Middle Jurassic trace fossils from the Ridang Formation in Sajia County,South Tibet,and their palaeoenvironmental significance

An ichnofauna consisting of 18 ichnospecies (one of them new) in 14 ichnogenera are described for the first time from the Middle Jurassic Ridang Formation in Sajia County, South Tibet. The ichnofauna can be subdivided into two ichnoassemblages in ascending stratigraphic order: the Palaeophycus–Megagrapton ichnoassemblage in the lower and middle parts of the Ridang Formation, followed by the Cosmorhaphe–Nereites–Paleodictyon ichnoassemblage in the upper Ridang Formation. Overall, the trace fossils occur in a middle–distal turbidite fan sequence, as evidenced by both sedimentological analysis and the composition of the trace fossils. Several subenvironments of the middle–distal fan system have been recognized on the basis of the spatial distribution of the trace fossils. Typically, the channel-fill deposits in the middle part of the turbidite fan lack trace fossils, the interchannel and upper channel-fill (levee) subenvironments of the middle turbidite fan contain abundant facies-crossing trace fossils, in contrast to the distal part of the turbidite fan where deep-water trace fossils are dominant. The ichnofauna is similar to typical flysch ichnofaunas from Europe and North America in characteristics, and is interpreted to represent a typical deep-sea Nereites ichnofacies. The presence of these deep-sea trace fossils therefore would suggest that a continental slope environment existed in southern Tibet during the Middle Jurassic and the study area was located in a slope-abyssal plain setting.     

Trace fossils from the Cambro-Ordovician cow head group,newfoundland, and their paleobathymetric implication

U-shaped burrows identified as the trace fossil Arenicolites occur in the Cambro-Ordovician Cow Head Group, a series of thin-bedded limestones interbedded with graptolitic shale and thick beds of limestone breccia and conglomerate. The lithology, limestone petrography, and trace fossils indicate deposition on a submarine slope of a slowly submerging carbonate platform. The limestone bed containing Arenicolites probably represents a period of slow deposition. The steeply inclined U-shaped burrows are assumed to have been formed by polychaete worms of the family Mochtyellidae which thrived in an argillaceous carbonate mud bottom of a carbonate platform slope, in depths exceeding 200 m. Although Arenicolites is believed to denote a shallow-water environment, its presence in the Cow Head extends the ecological niche of the Arenicolites-producing organisms into the outer shelf and continental slope. The domichnia of suspension feeders thus extends from shallow- to deep-water environments.     

Giant Bathysiphon (Foraminiferida) from Cretaceous turbidites, northern California

Straight-sided, tubular fossils occur together with a diverse assemblage of deep-water trace fossils in linegrained Franciscan turbidites at Point Saint George. Pacific Coast of California. Based on comparison with living abyssal organisms and on skeletal microstructure, these tubes are interpreted as recrystallized siliceous tests of the large abyssohenthic foraminiferid, Bathysiphon. Tubes found preserved in-place show that life orientation of the Franciscan species was vertical with the broader, mature end protruding several millimetres above the muddy seafloor. Positioned in this way the organisms probably were suspension feeders or carnivores. Bathysiphon and trace fossils taken together reflect a diverse deep-water benthic community that was disrupted (or locally eliminated) repeatedly by turbidity currents reaching the outer margins of a submarine fan. ▭ Bathysiphon, deep-water benthos, outer fan/basin floor, trace fossils, Franciscan Complex, flysch, Cretaceous.     

Evolution of pelagic swells from hardground analysis (Bathonian–Oxfordian, Eastern External Subbetic, southern Spain)

The Middle Bathonian to Middle Oxfordian interval in the Eastern External Subbetic (Betic Cordillera, SE Spain) is characterized by Ammonitico Rosso facies including various stratigraphic breaks. Five hardground-bounded units are recognized in relation to hiatuses in the ammonite record at the following stratigraphic boundaries: Hg1 (Lower–Middle Bathonian), Hg2 (Middle–Upper Bathonian), Hg3 (Lower–Middle Callovian), Hg4 (Middle–Upper Callovian), and Hg5 (Callovian–Oxfordian). Interesting features of these hardgrounds include their microfacies, ferruginous crusts and macro-oncoids, taphonomy of macroinvertebrates, trace fossils, neptunian dykes, and the hiatuses associated with each of them. The main hardgrounds (Hg1, Hg2, and Hg5) contain trace fossils of the Cruziana and Trypanites ichnofacies as well as abundant fossil macroinvertebrates with taphonomic features evidencing corrasion, early diagenesis, and reworking, indicating substrate evolution from softground to hardground. Neptunian dykes affected the trace fossils and ammonoid moulds, and their walls and the hardground surfaces were colonized by ferruginous microbial crusts. These features are characteristic of the External Subbetic pelagic swells, where the absence of sedimentation, sediment bypassing and erosion, and early diagenesis during relative sea-level falls produced hardgrounds. The neptunian dykes are indicative of tectonic activity in the areas of pelagic swells. Ferruginous crusts and macro-oncoids developed only on hardground surfaces and neptunian dykes walls prior to deposition of condensed bioclastic beds, which are interpreted as the first deposits after hardground development and are related to the onset of transgression. The varying ranges of the gaps as well as lateral facies changes are related to different local paleobathymetry controlled by the activity of listric faults.     

Silurian trace fossils in carbonate turbidites from the Alexander arc of southeastern Alaska

Early to Late Silurian (Llandovery‐Ludlow) body and trace fossils from the Heceta Formation of southeastern Alaska are preserved in the oldest widespread carbonates in the Alexander terrane. These fossils represent the earliest benthos to inhabit diverse shallow and deep subtidal environments in the region and are important indicators of early stages in benthic community development within the evolving Alexander arc. The ichnofossils are particularly significant because they add to a small but growing body of knowledge about trace fossils in deep‐water carbonates of Paleozoic age.

Carbonate turbidites that originated along a deep marine slope within the arc yield a low‐diversity suite of trace fossils consisting of five distinct biogenic forms. Simple burrows (Planolites, two forms), ramifying tunnels (Chondrites), and tiny cylindrical burrows (?Chondrites) represent the feeding activities (fodinichnia) of pre‐turbidite animals that burrowed in the lime mud before the influx of coarser sediment deposited by turbidity currents. These trace fossils are associated locally with cross‐cutting burrows created as domichnia (Palaeophycus). Rarer hypichnial burrows and endichnial traces were created by post‐turbidite animals that fed soon after the deposition of coarse detritus from turbidity flows.

Trace fossils in these deposits reflect much lower diversity levels than in Paleozoic siliciclastic turbidites. This difference may represent unfavorable environmental conditions for infaunas, differential preservation, or significant paleogeographic isolation of the Alexander terrane during the Silurian. Greater utilization of trace fossils in terrane analysis may help to resolve this issue and provide new data for reconstructing the paleogeography of circum‐Pacific terranes.     

Trace fossils in upper cretaceous argillaceous marine facies of the U.S. Western interior

Argillaceous strata of the Greenhorn and Niobrara depositional cycles contain an extensive, though spottily developed, record of tracemaking organisms. These beds are assignable to five facies, four of which represent the gradation from nearshore sandy shales to far offshore calcareous shales, the fifth representing anoxic or nearly anoxic bottom conditions. In strata studied by us the best potential for trace fossil preservation was in deposits characterized by pronounced textural variation, such as shales with sandstone interbeds, shales with thin lenses of siltstone or sandstone, or sandy and silty shales (= mudstones). In pure clayey shales and calcareous shales, trace fossils are preserved best in concretionary structures. Our study suggests that except for shales rich in organics, trace-making organisms were common and widespread in argillaceous muds of the Western Interior. Initial fluidity, high degree of compaction, and textural homogeneity are principal reasons for the poor record of trace makers in pure, clayey shales.     

The Ichnofossils of the Triassic Hope Bay Formation,Trinity Peninsula Group,Antarctic Peninsula

The Triassic Hope Bay Formation (Trinity Peninsula Group) includes a diverse ichnocoenosis in the Puerto Moro succession (Hope Bay, Antarctic Peninsula). The Hope Bay Formation is a thick turbidite succession with a minimum vertical exposure of 533 meters along the Hope Bay coast. The rocks are locally affected by contact metamorphism related to later arc magmatism. The ichnofossils are found mainly in thick- and thin-bedded sandstone-mudstone facies composed of a monotonous repetition of sandstone-mudstone cycles. The sandstones are usually medium grained, massive or parallel laminated; the mudstones are massive and rarely laminated. In the fine-grained rocks, mainly the mudstones, there are distinct densities of bioturbation, and at least six patterns were observed. The following ichnogenera were recognized: Arenicolites Salter 1857, Lophoctenium Richter 1850, Taenidium Heer 1877, Palaeophycus Hall 1847, Phycosiphon von Fischer-Ooster 1858 and Rhizocorallium Zenker 1836. All appear to be feeding-traces. The trace fossil assemblages occur mainly in black mudstones rich in organic material that suggest a low oxygen environment. The stratigraphic interval in which they occur is interpreted as progradational supra-fan lobes with channel fill and levee deposits. The thin-bedded turbidite and mudstone lithofacies, where the ichnofossils are abundant, is interpreted as a distal fan turbidite or levee deposit related to a long-term channel fill. This study is the first significant report of trace fossils in the Hope Bay Formation.     

Deep-water trace fossils in the Ilfjellet rift basin (Middle Ordovician), central Norwegian Caledonides

The late Early to early Middle Ordovician Fjellvollen Formation, Central Norwegian Caledonides, is a part of the Ilfjellet Group volcano-sedimentary succession formed in a rift basin that opened along the Laurentian margin. Depositional facies and trace fossils indicate the Nereites ichnofacies, typically found in distal turbidites and deep marine deposits. The recovered trace fossils include ?Alcyonidiopsis, Chondrites, Dictyodora, Gordia, Helminthoidichnites, Macaronichnus, Monomorphichnus, Nereites, Oikobesalon, Palaeophycus, Protovirgularia and Treptichnus. No body-fossils have been reported from the Fjellvollen Formation, but the trace fossils indicate the presence of varied epi- and infaunas of arthropods, bivalves, gastropods and polychaets. The abundance of meandering and looping trace fossils is comparable to what is found in the inferrably time-equivalent Vuddudalen Group farther north, although lack of graphoglyptids like Megagrapton in the Fjellvollen Formation may indicate more proximal, unstable depositional conditions in fan-fringe and adjacent basin-plain settings.     

Non-calcified warm-water marine macroalgae from the Ordovician strata of Spiti,Tethys Himalaya,India

The calcareous siltstones within the Ordovician section of the Takche Formation near Takche, Spiti region of Tethyan Himalaya, India, contain numerous specimens of non-calcified marine macroalgae in association with brachiopods, gastropods, tentaculitoids, and few trace fossils. The algal remains, representing five genera, are preserved as black or dark brown carbonaceous compression fossils, interpreted as warm-water marine macroalgae, namely, Inocladus sp., Callisphenus? sp., Algites sp. (siphonous algae), Fisherites sp., and Mastopora sp. (non-siphonous). Callisphenus is characterised by a radially symmetrical short pyriform thallus, with a central axis surrounded by short laterals whereas Inocladus sp. is characterised by an unsegmented simple thallus with internal parallel medullary siphons and cortical tubes. These algal remains, probably transported from a more near-shore living niche, co-occur with Cyclocrinitids, Tentaculitoids tube worms, trace fossils and brachiopods, suggesting that deposition of the studied units took place in low energy hydrodynamic conditions influenced by intermittent storm events. The study represents the first diversified macroalgal records from the Ordovician strata in the Tethyan realm of Indian subcontinent.     

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.     

贵州交榜留茶坡组化石组合特征及其生物地层学和演化意义*

埃迪卡拉纪—寒武纪之交见证了地球—生命系统不同圈层的重大变革, 是复杂多细胞生物演化的重要转折期。华南是开展相关研究的主要区域之一, 但前人工作主要集中在化石材料丰富的浅水台地相区, 深水区生物组成面貌尚未得到充分认识。本研究对斜坡相区贵州交榜剖面的留茶坡组进行了详细研究, 通过酸蚀和薄片观察发现了丰富的化石材料, 包括: 海绵骨针、软舌螺、可能的原牙形类(? Protohertzina sp.)和织金钉类(? Zhijinites sp.)、球形疑源类、Megathrix longus, 及不同类型的多细胞藻类, 亲缘关系未定的Poratusiramus sp.、球形化石和形态多样的丝状、片状化石等。该化石组合属于寒武纪纽芬兰世幸运期, 其中的骨骼化石以海绵骨针为主。化石组合中既有与浅水区共有分子, 也有深水区特有类群, 丰富了斜坡相区的化石记录, 具有潜在的地层对比和演化意义。     

The palaeoecology of the Ordovician Harding Sandstone (Colorado,U.S.A.)

The Middle Ordovician Harding Sandstone in Colorado, U.S.A. is the oldest formation known to have an environment rich in vertebrate fossils. In order to study the palaeoecology of these oldest vertebrates, a detailed analysis of both the sediments and the associated invertebrate fauna was made. Undulatory quartz, sandstone mineralogy, geochemistry, trace fossils, and ecological implications of the invertebrate fossils have been studied. The type of environment is not a typical one, but was probably a shallow-water marine (intertidal, or shallow subtidal), in a lagoon-like or estuarine—deltaic habitat, with changing salinity, and a generally warm climate.     

Ichnology and sedimentology of the early Permian deep-water deposits from the Lercara-Roccapalumba area (Western Sicily,Italy)

Summary Diverse and abundant trace fossils of the deep-waterNereites ichnofacies have been found in well-dated Early Permian deep-water turbidites (Lercara Formation) of western Sicily (Italy). Conodonts indicate a latest Artinskian to Cathedralian (late Early Permian) age. Microfossils (pelagic conodonts, albaillellid Radiolaria, paleopsychrospheric ostracods, foraminiferal associations dominated byBathysiphon), trace fossils (deep-bathyal to abyssalNereites ichnofacies) and sedimentologic data collectively indicate a deep-water environment for the Early Permian turbidites of the Lercara Formation. The dominance ofAgrichnium and of thePaleodictyon subichnogeneraSquamodictyon andMegadictyon suggests that this icnofauna is closely related in ichnotaxonomic composition to other late Paleozoic deep-water ichnofaunas. The occurrence ofAcanthorhaphe. Dendrotichnium andHelicoraphe, to date only reported from Cretaceous or Tertiary flysch deposits, suggests that the entire ichnofauna corresponds well to previously documented Silurian-Tertiary flysch ichnofaunas. Eight new ichnospecies and a new ichnosubgenus,Megadictyon, are described.     

Integrated sedimentological,ichnological and sequence stratigraphical studies of the Koti Dhaman Formation (Tal Group), Nigali Dhar Syncline,Lesser Himalaya,India: paleoenvironmental,paleoecological, paleogeographic significance

Abstract

Integrated ichnology, sedimentology and sequence stratigraphy of the Lower Quartzite Member to the Arkosic Sandstone Member of the Koti Dhaman Formation (Cambrian Series 2, Stage 4), Tal Group, Nigali Dhar Syncline, Lesser Himalayan lithotectonic zone are presented. Trilobite traces of Gondwanan affinity i.e., Cruziana salomonis, Cruziana fasciculata, Rusophycus dispar and Rusophycus burjensis are recorded along with Arenicolites isp. and Skolithos isp. from the Lower Quartzite Member. A rich and diverse ichnoassemblage attributed to the Cruziana ichnofacies is described for the first time from the Arkosic Sandstone Member of the same formation. Seven ichnofossil assemblages, i.e., Cruziana-Rusophycus, Planolites-Palaeophycus, Cruziana problematica, Diplichnites, Cochlichnus anguineus, Bergaueria perata and Psammichnites gigas have been recognized in the Lower Quartzite to Arkosic Sandstone members of the Koti Dhaman Formation. Seven sedimentary facies i.e., sandstone–shale facies (FT1), cross-bedded (trough and planar) sandstone (FT2), bedded sandstone facies (FT3), shale facies (FT4), shale–sandstone facies (FT5), shale-rippled sandstone facies (FT6) and planar and trough cross-laminated sandstone (FT7) and four facies associations FA1-FA4 are identified in the Koti Dhaman Formation. The formation contains shallowing upward parasequences of a tidal flat complex. Overall, two major events are recognized: i) the break in sedimentation between the Lower Quartzite Member and the overlying Shale Member probably related to forced-regressive event and ii) the facies shift from FT6 to FT7 of the Arkosic Sandstone Member represents an erosive transgressive event; the surface is interpreted as wave ravinement surface, which also serves as a sequence boundary. Integrated ichnology, sedimentology and sequence stratigraphic studies indicate that the Lower Quartzite Member was deposited in a shallow subtidal sand sheet complex and tidal flat complex; the Shale Member was deposited in a mud flat setting of a tidal flat complex, and the Arkosic Sandstone Member in a mixed-flat (tidal flat complex) to sand sheet complex front and margin (subtidal sand sheet complex). Overall, the lower to middle part of the Koti Dhaman Formation represents a tide-dominated shallow subtidal–intertidal to mud-flat subenvironments of the tidal flat complex. A palaeogeographic reconstruction of lower Cambrian (516–514?Ma) is presented based on the distribution of trilobite traces from the Lesser Himalaya and the Bikaner–Nagaur area of Peninsular India (eastern Gondwana), Egypt, Jordan, Turkey (western Gondwana) and Canada (Avalonia).     

Trace fossils of the arthropod Camptophyllia from the Westphalian (Carboniferous) rocks of Lancashire, UK and their palaeoenvironmental context

Two arthropod trace fossils are described and analysed from the Carboniferous Lower Westphalian (C. communis and basal A. modiolaris chronozones) coal-bearing strata of Lancashire. The biserial trackway Diplichnites triassicus consists of five overlapping en echelon sets of 7–9 tracks preserved as epichnia and hypichnia in lacustrine siltstones. The trackway suggests subaqueous in-phase walking by a multi-segmented producer with a body length of 35–40 mm, width 17–22 mm, and 7–9 appendages. Curved, clustered, or laterally repeated, hypichnial lobes with transverse striations on the base of ripple cross-laminated sandstone are identified as Rusophycus versans. This trace fossil is interpreted as shallow resting or furrowing burrows of a homopodous arthropod, 30–60 mm long, 15–30 mm wide, and probably the same kind of arthropod as produced D. triassicus.A review of contemporary arthropod body fossils from Lagerstätten in Lancashire favours the onisciform, or Arthropleura like arthropod Camptophyllia as a potential producer of both of these trace fossils in a lacustrine palaeoenvironment.This study integrates the analysis of sediments, trace fossils and body fossils for reconstructing the arthropod biota and ecology in Westphalian lacustrine and crevasse splay fluvial palaeoenvironments.     

Lithostratigraphy of the Lower Cambrian metaclastics and their age based on trace fossils in the Sand?kl? region, southwestern Turkey

In the Sand?kl? region of the Taurus Range of Turkey, greater than 3000 m in thickness metamorphosed siliciclastics and volcanics (Kocayayla Group) underlies the trilobite-and conodont-bearing Middle-Late Cambrian Hudai Quartzite and Çaltepe Formation.The Kocayayla Group, previously regarded as Infracambrian or Precambrian, is dated for the first time as Early Cambrian on the basis of trace fossils. Cruziana ?fasciculata, C. ?salomonis, ?Cruziana isp., ?Diplichnites isp., Monomorphichnus isp., Petalichnus isp., Rusophycus ?avalonensis, R. ?latus, Arenicolites isp., cf. Altichnus foeyni, Planolites isp., Skolithos isp., and ?Treptichnus isp. have been recognised. These trace fossils are considered Tommotian or younger in age but older than the overlying, trilobite and conodont bearing Middle Cambrian limestones of the Çaltepe Formation. The trace fossils were likely produced by trilobites, suspension feeding annelids and deposit feeding “worms”, probably polychaetes. Sections bearing abundant Skolithos represent the Skolithos ichnofacies, which is typical of high energy environments with loose sandy, well sorted to slightly muddy substrates in intertidal to shallow subtidal zones. The other trace fossils represent the Cruziana ichnofacies, which is typical of subtidal, poorly sorted and soft substrates, from moderate energy to low energy environments between the fairweather and storm wave base.The Kocayayla Group was deposited at an early stage in a shallow marine stable shelf condition. The shelf subsided in a later stage and was affected by normal faults along which mafic and felsic volcanic rocks erupted. The volcanic activity had ceased and a shallow marine clastic sedimentation took place in the final stage of the shelf development. The Kocayayla Group was deformed and metamorphosed before the deposition of the trilobite-bearing Middle-Upper Cambrian succession.     

New evidence of nearshore Mid-Triassic <Emphasis Type="Italic">Zoophycos</Emphasis>: morphological and paleoenvironmental characterization

Zoophycos is a well-known trace fossil common throughout the Phanerozoic. Paleozoic forms show important differences in morphology and habitat distribution with respect to the Jurassic, Cretaceous, and Cenozoic ones. Therefore, Early–Middle Triassic is considered a crucial time-span for the understanding of the evolution of this trace fossil. So far, Early Triassic Zoophycos is unknown and Middle Triassic forms were recorded only in deposits from Thuringia. The morphology and paleoenvironment of Zoophycos from the middle–upper Muschelkalk of the Iberian Range is herein described. The best-preserved trace fossils occur in a dolomicritic bed Ladinian in age, and are represented by small forms with a subcircular, slightly lobed outline and very little penetration depth. They were deposited in a very shallow, quiet-water environment with transition to supratidal/emerged areas. The low diversity of both trace fossils and skeletal remains point to stressful conditions related to strong salinity variations and/or poor water circulation. A comparison was made with Zoophycos from Anisian deposits of the Muschelkalk in Germany. This showed that both forms are quite simple and penetrate only the shallowest tiers, although they are different in whorl outline and lobe shape. This confirms that, notwithstanding the morphological variability of this group, Zoophycos still maintained a quite simple structure in the Triassic. A shallow-water environment was deduced for both localities, confirming that at least until the Early Jurassic Zoophycos had not definitively migrated toward deep-water areas.     

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.     

History of Ichnology: Early Ichnology Poems and Their Poets

In the early nineteenth century, the discovery of trace fossils fired the imagination of the discoverers and inspired them to compose unique poems. John Joly of Ireland wrote a poem about the invertebrate trace fossil Oldhamia that had been discovered in rocks around Bray Head. In the United States, the Reverend Edward Hitchcock discovered what he felt were giant bird tracks that later turned out to be reptile tracks. The traces inspired Hitchcock, who published a poem “The Sandstone Bird” in The Knickerbocker magazine under the pseudonym Poetaster. The poem is about a sorceress bringing the great sandstone bird back to life and probably represents the first ichnological poem.