山西兴县中奥陶统马家沟组五5亚段遗迹化石组合及其古环境意义

鄂尔多斯盆地东缘关家崖剖面奥陶系马家沟组五5亚段地层中保存大量无脊椎动物遗迹化石,可识别出居住迹、牧食迹、觅食迹三大类,共7个遗迹属、14个遗迹种,分别是Arenicolites isp.,Cylindricumisp.,Helminthopsis abeli,Helminthopsis isp.1,Helminthopsis isp.2,Lorenziniaisp.,Planolites isp.,Planolites beverleyensis,Planolites montanus,Teichichnus rectus,Thalassinoides isp.1,Thalassinoides isp.2,Thalassinoides isp.3,Thalassinoides isp.4。根据遗迹化石特征及其沉积环境,可划分3个遗迹组合:1、Helminthopsis-Planolites组合,该组合以觅食迹为主,部分为居住迹,出现在潮间带和潮下带;2、Thalassinoides-Teichichnus组合,该组合遗迹化石种类较单一,主要为觅食迹,分布于潮间带和潮上带;3、Thalassinoides-Helminthopsis组合,该组合出现在潮间带。基于遗迹化石组合的分布特点,提出山西兴县奥陶系马家沟组五5亚段的沉积环境模式。     

Ichnology of Lower Jurassic beach deposits in the Shemshak Formation at Shahmirzad,southeastern Alborz Mountains,Iran

A 19 m thick package of well-sorted lowermost Jurassic (Hettangian-Lower Sinemurian?) sandstones within the Shemshak Formation of the southeastern Alborz Mountains displays features characteristic of foreshore to upper shoreface environments such as tabular bedding, low-angle lamination, trough cross-stratification, parting lineation, and oscillation ripples. In contrast to most other beach successions recorded in the literature the sandstones contain a trace fossil assemblage characterised by low abundance but comparatively high diversity. The assemblage, comprising 14 ichnotaxa, is dominated by Palaeophycus heberti, Rhizocorallium irregulare, Gyrochorte comosa, and Parahaentzschelinia surlyki. Contrary to predictions, which assume a dominance of suspension-feeders in such high-energy environments, the trace fossil assemblage represents a variety of ethological groups ranging from suspension-feeders to deposit-feeders, detritus-feeders, scavengers, and a possible trap constructor (Ctenopholeus), whereby deposit-feeders predominate. This anomaly is explained by a high amount of organic detritus in the sediment, indicated by abundant plant material, and a position of the beach in the vicinity of a river mouth.     

The trace fossil Thalassinoides from the Upper Ordovician of Tuva

Traces of Thalassinoides (the tunnels of unknown burrowing organisms) are described from carbonates of the Khondelensky layers of the Upper Ordovician of Tuva. Hitherto, this fossil was unknown in the Ordovician of the USSR. They demonstrate great similarity with Thalassinoides from coeval deposits of the Great Basin, USA. The traces are assumed to have been made in terrigenous-carbonate sediments deposited on the areas of a gently sloping shelf in quiet water, below wave base. □ Upper Ordovician, terrigenous-carbonate sediments, burrows.     

Bay and shoreface benthic communities in the Lower Cretaceous

Lower Cretaceous marine rocks exposed in New Mexico, southcastcrn Colorado, Oklahoma, and Kansas contain well-preserved faunal assemblages that formed either as in-place, disturbed-neighborhood, or transported assemblages. Five faunal associations characterize lithofacies of the bay-to-shoreface depositional model and possess uniquc structures. The Nucula-Nuculana association represents a speciediverse, infaunal detritus-suspension community occupying the open-bay muddy substrate. The Corbula-Breviarca association was a species-dominant, infaunal suspension feeding community on the lower shoreface. The Texigryphaea-Lopha community formed biostromes on the shoreface. The mid-shoreface supported a species-diverse, infaunol suspension feeding community of Scabrotrigonia and Turritella . The Arenicolites trace fossil association characterizes the upper shoreface-beach habitat.     

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.     

A diverse deep‐marine Ichnofauna from the Eocene Tarcau sandstone of the Eastern Carpathians,Romania

The Paleocene to Middle Eocene Tarcau Sandstone at Buzau Valley, eastern Carpathians, Romania, records sedimentation in a turbidite system. These strata contain a diverse and abundant pre‐ and postdepositional ichnofauna consisting of 35 ichnogenera and 54 ichnospecies. The predepositional assemblage is rich in graphoglyptids and ornate grazing trails; simple grazing trails, resting traces, and feeding structures also occur. The predepositional assemblage includes Acan‐thorhaphe, Belorhaphe, Cardioichnus, Circulichnus, Coch‐lichnus, Cosmorhaphe, Desmograpton, Fustiglyphus, Gordia, Helicolithus, Helminthopsis, Helminthorhaphe, Lorenzinia, Megagrapton, Paleodictyon, Paleomeandron, Protopaleodictyon, Scolicia (S. strozzii), Spirorhaphe, Spirophycus, Treptichnus, and Urohelminthoida. The ich‐nodiversity, composition, ethology, and morphologic complexity of the predepositional association are indicative of the Nereites ichnofacies. The postdepositional association essentially consists of dwelling, feeding, and grazing traces, and is represented by Chondrites, Glockerichnus, Halopoa, Nereites, Ophiomorpha, Phycodes, Planolites, Polykampton, Scolicia(S. prisca. S. striata), Taenidium, Thalassinoides, and Zoophycos. Palaeophycus occurs in both assemblages. Allochthonous Teredolites is present in wood fragments, The postdepositional association includes elements of the Skolithos ichnofacies and facies‐crossing forms that are commonly present in deep‐marine deposits, Elements of the Skolithos ichnofacies are present not only in the most proximal parts of the turbidite system, but also in distal parts. The number of predepositional forms greatly exceeds postdepositional ones, reflecting a dominance of K‐selected over r‐selected population strategies in a stable environment. High levels of ichnodiversity in the Tarcau Sandstone are comparable with deep‐sea ichnofaunas from the Polish Carpathians and with other flysch trace‐fossil assemblages of similar age. This abundant and diverse Eocene ichnofauna supports the idea of extremely rich deep‐sea ichnofaunas in the Cenozoic.     

天山和昆仑—秦岭造山带志留系、石炭系和三叠系复理石相遗迹化石

在天山志留系,石炭系和东昆仑－西秦岭三叠系浊积岩系中遗迹化石发育,经研究计有：Helminthopsis hieroglyphica,Neonerietes biserialis.,N,uniserialis,palaeophycus isp.,P.serratus,P.striatus.P.tubularis,Paleodictyon imperfectum,Phycodes circinnatum,Phycosiphon incertum,Planolites annularis,P.beverleyensis,P.Montanus,Rhizocorallium ips.,Scalarituba missourensis,Skolithos ips.,?Spirorhaphe isp.,sublorenzinia ips.Tambia isp.,Taphrhelminthopsis auricularis,Teichichnus isp.,Thalassinoides isp.它们构成4种遗迹化石组合：Phycosiphon-Palaeophycus组合,Neonereites-Scalarituba组合,Paleodictyon组合和Phycodes Skolithos组合,分别代表局限缺氧深海盆地浊流沉积,半深海环境中－上扇沉积,多岛洋环境的中－下扇沉积,半深海环境的中扇浊流沉积。     

Sea-level dynamics and palaeoecological factors affecting trace fossil distribution in Eocene turbiditic deposits (Gorrondatxe section,N Spain)

Ichnological analysis of the upper Ypresian–lower Lutetian interval at the Gorrondatxe section (W Pyrenees, N Spain), reveals a relationship between sea-level dynamics and the eco-sedimentary factors influencing trace fossil assemblages. The 600 m thick section of deep-sea turbiditic deposits contains 41 ichnospecies belonging to 28 ichnogenera, which are typical of the Nereites ichnofacies, and mostly of the Paleodictyon ichnosubfacies, suggesting deposition in a basin plain to fan-fringe setting. The trace fossil diversity and abundance fluctuate, irrespective of turbidite frequency. These ichnological features are strongly affected by trophic level changes related partly to sea-level dynamics according to the sequence stratigraphic interpretations for the studied section. Temperature, oxygenation and substrate changes are also considered as relevant factors. Increased ichnodiversity, particularly among graphoglyptids, coincides with moderate oligotrophy and stable ecological conditions. Eutrophisation, lowered oxygenation and drop of temperature, typical of low sea level, can reduce ichnodiversity.     

Benthic foraminifers and paleoecology of a Holocene shelly concentration, Salado Basin, Argentina

Foraminiferal fossil assemblages of the shelly concentration, which represents the type section of Cerro de la Gloria Member of Las Escobas Formation, were analyzed for the first time. Taxonomic, quantitative and taphonomical analyses were made in order to obtain paleoenvironmental (physical as well biological) information. The complexity of the internal structure of the taphocoenoses was analyzed to infer the history of the final concentration process. The shell bed of Channel 15 corresponds to a shoreface longshore bar deposited in a brackish, unstable, wave-dominate coast. Shoreface and beach (foreshore) regressive facies were recognized. Taphonomic processes have modified the paleobiocoenoses by the selective preservation of autochthonous elements and by the addition of parautochthonous fauna from relict beachs and lagoons. Thus, the taphocoenoses is a within-habitat time-averaged assemblage composed of species that inhabit shallow shelf marine environments. Discrimination of autochthonous and parautochthonous fauna was possible based on taphonomic signatures of tests. The addition of the parautochthonous elements was related with longshore currents and littoral drift, and with high-energy events, probably with storm-waves, when erosion of the Pre-Mid Holocene substrate was more intense. Thus, the contribution of parautochthonous fauna is directly related with lithology and therefore, with dynamic of the paleoenvironment: in the shoreface, autochthonous fauna dominates in clastic sands with lamination and parallel stratification, whereas parautochthonous elements dominate in shoreface shelly gravels and in the foreshore sands. In the upper part of the section (beach facies), mainly parautochthonous elements related with erosion of the Pre-Mid Holocene substrate was recognized, since the shoreface was only periodically affected by marine processes, i.e., during storms.     

Ordovician Bathyal Trace Fossils From Metasiliciclastics in Central Norway and Their Sedimentological and Paleogeographical Implications

Numerous trace fossils are recognized in metasiliciclastic rocks of the Lower-Middle Ordovician Lower Hovin Group, Upper Ordovician Ekne Group and on roofing slates from an unknown locality (probably Ordovician) from the Trondheim region, central Norway. The trace fossil assemblages are dominated by meandering pascichnial forms, i.e., Helminthoidichnites in the Lower Hovin Group and Helminthoidichnites and Nereites in the slates. Protovirgularia, Dictyodora, ?Planolites and ?Palaeophycus are less common. Alcyonidiopsis, ?Trichophycus, Chondrites, cf. Chondrites, Gordia, ?Phycodes, ?Helminthopsis, cf. Naviculichnium, Treptichnus, Saerichnites, Megagrapton and ?Paleodictyon (Squamodictyon) are rare. The trace fossils were collected or observed at 17 different localities and represent assemblages belonging to the Nereites ichnofacies (deep-sea flysch deposits with thinly bedded turbidites). They reflect a distal Nereites subfacies (fan-fringe or basin-plain deposits) transitional to a Nereites/Paleodictyon subfacies (proximal fan facies). The trace fossil assemblages indicate an opportunistic style of colonization related to fluctuations in food supply introduced by turbidity currents.     

Small Theropod Track Assemblages from Middle Jurassic Eolianites of Eastern Utah: Paleoecological Insights from Dune Ichnofacies in a Transgressive Sequence

New discoveries show that very small theropod tracks (cf. Wildeichnus) are abundant in the upper part of the Moab Member, recently assigned to the Curtis Formation (formerly considered part of the Entrada Formation) in the Mid-?Late Jurassic of eastern Utah. The tracks represent a distinct small-theropod ichnofacies associated with eolian dune deposits that is easily differentiated from the water-lain beds of the overlying Megalosauripus-Therangospodus ichnofacies, which comprises the single-surface Moab megatracksite. Pterosaur track assemblages, representing the Pteriachnus ichnofacies, are found a few meters above the megatracksite surface in the upper tongue of the Summerville Formation.

The small theropod ichnofacies is reminiscent of other early Mesozoic dune facies ichnofaunas from the Wingate and Navajo formations (Late Triassic and Early Jurassic) where small theropod tracks occur in association with other small tetrapod footprints. All such examples evidently represent a recurrent dune facies ecosystem dominated by diminutive vertebrates. Because the small theropod ichnofacies is one of three ichnofacies found in a thin stratigraphic sequence (<20 m) that contains no body fossils, it is clear that vertebrate tracks play an important role in providing insight into the paleoecology of units previously considered devoid of any useful fossil evidence. The three successive ichnofacies represent a transgressive transition from sand dunes, through sandy shoreline to shallow marine environments, each with its quite distinct vertebrate fauna.     

Trace fossil analysis of lacustrine facies and basins

Two ichnofacies are typical of lacustrine depositional systems. The Scoyenia ichnofacies characterizes transitional terrestrial/nonmarine aquatic substrates, periodically inundated or desiccated, and therefore is commonly present in lake margin facies. The Mermia ichnofacies is associated with well oxygenated, permanent subaqueous, fine-grained substrates of hydrologically open, perennial lakes. Bathymetric zonations within the Mermia ichnofacies are complicated by the wide variability of lacustrine systems. Detected proximal–distal trends are useful within particular lake basins, but commonly difficult to extrapolate to other lakes. Other potential ichnofacies include the typically marine Skolithos ichnofacies for high-energy zones of lakes and substrate-controlled, still unnamed ichnofacies, associated to lake margin deposits. Trace fossils are useful for sedimentologic analysis of event beds. Lacustrine turbidites are characterized by low-diversity suites, reflecting colonization by opportunistic organisms after the turbidite event. Underflow current beds record animal activity contemporaneous with nearly continuous sedimentation. Ichnologic studies may also help to distinguish between marine and lacustrine turbidites. Deep-marine turbidites host the Nereites ichnofacies that consists of high diversity of ornate grazing traces and graphoglyptids, recording highly specialized feeding strategies developed to solve the problem of the scarcity of food in the deep sea. Deep lacustrine environments contain the Mermia ichnofacies, which is dominated by unspecialized grazing and feeding traces probably related to the abundance and accessibility of food in lacustrine systems. The lower diversity of lacustrine ichnofaunas in comparison with deep-sea assemblages more likely reflects lower species diversity as a consequence of less stable conditions. Increase of depth and extent of bioturbation through geologic time produced a clear signature in the ichnofabric record of lacustrine facies. Paleozoic lacustrine ichnofaunas are typically dominated by surface trails with little associated bioturbation. During the Mesozoic, bioturbation depth was higher in lake margin facies than in fully lacustrine deposits. While significant degrees of bioturbation were attained in lake margin facies during the Triassic, major biogenic disruption of primary bedding in subaqueous lacustrine deposits did not occur until the Cretaceous.     

A nearshore–offshore trend in acritarch distribution from the Early–Middle Ordovician of the Yangtze Platform, South China

The stratigraphical interval of the late Early Ordovician Didymograptus deflexus and the early Middle Ordovician Azygograptus suecicus graptolite Biozones was investigated from seven sections from the upper Yangtze Platform, southern China. These are located on different parts of the platform, between the nearshore environments of the Kunming area, Yunnan Province, and the offshore carbonate shelf of the Yichang area, Hubei Province. The assemblages recovered from the different parts of the platform vary both in terms of diversity and composition. The nearshore environments show low diversity assemblages with about 10 acritarch species, whereas the offshore shelf environments reflect higher diversities with about 40 species. The composition of the assemblages also changes from simple morphologies (micrhystrids, leiosphaerids, fusiform acritarchs) in nearshore environments to specimens with longer and more complexly branched processes on the shelf. The polygonomorph acritarchs are common over all the upper Yantze Platform, while the acanthomorph genera Baltisphaeridium and Peteinosphaeridium are the most abundant taxa on the offshore carbonate shelf area. Phylogenetic or sea-level changes are probably not responsible for the compositional and diversity changes that occurred during the investigated interval. This study confirms previous interpretations that poorly diversified Palaeozoic acritarch assemblages occur in neritic environments and more complex, highly diversified assemblages are found on the shelf.     

Latest Ordovician brachiopod and trilobite assemblage from Yuhang,northern Zhejiang,East China: a window on Hirnantian deep-water benthos

A moderately diverse brachiopod and trilobite assemblage, the Leangella–Dalmanitina (Songxites) Assemblage, occurs in the upper Yankou Formation (Hirnantian, probably equivalent to the Normalograptus persculptus Biozone) at Shizi Hill, Yuhang, west of Hangzhou, northern Zhejiang, E China. The brachiopods are rare, characterised by minute, thin shells with very small body cavities, preserved in mudstones as moulds. They may have inhabited quiet, deep-water and dysaerobic slope environments with low levels of nutrients, equivalent to Benthic Assemblage 5. Most genera were adapted for life in deep water and either remained there or alternatively migrated into relatively shallower habitats to evade perturbations during the first phase of the end Ordovician extinctions. The slope environments were recolonised from outer shelf and upper slope communities during the early Hirnantian, but isolated biotas may also have survived in deeper-water habitats by reducing their population size and diversity during the crisis. The Leangella–Dalmanitina (Songxites) Assemblage provides an unique Hirnantian window through which we can monitor the changes in the deep-water biofacies following the first phase of the extinctions. Significantly, parts of the deep water marine environment may have survived intact, the end Ordovician extinctions.     

Controls on trace fossil diversity in an Early Cambrian epeiric sea: new perspectives from northwest Scotland

The Lower Cambrian Eriboll Formation of northwest Scotland is renowned for the high density, low diversity trace fossils (Skolithos ichnofacies) found in its upper Pipe Rock Member. Ichnofabric analysis of the member indicates that relatively small examples of Skolithos terminating at the same foreset boundary were formed during a brief colonization window after a single depositional event, that particularly long Skolithos specimens are equilibrichnia, and that palimpsests of Skolithos represent the marginal, slightly deeper water fringes of the Pipe Rock Member depositional environment. Nearest neighbour analysis, however, suggests that such palimpsests were uncommon. A much more diverse trace fossil assemblage is present in the overlying Fucoid Member (An t‐Sròn Formation), comprising Cruziana barbata, Dactylophycus, Didymaulichnus, Halopoa imbricata, ?Margaritichnus, Monocraterion, Monomorphichnus, Palaeophycus striatus, P. tubularis, ?Phycodes, Planolites montanus, ?Polarichnus, Rusophycus ramellensis, ?Psammichnites, Skolithos and various unidentified traces, and represents the Cruziana ichnofacies. Above the Fucoid Member, the Salterella Grit Member ichnofauna is more impoverished, yielding only Cruziana, Monocraterion, Rusophycus, Skolithos and ?Spirophyton. The ichnological variations between the Pipe Rock, Fucoid and Salterella Grit members are interpreted as being driven by changes in sea level. The low trace fossil diversity in the Pipe Rock Member indicates opportunistic colonization of laterally extensive, shoreface sediments deposited by regular influxes of terrigenous material, which were overlain by more distal, ichnologically diverse sediments (Fucoid Member) as sea level rose. A minor regression then caused an increase in terrigenous sediment input, producing an impoverished, proximal Cruziana ichnofacies (Salterella Grit Member).     

Trace fossils in fluvial deposits of the uppermost Stockton Formation (Late Triassic), Newark Basin,New Jersey

Abstract

Fluvial deposits of the uppermost Stockton Formation (Late Triassic), Newark Basin, west-central New Jersey have yielded an assemblage of trace fossils. Dominated by burrows, specimens include Cochlichnus anguineus, Helminthoidichnites tenuis, Planolites beverleyensis, Scoyenia gracilis, Spongeliomorpha carlsbergi, Treptichnus bifurcus, Treptichnus pollardi, plant remains, and an undetermined vertebrate trace fossil. The assemblage belongs to the Scoyenia ichnofacies. On the basis of stratification and primary sedimentary structures, the beds are interpreted as deposits in a meandering stream environment. Larval insects, wormlike forms, and arthropods are probably responsible for most of the animal traces in wet or moist channel, floodplain, and point bar sediments subject to subaerial exposure.     

Tetrapod Ichnofacies: A New Paradigm

We recognize three fundamental terms in ichnology: (1) ichnoassemblage, which is an assemblage of ichnofossils conceptually equivalent to an assemblage of body fossils; (2) ichnocoenosis, which is a trace fossil assemblage produced by a biological community that can be characterized by morphological criteria; and (3) ichnofacies, which refers to recurrent ichnocoenoses that represent a significant portion of Phanerozoic time. There are two different kinds of ichnofacies, ethoichnofacies (mostly invertebrate ichnofacies) and biotaxonichnofacies (mostly tetrapod ichnofacies). Nonmarine invertebrate ichnologists now recognize five archetypal ichnofacies (Mermia, Skolithos, Scoyenia, Coprinisphaera, Psilonichnus) to which we add the Octopodichnus ichnofacies. We propose a coherent and consistent classification and nomenclature for tetrapod ichnofacies. We name five archetypal vertebrate ichnofacies for nonmarine environments: Chelichnus, Grallator, Brontopodus, Batrachichnus and Characichnos ichnofacies.     

Stable deep-sea macrobenthic trace maker associations in disturbed environments from the Eocene Lefkara Formation,Cyprus

Ichnological analysis of Eocene deep-pelagic whitish chalky calcilutites interstratified with high-energy calcarenite beds in the lower part of the Petra Tou Romiou section (southern Cyprus) was conducted to interpret the development and evolution of the trace maker associations during calcilutite deposition after high-energy episodes. The trace fossil assemblage from the chalky calcilutites consists of Chondrites isp. (Chondrites intricatus and Chondrites targionii), Planolites isp., Taenidium isp., Thalassinoides isp., and Zoophycos isp., typical of the Zoophycos ichnofacies. A composite chalky ichnofabric reveals a multi-tiered association of burrowing animals: the uppermost tier determines a mottled background, the upper tier shows the highest trace fossil abundance and diversity (Planolites, Taenidium and Thalassinoides), the middle tier features Zoophycos and large Chondrites, and the deepest tier consists mainly/exclusively of small Chondrites. This ichnofabric has an autocomposite character, associated with bioturbation by a single ichnocoenosis and gradual upward migration of the tiered macrobenthic community as the pelagic calcilutite sedimentation slowly progresses. There are no changes in the trace fossil assemblage between or within calcilutite intervals, regardless of the associated calcarenite beds. This supports a stable, mature, background calcilutite trace maker association, which recovers shortly after the deposition of high-energy calcarenites. In turn, there would have been a rapid re-establishment of paleoenvironmental conditions during pelagic calcilutite accumulation after episodic deposition of any calcarenitic material.     

Uniformity in marine invertebrate ichnology

Relationships between ichnology and uniformitarianism are perhaps less complicated than those of their sister subdisciplines, paleontology and paleoecology. Trace fossils are manifestations of benthic behavior; and these traits, although evolving in significant ways, have remained stable over longer spans of time than individual species of invertebrates. The fossil record of behavior in fact originated earlier than the fossil record of invertebrate body parts. Although macroinvertebrates and their traces exhibit tremendous diversity of form and function, these fit into a relatively small number of behavioral patterns. The patterns, in turn, may correlate with prevailing environmental conditions, resulting in gradients among trace fossil assemblages, or ichnofacies. Behavioral patterns and characteristic ichnofacies therefore constitute the main basis for uniformity in ichnology. Thus, the most fundamental questions are: What is the specific function represented by the trace? How will it change as the tracemaker is influenced by other genetic, physiologic, or ecologic stimuli? In which facies will it likely occur? and what preservational biases are apt to modify the fossil record of this behavior and its environmental distribution? Approached from this standpoint, the present is indeed a key to the ichnologic past, and vice versa. In practice, however, the present has been studied considerably less than its importance would dictate.