Geology topics

Luis A. Buatois

Publications and source records attributed to Luis A. Buatois.

9 recordsLinked to original sources

USGS2020

Quantifying ecospace utilization and ecosystemengineering during the early Phanerozoic—The role of bioturbation and bioerosion

The Cambrian explosion (CE) and the great Ordovician biodiversification event (GOBE) are the two most important radiations in Paleozoic oceans. We quantify the role of bioturbation and bioerosion in ecospace utilization and ecosystem engineering using information from 1367 stratigraphic units. An increase in all diversity metrics is demonstrated for the Ediacaran-Cambrian transition, followed by a decrease in most values during the middle to late Cambrian, and by a more modest increase during the Ordovician. A marked increase in ichnodiversity and ichnodisparity of bioturbation is shown during the CE and of bioerosion during the GOBE. Innovations took place first in offshore settings and later expanded into marginal-marine, nearshore, deep-water, and carbonate environments. This study highlights the importance of the CE, despite its Ediacaran roots. Differences in infaunalization in offshore and shelf paleoenvironments favor the hypothesis of early Cambrian wedge-shaped oxygen minimum zones instead of a horizontally stratified ocean.

Science Advances↗

USGS2008

Trace fossils and sedimentary facies from a Late Cambrian‐Early Ordovician tide‐dominated shelf (Santa Rosita Formation, northwest Argentina): Implications for ichnofacies models of shallow marine successions

The Santa Rosita Formation is one the most widely distributed lower Paleozoic units of northwest Argentina. At the Quebrada del Salto Alto section, east of Purmamarca, Jujuy Province, it is represented by four sedimentary facies: thick‐bedded planar cross‐stratified quartzose sandstones (A), thin‐bedded planar cross‐stratified quartzose sandstones and mudstones (B), wave‐rippled sandstones and bioturbated mudstones (C), and black and greenish gray shales (D). Paleocurrent data, sandstone architecture, and sedimentary structures from faciès A and B indicate bipolar/bimodal paleoflows, suggesting the action of tidal currents. The succession is interpreted as that of a tide‐dominated shelf, with only secondary influence of wave processes. Trace fossils are restricted to facies B and C. The Cruziana ichnocoenosis is preserved on the soles of thin‐bedded planar cross‐stratified quartzose sandstones (faciès B). This ichnocoenosis consists of Conostichus isp., Cruziana omanica, C. semiplicata, C. cf. tortworthi, Cruziana isp. Helminthopsis abeli, Monomorphichnus bilinearis, M. multilineatus, Palaeophycus tubularis, Rusophycus carbonarias, R. latus , and R. isp. The occurrence of Cruziana semiplicata , C. omanica, C. cf. tortworthi , and Rusophycus latus supports a Late Cambrian‐Tremadoc age. Slabbing of Cruziana shows complex interactions between biologic and sedimentologic processes, and suggests a predominance of exhumed traces, washed out and recast by tractive sand deposition. Sandstone soles are densely packed with biogenic structures and exhibit distinctive clusters of Rusophycus isp. that most likely represent trilobite nesting burrows. The Cruziana ichnocoenosis records the resident fauna of a protected, lower intertidal to subtidal interbar setting. The Skolithos ichnocoenosis is represented by high to low density vertical burrows of Skolithos linearis , which extend downwards to the quartzose sandstone soles of faciès B and cross the Cruziana ichnocoenosis. The Skolithos ichnocoenosis represents colonization by suspension‐feeding organisms following a major change in environmental conditions, related to the migration of lower intertidal to subtidal sandwaves. The Planolites ichnocoenosis consists exclusively of Planolites montanus within mudstones overlying wave‐rippled sandstones (facies C). The Planolites ichnocoenosis records opportunistic colonization by inf aunal deposit feeders that mined the organic‐rich fine‐grained sediment during the waning phase of storms that scoured organic detritus from the sea bottom. The section records, from base to top, a Cruziana‐Skolithos ichnofacies zone, a Skolithos ichnofacies zone and an unbioturbated zone typified by the thick‐bedded cross‐stratified quartzose sandstone (fades A). This trend reflects progressively higher energy conditions linked to the establishment of a large sand wave complex. The presence of a mixed Cruziana‐Skolithos ichnofacies in the lower interval reflects changes in substrate and energy levels, rather than water depth. Accordingly, contrasting ichnocoenoses from interbars (Cruziana) and sandwaves (Skolithos) must be considered an example of ichnofacies controlled by local parameters instead of general bathymétrie trends. Conversely, the vertical replacement of the Cruziana ichnofacies by the Skolithos ichnofacies towards the middle interval of the section reflects the environmental changes associated with the transition between the intertidal and subtidal zones. As overall tidal energy increases from supratidal to subtidal settings, the Skolithos ichnofacies tends to occur seaward of the Cruziana ichnofacies in tide‐dominated shallow marine environments. Therefore, onshore‐offshore ichnofacies replacement in tide‐dominated shallow seas is opposite to that in wave‐dominated marine settings.

Ichnos: An International Journal for Plant and Ani↗

USGS1999

The insect trace fossil Tonganoxichnus from the middle Pennsylvanian of Indiana: Paleobiologic and paleoenvironmental implications

The ichnogenus Tonganoxichnus , produced by one or more monuran insect taxa, is now recorded from the Middle Pennsylvanian Mansfield Formation of Indiana. Tonganoxichnus is a resting trace that has three important implications. First, it represents a recurrent behavioral pattern in Upper Carboniferous to Lower Permian marginal marine environments of North America. Second, it provides finely resolved anatomical information for axial and appendicular body structures and behaviors that are difficult to determine from body‐fossil material alone. Third, integrated sedimentologic and ichnologic observations indicate that the Tonganoxichnus assemblage, inclusive of other ichnotaxa, is common in tidal rhythmites that were developed under freshwater conditions, probably in the innermost part of estuarine systems, close to or at the fluvioestuarine transition.

Ichnos: An International Journal for Plant and Ani↗

USGS1998

Contrasting behavioral and feeding strategies recorded by tidal-flat bivalve trace fossils from the Upper Carboniferous of eastern Kansas

Upper Carboniferous tidal-flat deposits near Waverly, eastern Kansas (Stull Shale Member, Kanwaka Shale Formation), host abundant and very well-preserved trace fossils attributed to the activity of burrowing bivalves. Thin shell lenses with an abundant bivalve fauna area associated with the ichnofossil-bearing beds and afford an unusual opportunity to relate trace fossils to their makers. Two distinctive life and feeding strategies can be reconstructed on the basis of trace fossil analysis and functional morphology. Lockeria siliquaria hyporeliefs commonly are connected with vertical to inclined, truncated endichnial shafts in the absence of horizontal locomotion traces. These structures record vertical and oblique displacement through the sediment, and suggest relatively stable domiciles rather than temporary resting traces as typically considered. Crowded bedding surfaces displaying cross-cutting relationships between specimens of L. siliquaria and differential preservation at the top (concave versus convex epireliefs) record a complex history of successive events of colonization, erosion, deposition, and recolonization (time-averaged assemblages). Irregujlar contours of some large hypichnia indicate the cast of the foot, while other outlines closely match the anterior area of Wilkingia, its suggested tracemaker. Relatively stable, vertical to inclined life positions and dominanit vertical mobility suggest a filter-feeding strategy. Moreover, the elongate shell and pallial sinus of Wilkingia providfe a strong independent line of evidence for an opisthosiphonate, moderately deep-tier inhabitant. Wilingia may represent a pioneer attempt at siphon-feeding in the late Paleozoic, preceding the outcome of the Mesozoic infaunal radiation. A second strategy is represented by Lockeia ornata and association locomotionm and locomotion/feding structures. Lockeia ornata is commonly connected with chevron locomotion traces that record the bifurcated foot of a protobranch bivalve. Lockeia ornata exhibits distinctive, fine, parallel lines that mimic the ornamentation of Phestia, a nuculanid protobranch bivalve. Rosary and radial structures give evidence of a patterned search for food. Lockeia ornata and associated Protovirgularia record dominant horizontal locomoton and suggest the activity of deposit-feeding bivalves. Morphologic variability of Protovirgularia was controlled by substrate fluidity, which was dependent on sediment heterogeneity and tidal-cycle dynamics. This study demonstrates that detailed analysis of bivalve traces provides valuable information on bivalve ethology and paleoecology, evolutionary innovations, environmental dynamics, and substrate fluidity.

Kansas↗

USGS1998

The ichnologic record of the continental invertebrate invasion; evolutionary trends in environmental expansion, ecospace utilization, and behavioral complexity

The combined study of continental trace fossils and associated sedimentary facies provides valuable evidence of colonization trends and events throughout the Phanerozoic. Colonization of continental environments was linked to the exploitation of empty or under-utilized ecospace. Although the nonmarine trace fossil record probably begins during the Late Ordovician, significant invasion of nonmarine biotopes began close to the Silurian-Devonian transition with the establishment of a mobile arthropod epifauna (Diplichnites ichnoguild) in coastal marine to alluvial plain settings. Additionally, the presence of vertical burrows in Devonian high-energy fluvial deposits reflects the establishment of a stationary, deep suspension-feeding infauna of the Skolithos ichnoguild. The earliest evidence of plant-arthropod interaction occurred close to the Silurian-Devonian boundary, but widespread and varied feeding patterns are known from the Carboniferous. During the Carboniferous, permanent subaqueous lacustrine settings were colonized by a diverse, mobile detritus-feeding epifauna of the Mermia ichnoguild, which reflects a significant palaeoenvironmental expansion of trace fossils. Paleozoic ichnologic evidence supports direct routes to the land from marginal marine environments, and migration to lakes from land settings. All nonmarine sedimentary environments were colonized by the Carboniferous, and subsequent patterns indicate an increase in ecospace utilization within already colonized depositional settings. During the Permian, back-filled traces of the Scoyenia ichnoguild record the establishment of a mobile, intermediate-depth, deposit-feeding in-fauna in alluvial and transitional alluvial-lacustrine sediment. Diversification of land plants and the establishment of ecologically diverse plant communities through time provided new niches to be exploited by arthropods. Nevertheless, most ot the evolutionary feeding innovations took place relatively early, during the Late Palaeozoic or early Mesozoic. A stationary deep unfauna, the Camborygma ichnoguild, was developed in Triassic transitional alluvial-lacustrinbe deposits. Terrestrial environments hosted the rise of complex social behavioral patterns, as suggested by the probable presence of hymenopteran and isopteran nests in Triassic paleosols. An increase in diversity of trace fossils is detected in Triassic-Jurassic eolian deposits, where the ichnofauna displays more varied behavioral patterns than their Paleozoic counterparts. Also, a mobile, intermediate-depth, deposit-feeding infauna, the Vagorichnus ichnoguild, was established in deep lake environments during the Jurassic. In contrast to Paleozoic permanent subaqueous assemblages typified by surface trails, Jurassic ichnocoenoses are dominated by infaunal burrows. High density of infaunal deposit-feeding traces of the Planolites ichnoguild caused major disruption of lacustrine sedimentary fabrics during the Cretaceous. Most insect mouthpart classes, functional feeding groups, and dietary guilds were established by the end of the Cretaceous. Diversification of modern insects is recorded by the abundance and complexity of structures produced by wasps, bees, dung-beetles, and termites in Cretaceous-Tertiary paleosols. The increase in bioturbation migrated from fluvial and lake-margin settings to permanent subaqueous lacustrine environments through time.

Palaios↗

USGS1997

The paradox of nonmarine ichnofaunas in tidal rhythmites; integrating sedimentologic and ichnologic data from the Late Cretaceous of eastern Kansas, USA

The occurrence of trace fossil assemblages dominated by arthropod trackways and surface grazing trails within Carboniferous tidal rhythmites has puzzled sedimentologists and ichnologists, who interpreted them either as marine or nonmarine. The Virgilian (Stephanian) Tonganoxie Sandstone Member (Stranger Formation) at Buildex Quarry (eastern Kansas) consists, for the most part, of planar-laminated coarse-grained siltstones deposited on an upper tidal flat, close to or at the fluvial-estuarine transition of a macrotidal estuarine paleovalley. Recurrent thickness fluctuations demonstrate the strong influence of tidal processes and provide evidence that these deposits are tidal rhythmites, with thicker strata representing spring tides and thinner ones recording neap tides. The Buildex sequence hosts a moderately diverse ichnofauna composed of arthropod trackways (Dendroidichnites irregulare, Diplichnites gouldi, Diplopodichnus bifurcus, Kouphichnium isp., Mirandaichnium famatinense, Stiallia pilosa, Stiaria intermedia), grazing traces (Gordia indianaensis, Helminthoidichnites tenuis, Helminthopsis hieroglyphica), subsurface feeding traces (Treptichnus bifurcus, T. pollardi, irregular networks), apterygote insect resting and feeding traces (Tonganoxichnus buildexensis, T. ottawensis), fish traces (Undichna britannica, U. simplicitas), and tetrapod trackways. In contrast to trace fossil assemblages from brackish-water estuarine settings, the Buildex ichnofauna is characterized by moderate to relatively high ichnodiversity, ichnotaxa commonly present in terrestrial/freshwater environments, dominance of surface trails and absence of burrows, dominance of temporary structures produced by a mobile deposit-feeder fauna, a mixture of traces belonging to the Scoyenia and Mermia ichnofacies, moderate density of individual ichnotaxa, and absence of monospecific suites. This ichnofauna is thought to record the activity of a typical freshwater/terrestrial benthos. The presence of this mixed freshwater/terrestrial ichnofauna in tidal rhythmites is regarded as indicative of tidal flats that were developed in the most proximal zone of the inner estuary under freshwater conditions, more precisely in a zone between the maximum limit of landward tidal currents and the salinity limit further towards the sea. Although lithofacies distribution in estuarine valleys is mainly salinity-independent, the distribution of benthos is not. Accordingly, ichnologic studies have the potential to provide a high-resolution delineation of fluvio-estuarine transitions.

Kansas↗

USGS1996

Grazing trails formed by soldier fly larvae (Diptera: Stratiomyidae) and their paleoenvironmental and paleoecological implications for the fossil record

Recent trails formed by soldier fly larvae (Díptera: Stratiomyidae) were examined in a shallow pond in the floodplain of a braided river in Jujuy Province, northwestern Argentina. Collected specimens were identified as Stratiomys convexa van der Wulp. Simple, irregularly meandering trails were produced across the surface of a muddy‐silty substrate. Since soldier fly larvae extend their caudal respiratory tube to the water‐air interface, they are restricted to extremely shallow water. The presence of benthic algal remains within the mouthparts of the larvae suggests a feeding habit of algal grazing. If preserved, these trails would be included in the ichno‐genus Helminthopsis, a common element in ancient freshwater ichno‐faunas. Helminthopsis preserved in pond and lacustrine margin deposits younger than Late Jurassic is regarded as one possible trace fossil analogue of the trails documented herein. Additionally, it is suggested that larvae of many aquatic Diptera with similar ecologic restrictions are potential tracemakers of Helminthopsis and other simple trails in these environments, particularly in post‐Paleozoic deposits. Studies of modern shallow aquatic habitats and reex‐amination of the ichnologic record stress the importance of fly larvae as tracemakers in lake margin and pond ecosystems. Ecologic requirements of soldier fly larvae make them inappropriate analogues of Helminthopsis tracemakers in deeper water, lacustrine settings.

Ichnos: An International Journal for Plant and Ani↗

USGS1996

Trace fossils from Jurassic lacustrine turbidites of the Anyao Formation (Central China) and their environmental and evolutionary significance

The Lower Jurassic Anyao Formation crops out near Jiyuan city, western Henan Province, central China. It is part of the infill of the nonmarine early Mesozoic Jiyuan‐Yima Basin. In the Jiyuan section, this unit is about 100 m thick and consists of laterally persistent, thin and thick‐bedded turbidite sandstones and mudstones displaying complete and base‐or top‐absent Bouma sequences, and thick‐bedded massive sandstones. The Anyao Formation records sedimentation within a lacustrine turbidite system developed in a pull‐apart basin. Processes involved include high and low density turbidity currents, sometimes affected by liquefaction or fluidization. Facies analysis suggests that this succession is formed by stacked aggradational turbidite lobes. The absence of thick mudstone packages indicates that background sedimentation was subordinate to high frequency turbidite deposition. The Anyao Formation hosts a moderately diverse ichnofauna preserved as hypichnial casts on the soles of thin‐bedded turbidite sandstones. The ichnofauna consists of Cochlichnus anguineus, Hel‐minthoidichnites tenuis, Helminthopsis abeli, H. hieroglyphica, Mono‐morphichnus lineatus, Paracanthorhaphe togwunia, Tuberculichnus vagans, Vagorichnus anyao, tiny grazing trails, and irregularly branching burrows. Vagorichnus anyao occurs not only as a discrete trace, but also as a compound ichnotaxon intergrading with Gordia marina and Tuberculichnus vagans. Both predepositional and post‐depositional traces are present on the soles of turbidites. This ichnofauna comprises both feeding and grazing traces produced by a deposit‐feeding lacustrine benthic biota. Crawling traces are rare. Although certain ichnofossils (e.g. V. anyao, P. togwunia) show overall similarities with deep‐sea agrichnia, they differ in reflecting remarkably less specialized feeding strategies, displaying overcrossing between specimens (and to a lesser extent, self‐crossing), and in the case of V’ anyao recording post‐turbidite burrowing activity. The development of less specialized strategies than those displayed by deep‐marine ichnofaunas may be related to less stable conditions, typical of lake settings. Oxyenation, energy, sedimentation rate (both event and background), food supply, soft‐sediment deformation and erosion rate have mainly influenced trace‐fossil distribution. Turbidity currents would have ensured oxygen (as well as food) supply to deep lake settings, thus allowing the establishment of a moderately diverse biota. Biogenic structures were mostly confined to the outer, low energy areas. High sedimentation rates and strong erosion precluded preservation of ichnofossils in inner lobe settings. The Anyao ichnofauna is of significance in furthering knowledge of the colonization of deep lakes throughout the stratigraphie record and in identification of additional nonmarine ichnofacies. The ana‐lyzed ichnofauna resembles late Paleozoic lacustrine assemblages described from different localities around the world and is regarded as a Mesozoic example of the Mermia ichnofacies. However, when compared with Paleozoic assemblages, the Anyao ichnofauna shows a clear dominance of burrows over surface trails, deeper burrowing penetration, larger size, and presence of relatively more complex structures. The high burrow/surface trail ratio may be indicative of lower preservation potential in the latter, thus reflecting a tap‐honomic overprint. In contrast to the Paleozoic examples, the establishment of a relatively well‐developed lacustrine infauna may have precluded preservation of surface trails. Burrower activity probably obliterated biogenic structures formed close to the sediment‐water interface.

Ichnos: An International Journal for Plant and Ani↗

USGS1996

Taxonomic reassessment of the ichnogenus Beaconichnus and additional examples from the Carboniferous of Kansas, U.S.A.

The ichnogenus Beaconichnus (Gevers 1973), an arthropod trace fossil, includes very different forms that comprise five ichnospecies, namely B. darwi‐nunt (Gevers 1971), B. gouldi (Gevers 1971), B. ahtarcticum (Gevers 1971), B. giganteum Gevers and Twomey 1982, and B. wrrighti Gevers and Twomey 1982. The original diagnosis of Beaconichnus is rather vague and potentially may accommodate virtually every arthropod trackway described from the fossil record. In view of these problems, the validity of Beaconichnus is reassessed and each of its ichnospecies is reviewed. We conclude that B. darwinum is a junior synonym of Diplopodichnus biformis Brady 1947; B. antarcticum should be regarded as Palmich‐niunt antarcticum; and B. wrighti is a nomen nudum. Additionally, we agree with previous proposals in considering B. gouldi as the senior synonym of B. giganteum , and including it in Diplichnites Dawson 1873. Therefore, we suggest that the ichnogenus Beaconichnus is best disregarded. Additionally, we describe specimens collected from the Late Carboniferous Tonganoxie Sandstone Member (Stranger Formation) of eastern Kansas, ascribed herein to Diplopodichnus biformis and Diplichnites gouldi , which include examples of intergradations between both ichnotaxa, and provide synonymy lists for both ichnospecies.

Kansas↗