Geology topics

C.G. Maples

Publications and source records attributed to C.G. Maples.

8 recordsLinked to original sources

USGS2016

Ichnology of an Upper Carboniferous fluvio-estuarine paleovalley: The Tonganoxie Sandstone, Buildex Quarry, Eastern Kansas, USA

Tidal rhythmites of the Tonganoxie Sandstone Member (Stranger Formation, Douglas Group) at Buildex Quarry, eastern Kansas, contain a relatively diverse ichnofauna. The assemblage includes arthropod locomotion ( Dendroidichnites irregulare, Diplichnites gouldi types A and B, Diplopodichnus biformis, Kouphichnium isp., Mirandaichnium famatinense , and Stiaria intermedia ), resting ( Tonganoxichnus buildexensis ) and feeding traces ( Stiallia pilosa, Tonganoxichnus ottawensis ); grazing traces ( Gordia indianaensis, Helminthoidichnites tenuis, Helminthopsis hieroglyphica ); feeding structures ( Circulichnis montanus, Treptichnus bifurcus, Treptichnus pollardi , irregular networks), fish traces ( Undichna britannica, Undichna simplicitas ), tetrapod trackways, and root traces. The taxonomy of some of these ichnotaxa is briefly reviewed and emended diagnoses for Gordia indianaensis and Helminthoidichnites tenuis are proposed. Additionally, the combined name Dendroidichnites irregulare is proposed for nested chevron trackways. Traces previously regarded as produced by isopods are reinterpreted as myriapod trackways ( D. gouldi type B). Trackways formerly interpreted as limulid crawling and swimming traces are assigned herein to Kouphichnium isp and Dendroidichnites irregulare , respectively.

Journal of Paleontology↗

USGS2000

A new ichnospecies of Nereites from carboniferous tidal-flat facies of eastern Kansas, USA: Implications for the Nereites-Neonereites debate

Predominantly horizontal, gently curved to slightly sinuous traces constituting uniserial rows of imbricated, subspherical sediment pads occur in Pennsylvanian tidal-flat facies of eastern Kansas. These traces exhibit a complex, actively filled internal structure. The presence of a median tunnel enveloped by overlapping pads of reworked sediment indicates that these biogenic structures should be included in the ichnogenus Nereites MacLeay in Murchison, 1839. A new ichnospecies, N. imbricata , is erected. Externally, Nereites imbricata differs from the other Nereites ichnospecies by the large, tightly packed, imbricated pads that commonly result in an annulated appearance on bedding-planes. Internally, obliquely arranged, arcuate laminae envelope the median tunnel and tend to follow the outline of the external semispherical pads. Additionally, the behavioral pattern reflected by N. imbricata is less specialized than that of the other Nereites ichnospecies. Eione monoliformis Tate, 1859 resembles N. imbricata in general appearence, but lack the diagnostic Nereites internal structure, and is invariably preserved as positive epireliefs. Occurrence of Nereites imbricata as both median tunnels surrounded by reworked sediment ( Nereites preservation) and uniserial rows of imbricated sediment pads ( Neonereites preservation) supports the notion that Neonereites Seilacher, 1960 is a preservational variant of Nereites . The ichnogenus Nereites is an eurybathic form and is a common component of Paleozoic shallow-marine facies.

Kansas↗

USGS1999

The origin and paleoecologic significance of the trace fossil Asteriadtes in the Pennsylvanian of Kansas and Missouri

The trace fossil Asteriacites , recorded in Cambrian to Recent shallow- and deep-marine facies, is traditionally interpreted as the resting trace of asterozoans. Well-preserved specimens of A. lumbricalis are abundant in Pennsylvanian (Upper Carboniferous) shallow- and marginal-marine siliciclastic deposits of eastern Kansas and western Missouri. Detailed morphologic analysis of these specimens suggests that they record the activities of mobile epifaunal ophiuroids. Evidence of a brittle star (ophiuroid) producer rather than sea star (asteroid) is provided by (1) trace-fossil morphologic features reflecting the anatomy of the producer (e.g., well-differentiated central structure, slender vermiform arms) and ophiuroid burrowing technique (e.g., proximal arm expansion, arm branching), and (2) mode of occurrence (e.g., gregarious behavior, horizontal and vertical repetition). Vertical and horizontal repetition produces complex aggregates of A. lumbricalis that are interpreted either as escape structures (fugichnia) or as feeding structures, respectively. Ophiura texturata is proposed as a modern analogue for the A. lumbricalis producer, based on inferred life habit and feeding behavior. Asteriacites lumbricalis is present in two different intertidal trace-fossil assemblages. The first assemblage is characterized by high diversity and records tidal flats developed outside of embayments under normal marine conditions. The second assemblage consists of A. lumbricalis together with a few other ichnotaxa and represents a depauperate association that developed in restricted tidal flats within an embayment or estuarine setting. This challenges the conventional view of Asteriacites as a normal-marine salinity indicator. Some echinoderms, and particularly asterozoans, penetrate and inhabit modern environments of depressed salinity. The presence of Asteriacites in Pennsylvanian marginal-marine facies of Kansas and Missouri provides evidence that ophiuroids had adapted to brackish-water conditions by the late Paleozoic.

Kansas, Missouri↗

USGS1998

The ichnogenus Curvolithus revisited

The ichnogenus Curvolithus Fritsch, 1908, originally described from the Ordovician of the Prague Basin, typically comprises ribbonlike or tonguelike, flattened, endostratal traces with three rounded lobes on the upper surface. However, considerable confusion persists regarding the ichnotaxonomic status and diagnostic features of its ichnospecies. The type specimens of this ichnotaxon, overlooked in most subsequent reports, are redescribed herein. Curvolithus multiplex Fritsch, 1908, the type species, is retained for specimens with a trilobate upper surface and a quadralobate lower surface, in contrast to the criteria adopted by subsequent authors. The other ichnospecies originally proposed from the type locality, C. gregarius Fritsch, 1908, actually consists of a series of grouped parallel scratch marks forming ridges and should be removed from Curvolithus. Subsequently, four ichnospecies were defined: C.? davidis Webby 1970; C. annulatus Badve and Ghare 1978; C. aequus Walter et al. 1989; and C. manitouensis Maples and Suttner 1990. Curvolithus? davidis shows the typical trilobation of Curvolithus apparently in its lower surface, but the morphology of the upper surface is uncertain. Accordingly, it does not warrant ichnospecific assessment, and is regarded as a nomen dubium. The nature of the annulations on the trilobate upper surface of C. annulatus is unclear, and this ichnospecies is also best considered as a nomen dubium. Curvolithus aequus has a bilobate lower surface and probably represents washed out specimens of Didymaulichnus. Finally, C. manitouensis comprises specimens with a smooth, trilobate upper surface and a smooth, quadralobate lower surface, and is best regarded as a junior synonym of C. multiplex. Curvolithus multiplex has been used incorrectly for Curvolithus with a trilobate upper surface and a trilobate to unilobate lower surface. The new ichnospecies, Curvolithus simplex, is proposed herein for such traces. Curvolithus is interpreted as a locomotion trace (Repichnia) of endostratal carnivores, possibly gastropods, flatworms, or nemerteans. Curvolithus is a component of the Cruziana ichnofacies in shallow-marine facies, either of normal salinity or slightly brackish, in the latter case typically associated with fan deltas.

Journal of Paleontology↗

USGS1997

Tonganoxichnus, a new insect trace from the Upper Carboniferous of eastern Kansas

Upper Carboniferous tidal rhythmites of the Tonganoxie Sandstone Member (Stranger Formation) at Buildex Quarry, eastern Kansas, USA, host a relatively diverse arthropod-dominated ichnofauna. Bilaterally symmetrical traces displaying unique anterior and posterior sets of morphological features are well represented within the assemblage. A new ichnogenus, Tonganoxichnus , is proposed for these traces. T. buildexensis , the type ichnospecies, has an anterior region characterized by the presence of a frontal pair of maxillary palp impressions, followed by a head impression and three pairs of conspicuous thoracic appendage imprints symmetrically opposite along a median axis. The posterior region commonly exhibits numerous delicate chevron-like markings, recording the abdominal appendages, and a thin, straight, terminal extension. T. buildexensis is interpreted as a resting trace. A second ichnospecies, T. ottawensis , is characterized by a fan-like arrangement of mostly bifid scratch marks at the anterior area that records the head- and thoracic-appendage backstrokes against the substrate. The posterior area shows chevron-like markings or small subcircular impressions that record the abdominal appendages of the animal, also ending in a thin, straight, terminal extension. Specimens display lateral repetition, and are commonly grouped into twos or threes with a fix point at the posteriormost tail-like structure. T. ottawensis is interpreted as a jumping structure, probably in connection with feeding purposes. The two ichnospecies occur in close association, and share sufficient morphologic features to support the same type of arthropod producer. T. buildexensis closely mimics the ventral anatomy of the tracemaker, whereas T. ottawensis records the jumping abilities of the animal providing significant ethologic and paleoecologic information. The presence of well-differentiated cephalic, thoracic, and abdominal features, particularly in T. buildexensis , resembles the diagnostic tagmosis and segmentation of insects. Detailed analysis of trace morphology and comparison with described Paleozoic insect fossils and extant related forms suggest a monuran as the most likely tracemaker.

Kansas↗

USGS1996

A camerate-rich late carboniferous (Moscovian) crinoid fauna from volcanic conglomerate, Xinjiang, People's Republic of China

A low-diversity camerate-rich crinoid fauna from the Qijiagou Formation, Taoshigo Valley near Turpan, Xinjiang-Uygar Autonomous Region, China was collected during field work in May, 1993. The crinoid fauna is dominated by species of Platycrinites. Other camerate crinoids include a species in the Paragaricocrinidae, Actinocrinites, a hexacrinitid, and an acrocrinoid. The only other non-North American occurrence of this latter family is Springeracrocrinus from the Moscovian of Russia. In addition to the camerates, there are several advanced cladid inadunates more typical of Upper Carboniferous crinoid faunas, including an erisocrinoid (possibly Sinocrinus), Graphiocrinus, ?Cromyocrinus, and an agassizocrinoid (Petschoracrinus) represented by partly fused infrabasal cones. A single radial plate with angustary facet may represent a cyathocrinoid, There also is a catillocrinoid, assigned here to Paracatillocrinus. The fauna, which resembles Moscovian crinoids described from Russia, is preserved in graded volcanic conglomeratic debris flows that overlie a carbonate mound and contain clasts up to 3 m in dimension. The crinoids are fragmentary, with many calyces seemingly torn into two or three pieces and dumped in with the pyroclastic debris. Camerates are represented by large thecal scraps consisting of numerous plates, or by large individual plates or circlets. Other fossils include rare solitary rugose corals, tabular bryozoans, Neospirifer, and other fragmentary brachiopods. We suspect that the crinoids may have been swept off of a nearby carbonate mound and deposited as debris-flow bedload.

Journal of Paleontology↗

USGS1989

Response of selected binomial coefficients to varying degrees of matrix sparseness and to matrices with known data interrelationships

Numerous departures from ideal relationships are revealed by Monte Carlo simulations of widely accepted binomial coefficients. For example, simulations incorporating varying levels of matrix sparseness (presence of zeros indicating lack of data) and computation of expected values reveal that not only are all common coefficients influenced by zero data, but also that some coefficients do not discriminate between sparse or dense matrices (few zero data). Such coefficients computationally merge mutually shared and mutually absent information and do not exploit all the information incorporated within the standard 2 ?? 2 contingency table; therefore, the commonly used formulae for such coefficients are more complicated than the actual range of values produced. Other coefficients do differentiate between mutual presences and absences; however, a number of these coefficients do not demonstrate a linear relationship to matrix sparseness. Finally, simulations using nonrandom matrices with known degrees of row-by-row similarities signify that several coefficients either do not display a reasonable range of values or are nonlinear with respect to known relationships within the data. Analyses with nonrandom matrices yield clues as to the utility of certain coefficients for specific applications. For example, coefficients such as Jaccard, Dice, and Baroni-Urbani and Buser are useful if correction of sparseness is desired, whereas the Russell-Rao coefficient is useful when sparseness correction is not desired. ?? 1989 International Association for Mathematical Geology.

Mathematical Geology↗

USGS1989

The potential of paleozoic nonmarine trace fossils for paleoecological interpretations

Many Late Paleozoic environments have been interpreted as marine because of the co-occurrence of supposedly exclusively marine trace fossils. Beginning in the Late Ordovician, however, nonmarine trace-fossil diversity increased throughout the Paleozoic. This diversification of nonmarine organisms and nonmarine trace fossils was especially prevalent in Devonian and later times. Diversification of freshwater organisms is indicated by the large number of freshwater fish, arthropods, annelids and molluscs that had developed by the Carboniferous. In addition to diverse freshwater assemblages, entirely terrestrial vertebrate and invertebrate ecosystems had developed by the Devonian. This rapid diversification of freshwater and terrestrial organisms is inherently linked to development and diversification of land plants and subsequent shedding of large quantities of organic detritus in nonmarine and marginal-marine areas. Nearshore marine organisms and their larvae that are able to tolerate relatively short periods of lowered salinities will follow salt-water wedges inland during times of reduced freshwater discharge. Similarly, amphidromous marine organisms will migrate periodically inland into nonmarine environments. Undoubtedly, both of these processes were active in the Paleozoic. However, both processes are restricted to stream/distributary channels, interdistributary bays, or estuaries. Therefore, the presence of diverse trace-fossil assemblages in association with floodplain deposits is interpreted to reflect true nonmarine adaptation and diversity. Conversely, diverse trace-fossil assemblages in association with stream/distributary channel deposits, interdistributary-bay deposits, or estuarine deposits may reflect migration of salt-water wedges inland, or migration of marine organisms into freshwater environments (amphidromy), or both.

Palaeogeography, Palaeoclimatology, Palaeoecology↗