamping, the subsutural nodes and thick shell were probably effective against predation; repaired injuries indicate failed predatory attacks. Semizona shows morphological similarities with some pleurotomariin vetigastropods, and with the family Pseudophoridae Miller, 1889.     

Benthic palaeoecology of Danian deep-shelf bryozoan mounds in the Danish Basin

Early Danian cool-water bryozoan mounds exposed in the coastal cliff Stevns Klint in Denmark were formed shortly after the Cretaceous–Tertiary mass extinction. They represent a relatively deep-water, highly diverse benthic ecosystem within the epeiric seaway that covered the Danish Basin. The mounds are 50–110 m long and reached a height of about 5–10 m above the seafloor; they are asymmetrical with a steep southern and a gentle northern flank, and were dominated by small suspension feeders. The benthic elements generally occur as fragments set in a carbonate mud matrix. The main skeletal contributors are delicate branching bryozoans with minor contributions of bryozoan sheets, and nodular/arborescent bryozoans. Locally abundant octocorals occur on the mound crests and upper parts of the steep flanks. Echinoids are present in minor amounts, but are locally abundant. Serpulids, crinoids, asteroids, brachiopods, bivalves, massive calcareous sponges, and benthic foraminifers are generally minor contributors to the benthic mound fauna. Influx of planktonic foraminifers, coccoliths and other planktonic organisms was high and was probably a major source of nutrient supply to the mainly suspension-feeding benthic fauna.

The faunal association reflects a relatively low energy environment with a high, possibly seasonal influx of particulate nutrients. The best growth conditions with respect to nutrient influx were on the mound crest and upper steep flank reflected by the diverse and relatively largest benthic faunal elements. Periodic reworking and winnowing occurred across the entire mound structure but most prominent on the gentle northern flanks limiting the benthic growth and notably the colony density and size of delicate branching bryozoans. Vagile benthic faunas were also adapted to different areas on the mound. Irregular echinoids preferred the intermound areas within fine-grained wackestone–packstone facies where they ploughed through the sediment, whereas regular echinoids were epifaunal and preferred the upper parts of the mounds, possibly feeding mainly on bryozoans. Skeletons of both groups became concentrated at the toe of the steep flanks and in the intermound areas by physical reworking during major storms.

Changes in faunal composition on the mound crests occurred rhythmically on both small and large scale during mound growth. Rhythmically recurring faunal assemblages reflect alternating hydrodynamic conditions on the seafloor with respect to nutrient influx and energy, which probably were linked to short-term seasonal and long-term climatic variations; the long-term alternation may be within the Milankovitch frequency band. Blooming events of bryozoan sheets resulted from relatively short periods with large amounts of available food and suitable substrate. Successful colonisation by octocorals on the other hand reflected longer-term favourable conditions on the mounds possibly associated with overall higher energy levels.

A possible Pleistocene analogue to the bryozoan-dominated Danian mounds occurs at the shelf-slope break of the Great Australian Bight. Both of these cool-water mound systems deviate from most other biogenic mounds known from the fossil record in their non-cemented nature, regular geometry and a lack of core and flank facies.     

A microbial model for the Lower Devonian stromatactis mud mounds of the Montagne Noire (France)

Summary Lower Devonian mud mounds and stromatactis fabrics are exceptionally well exposed in quarry walls and industrially sawed blocks in the Montagne Noire in southern France. Interlayered red biomicrites and white to grey sparitic calcites form mounds up to 70 m high. The red biomicrites contain predominantly bryozoans, sponges and echinoderms. The sparitic layers show typical features of stromatactis fabrics, as outlined byBathurst (1982). We recognize two types of stromatactis fabrics: (1) Stromatactis type A: exentsive cavity systems filled by multiple cement generations, which are interpreted to be related to microbial mats, and (2) Stromatactis type B: smaller patches of blocky spar which are mainly diagenetic in origin, but show characteristic features of stromatactis. Type A is far more important in terms of rock volume. The cyclic interlayering of red biomicrites and sparitic layers is supposed to result from frequent changes in the composition of the mound biota. The bryozoan/sponge community was displaced by short term propagations of microbial mats during times of extremely low sedimentation. Sedimentation and thus the biotic community was probably determined by high frequency (6th order) sea level changes. Despite these changes, mound growth continued, because once established the ecological advantage over the surroundings was maintained by both communities alternating with each other. The microbial mats and the cavities they left after their decay were important for the stabilization of the mounds, the latter allowing for enormous quantities of dissolved carbonate to be transported and precipitated. We anticipate a close interrelation between mound formation and stromatactis formation, and we believe that it is not incidential that both, mud mounds and stromatactis, are mainly restricted to the same interval, namely the Paleozoic.     

Subsurface microbiology and biogeochemistry of a deep, cold-water carbonate mound from the Porcupine Seabight (IODP Expedition 307)

The Porcupine Seabight Challenger Mound is the first carbonate mound to be drilled (∼270 m) and analyzed in detail microbiologically and biogeochemically. Two mound sites and a non-mound Reference site were analyzed with a range of molecular techniques [catalyzed reporter deposition-fluorescence in situ hybridization (CARD-FISH), quantitative PCR (16S rRNA and functional genes, dsrA and mcrA ), and 16S rRNA gene PCR-DGGE] to assess prokaryotic diversity, and this was compared with the distribution of total and culturable cell counts, radiotracer activity measurements and geochemistry. There was a significant and active prokaryotic community both within and beneath the carbonate mound. Although total cell numbers at certain depths were lower than the global average for other subseafloor sediments and prokaryotic activities were relatively low (iron and sulfate reduction, acetate oxidation, methanogenesis) they were significantly enhanced compared with the Reference site. In addition, there was some stimulation of prokaryotic activity in the deepest sediments (Miocene, > 10 Ma) including potential for anaerobic oxidation of methane activity below the mound base. Both Bacteria and Archaea were present, with neither dominant, and these were related to sequences commonly found in other subseafloor sediments. With an estimate of some 1600 mounds in the Porcupine Basin alone, carbonate mounds may represent a significant prokaryotic subseafloor habitat.     

Middle paleozoic waulsortian-type mud mounds in Southern Fergana (Southern Tien-Shan,commonwealth of independent states): The shallow-water atoll model

Summary Several Waulsortian-type mud mounds nearly 500 m thick and about 5 km long occur in the Middle Paleozoic carbonate section of the Aktur nappe in the mountains on the right bank of Isfara river. These buildups form a well developed barrier system that stretches along the South Ferganian carbonate platform margin and divides the carbonate complex into a fore-reef and a back-reef part. The time of the mounds' most active growth was from the Late Silurian (Ludlow) to the Middle Devonian (Eifel). Three main facies types can be recognized in the mud mounds: 1. micritic core facies, 2. sparitic flank facies and 3. loferitic capping facies. The central massive or crudely bedded part of the mounds consists of white or light grey clotted micrite. Macrofossils are rare. The sparitic flank facies in contrast consists of coarse and densely packed crinoidal wackestone-floatstones with some brachiopod shell debris. Solitary rugose corals, tabulate corals, stromato-poroids and fragments of mollusks are also abundant. The tops of the mounds are usually covered with loferitic pelmicrites or oolitic grainstone caps. Stromatactis-like structures are very rare and poorly developed in the South Ferganian mud mounds. However, almostin all such mounds horizons of calcitic breccias can be found. In order to explain all the features found in the Fergana mounds an ‘atoll-like’ model has been proposed which starts the evolution of the mud mounds with a small nucleus bioherm. The main stage of the evolution corresponds to an atoll-like structure developing on the surface of shallow water platforms. White clotted micrite of the mound core facies is interpreted as a accumulation of fine-grained sediment in an inner lagoon flanked by crinoidal bar deposits. The mound flank facies represents the atoll rim deposits from where the carbonate mud is derived. The capping loferitic facies is considered as tidal flat deposit that developed on top of the buildups during the last stage of its evolution. The knoll shape of the mounds is explained by the retreat of the atoll flanking crinoidal bars back into the inner lagoon during the rise in sea level. Stromatactis-like structures of small cavities filled with sparry calcite owe their existence to burrowing organisms. Calcitic breccias are interpreted as paleokarst collapse breccias. They indicate that the tops of the mud mound became subaerially exposed. Other evidence for a subaerial exposure can be seen in the occurrence of Variscian ‘black and white’ limestone gravel on the tops of some mud mounds. According toWard et al. (1970) these sediments were produced above the sea level at the edge of hypersaline lakes situated on islands.     

Symbiosis between gastropods and bryozoans in the late Ordovician of Cumbria, England

Five examples of symbiosis between gastropods and trepostome bryozoans are described from the Ashgill (late Ordovician) of Cumbria (England). The gastropods are invariably found associated with the bryozoans. whereas the bryozoans may be free-living. Encrustation is considered to have taken place, in most cases, on mature, living gastropod shells, resulting in the trepostome utilizing the shell as a surrogate basal disc. Three specimens show encrustation on an empty gastropod shell, causing the trepostome to develop a basal disc similar to non-encrusting forms. The bryozoan colony probably benefited from the symbiotic relationship by increased water flow over the colony, caused by gastropod locomotion, whereas the gastropod was afforded protection from predators. The new species Spiroecus nidhoeggi. Diplotrypa hvergelmi and Monotrypa fontinalis are described.     

Oxygen minimum zone and internal waves as potential controls on location and growth of Waulsortian mounds (Mississippian, Sacramento Mountains, New Mexico)

Summary Lower Mississippian Waulsortian mounds in the Sacramento Mountains grew on a south-dipping homoclinal ramp at depths ranging from approximately 110 to 250 m, a setting in which nutrient sources and pathways are poorly understood in ancient carbonate depositional systems. Lithologic, biotic, and chemical data suggest that the mounds grew in an area on the ramp within a dysoxic oxygen minimum zone (OMZ) resulting from the concentration of organic matter below a thermocline. The abundance of organic matter there, perhaps a consequence of upwelling, enhanced the productivity of the major sediment contributors to the mounds—sponges, pelmatozoans, bryozoans, and heterotrophic carbonate-producing microbes. The siting and growth of individual mounds within the OMZ is best explained by two factors. One is the positive low-relief intra-ramp topography on and around which the mounds grew. The other is that nutrient supply for carbonate producing microbes was concentrated at the sites of mounds growth by internal waves on the pycnocline coincident with the thermocline. The internal waves mixed the nutrient-rich water of the OMZ with the better-oxygenated adjacent water mass, stirred the substrate and resuspended organic matter so that it was more available for the primarily suspension-feeding macrofauna both above and below the pycnocline, and generated local vertical mixing. Because of initial intra-ramp topography and subsequently increased relief as the mounds grew, internal waves focused and localized these processes, thus enhancing carbonate production at individual mound sites in a positive feed-back loop.     

Anatomy of carbonate mounds from the Middle Anisian of Nakhlak (Central Iran): architecture and age of a subtidal microbial-bioclastic carbonate factory

The Anisian succession of Nakhlak (in Central Iran) is characterized by a siliciclastic succession with minor carbonate units, with massive carbonate mounds up to 50?m thick in its upper part. The mounds, constrained in age to the late Bithynian (Ismidicus Zone) by ammonoids and conodonts, are characterized by a flat top and a lateral pinch-out marked by clinostratified slopes (about 15° in dip). Stratigraphic and microfacies analyses document an inner part of the mound characterized by massive microbial carbonates with open-space structures (stromatactis) filled with fine-grained internal sediments and marine cements. Isolated sponges (up to 5?cm), serpulids and bryozoans are present, which grew on the calcimicrobial limestone. A narrow bioclastic margin (mainly with crinoids and brachiopods) produces most of the slope facies (consisting of bioclastic grainstone and packstone, with intraclasts from the inner part of the mounds) which interfinger basinward with volcaniclastic sandstones. The demise of carbonate productivity is marked on the top of the carbonate mounds by a condensed surface, rich in ammonoids, glaucony grains, and articulated crinoids, documenting a rapid drowning. Paleolatitude data support deposition in a tropical setting, and sedimentological constraints indicate deposition close to the fair-weather wave base, within the photic zone. The late Bithynian Nakhlak carbonate mounds developed before the appearance (documented since the Pelsonian in different parts of the world) of scleractinians which, despite the favorable environmental conditions, are absent at Nakhlak. The Nakhlak mounds thus represent one of the last occurrences of the microbial factories (which developed after the Permo-Triassic extinction event and persisted for most of the Middle Triassic, but with a gradually increasing role played by scleractinians) before the first appearance of the Mesozoic corals.     

Mineralogy of Arctic bryozoan skeletons in a global context

Bryozoans are major carbonate producers in some ancient and Recent benthic environments, including parts of the Arctic Ocean. Seventy-six species of bryozoans from within the Arctic Circle have been studied using XRD to determine their carbonate mineralogies and the Mg content of the calcite. The majority of species were found to be calcitic, only four having bimineralic skeletons that combined calcite and aragonite, and none being entirely aragonitic. In almost all species, the calcite was of the low- (<4 mol% MgCO₃) or intermediate-Mg (4–11.99 mol% MgCO₃) varieties. Previous regional studies of bryozoan biomineralogy have found higher proportions of bimineralic and/or aragonitic species in New Zealand and the Mediterranean, with a greater number of calcitic species employing intermediate- and high-Mg calcite. The Antarctic bryozoan fauna, however, has a similar mineralogical composition to the Arctic. The lesser solubility of low-Mg calcite compared to both Mg calcite and aragonite in cold polar waters is most likely responsible for this latitudinal pattern. However, it is unknown to what extent environmental factors drive the pattern directly through eliciting an ecophenotypic response from the bryozoans concerned or the pattern reflects genetic adaptations by particular bryozoan clades.     

From sediment to rock: diagenetic processes of hardground formation in deep-water carbonate mounds of the NE Atlantic

Modern cool-water carbonate mounds topped by corals form an extended reef belt along the NW European continental margin at 200–1200 m water depth. An essential element of mound growth are hardgrounds which provide a stable substratum for mound-building invertebrate colonisation and stabilise the inclined mound flanks. Evaluating the degree of lithification and the slope stability against erosion represents an important task within the ESF programme MOUNDFORCE under the umbrella of EUROMARGINS. Sampling of hardgrounds during RV Meteor cruises M61-1 and -3 in 2004 by means of the IFM-GEOMAR TV-grab and the Bremen ROV QUEST focused on carbonate mounds of the Porcupine Seabight and northwestern Rockall Bank off Ireland. Lithified carbonates of mid-Pleistocene age were exhumed during the Holocene and are now exposed on the top and flanks of numerous carbonate mounds showing a patchy to dense colonisation by living corals and associated invertebrates. The sediments, composed of foraminiferal–nannoplankton oozes and admixed mound-derived invertebrate skeletons, range from partly lithified chalks to dense micritic limestones. These wackestones to packstones clearly differ from bacterially induced authigenic carbonate crusts typical of hydrocarbon seep settings by showing current-induced sedimentary structures, a non-luminescing matrix indicating oxic pore fluids, and a marine isotopic signature lacking any depleted carbon regime which is typical of anaerobic methane oxidation. The carbonate lithification is driven by carbonate ion diffusion from supersaturated seawater into the pore fluids in the studied areas. Vigorous bottom currents were the ultimate control not only of carbonate cementation by enhancing the diffusion process and supporting a pumping mechanism, but also of hardground formation and mound shaping by exhuming lithified carbonates and preventing fine-grained sediment accumulation at the downslope mound flanks.     

Distribution, seasonal use, and predation of incubation mounds of Orange-footed Scrubfowl on Komodo Island, Indonesia

ABSTRACT.   Megapodes are unique in using only heat from the environment, rather than body heat, to incubate their eggs as well as the precocious independence of their chicks on hatching. Of 22 recognized species of megapodes, 9 are listed as threatened due to factors including habitat loss and fragmentation, and predation on eggs and chicks. Orange-footed Scrubfowl ( Megapodius reinwardt ) are conspicuous components of the Oriental/Austral avifauna that inhabit the monsoon forests of the Lesser Sunda chain of islands in Indonesia. We examined the abundance, patterns of distribution, physical characteristics, seasonal activity, and predation risk of incubation mounds of Orange-footed Scrubfowl on Komodo Island in eastern Indonesia. We surveyed 13 valleys on Komodo Island from April 2002 to January 2005 and located 113 tended and 107 untended incubation mounds. Densities of scrubfowl mounds in our study were similar to that reported by investigators during the 1970s, suggesting little change in the scrubfowl population since then. Most scrubfowl mounds were on sandy or loamy soils in open monsoon forest with little overhead shade, and placement of mounds in such areas may ensure adequate temperatures for egg incubation. Although some mounds were tended during all months, mound use peaked during the late wet season in March. During the dry season (April–November), only a few mounds were tended. Komodo dragons ( Varanus komodoensis ) and wild pigs ( Sus scrofa ) were the primary predators of scrubfowl eggs, with no indication of egg predation by humans. The valley with the largest number of untended mounds in our study also had the largest number of active Komodo dragon nests. This suggests an effect of Komodo dragons on scrubfowl numbers, but additional study is needed.     

Facies belts and communities of the arctic Vesterisbanken Seamount (Central Greenland Sea)

Summary The Arctic Vesterisbanken Seamount, situated far offshore in the central Greenland Sea, provides a unique facility for studing modern cold water siliceous carbonate deposits. A nearly year round sea ice cover, which retreats on average only during two months, and a rather constant temperature and salinity structure of the water column characterize the Arctic conditions of the area. Despite predominantly oligotrophic conditions with a pronounced food supply from the pelagic realm only during the ice-free season, the seamount is covered extensively by extended sponge-bryozoan constructions. Three distinct facies belts reveal a pronounced depth zonation which depends on variations in downslope food transfer and which is specifically effective due to the development of aTaylor current regime over the seamount: i) the crest facies from the summit at −133m to −260 m, ii) the shallow slope facies from −260 m to −400 m, iii) the deep slope facies from −400 m down to the abyssal plain at about— 3.000 m. Different biogenic structures and communities are found within these facies belts, including widely extended biogenic mats, sponge bryozoan-serpulid buildups with mounds, hedges, spurs and flatcake-like structures, bryozoan thickets and sponge-crinoid mounds. Depth zonation, internal structure and controlling parameters in the formation of these biogenic structures are discussed in the context of their significance as a modern end member of the Foramol facies and their implication for the fossil record. In addition, the younger volcanic and hydrothermal history of the seamount is presented with special reference to its bearing on Holocene biogenic colonization patterns.     

Coral-rudist bioconstructions in the Upper Cretaceous Haidach section (Gosau Group; Northern Calcareous Alps, Austria)

Summary In the area of Haidach (Northern Calcareous Alps, Austria), coral-rudist mounds, rudist biostromes, and bioclastic limestones and marls constitute an Upper Cretaceous shelf succession approximately 100 meters thick. The succession is part of the mixed siliciclasticcarbonate Gosau Group that was deposited at the northern margin of the Austroalpine microplate. In its lower part, the carbonate succession at Haidach comprises two stratal packages that each consists, from bottom to top, of a coral-rudist mound capped by a rudist biostrome which, in turn, is overlain by bioclastic limestones and, locally, marls. The coral-rudist mounds consist mainly of floatstones. The coral assemblage is dominated by Fungiina, Astreoina, Heterocoeniina andAgathelia asperella (stylinina). From the rudists, elevators (Vaccinites spp., radiolitids) and recumbents (Plagioptychus) are present. Calcareous sponges, sclerosponges, and octocorals are subordinate. The elevator rudists commonly are small; they settled on branched corals, coral heads, on rudists, and on biolastic debris. The rudists, in turn, provided settlement sites for corals. Predominantly plocoid and thamnasteroid coral growth forms indicate soft substrata and high sedimentation rates. The mounds were episodically smothered by carbonate mud. Many corals and rudists are coated by thick and diverse encrustations that indicate high nutrient level and/or turbid waters. The coral-rudist mounds are capped byVaccinites biostromes up to 5 m thick. The establishment of these biostromes may result from unfavourable environmental conditions for corals, coupled with the potential of the elevator rudists for effective substrate colonization. TheVaccinites biostromes are locally topped by a thin radiolitid biostrome. The biostromes, in turn, are overlain by bioclastic limestones; these are arranged in stratal packages that were deposited from carbonate sand bodies. Approximately midsection, an interval of marls with abundantPhelopteria is present. These marls were deposited in a quiet lagoonal area where meadows of sea grass or algae, coupled with an elevated nutrient level, triggered the mass occurrence ofPhelopteria. The upper part of the Haidach section consists of stratal packages that each is composed of a rudist biostrome overlain by bioclastic wackestones to packstones with diverse smaller benthic foraminifera and calcareous green algae. The biostromes are either built by radiolitids,Vaccinites, andPleurocora, or consist exclusively of radiolitids (mainlyRadiolites). Both the biostromes and the bioclastic limestones were deposited in a low-energy lagoonal environment that was punctuated by high-energy events.In situ-rudist fabrics typically have a matrix of mudstone to rudistclastic wackestone; other biogens (incl. smaller benthic foraminifera) are absent or very rare. The matrix of rudist fabrics that indicate episodic destruction by high-energy events contain a fossil assemblage similar to the vertically associated bioclastic limestones. Substrata colonized by rudists thus were unfavourable at least for smaller benthic foraminifera. The described succession was deposited on a gently inclined shelf segment, where coral-rudist mounds and hippuritid biostromes were separated by a belt of bioclastic sand bodies from a lagoon with radiolitid biostromes. The mounds document that corals and Late Cretaceous elevator rudists may co-occur in close association. On the scale of the entire succession, however, mainly as a result of the wide ecologic range of the rudists relative to corals, the coral-dominated mounds and the rudist biostromes are vertically separated.     

Basalt mounds and adjacent depressions attract contrasting biofacies on a volcanically active Middle Miocene coastline (Porto Santo, Madeira Archipelago, Portugal)

Small basalt mounds with encrusting corals and inter-mound carbonate sandy zones with abundant rhodoliths corresponding to an ancient intertidal to shallow-water sea floor are exhumed from overlying volcaniclastic deposits and basalt lava flows at Pedra de água on Ilhéu de Cima off Porto Santo, one of the islands of the northeastern Atlantic Madeira Archipelago (Portugal). The mounds rise above the surrounding surface to attain a height of about half a meter. The mounds exhibit an in situ assemblage of hermatypic corals, dominated by Tarbellastrae and Solenastrea. They formed as massive (4.2?×?1.9?m average length), isolated patches in a protected bay close to shore eroded from an uneven basalt substrate dated to the Middle Miocene (14–15?Ma). The slightly deeper zones between basalt mounds, which alternate with them over a distance of more than 20?m, are covered mainly by coarse carbonate sand on which rhodoliths up to 14.8?cm in diameter are preserved in situ. Many rhodoliths have grown around a basalt core, which indicates a local, near-shore source for development. Complete burial of the elevated coral settlements and intervening low zones populated by rhodoliths occurred when volcanic lapilli and other tephra catastrophically buried this part of the rocky shore. The rhodoliths and coral assemblages exposed in an area of 12?m² were canvassed systematically using census quadrats to quantify community relationships.     

塔里木板块塔中区上奥陶统良里塔格组的生物礁类型

塔里木板块塔中Ⅰ号坡折带附近上奥陶统良里塔格组取芯井段中可识别多种生物礁灰岩类型,包括珊瑚骨架/障积岩、海绵骨架/绑结岩、苔藓虫绑结岩、钙藻障积岩、钙质菌藻障积/绑结岩等礁灰岩类,藉此可归纳出珊瑚礁、珊瑚-钙藻礁、层孔虫礁、层孔虫-钙藻礁、珊瑚-层孔虫-钙藻礁、苔藓虫礁丘、钙藻礁丘、灰泥丘和微生物礁等生物建造单元。这些礁体的时空分布模式与古环境分异相关联,纵向上具有灰泥丘向珊瑚-层孔虫-钙藻礁至苔藓虫礁丘和钙藻礁的群落结构更替趋势;空间分布则向台地北缘,即I号坡折带延伸显示由低能带灰泥丘向高能带珊瑚-层孔虫-钙藻礁的相变,而且高能带珊瑚-层孔虫-钙藻主体礁和环其周缘相对低能带的钙藻礁丘、灰泥丘等在一定范围内构成造礁群落结构分异。     

Microbial mats associated with bryozoans (Coorong Lagoon, South Australia)

Summary Bryostromatolites are laminated carbonate rocks composed of bryozoan zoarial laminae. The laminated texture is frequently caused by patterns of bryozoan self overgrowth as a regular defensive tactic against microbial fouling. In the Coorong Lagoon (South Australia), another type of bryostromatolite is present where the laminated growth of the weakly calcifying bryozoan speciesConopeum aciculata is postmortally stabilized by cyanobacterial mats at the surface, and fungal mats settling in the zooecial cavities. A tough extracellular slime network produced by benthic cyanobacteria is a trap for sediment particles, provides a method of adhesion to the bryozoan substrate, and produces a biological lamination by the vertical stratification of dead bryozoan skeletons. These slimes are also important for the preservation of cell structures and for their fossilization. Seasonal fluctuations in salinity and water level are the most important regional control factors, causing a phase displacement in the growth optima of microbial mats and bryozoans, thereby resulting in a rigid bryostromatolitic fabric.     

Iron microbial communities in Belgian Frasnians carbonate mounds

Summary The Belgian Frasnian carbonate mounds occur in three stratigraphic levels in an overall backstepping succession. Petit-Mont and Arche Members form the famous red and grey “marble” exploited for ornamental stone since Roman times. The evolution and distribution of the facies in the mounds is thought to be associated with ecologic evolution and relative sea-level fluctuations. Iron oxides exist in five forms in the Frasnian mounds; four are undoubtedly endobiotic organized structures: (1) microstromatolites and associated forms (blisters, veils...), possibly organized in “endostromatolites”; (2) hematitic coccoids and (3) non dichotomic filaments. The filaments resemble iron bacteria of theSphaerotilus-Leptothrix “group”; (4) networks of dichotomic filaments ascribable to fungi; (5) a red ferruginous pigment dispersed in the calcareous matrix whose distribution is related to the mound facies type. The endobiotic forms developed during the edification of the mounds, before cementation by fibrous calcite. The microbial precipitation of iron took place as long as the developing mounds were bathed by water impoverished in oxygen.     

Late Ordovician carbon isotope trend in Estonia, its significance in stratigraphy and environmental analysis

Carbon isotope changes during most of Late Ordovician time (from the mid-Caradoc Kinnekulle K-bentonite until the beginning of the Silurian) were investigated. As the corresponding sequence of rocks is stratigraphically nearly complete in Estonia, an attempt was made to use it to elaborate the general pattern of carbon isotope changes in the Late Ordovician. Complications were caused by several local or regional hiatuses in the middle and late Caradoc and Hirnantian. A total of 385 whole rock samples were studied from eight drill cores in northern and central Estonia. The following positive carbon isotope events were observed: (1) the mid-Caradoc excursion (peak δ¹³C value 2.2‰) in the uppermost part of the Keila Stage, also known in Sweden; (2) the first late Caradoc excursion (1.9‰) in the lower part of the Rakvere Stage; (3) the second late Caradoc excursion (2.4‰) in the upper part of the Nabala Stage; (4) the early Ashgill excursion (2.5‰) in the lowermost part of the Pirgu Stage; (5) the widely known large Hirnantian excursion (in Estonia the peak value reaches 6.7‰) in the Porkuni Stage. The study interval comprises a long (10 Ma) period characterized by low-magnitude carbon isotope changes and a following brief (2 Ma) interval with large changes. No obvious lithological preference for hosting the positive shifts was recorded. In principle, the δ¹³C values exceeding the background values may occur in all types of rocks present in a sedimentary basin. Several δ¹³C positive excursions (values 1.5‰ to 3‰) in the Mohawkian of North America are evidence that the minor Caradoc and early Ashgill δ¹³C positive shifts in Baltoscandia may have counterparts in Laurentia. If correctly correlated, these shifts may have global significance. The Hirnantian excursion is usually linked to a major glacial event, even if some carbon cycling mechanisms are not completely understood. The environmental causes suggested for the earlier minor shifts range from global climatic and glacial events to very local changes in basin regime and sea level. Our study supports the primary role of climatic or climatically triggered oceanic processes.     

Reefal and mud mound facies development in the Lower Devonian La Vid Group at the Colle outcrops (León province, Cantabrian Zone, NW Spain)

In the locality of Colle (Cantabrian Zone, NW Spain), the upper part of the Valporquero Shale Formation (Emsian, La Vid Group) contains an interval of shales and marlstones (barren, greenish-grey shales and fossiliferous, greenish-grey or reddish shales/marlstones) with beds and packages of homogeneous and cross-bedded skeletal limestones. Metre-scale mud mounds and coral biostromes occur encased in the fossiliferous reddish and greenish-grey shale/marlstones, respectively, with the coral biostromes overlying conspicuous skeletal limestone bodies. These rocks were deposited on a carbonate ramp, ranging from above storm wave base for the cross-bedded skeletal limestones to below the storm wave base for the remaining deposits, organic buildups included. The vertical stacking of these facies and the occurrence of the two types of buildups are interpreted to reflect the interplay among several (possibly 4th and 5th) orders of relative sea-level variations, during a 3rd-order highstand. Coral biostromes occur in early 5th-order transgressive system tracts developed within late 4th-order highstand, and are interpreted to have thrived on a stable granular substrate (skeletal limestones) in non-turbid waters, being later aborted by the onset of muddy sedimentation. Biostrome features suggest that they developed under environmental conditions essentially different from those related to the sedimentation of their granular substrate. Mud mounds occur in 5th-order transgressive and early highstand system tracts tied to early 4th-order sea-level rise. Field relationships suggest that mud mounds grew coevally with muddy sedimentation, with high-frequency variations in carbonate vs. terrigenous mud sedimentation influencing their development.An erratum to this article can be found at