Why barren intervals? A taphonomic case study of the Scandinavian Alum Shale and its faunas

The Scandinavian Alum Shale Formation (Middle Cambrian to Lower Ordovician) accumulated under generally low oxygen concentrations. Syndepositional changes in the oxygen concentrations of the bottom water are reconstructed on the basis of the fossil fauna. Under relatively high oxygen concentrations, brachiopods and non-olenid polymerid trilobites inhabited the sea floor. Under lower oxygen concentrations the fauna was dominated by agnostids and at lowest oxygen levels by olenid trilobites. The enrichments of vanadium relative to nickel, as well as the enrichment of sulphur, match these faunal changes. A geochemical classification of the dysoxic environment is presented. The abundance of calcareous fossils decreases with increasing bottom water oxygen concentrations, indicating that the preservation of calcareous hard parts is most likely at the lowest oxygen concentrations. The poor preservation of calcareous fossils at relatively high oxygen concentrations is explained by the generation of corrosive pore waters during the reoxidation of sulphide compounds. Trilobitic and non-trilobitic intervals alternate up through the shale. Non-trilobitic intervals are either barren or contain non-calcareous fossils (phosphatic brachiopods, phosphatic 'ostracodes' and graptolites). The stratigraphical variation of trilobitic and non-trilobitic intervals is interpreted to reflect major changes in oxygen levels that might be linked to sea-level and climatic fluctuations.     

Cambrian high-resolution biostratigraphy and carbon isotope chemostratigraphy in Scania, Sweden: first record of the SPICE and DICE excursions in Scandinavia

A core drilling (Andrarum‐3), from the classical locality at Andrarum, Scania, southernmost Sweden, penetrated a 28.90‐m‐thick Cambrian succession. The core comprises dark grey to black, finely laminated mudstones and shales with early concretionary carbonate lenses (stinkstones or orsten) and a few primary carbonate beds. The middle Cambrian (provisional Series 3) part of the core comprises 17.35 m, whereas the Furongian Series (upper Cambrian) part covers the remaining 11.55 m. Nineteen trilobite and two phosphatocopine genera are present in the middle Cambrian, whereas the less diverse Furongian interval yielded four trilobite and three phosphatocopine genera. Other, less frequent, faunal elements include conodonts (s. l.), brachiopods, sponge spicules, bradoriids, and coprolites. Trilobites and phosphatocopines were used to subdivide the core into seven biozones ranging from the Ptychagnostus atavus Zone to the Parabolina spinulosa Zone (P. spinulosa Subzone). Carbon isotopic analyses (δ¹³C_org) through the core show two important excursions, the negative DrumIan Carbon isotope Excursion (DICE) in the Pt. atavus Zone, and the Steptoean Positive Carbon Isotope Excursion (SPICE) beginning near the first appearance of Glyptagnostus reticulatus and extending upward into the Olenus and Agnostus (Homagnostus) obesus Zone. The DICE displays a peak value, in the samples at hand, of –30.45‰δ¹³C_org in the lower part of the P. atavus Zone. The δ¹³C_org values increase through the overlying L. laevigata and A. pisiformis zones and display peak values of c. –28.00‰δ¹³C_org in the lowermost Furongian Olenus wahlenbergi and O. attenuatus subzones. Thereafter the values decrease significantly through the O. scanicus Subzone. Both isotopic excursions have been documented from several palaeocontinents, but never before from Baltica. Moreover, for the first time these excursions are recorded from organic matter in an alum shale setting. The recorded shift of +1.50–2.00‰δ¹³C_org is approximately half the magnitude of the SPICE documented from other regions. This discrepancy may be related to temporal variations in the type, origin, or diagenesis of the organic fraction analysed.     

Trilobite biofacies and sequence stratigraphy: an example from the Upper Ordovician of Oklahoma

There have been surprisingly few empirical investigations of the fundamental principle that the architecture of depositional sequences exerts considerable control on observed patterns of faunal distribution and replacement. In this paper, we examine trilobite associations in two sequences of the Upper Ordovician (Sandbian) Bromide Formation of southern Oklahoma. Cluster analysis and ordination of genus abundance data identified five lithofacies‐related biofacies that are also differentiated by diversity patterns. Biofacies of the transgressive system tract (TST) of successive sequences are more similar to each other than they are to biofacies in the highstand systems tract (HST) of the same sequence. This similarity likely records dominance of large, robust convex sclerites in taphonomically degraded samples from condensed, strongly winnowed grainstone and rudstone. Horizons with articulated exoskeletons of isoteline trilobites preserved by obrution deposits occur most commonly in the early HST and record behavioural aggregations. Grainstone and rudstone of the later HST are less winnowed than those of the TST and show less fragmentation and sorting of sclerites. These changes in taphonomic conditions preserve ecological patterns more clearly. In most biofacies, rarefied alpha diversity (samples) and gamma diversity (biofacies) of middle‐ and outer‐ramp HST deposits are greater than in the TSTs, and biofacies replace each other down ramp. Diversity patterns do not agree with model predictions and other data sets that indicate low beta and high alpha diversity in the TST, likely because of taphonomic degradation. Vertical replacement of biofacies is expressed by the appearance of peritidal facies in which trilobites are rare. Biofacies shifts also characterize sequence boundaries and are most profound in the inner‐ramp successions characterized by sharp facies offsets. Comparison with bathymetrically similar deposits in the Taconic foreland basin showed similar diversity trends along environmental gradients, with some differences in shallow‐water settings attributed to taphonomic differences.     

Lower-Middle Cambrian boundary in open shelf facies of the Siberian Platform

In the Early and Middle Cambrian (of traditional usage), three broad facies belts were developed over the Siberian Platform. The lithofacies belts comprise evaporitic-carbonate, reef-shoal, and open-marine environments.Trilobites assemblages are most diverse in the open-marine lithofacies (Judoma-Olenek facies), represented especially by the Kuonamka Formation, in the eastern part of the platform. Species, genera and families of trilobites gradually increased through the Middle-Cambrian boundary interval in the Kuonamka Formation. Protolenidae dominated in the time represented by the Lermontovia Zone. In strata assigned to the Anabaraspis Zone, the protolenids disappear, the paradoxidids appear, and the diversity of dorypygids increases. The number of trilobite families increases in the Oryctocara and Kounamkites zones.Well represented in the Kuonamka formation of the eastern Siberian Platform are three levels of trilobites that have potential for global correlation. They are the Oryctocephalus reticulatus (=O. indicus latus), Oryctocephalus indicus, and Ovatoryctocara granulatus levels. The Lower-Middle Cambrian boundary in the South China correlates to the lower part of the Kounamkites Zone of the Siberian Platform.     

Names for trace fossils: a uniform approach

The taxonomic treatment of trace fossils needs a uniform approach, independent of the ethologic groups concerned. To this aim, trace fossils are rigorously defined with regard to biological taxa and physical sedimentary structures. Potential ichnotaxobases are evaluated, with morphology resulting as the most important criterion. For trace fossils related to bioerosion and herbivory, substrate plays a key role, as well as composition for coprolites. Size, producer, age, facies and preservation are rejected as ichnotaxobases. Separate names for undertracks and other poorly preserved material should gradually be replaced by ichnotaxa based on well-preserved specimens. Recent traces may be identified using established trace fossil taxa but new names can only be based on fossil material, even if the distinction between recent and fossil may frequently remain arbitrary. It is stressed that ichnotaxa must not be incorporated into biological taxa in systematics. Composite trace fossil structures (complex structures made by the combined activity of two or more species) have no ichnotaxonomic standing but compound traces (complex structures made by one individual tracemaker) may be named separately under certain provisions. The following emendations are proposed to the International Code of Zoological Nomenclature: The term 'work of an animal' should be deleted from the code, and ichnotaxa should be based solely on trace fossils as defined herein.     

Paleoceanography of the Late Cretaceous (Maastrichtian) Western Interior Seaway of North America: evidence from Sr and O isotopes

Well-preserved fossils of the Late Cretaceous Western Interior Seaway (WIS) of North America have been analyzed for Sr concentration and Sr and O isotopes in order to decipher paleosalinities and paleotemperatures. The samples are from four biofacies within the Seaway (late Maastrichtian): offshore Interior (Pierre Shale), nearshore Interior (Fox Hills Formation), brackish (reduced salinity; Fox Hills Formation) and freshwater (Hell Creek Formation). Samples were also obtained from the Severn Formation of Maryland (considered to be representative of the open ocean). All biofacies (except the freshwater) are demonstrably within the Jeletzkytes nebrascensis ammonite zone (<1 Ma duration). The ⁸⁷Sr/⁸⁶Sr ratios show significant and systematic decreases from marine (mean±1 S.D.=0.707839±0.000024) to brackish facies (mean±1 S.D.=0.707677±0.000036), consistent with dilution by freshwater with a lower ⁸⁷Sr/⁸⁶Sr ratio than seawater. Such variation disallows using the ⁸⁷Sr/⁸⁶Sr ratios of fossil shell material to assign ages to fossils from the Late Cretaceous WIS without knowledge of the salinity in which the organism grew. The Sr isotope ratios for scaphitid ammonites within a single biofacies are similar to each other and different from those for scaphites in other biofacies, implying that these organisms are restricted in their distribution during life. The ⁸⁷Sr/⁸⁶Sr values of freshwater unionid mussels range widely and are not compatible with the freshwater endmember ⁸⁷Sr/⁸⁶Sr ratio required by the trend in ⁸⁷Sr/⁸⁶Sr vs. biofacies established from the other samples. Paleosalinities for the biofacies are estimated to range from 35‰ in the open marine to a minimum of 20‰ in the brackish, based on the presence of cephalopods in all four facies and the known salinity tolerance of modern cephalopods. Producing reasonable ⁸⁷Sr/⁸⁶Sr values for the freshwater endmember of a ⁸⁷Sr/⁸⁶Sr vs. 1/[Sr] plot requires a Sr concentration 0.2-0.5 that of seawater for the dominant freshwater input to the WIS. Such high Sr concentrations (relative to seawater) are not observed in modern rivers, and we suggest that the brackish environment in the WIS arose through the mixing of freshwater and seawater in a nearshore aquifer system. Reactions of the solution with aquifer solids in this ‘subterranean estuary’ [Moore, Mar. Chem. 65 (1999) 111-125] produced brackish water with the Sr concentration and isotopic composition recorded in the brackish biofacies. δ¹⁸O values of the fossils show decreases from the marine to brackish biofacies consistent with increasing temperatures (from ∼13 to 23°C) or, if temperatures were relatively constant, to a decrease in the δ¹⁸O of the water in which the shell formed. The latter interpretation is consistent with less-than-fully marine salinities in the nearshore biofacies, but both changes in temperature and the isotopic composition of the water may have occurred in this environment.     

Traces of predation in the Cambrian

Series two marks a revolution in Cambrian predation when new predators and new predation methods appeared, which led to general increase in predation intensities and in the diversity of prey groups. The number of bored taxa and taxa with the predation scars is similar in the Cambrian. Most of the borings are associated with brachiopods and most of the scars with trilobites. Brachiopods, arthropods, molluscs, cnidarians and echinoderms were the most common prey in the Cambrian. The Cambrian record of predation is dominated by damage inflicted on brachiopods and trilobites. The fossils with predation signs are known from a majority of paleocontinents and all the Cambrian series.     

贵州湄潭志留纪初期三叶虫动物群及其意义*

志留纪兰多维列世(Llandovery)鲁丹期(Rhuddanian)是奥陶纪末生物大灭绝后的残存期和复苏期。志留纪初期冈瓦纳大陆边缘壳相地层稀少,多数地区为沉积间断或笔石相地层,研究底栖壳相生物残存-复苏期的宏演化普遍缺乏理想材料,而华南上扬子区贵州湄潭地区发育了志留纪早期的壳相地层,即五里坡层(鲁丹阶中部)和牛场组(鲁丹阶上部),为探索这一关键地史时期三叶虫动物群宏演化型式及其背景机制提供了依据。贵州湄潭岩坪剖面和高江剖面的五里坡层和牛场组共发现三叶虫7目11科15属(含亚属)17种(含1新种、3未定种),根据其属级分类单元的时空分布规律,将这些三叶虫识别为5种宏演化类型:即减缩幸存型、扩增幸存型、复活幸存型、新生型和死支漫步型。不同类型的属级分类单元在大灭绝中具有不同的宏演化型式,体现出其应对灾变而采取的不同的生存策略。减缩幸存型和复活幸存型是大灭绝后生态系统复苏和再次辐射的主要源泉,它们的发展在一定程度上影响着整个生态系统的宏演化进程;新生型的出现则标志着大灭绝后环境的实质性改善,三叶虫的全面复苏也随之到来。     

湘西北晚二叠世-早三叠世早期牙形石古生态

通过对牙形石器官的对称性、相分布和地球化学特征的研究,探讨湘西北晚二叠世至三叠纪初牙形动物的生态分布.按器官所包括不同对称型分子的比例,牙形动物器官的对称性可分为4级,器官的对称性越高,动物运动能力越强.湘西北晚二叠世一三叠纪初地层可分为6种沉积相,即盆地相、盆缘-台坡相、开阔台地相、边缘浅滩相、局限台地相和泥坪相.具不同对称级器官的属种在6种沉积相中的差异分布,反映了牙形动物的3种生态类型:自由游泳型、浮游型和底栖型.牙形石地球化学组分的变化与当时环境演变相吻合.随水深增加,化石中的P含量升高,而Ca、s、sr的含量降低;Al、Fe和Ba在近岸浅水环境的牙形石中富集;而Mg的富集指示高盐环境.基于上述研究,划分了4个牙形石相,建立了一个组合横向替代的牙形动物生态分布模式.     

Cambrian biostratigraphy of the Bowers back-arc basin,Northern Victoria Land,Antarctica — A review

The Bowers Mountains in Northern Victoria Land contain the richest Cambrian Series 3 (Miaolingian, middle Cambrian) and Cambrian Series 4 (Furongian, late Cambrian) fossiliferous successions in Antarctica. Almost all the fossils are found within the Bowers Supergroup, which outcrops within the Bowers Terrane, a fault-bounded northwest-southeast oriented strip in Northern Victoria Land. The fossils provide the main age control on the history and evolution of the Bowers volcanic arc and back-arc basin. The great bulk of the fossils occur within the Spurs Formation. The fossil assemblages are dominated by agnostoids and polymerid trilobites with most ranging in age from Drumian to Paibian, although one fauna is of Jiangshanian age. Over 40 agnostoid taxa and over 100 polymerid trilobite taxa have been recorded from the rocks of the Bowers Supergroup. The youngest fauna occurs within the adjacent Robertson Bay Terrane, where a limited fauna of polymerid trilobites and conodonts from within a limestone olistolith have a very late Cambrian or early Ordovician age. Faunal affinities are mainly with Australia, New Zealand, North and South China and the Himalaya with lesser ties to Iran, Kazakhstan, Siberia and Laurentia.     

Facies of a Lower Ordovician carbonate shelf (Mungok Formation: Taebaeksan Basin,Korea)

Summary The lithologic associations within the Lower Ordovician Mungok Formation in Korea define four depositional facies that formed across a continental margin fringing the Sino-Korean block: these facies represent lagoonal/restricted marine, shoal, inner shelf, and outer shelf environments. The stacking pattern of these facies reveals two systems tracts composed of five depositional sequences. The lower highstand systems tract consists of the lagoonal/restricted marine and shoal facies, whereas the upper lowstand systems tract comprises, in ascending order, inner shelf, outer shelf, and inner shelf facies. Three trilobite biofacies are recognized in the Mungok Formation: i.e.,Yosimuraspis, Kainella, andShumardia biofacies in ascending order. TheYosimuraspis Biofacies is dominated byYosimuraspis but also containsJujuyaspis andElkanaspis. The predominance of the endemic eponymous taxon suggests a lagoonal/restricted marine environment. The nearly monotaxicKainella Biofacies, which comprises pandemic genera such asKainella and occasionallyLeiostegium, may represent a less restricted environment than theYosimuraspis Biofacies. TheShumardia Biofacies occurs in the marlstone/shale lithofacies through relatively thick stratigraphic interval and is dominated by cosmopolitan trilobite taxa with some endemic species. The lithofacies and cosmopolitan trilobite assemblage of theShumardia Biofacies indicate that it occupied an outer shelf environment. The vertical succession of lithofacies and trilobite biofacies in the Mungok Formation records in general a shift from a restricted, shallow water environment to deeper-water environment.     

Baring it all: undressing Cambrian ‘Orsten’ phosphatocopine crustaceans using synchrotron radiation X‐ray tomographic microscopy

Synchrotron radiation X‐ray tomographic microscopy (SRXTM) was used to virtually dissect and peel the shields off of the microscopic, bivalved phosphatocopine crustaceans in the Cambrian ‘Orsten’ type of preservation of Sweden. Doing so opened up for an array of concealed internal structures to be observed in a fully enclosed specimen of Hesslandona ventrospinata and a semi‐enclosed specimen of Hesslandona angustata. For comparison, also a head‐larva stage specimen of H. angustata, with shields in ‘butterfly position’, was analysed. The X‐ray tomographic data sets revealed excellently preserved structures, such as labrum, sternum, antennae, mandibular and post‐mandibular limbs with their minute setae, all of which were more or less disguised by the enclosing shields. This, moreover, allowed assignment to growth stages of the specimens, which is impossible based solely on external morphology and size. Micro‐spherules observed inside the shields of the semi‐enclosed H. angustata specimen may represent remains of food particles, and the feeding biology of phosphatocopines is discussed in detail. Our analyses suggest that phosphatocopines were particle feeders. The SRXTM technique offers the ability to three‐dimensionally reconstruct the morphology in high resolution, construct virtual serial sections and study concealed structures. The resulting data allow for new structures to be revealed for previously known taxa and for new taxa to be identified, with the added benefit of not destroying the specimens in the process. Hence, we do not longer have to rely on serendipitous finds of broken and/or open phosphatocopine specimens to elucidate their diagnostic ventral morphology.     

Cambrian (Series 2 to Miaolingian) platform facies from central Sonora,Mexico and the regional correlation

This study provides new insights about depositional paleoenvironments through siliciclastic microfacies, carbonate microfacies, and biofacies analysis from sedimentary formations of the lower and middle Cambrian (Stage 4–Wuliuan), exposed in central Sonora, northern Mexico. Results of the petrographic analysis of 48 samples revealed the following lithologies: quartzarenite, oncolytic rudstone, grainstone-packstone, wackestone, mudstone, and to a lesser extent sandy limestone. Two siliciclastic microfacies were identified: (A) quartzarenite with cross-bedded and horizontal stratification deposited in an intertidal and supratidal environment; and (B) massive quartzarenite with Skolithos ichnofacies deposited in subtidal and intertidal environments. Four carbonate microfacies were identified: microfacies 1 is a sandy limestone with trilobite fragments; microfacies 2 is a grainstone with intraclasts, salterellids, hyolithids, trilobites, and echinoderms plates; microfacies 3 is an oncolytic rudstone consisting of microbes and abundant echinoderms plates; and microfacies 4 is a packstone-grainstone with abundant ooids, trilobite fragments, and echinoderm plates. Two biofacies were identified: Agnostid-polymeroid biofacies with predominance of the trilobites Pentagnostus, Bathyuriscus, Oryctocephalites, and Elrathina; and Pagetia biofacies with abundant trilobites of the genera Pentagnostus, Pagetia and Elrathina. It is concluded by the sedimentation model that changes in sea level is the most important parameter in determining the siliciclastic microfacies, carbonate microfacies and biofacies; as well as the depositional environments that vary from the coastline (subtidal to supratidal) to shallow-water open circulation marine platform with low and high energy waters. The Cambrian deposits of northern Mexico are correlated with the deposits of California and Nevada (USA), as well as to the Precordillera (Argentina), where the species in common show a strong affinity.     

Ladinian carbonates of the Cabo Cope Unit (Betic Cordillera,SE Spain): a tethys-maláguide palaeogeographic gateway

Summary The Cabo Cope Unit, which outcrops east of Aguilas (Murcia), belongs to the Maláguide tectonic Complex (Betic Internal Zone) and displays stratigraphic characteristics of particular interest, including Triassic bioclastic carbonate beds which are not common in the Maláguide units. Biostratigrafic fossils have been found in these beds and may correlate with Triassic alpine biofacies. Alpine fauna fossils only appeared in those palaeogeographic units of the Internal Zone of the Cordillera referred to as Alpujárride units, while the influence of the Sephardic faunal province is evident in almost all the cordillera. For these reasons it is noteworthy that new alpine fauna fossils have been found in an Internal Zone unit in which relevant fossils rarely appear. The Triassic succession of the unit studied in this paper can be subdivided into two members: a lower one, which is clastic and contains thick gypsum beds, and an upper one, consisting of carbonate rocks. The lower member has been interpreted as a fluvial-coastal deposit. The upper member is interpreted as a sequence of carbonate ramp deposits. This ramp evolved into a shallow platform with tidal flats typical of a coastal zone. The bivalve fossilsDaonella cf.lommeli (Wissmann) and “Posidonia” sp. have been found in the carbonate member, along with the conodontSephardiella mungoensis (Diebel). These fossils are of the Late Ladinian age and have been found only in this outcroup of the Betic Cordillera. The presence of this fossil assemblage, which belongs to the alpine faunal province, indicates a connection during the Late Ladinian between the Tethys sea and this area of the Maláguide palaeogeographic domain. The palaeogeographic location of the Cabo Cope Unit during the Middle Triassic was at the south-easternmost part of the Betic Basin, implying that the connection between the Tethys and the Betic Basin was established in the easternmost domains of the basin.     

Lower Cambrian trace fossil evidence for predation on trilobites

Predation upon trilobites previously has been inferred from large coprolites containing trilobite fragments, and from specimens of trilobites with healed wounds. The discovery of large burrows ( Dolopichnus gulosus , n. ichnogen., n. ichnosp.) in micritic quartz arenite of the Lower Cambrian Poleta Formation in Esmeralda County, Nevada, suggests that sea anemones preyed upon trilobites. Dolopichnus n. ichnogen., vertical cylindrical burrows with a central cylindrical core, is interpreted as dwelling burrows of sea anemones. In the specimens studied, the core contains coarser-grained material, and in one series of burrows, is composed of trilobitc fragments and micrite pellets. cemented with sparite. The central cylinder is interpreted to be a cast of the sea anemone's coelenteron, which in some specimens contains stomach contents.     

The Furongian (upper Cambrian) Alum Shale of Scandinavia: revision of zonation

The zonation of the Furongian Alum Shale in Scandinavia, based on olenid trilobites, is reviewed and revised. The current scheme is rooted in a detailed zonation introduced in the late 1950s with subzones that subsequently have been elevated to zonal rank. Ten of these zones are difficult to recognize in all Alum Shale districts, and a revised zonation is proposed, focused on unambiguous identification throughout Scandinavia. The difficulties in recognizing zones in some districts mostly relate to biofacies differentiation. Representatives of Ctenopyge are, for instance, common in palaeo-offshore areas, whereas pelturines are rare in these settings and vice versa in palaeo-inboard settings. The following modifications of the olenid zonation are proposed: the Olenus scanicus Zone is renamed the O. scanicus–O. rotundatus Zone; the Ctenopyge similis and Ctenopyge spectabilis zones are replaced by the Sphaerophthalmus modestus–Sphaerophthalmus angustus Zone; the Ctenopyge tumida Zone is renamed the Peltura acutidens–Ctenopyge tumida Zone; the Peltura scarabaeoides Subzone is restored (as a zone) and replaces the Ctenopyge bisulcata and Ctenopyge linnarssoni zones. The Parabolina heres megalops (Sub)Zone is reinstated and replaces the Peltura paradoxa Zone; the Acerocarina granulata and P. costata zones are combined as the Acerocarina granulata–Peltura costata Zone. In addition, the name Proceratopyge nathorsti–Simulolenus alpha Zone is suggested for the polymerid zone corresponding to the upper Miaolingian Agnostus pisiformis Zone. The proposed changes reduce the number of Furongian Zones to 23, allocated to six superzones. No subzones are recognized, but some zones can potentially be subdivided for improved local correlation. The stratigraphical ranges of all Furongian olenid trilobites and agnostoids described from Scandinavia are summarized.     

Coral assemblages, biofacies, and ecological zones in the mid-Holocene reef deDosits of the Enriquillo Valley, Dominican Republic

Stemann, T. A. & Johnson, K. G. 1992 07 15: Coral assemblages, biofacies. and ecological zones in the mid-Holocene reef deposits of the Enriquillo Valley, Dominican Republic. A large, subaerially exposed mid-Holocene reef in the Enriquillo Valley (southwest Dominican Republic) provides an excellent opportunity to examine the relationship between reefal ecology and reefal deposits. Coral species richness and diversity in the Enriquillo reef are comparable to that found in the recent of the Caribbean, and ecological zonation comprised of a shallow-water branching coral zone and a deeper water mixed-coral zone is apparent. Similar zonation and diversity patterns have been recognized on living Caribbcan reefs with moderate wave exposure. Three statistically discrete biopdcies can be discriminated in the Enriquillo deposits using quadrat point-counting techniques commonly used to census modern reefs. They include a facies dominated by Acropora cervicornis, a low diversity assemblage with abundant, large colonies of Siderastrea siderea and Stephanocoenia intersepta, and a higher diversity assembbdge composed of various taxa including Montastraea spp., Colpophyllia spp., and Agaricia spp. Each facies can be recognized at scales of 1–3 m², though in some cases they extend for more than 20 m². In general, the A. cervicornis facies is spatially segregated from the other two biofacies. although neither the shallow nor the deep-water ecological zone is comprised of a single reef biofacies. Rather, the biofacies described here appear to represent distinct micro-environments resulting from ecological variation at a subzonal scale. Micro-environments of similar scale are most likely preserved in other reef deposits. Recognition of these subzonal biofacies may have important consequences for the stratigraphical and paleoccological interpretation of fossil reefs. Corals, biofacies, reef zonation, coral communities, fossil reefs.     

Trace and soft body fossils from the Pedroche Formation (Ovetian, Lower Cambrian of the Sierra de Córdoba, S Spain) and their relation to the Pedroche event

The low Lower Cambrian rocks from the Sierra de Córdoba contain one of the best successions in Europe, which consists of well exposed mixed facies with abundant fossil assemblages showing long stratigraphical ranges throughout the Pedroche Formation. These assemblages include diverse Ovetian archaeocyaths, trilobites, small shelly fossils, calcimicrobes, trace fossils and stromatolites. Trace fossils are still poorly known, and thus they are the main objective of this work. Ichnological data are obtained from the Arroyo de Pedroche 1, Arroyo de Pedroche 2 and Puente de Hierro sections. Trace fossils include the ichnogenera Bergaueria, aff. Bilinichnus, Cochlichnus, aff. Cosmorhaphe?, Cylindrichnus, Dactyloidites, Dimorphichnus, Diplichnites, Monocraterion, Palaeophycus, aff. Phycodes, Planolites, Psammichnites, Rusophycus, Skolithos, Torrowangea and Treptichnus, as well as faecal pellets, meniscate trace fossils and others. They are abundant in shales and sandstones, and indicate important changes in the benthic conditions with respect to the underlying Torreárboles Formation. Changes in fossil assemblages within Member I of the Pedroche Formation indicate palaeoecological disruptions, which led to the disappearance of numerous archaeocyath species and the decrease of stromatolite biodiversity. This was followed by dominance of trilobite and brachiopod assemblages, accompanied by trace fossils of the Psammichnites ichnosp. A ichnoassociation. This biotic turnover (Pedroche event) occurred at the lower part of the archaeocyath Zone III, within the Bigotina bivallata biozone. The diagnoses of the ichnospecies Cochlichnus anguineus and Dactyloidites cabanasi are emended.     

湖北京山早三叠世有孔虫动物群的发现及其意义

本文首次报道了湖北京山地区早三叠世有孔虫动物群,计６属１５种,其中包括４新种,在对该动物群分析基础上,作者建立了Ａｕｌｏｔｏｒｔｕｓｃｈｉａｌｉｎｇｃｈｉａｎｇｅｎｓｉｓ－Ｄｉｃｈｏｓｐｉｒａｓｉｎｅｎｓｉｓ组合带,通过对其古生态特征及生物相研究,揭示了该动物群的生活习性与生态环境的关系,简述了该有孔虫动物群的发现在地层划分对比及油气勘探中的意义。     

Biotic structure and morphology of patch reefs from South China (Ningqiang Formation, Telychian, Llandovery, Silurian)

Summary Ningqiang Formation (late Telychian, Llandovery, Silurian), characterized by nearly 3000 m of shales in tercalated with carbonates, is situated between Ningqiang (S. Shaanxi Province) to Guangyuan (N. Sichuan Province) adjacent to the northwest margin of the Yangtze Platform. The high diversity “Xiushan Fauna”, and abundant reef development, illustrate a relatively warm and persistent shallo marine environment in these early Silurian sediments. The sequence shows reef radiation after recovery from the end Ordovician mass extinction envents. Multiple horizons of reef-building occurred within a relatively short geological interval and resulted in more than 30patch reefs up to 200 m in diameter and 1–50 m vertically, composed of abundant fossils. Reef biota include frame-building corals, stromatoporoids, bryozoans, and microbialites, and reef-associated oranisms such as crinoids, brachiopods, trilobites, gastropods, nautiloids and ostracods. Three reefrelated biotic associations are recognised: a) reefs dominated by framework with crinoids and microbia; b) reefs dominated by only crinoids and microbia; and c) crinoiddomainated facies. Seven representative reef examples illustrate different morphologies and growth styles. A high terrigenous debris input and shallow epicontinental ramp, which lacked obvious topographic variation, were major controls which resulted in rather simple reefs; sedimentation was apparently the main constraint on lateral and vertical extension of reefs, and prevented large-scale reef complexes developing.