The convergence of the discrete ordinates method for integral equations of anisotropic radiative transfer

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Part A: General Sequence Stratigraphy and Conodont Biostratigraphy (including new species) of the Uppermost Carboniferous (upper Gzhelian) to Lower Permian (lower Artinskian) from the North American Midcontinent

The uppermost Wabaunsee, Admire, Council Grove, and lower Chase Groups of Kansas, Oklahoma, and Nebraska are placed into three third-order depositional sequences: a Gzhelian late-highstand sequence set, a Council Grove transgressive and highstand sequence set, and a Chase transgressive sequence set. Sequences are defined by bounding maximum-exposure surfaces and are placed within the zone of exposure surfaces (typically, stacked paleosols). Conodonts are abundant in open-marine deposits and most marine units have a differing and characteristic faunal make-up. Eleven species are described as new: Streptognathodus binodosus, S. denticulatus, S. elongianus, S. florensis, S. lineatus, S. nevaensis, S. postconstrictus, S. postelongatus, S. robustus, S. translinearis, and S. trimilus

Part B: Conodont Distribution, Systematics, Biostratigraphy, and Sequence Stratigaphy of the Uppermost Carboniferous and Lower Permian (uppermost Wabaunsee, Admire, Council Grove, and lower Chase Groups) from the North American Midcontinent

aximum-marine flooding levels and marine-condensed sections from uppermost Carboniferous and Lower Permian fourth-order (0.1-1 m.y.) depositional sequences of the North American midcontinent reveal a rich stratigraphic succession of species of Streptognathodus and Sweetognathus conodonts that permits high-precision correlation of the Carboniferous-Permian boundary as well as the Asselian-Sakmarian and Sakmarian-Artinskian boundaries. Eleven new species of Streptognathodus are described: Streptognathodus binodosus, S. denticulatus, S. elongianus, S. florensis, S. lineatus, S. nevaensis, S. postconstrictus, S. postelongatus, S. robustus, S. translinearis, and S. trimilus. Seventeen species are redescribed and clarified and include Streptognathodus alius, S. barskovi, S. bellus, S. brownvillensis, S. conjunctus, S. constrictus, S. elongatus, S. farmeri, S. flexuosus, S. fuchengensis, S. fusus, S. invaginatus, S. isolatus, S. longissimus, S. minacutus, S. nodulinearis, and S. wabaunsensis. The correlated level of the Carboniferous-Permian boundary is recognized in the lower part of the Red Eagle Depositional Sequence based on the introduction of Streptognathodus isolatus Chernykh, Ritter, and Wardlaw; Streptognathodus minacutus Barskov and Reimers; Streptognathodus invaginatus Reshetkova and Chernykh; Streptognathodus fuchengensis Zhao; and Streptognathodus nodulinearis Reshetkova and Chernykh. The correlated Carboniferous-Permian boundary occurs in the depositional sequence that represents the maximum-marine highstand of the Council Grove Composite Third Order Sequence. This level represents a significant marine-flooding event that should be correlatable in numerous shelfal sections throughout the world. Although the Asselian-Sakmarian boundary has not been rigorously defined, Sweetognathus merrilli has been informally utilized as a Sakmarian indicator. Due to the ecologically controlled distribution of species of Sweetognathus, we prefer to use a species of Streptognathodus as a defining species. We propose that Streptognathodus barskovi (Kozur) Reshetkova be considered as a potentially defining or ancillary defining species for the Sakmarian Stage. In the North American midcontinent, Streptognathodus barskovi appears in the same depositional sequence with Sweetognathus merrilli in the Eiss (Lower Bader) Depositional Sequence. Historically, Sweetognathus whitei has been used to mark the Sakmarian-Artinskian boundary. In our succession Sweetognathus whitei and Streptognathodus florensis appear in the basal part of the Barneston Depositional Sequence. We suggest that Streptognathodus florensis be further investigated as a possible defining or ancillary defining taxon for the base of the Artinskian Stage. This depositional sequence also forms the maximum-marine highstand of the Chase Third-Order Composite Depositional Sequence suggesting that this level is a significant marine-flooding event that should be widely traceable in numerous shelfal sections

Part B: Conodont Distribution, Systematics, Biostratigraphy, and Sequence Stratigaphy of the Uppermost Carboniferous and Lower Permian (uppermost Wabaunsee, Admire, Council Grove, and lower Chase Groups) from the North American Midcontinent

aximum-marine flooding levels and marine-condensed sections from uppermost Carboniferous and Lower Permian fourth-order (0.1-1 m.y.) depositional sequences of the North American midcontinent reveal a rich stratigraphic succession of species of Streptognathodus and Sweetognathus conodonts that permits high-precision correlation of the Carboniferous-Permian boundary as well as the Asselian-Sakmarian and Sakmarian-Artinskian boundaries. Eleven new species of Streptognathodus are described: Streptognathodus binodosus, S. denticulatus, S. elongianus, S. florensis, S. lineatus, S. nevaensis, S. postconstrictus, S. postelongatus, S. robustus, S. translinearis, and S. trimilus. Seventeen species are redescribed and clarified and include Streptognathodus alius, S. barskovi, S. bellus, S. brownvillensis, S. conjunctus, S. constrictus, S. elongatus, S. farmeri, S. flexuosus, S. fuchengensis, S. fusus, S. invaginatus, S. isolatus, S. longissimus, S. minacutus, S. nodulinearis, and S. wabaunsensis. The correlated level of the Carboniferous-Permian boundary is recognized in the lower part of the Red Eagle Depositional Sequence based on the introduction of Streptognathodus isolatus Chernykh, Ritter, and Wardlaw; Streptognathodus minacutus Barskov and Reimers; Streptognathodus invaginatus Reshetkova and Chernykh; Streptognathodus fuchengensis Zhao; and Streptognathodus nodulinearis Reshetkova and Chernykh. The correlated Carboniferous-Permian boundary occurs in the depositional sequence that represents the maximum-marine highstand of the Council Grove Composite Third Order Sequence. This level represents a significant marine-flooding event that should be correlatable in numerous shelfal sections throughout the world. Although the Asselian-Sakmarian boundary has not been rigorously defined, Sweetognathus merrilli has been informally utilized as a Sakmarian indicator. Due to the ecologically controlled distribution of species of Sweetognathus, we prefer to use a species of Streptognathodus as a defining species. We propose that Streptognathodus barskovi (Kozur) Reshetkova be considered as a potentially defining or ancillary defining species for the Sakmarian Stage. In the North American midcontinent, Streptognathodus barskovi appears in the same depositional sequence with Sweetognathus merrilli in the Eiss (Lower Bader) Depositional Sequence. Historically, Sweetognathus whitei has been used to mark the Sakmarian-Artinskian boundary. In our succession Sweetognathus whitei and Streptognathodus florensis appear in the basal part of the Barneston Depositional Sequence. We suggest that Streptognathodus florensis be further investigated as a possible defining or ancillary defining taxon for the base of the Artinskian Stage. This depositional sequence also forms the maximum-marine highstand of the Chase Third-Order Composite Depositional Sequence suggesting that this level is a significant marine-flooding event that should be widely traceable in numerous shelfal sections

Part A: General Sequence Stratigraphy and Conodont Biostratigraphy (including new species) of the Uppermost Carboniferous (upper Gzhelian) to Lower Permian (lower Artinskian) from the North American Midcontinent

The uppermost Wabaunsee, Admire, Council Grove, and lower Chase Groups of Kansas, Oklahoma, and Nebraska are placed into three third-order depositional sequences: a Gzhelian late-highstand sequence set, a Council Grove transgressive and highstand sequence set, and a Chase transgressive sequence set. Sequences are defined by bounding maximum-exposure surfaces and are placed within the zone of exposure surfaces (typically, stacked paleosols). Conodonts are abundant in open-marine deposits and most marine units have a differing and characteristic faunal make-up. Eleven species are described as new: Streptognathodus binodosus, S. denticulatus, S. elongianus, S. florensis, S. lineatus, S. nevaensis, S. postconstrictus, S. postelongatus, S. robustus, S. translinearis, and S. trimilus

Correlation and high-resolution timing for Paleo-tethys Permian-Triassic boundary exposures in Vietnam and Slovenia using geochemical, geophysical and biostratigraphic data sets

Two Permian-Triassic boundary (PTB) successions, Lung Cam in Vietnam, and Lukač in Slovenia, have been sampled for high-resolution magnetic susceptibility, stable isotope and elemental chemistry, and biostratigraphic analyses. These successions are located on the eastern (Lung Cam section) and western margins (Lukač section) of the Paleo-Tethys Ocean during PTB time. Lung Cam, lying along the eastern margin of the Paleo-Tethys Ocean provides an excellent proxy for correlation back to the GSSP and out to other Paleo-Tethyan successions. This proxy is tested herein by correlating the Lung Cam section in Vietnam to the Lukač section in Slovenia, which was deposited along the western margin of the Paleo-Tethys Ocean during the PTB interval. It is shown herein that both the Lung Cam and Lukač sections can be correlated and exhibit similar characteristics through the PTB interval. Using time-series analysis of magnetic susceptibility data, high-resolution ages are obtained for both successions, thus allowing relative ages, relative to the PTB age at ~252 Ma, to be assigned. Evaluation of climate variability along the western and eastern margins of the Paleo-Tethys Ocean through the PTB interval, using d18O values indicates generally cooler climate in the west, below the PTB, changing to generally warmer climates above the boundary. A unique Black Carbon layer (elemental carbon present by agglutinated foraminifers in their test) below the boundary exhibits colder temperatures in the eastern and warmer temperatures in the western Paleo-Tethys Ocean.ReferencesBalsam W., Arimoto R., Ji J., Shen Z, 2007. Aeolian dust in sediment: a re-examination of methods for identification and dispersal assessed by diffuse reflectance spectrophotometry. International Journal of Environment and Health, 1, 374-402.Balsam W.L., Otto-Bliesner B.L., Deaton B.C., 1995. 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Conodont biostratigraphy of the Permian-Triassic boundary sequence at Lung Cam, Vietnam

The occurrences of a few specimens of Clarkina and many specimens of Hindeodus at the Permian-Triassic boundary section at Lung Cam, Vietnam allow accurate graphic correlation to the P-T boundary stratotype at Meishan, China. One species of Clarkina, ten species and two subspecies of Hindeodus, and the apparatuses of Hindeodus latidentatus and Merrillina ultima are described and illustrated

Identifying globally synchronous Permian–Triassic boundary levels in successions in China and Vietnam using Graphic Correlation

© 2017 Elsevier B.V. Understanding the timing and correlation of significant global events in Earth history is facilitated by the Global Boundary Stratotype Section and Point (GSSP) concept, along with multi-proxy correlation techniques. As an example, the Permian–Triassic boundary (PTB) GSSP is used herein to correlate three PTB successions in east and southeast Asia. The PTB is defined using the First Appearance Datum (FAD) of the conodont Hindeodus parvus at the Meishan D section in China. By definition then, Meishan D is the only section on Earth where the FAD of H. parvus represents the beginning of the Triassic, at ~ 251.88 Ma, and thus the end of the Permian. Therefore, when correlating strata in any other section back to the PTB using biostratigraphic data, the local Lowest Observed Occurrence Point (LOOP) of H. parvus will probably not equate precisely to the defined FAD GSSP level (the PTB) for the beginning of the Triassic at Meishan D. The Graphic Correlation method, applied to PTB sites in China and Vietnam, is used herein to demonstrate that LOOPs of H. parvus in other successions are not equivalent in time to the PTB FAD. The LOOP and Highest Observed Occurrence Point (HOOP) for conodont data at two other successions studied, Huangzhishan in China, and Lung Cam in Vietnam, are used to determine the approximate level where the Triassic begins in these successions, resulting in high-resolution correlation among the sections and correlation back to the PTB GSSP level. It is demonstrated that when critical biostratigraphic data are missing, multiple proxy correlation techniques, geochemical, geophysical and, in some regional instances, unique lithostratigraphic information such as coeval ash beds, can be used to aid in locating the boundary in successions that are not the defining GSSP. LOOP and HOOP data are used to establish a Line of Correlation to differentiate between a defining PTB H. parvus FAD versus the H. parvus LOOP in secondary successions, and to project the PTB FAD into secondary sections to define the PTB at these localities. In addition, the timing of H. parvus arrivals at these sections is used to establish rough dispersal rates and patterns in the region