遗迹化石Chondrites的指相意义和阶层分布

介绍和评述Chondrites的基本特征和流行的成因解释 ,记述最近发现于美国犹他州中西部北美下 中奥陶统之交层型剖面上的Chondrites遗迹组构的不寻常特征和属性 :细小的Chondrites被所有与之共生的遗迹化石交切 ,形成于水与沉积物界面附近缺氧的早期软底质中 ,Chondrites是形成最早和最浅的遗迹阶层。流行的遗迹相和遗迹阶层模式的不足是 :前者在操作上 ,简单地将遗迹化石及其组合处理为同沉积或准同沉积的物理沉积构造 ,忽略了造迹活动的多阶段和多阶层的特点 ;后者的资料基础仅依据中生代以来的地层记录 ,对重大生物 环境事件和造迹生物生态习性演化对遗迹阶层形成和分布的影响注重不够。指出Chondrites的阶层分布和对古氧相的示踪在古生代与中生代有重要差别     

Environmental distribution of trace fossils in the Jurassic of Kachchh (Western India)

Summary Trace fossils occur abundantly in Middle Jurassic rocks of the Kachchh Basin. They are found in environments ranging from beach sequences down to central parts of the basin. For stratinomic reasons, they are particularly well preserved in storm deposits. Their distribution pattern exhibits a clear relationship to the hydrodynamic conditions and, secondarily, to bathymetry, and follows the classic ichnofacies concept ofSeilacher (1967). High energy nearshore areas and submarine shoals are represented by members of the Skolithos ichnofacies such asOphiomorpha nodosa, Arenicolites, Diplocraterion parallelum, andRhizocorallium jenense. The storm-influenced ramp contains both members of the Cruziana ichnofacies (e.g.Rhizocorallium irregulare, Thalassinoides suevicus, Taenidium serpentinum, Chondrites) and the Skolithos ichnofacies (in particularOphiomorpha). The former were produced during interstorm phases, the latter are of post-storm origin. Carbonate ramp environments of low to intermediate energy also contain members of the Cruziana ichnofacies, whilst equivalent siliciclastic environments are characterized by a low-diversity Zoophycos ichnofacies. Low energy basinal environments of fine-grained substrates contain an impoverished Cruziana ichnofacies consisting ofChondrites, Trichichnus andThalassinoides suevicus. 32 ichnotaxa are briefly described, among themSphaerichnus lobatus ichnogen. et ichnosp. nov.     

Diverse tiering patterns in Paleogene flysch trace fossils,Magura nappe,Carpathian Mountains,Poland

Diversified tiering patterns of trace fossils were observed in three Paleogene lithostratigraphic units of the Magura nappe: the Szczawnica Formation (Paleocene‐early Eocene); the Belove?a beds (middle Eocene); and the Piwniczna Sandstone Member of the Magura Formation (middle‐upper Eocene). Sediments of the first unit were deposited under oxygen‐poor conditions, and those of the second and third units under well‐aerated conditions. Thick‐bedded turbidites and fluxoturbidites of the third unit accumulated quickly, in contrast to ‘normal flysch’ of the first and second units. Analyses of tiering patterns show a thickening of tiers following the improvement of sediment oxygenation. Slowly accumulated deposits of ‘normal’ flysch exhibit a more mature, well‐developed tiering pattern than those which accumulated quickly.     

Infaunal communities and tiering in Early Palaeozoic nearshore clastic environments: trace-fossil evidence from the Cambro-Ordovician of New South Wales

Understanding of the palaeoecology of Early Palaeozoic shallow-marine communities in sandy habitats is incomplete. Reasons for this include the poor preservation of body fossils and the dominance of Skolithos piperock in sandstones of that age. Cambrian and Ordovician deposits preserving diverse nearshore trace-fossil assemblages are therefore of critical importance for assessing the early evolution of marine ecosystems. The basal part of the Cambro-Ordovician Bynguano Formation of the Mootwingee area (New South Wales, Australia) is a series of interbedded sandstones and mudstones, which were deposited under nearshore conditions. These strata provide an early example of the Arenicolites ichnofacies. Two ichnocoenoses are distinguished in the sandstones of this unit. A 'predepositional' ichnocoenosis, which reflects the benthic community prior to episodes of sand deposition, includes dense aggregations of Rusophycus with rare Planolites. The 'postdepositional' ichnocoenosis is more diverse and includes Thalassinoides, Arenicolites (various types), Monocraterion, Skolithos, Trichichnus , and epichnial grooves. The tiered structure developed in this ichnocoenosis is preserved as a 'frozen tiered profile' and is characterised by a Thalassinoides tier, 10–30 cm in depth, which is cross-cut by Skolithos and Arenicolitesin the middle tier, and by Arenicolites and Trichichnusin the shallowest tier. The pattern of tiering indicates that a complex ecosystem of opportunistic organisms, capable of exploiting shifting substrates, had evolved by the earliest Ordovician. □ Predepositional, postdepositional frozen tier profile, ichnocoenosis, nearshore clastics, RUSOPHYCUS, Cambro-Ordovician, Bynguano Formation, Mootwingee, New South Wales.     

Ediacaran–Cambrian bioturbation did not extensively oxygenate sediments in shallow marine ecosystems

The radiation of bioturbation during the Ediacaran–Cambrian transition has long been hypothesized to have oxygenated sediments, triggering an expansion of the habitable benthic zone and promoting increased infaunal tiering in early Paleozoic benthic communities. However, the effects of bioturbation on sediment oxygen are underexplored with respect to the importance of biomixing and bioirrigation, two bioturbation processes which can have opposite effects on sediment redox chemistry. We categorized trace fossils from the Ediacaran and Terreneuvian as biomixing or bioirrigation fossils and integrated sedimentological proxies for bioturbation intensity with biogeochemical modeling to simulate oxygen penetration depths through the Ediacaran–Cambrian transition. Ultimately, we find that despite dramatic increases in ichnodiversity in the Terreneuvian, biomixing remains the dominant bioturbation behavior, and in contrast to traditional assumptions, Ediacaran–Cambrian bioturbation was unlikely to have resulted in extensive oxygenation of shallow marine sediments globally.     

Trace fossils of the Jurassic,blue Lias,Lyme Regis,Southern England

The Lower Jurassic, Blue Lias Formation at Lyme Regis, Dorset, England is rhythmically bedded with symmetrical rhythms consisting of laminated black shale followed by dark then pale marls (sometimes cemented into pale limestones) and back to laminated black shale. Its trace fossil fauna includes nine ichno‐genera and represents a shallow shelf paleoenviron‐ment. The ichnofauna occurs in three assemblages named after consistently occurring ichnogenera. A Chondrites assemblage (diversity = 1 ichnogenus) and a Chondrites‐Arenicolites assemblage (diversity = 2–3 ichnogenera) are typical of dark marls but may penetrate tops of laminated black shales. A thalassi‐noides‐Chondrites‐Arenicolites assemblage (diversity up to 7 ichnogenera) is typical of pale marls or limestones. Blue Lias limestones are diagenetic: dark laminated limestones and pale bioturbated limestones are cemented equivalents of laminated black shales and pale marls, respectively. However, pale burrow fills in darker sediments and vice versa confirm the rhythms are primary. Rhythms represent redox cycles, fluctuating from anoxic laminated black shales lacking mac‐robenthos or infauna (bioturbation index = 0) to oxic, bioturbated, pale marls or limestones with large mac‐robenthos such as Gryphaea or Plagiostoma and diverse infauna (bioturbation index = 5).     

Ethologic and ontogenic significance of the Pliocene trace fossil Sinusichnus sinuosus from the northwestern Mediterranean

The trace fossil Sinusichnus sinuosus Gibert 1996 is described and interpreted as an open burrow system, attributed to a crustacean tracemaker, that shares some features with fodinichnial networks, such as Thalassinoides and Ophiomorpha , and with graphoglyptid burrows, such as Protopaleodictyon and Cosmorhaphe. These similarities suggest that Sinusichnus could have been produced by an animal combining deposit-feeding and farming (or trapping) strategies. The Sinusichnus record has yielded juvenile and adult burrows, often in close association. On account of minor morphologic differences between the two, juvenile tracemakers could have employed an agrichnial feeding strategy, whereas adults could have employed fodinichnial feeding.     

Lower Miocene bathyal and submarine canyon ichnocoenoses from Northland, New Zealand

Thalassinidean crustacean remains ( Callianassa ) are recorded from lower Miocene burrow networks belonging to the ichnogenus Thalassinoides . They were produced at mid bathyal depths of 1000–3000 m. Mid to lower bathyal basinal sediments and inferred outer neritic to upper bathyal submarine canyon sediments contain sparse ichnocoenoses composed entirely of feeding and dwelling structures, produced by burrowing polychaetes, echinoids and possibly sipunculoids and also by bivalves escaping burial during rapid sedimentation. These two ichnocoenoses are similar to those of proximal turbidite sequences, and this is considered a response to similar rates of sedimentation, water agitation and coarseness of sediment rather than a similarity in depth. An outer neritic to upper bathyal canyon wall ichnocoenosis was developed in semi-consolidated lutites and arenites by burrowing polychaetes, decapod Crustacea (shrimps and crabs) and possibly amphipods and other organisms. Inclined, but randomly oriented Rhizocorallium occur in the canyon wall, and their presence at these depths is explained by inferred abnormally high water turbulence and abundant suspended food matter as well as a favourable semi-consolidated lutite substrate.     

The effects of increased flow and fine sediment on hyporheic invertebrates and nutrients in stream mesocosms

相似文献   

Zoophycos composite ichnofabrics and tiers from the Permian neritic facies in South China and south‐eastern Australia

Gong, Y.‐M., Shi, G.R., Zhang, L.‐J. & Weldon, E.A. 2009: Zoophycos composite ichnofabrics and tiers from the Permian neritic facies in South China and south‐eastern Australia. Lethaia, Vol. 43, pp. 182–196. Zoophycos composite ichnofabrics (ZCI) comprising two or more suites of the same form of Zoophycos are widespread and densely distributed in Early and Middle Permian (Cisuralian–Guadalupian) neritic limestones (Qixia and Maokou Formations) of palaeotropical origin in the Laibin area, Guangxi, South China. Similar ZCI also occur in neritic greywackes of glaciomarine origin from the Middle Permian (Guadalupian) Westley Park Sandstone Member (Broughton Formation) in the southern Sydney Basin, south‐eastern Australia. Zoophycos from both regions consists of planar spreite with major and minor lamellae and a cylindrical tunnel interpreted as a marginal tube and/or axial shaft. The cylindrical tunnel is herein considered to be an essential component of Zoophycos, and thus can be used to define and characterize the morphological variability of Zoophycos. It is suggested that the variation of spreite and major and minor lamellae originated from the different morphologies and migration manners of the cylindrical tunnel. The shallowest, shallow, middle and deepest Zoophycos tiers have been distinguished in ZCI on the basis of cross‐cutting relationships, the soft‐sediment deformation and the contrast in colour between Zoophycos and its host rock. The multiple tiers may represent the substrate consistency spectrum from a softground through a stiffground to a firmground. The different Zoophycos tiers may have been constructed by tracemakers of either different or the same taxonomic affinities in response to the gradual accretion and lithification of sediment layers on the seafloor. The tracemakers appeared to be very sensitive to neither climate nor lithology. The width of the planar spreiten of Zoophycos decreases slightly with the depth of tiering in ZCI. □Composite ichnofabric, Permian, South China, south‐eastern Australia, tier, Zoophycos.     

Ichnology of deep‐sea fan overbank deposits of the Ganei slates (Eocene,Switzerland)— a classical flysch trace fossil locality studied first by Oswald Heer

Ganei (Switzerland) is a classical locality for trace fossils. At this site, Heer (1877) described a large number of trace fossils, several of which were new taxa. The trace fossils occur in thin‐bedded turbidites in which the basal divisions of the Bouma sequence are typically absent; the turbidites are assigned to the Ganei Slates and are Eocene in age. They are interpreted to have been deposited in an overbank environment within an upper to middle fan area distal to a channel. Two trace‐fossil associations occur: the first (I) is characterized by bulldozing organisms producing biodeformational structures, Scolica, and Nereites irregularis; the second (II) association shows a distinct tiering pattern with near‐surface graphoglyptids and a mixed layer with simple tubes such as cf. Palaeophycus and Planolites, plus patterned tubes such as Nereites cirrinalis, and Chondrites. Deeper turbidite layers were colonized by Chondrites and Gyro‐phyllites. All trace fossils show a normal size spectrum compared to previously studied trace‐fossil associations, so the degree of oxygenation probably did not influence the composition of either trace‐fossil association. Seafloor sediment was probably soft and did not affect the trace‐fossil associations. Sedimentation rate and event frequency did not change and are estimated to have been in a range of 5–10 cm/1000 years and 2–5 events per 1000 years, respectively. The composition of trace‐fossil associations I and II is therefore interpreted to have been controlled by the benthic food content being higher for trace‐fossil association I than for II.     

Dendroid morphology and growth patterns: 3-D computed tomographic reconstruction

This paper analyzes the growth patterns of dendrolite in the Zhangxia Formation (Middle Cambrian), Shandong Province, China, using the technique of 3-D computed tomographic reconstruction. Dendroids are classified into V-dendroids, columnar dendroids, and arborescent dendroids, based on morphological characteristics. The means of interconnection between dendroids are classified into trunks, nodules, shoots, and fingers. Stacking and tiering control the gross morphology and structural framework of dendrolite. Stacking is a process of vertical growth, in which V-dendroids create a staircase-like structure. Tiering occurs when a layer of dendroids is covered by sediment, and then partially eroded, allowing a new layer of dendroids to form.A comprehensive blueprint of the structural divisions of dendrolite is presented, according to scale, being divided into micro-, meso-, macro-, and megastructures. The mesostructure, which includes individual dendroids and their combined structures, is subsequently divided into primary (V-dendroid), secondary (columnar and arborescent dendroid), and tertiary (stair and tier) structures and a basic growth model is provided for V-dendroids. The stages of V-dendroid growth are: 1) trunk extension and base expansion, 2) divergence, 3) expansion and convergence, followed by repetition of stages 2 and 3, until 4) growth completion, followed by the subsequent emergence of a new dendroid by either stacking or tiering. This development of systematically ordered structures is suggestive of the reaction of microbial colonies to external environmental conditions.     

A day and a night in the life of a cleft-foot clam: Protovirgularia-Lockeia-Lophoctenium

A remarkable specimen of a compound trace fossil in Pennsylvanian sandstone comprises three very different ichnotaxa in conjunction: Protovirgularia dichotoma, Lockeia siliquaria and Lophoctenium isp. The combined activities represented by these ichnotaxa reflect the locomotion, resting and feeding behavior of a cleft-foot, protobranch clam (bivalve) that burrowed through the sediment, paused five times to deposit-feed, and then burrowed on to a new location, possibly as a reaction to a depositional event. It is estimated that the complete trace fossil was made in 24 hours or less. The three ichnotaxa also provide morphologic details of the bivalve's shell and soft parts (foot and labial palps).     

Ecospace utilization in early Phanerozoic deep-marine environments: deep bioturbation in the Blakely Sandstone (Middle Ordovician), Arkansas, USA

Ichnofabric analysis of alternating light and dark-coloured mudstone layers in the Blakely Sandstone (Middle Ordovician) at Crystal Springs Landing, Lake Ouachita (west of Hot Springs, western Arkansas, USA) reveals two equilibrium palaeoichnocoenoses. The first was emplaced under variable, but low, oxygen levels during deposition of the dark-coloured layers; small diameter transition layer burrows overprint a mixed layer ichnofabric. The transition layer infauna was tiered with abundant Chondrites representing the deeper of two shallow tiers. Light-coloured layers accumulated during prolonged intervals in which the sediments were oxygenated to a greater extent and depth. Preservation of a mixed layer ichnofabric within them is the result of limited, but deep (up to at least 400 mm), reworking subsequently in the transition layer by an equilibrium community. These transition layer trace fossils are not tiered. If representative of oxygenated sediment columns in Ordovician deep-marine environments, an extensive volume of infaunal ecospace was colonized (in this case by deposit feeders); its more efficient use subsequently, including vertical partitioning of the infaunal community into specific environmental niches (tiering), could have accommodated increases in diversity and community complexity. Changes over time in the maximum depth to which sediments were bioturbated, alone, would therefore be a poor measure of the extent of ecospace utilization.     

Sediment-Associated Phototoxicity to Aquatic Organisms

Phototoxicity is a two to greater than 1000-fold increase in chemical toxicity caused by ultraviolet radiation (UV), which has been demonstrated in a broad range of marine and freshwater fish, invertebrates, and other aquatic organisms in water column exposures. Field collected sediments containing polycyclic aromatic hydrocarbons (PAHs) and other contaminants are phototoxic to sediment-dwelling organisms in laboratory tests, but in situ or field investigations of phototoxicity have not been reported. Sediment provides a pathway for the bioaccumulation of phototoxic chemicals through contact with and ingestion of bedded and suspended sediment, and maternal transfer, but risks are uncertain. Risks from sediment-associated phototoxicity will be greatest in areas of both high contaminant exposure (e.g., surficial and suspended sediments in harbors, outfall areas, and spill sites), and high UV exposure (e.g., high optical clarity or shallow depths). Organisms and life-stages most at risk will be those translucent to UV that inhabit the photic zone and near shore areas, but benthic organisms may have generally low UV exposure because of life history and morphological characteristics. Site-specific assessments are needed to characterize risks both spatially and temporally because of heterogeneous sediment contamination and large differences in species sensitivity and exposure pathways.     

Relative roles of stream flow and sedimentary conditions in controlling hyporheic exchange

Hyporheic exchange is often controlled by subsurface advection driven by the interaction of the stream with sedimentary pore water. The nature and magnitude of the induced exchange flow is dependent on the characteristics of both the stream flow and the sediment bed. Fundamental hydrodynamic theory can be applied to determine general relationships between stream characteristics, sediment characteristics, and hyporheic exchange rates. When the stream bed is fine enough to allow application of Darcy's Law, as with sand beds, the induced advective exchange can be calculated from fundamental hydrodynamic principles. Comparison with a wide range of experimental results demonstrates the predictive capability of this theory. Coarser sediments such as gravels are more complex because they admit turbulent interactions between the stream and subsurface flows, which can produce considerable exchange even when the bed surface is flat and no flows are induced by the bed topography. Even for this case, however, scaling arguments can still be used to determine how exchange rates vary with stream and sedimentary conditions. Evaluation of laboratory flume experiments for a wide range of stream conditions, bed sediment types including sand and gravel, and bed geometries demonstrates that exchange scales with the permeability of the bed sediments and the square of the stream velocity. These relationships occur due to fundamental hydrodynamic processes, and were observed to hold over almost five orders of magnitude of exchange flux. Such scaling relationships are very useful in practice because they can be used to extend observed hyporheic exchange rates to different flow conditions and to uniquely identify the role of sedimentary conditions in controlling exchange flux.     

Paleoecology of a large Early Cambrian bioturbator

The Lower Cambrian Poleta Formation in the White-Inyo Mountains of eastern California contains well-preserved and laterally extensive exposures of the large looping and meandering trace fossil Taphrhelminthopsis nelsoni n.isp. Such traces are typical features on upper bed surfaces of Lower Cambrian shallow marine sandstones and occur with Ediacaran fossils at other localities. Morphologic, sedimentologic and goniogram analyses suggest that the inferred tracemaker was a large soft-bodied echinozoan- or mollusc-grade animal with a volume greater than 14 cm³ that actively grazed or ingested sediment at the sediment-water interface. Although portions of these traces appear to reflect relatively 'complex' behavior, looping patterns are not periodic as expected for a systematic foraging strategy. T. nelsoni traces are patchy in distribution and commonly associated with suspect-microbial features, suggesting that tracemakers may have been targeting microbial-based or related concentrations of food resources. Such behavioral patterns are typical of shallow late Neoproterozoic-early Cambrian settings, and like suspect-microbial structures are later restricted to deep marine or stressed settings.