Spore-Pollen Biostratigraphy and Paleoecology of Mesozoic and Lower Tertiary Samples from the Surghar and Salt Ranges, Northern Pakistan

Total Page:16

File Type:pdf, Size:1020Kb

Spore-Pollen Biostratigraphy and Paleoecology of Mesozoic and Lower Tertiary Samples from the Surghar and Salt Ranges, Northern Pakistan Spore-Pollen Biostratigraphy and Paleoecology of Mesozoic and Lower Tertiary Samples from the Surghar and Salt Ranges, Northern Pakistan By N.O. Frederiksen, U.S. Geological Survey T.P. Sheehan, U.S. Geological Survey V.A.S. Andrle, U.S. Geological Survey Chapter D of Regional Studies of the Potwar Plateau Area, Northern Pakistan Edited by Peter D. Warwick and Bruce R. Wardlaw Prepared in cooperation with the Geological Survey of Pakistan, under the auspices of the U.S. Agency for International Development, U.S. Department of State, and the Government of Pakistan Bulletin 2078–D U.S. Department of the Interior U.S. Geological Survey iii Contents Abstract ........................................................................................................................................................D1 Introduction.....................................................................................................................................................1 Acknowledgments ................................................................................................................................1 Previously Reported Ages of Formations ..................................................................................................1 Determination of Spore-Pollen Ages ..........................................................................................................3 Palynological Methods .................................................................................................................................5 Sample Analyses............................................................................................................................................5 Makarwal Coal Field .............................................................................................................................5 Nammal Pass Section ..........................................................................................................................6 Nammal Dam Section ..........................................................................................................................7 Kuraddi Section .....................................................................................................................................7 Samples from the Central and Eastern Salt Range .........................................................................8 Arara Section.........................................................................................................................................9 Nila Wahan Section ..............................................................................................................................9 Drill Hole 9, Khairpur Area ...................................................................................................................9 Nammal Formation ......................................................................................................................9 Patala Formation ..........................................................................................................................9 Lockhart Limestone ...................................................................................................................10 Drill Hole 34, Basharat Area ..............................................................................................................10 Discussion and Conclusions ......................................................................................................................11 References Cited..........................................................................................................................................12 Appendix D1. Alphabetical List of Species Mentioned in this Report ................................................14 Plates [Plates follow Appendix D1] D1. Permian and Jurassic or Early Cretaceous spores and gymnosperm pollen from the Salt Range. D2. Late Jurassic or Early Cretaceous, probably middle Cretaceous, and Paleocene spores and pollen from the Surghar and Salt Ranges. D3. Spores and angiosperm pollen from the Patala Formation of the Salt Range. D4. Angiosperm pollen from the Patala and Nammal Formations of the Salt Range. Figures D1. Map showing the Salt Range study area and selected regional features .......................D2 D2. Map of the Salt Range study area in northern Pakistan showing sample localities discussed in this report ...............................................................................................................2 iv D3. Range chart for 27 stratigraphically significant pollen species and species groups in a composite section for the upper Paleocene of the Lower Indus coal region, Sindh Province .................................................................................................................4 D4–D8. Diagrams showing analyses of spore-pollen assemblages from the— D4. Hangu and Patala Formations of Lumshiwal Nala in the Makarwal coal field .........6 D5. Hangu Formation of Nammal Pass and the Patala Formation of the Nammal Dam, Arara, Kuraddi, and Nila Wahan sections .............................................................7 D6. Patala Formation of various sections in the central and eastern Salt Range ...........8 D7. Patala Formation of drill hole 9, Khairpur area ...............................................................9 D8. Patala and Nammal Formations of drill hole 34, Basharat area ................................10 D9. Diagram showing composite analyses of spore-pollen assemblages from the Hangu, Patala, and Nammal Formations of the Surghar and Salt Ranges .......................11 Table D1. Some stratigraphic units in Sindh Province and in the Surghar and Salt Ranges, Pakistan .......................................................................................................................................D3 Spore-Pollen Biostratigraphy and Paleoecology of Mesozoic and Lower Tertiary Samples from the Surghar and Salt Ranges, Northern Pakistan By N.O. Frederiksen, T.P. Sheehan, and V.A.S. Andrle Abstract ments and can generally be given an age assignment using marine megafossils or microfossils. However, some of the Mesozoic and The conglomerate at the base of the Basharat drill hole 34 Paleocene formations of the region are predominantly nonmarine; (eastern Salt Range), thought to represent the Tobra Formation although marine fossils have been found in these formations in (Permian), contained Permian pollen grains and spores that certain areas, many outcrops lack such fossils. Spores and pollen may be indigenous or may be reworked; thus, the age of this are therefore most useful in providing ages and correlations of conglomerate is uncertain. mainly nonmarine units. Previously published Tertiary spore Two samples from the lower part of Lumshiwal Nala and pollen work in the region includes a description of some late (Makarwal coal field, Surghar Range), probably from the Paleocene or Eocene species from Dandot, in Jhelum District, Lumshiwal Formation, were assigned Late Jurassic to Early Punjab, by Vimal (1952) and a description of many Paleocene spe- Cretaceous and middle Cretaceous (approximately Aptian to cies from northern and southern Pakistan by Frederiksen (1994). Albian) ages, respectively. In the present study of spores and pollen from the Surghar and Salt Ranges, 1 sample was analyzed from the Rocks from the shallow subsurface of the Kuraddi sec- Tobra Formation(?) (Permian(?)), 2 from the Lumshiwal For- tion in the western Salt Range, thought to be possibly from the mation (Mesozoic), 7 from rocks thought at least tentatively Paleocene Hangu Formation, contained spores and pollen grains to represent the Hangu Formation (Paleocene), 26 from the probably of Jurassic to Early Cretaceous age; therefore, these Patala Formation (mainly or entirely Paleocene), and 2 from samples were probably from the Mesozoic Datta Formation. the Nammal Formation (Eocene(?)). Spore-pollen species Rocks mapped as the Hangu Formation at Lumshiwal Nala mentioned in the text and figures are listed in appendix D1. (Surghar Range) and Nammal Pass (western Salt Range) are Many taxa studied are shown in plates D1–D4. Paleocene in age. All analyzed samples of the Patala Formation from the Salt Range appear to be late Paleocene in age and con- tain pollen assemblages similar to those of the Lakhra Formation Acknowledgments of Sindh Province. The Patala assemblages are no older than those from the uppermost part of the Bara Formation of Sindh Prov- This work was done as part of the Coal Resources Explo- ince. Paleocene coal beds in the Hangu and Patala Formations ration and Assessment Program (COALREAP), a collaborative were undoubtedly deposited in or near brackish water because program between the U.S. Geological Survey and the Geologi- dinoflagellate cysts and brackish-water palm pollen of the genus cal Survey of Pakistan. This cooperative program is under the Spinizonocolpites were found in the associated detrital rocks. auspices of the U.S. Agency for International Development Two samples from the Nammal Formation (lower and the Government of Pakistan. Most samples discussed in Eocene(?)) of the Basharat drill hole 34 (eastern Salt Range) had this paper were collected by Frederiksen; however, many of low-diversity spore and pollen assemblages that did not include the Patala samples from the central and eastern Salt Range any species known to be restricted to the Eocene, although some were collected by
Recommended publications
  • Devonian Bryozoans of the Holy Cross Mountains, Poland
    ACT A PAL A EON T 0 LOG ICA POLONICA Vol. XVIII 1973 No.4 MARIA KIEPURA DEVONIAN BRYOZOANS OF THE HOLY CROSS MOUNTAINS, POLAND. PART II. CYCLOSTOMATA AND CYSTOPORATA Abstract. - Descriptions are given of 33, species of Middle Devonian Bryozoa from the Holy Cross Mts., belonging to the orders Cyclostomata and Cystoporata. Cyclo­ stomata are represented by 26 species (4 new: Corynotrypa (Corynotrypa) skalensis, C. (C.) basiplata, Stomatopora varigemmata and Diversipora bitubulata n. gen.). Cystoporata are represented by 7 new species: Ceramoporella orbiculata, C. grandi­ cystica, Favositella integrimuralis, Fistulipora boardmani, F. emphantica, Cyclotrypa nekhoroshevi and Fistuliramus astrovae. The systematic assignment of the genus Hederella Hall, 1881 has been discussed and the "tabulate-like" microstructure of the zooecial walls of this genus examined. In addition, the epifauna and associated assemblages have been characterized as well as the geological and palaeoecological conditions in which the described Bryozoa occurred. INTRODUCTION Among the Middle Devonian Bryozoa of the Holy Cross Mts., the present author has, up to now, described Ctenostomata (Kiepura, 1965). The present paper is a continuation of her investigations on the Middle Devonian Bryozoa of this region and contains descriptions of 33 species belonging to 9 genera of the orders Cyclostomata and Cystoporata occur­ ring in the Grzegorzowice - Skaly profile. The bryozoan collection of the Palaeozoological Institute of the Polish Academy of Sciences also contains a rich material representing the orders Trepostomata and Cryptostomata from the Middle Devonian of the Holy Cross Mts., which will be described at a future date. The material described in the present paper was collected by the author during several years of fieldwork (1950-1954).
    [Show full text]
  • Database of Bibliography of Living/Fossil
    www.shark-references.com Version 16.01.2018 Bibliography database of living/fossil sharks, rays and chimaeras (Chondrichthyes: Elasmobranchii, Holocephali) Papers of the year 2017 published by Jürgen Pollerspöck, Benediktinerring 34, 94569 Stephansposching, Germany and Nicolas Straube, Munich, Germany ISSN: 2195-6499 DOI: 10.13140/RG.2.2.32409.72801 copyright by the authors 1 please inform us about missing papers: [email protected] www.shark-references.com Version 16.01.2018 Abstract: This paper contains a collection of 817 citations (no conference abstracts) on topics related to extant and extinct Chondrichthyes (sharks, rays, and chimaeras) as well as a list of Chondrichthyan species and hosted parasites newly described in 2017. The list is the result of regular queries in numerous journals, books and online publications. It provides a complete list of publication citations as well as a database report containing rearranged subsets of the list sorted by the keyword statistics, extant and extinct genera and species descriptions from the years 2000 to 2017, list of descriptions of extinct and extant species from 2017, parasitology, reproduction, distribution, diet, conservation, and taxonomy. The paper is intended to be consulted for information. In addition, we provide data information on the geographic and depth distribution of newly described species, i.e. the type specimens from the years 1990 to 2017 in a hot spot analysis. New in this year's POTY is the subheader "biodiversity" comprising a complete list of all valid chimaeriform, selachian and batoid species, as well as a list of the top 20 most researched chondrichthyan species. Please note that the content of this paper has been compiled to the best of our abilities based on current knowledge and practice, however, possible errors cannot entirely be excluded.
    [Show full text]
  • Fossil Microbial Shark Tooth Decay Documents in Situ Metabolism Of
    www.nature.com/scientificreports OPEN Fossil microbial shark tooth decay documents in situ metabolism of enameloid proteins as nutrition source in deep water environments Iris Feichtinger1*, Alexander Lukeneder1, Dan Topa2, Jürgen Kriwet3*, Eugen Libowitzky4 & Frances Westall5 Alteration of organic remains during the transition from the bio- to lithosphere is afected strongly by biotic processes of microbes infuencing the potential of dead matter to become fossilized or vanish ultimately. If fossilized, bones, cartilage, and tooth dentine often display traces of bioerosion caused by destructive microbes. The causal agents, however, usually remain ambiguous. Here we present a new type of tissue alteration in fossil deep-sea shark teeth with in situ preservation of the responsible organisms embedded in a delicate flmy substance identifed as extrapolymeric matter. The invading microorganisms are arranged in nest- or chain-like patterns between fuorapatite bundles of the superfcial enameloid. Chemical analysis of the bacteriomorph structures indicates replacement by a phyllosilicate, which enabled in situ preservation. Our results imply that bacteria invaded the hypermineralized tissue for harvesting intra-crystalline bound organic matter, which provided nutrient supply in a nutrient depleted deep-marine environment they inhabited. We document here for the frst time in situ bacteria preservation in tooth enameloid, one of the hardest mineralized tissues developed by animals. This unambiguously verifes that microbes also colonize highly mineralized dental capping tissues with only minor organic content when nutrients are scarce as in deep-marine environments. Teeth and bones are ofen the only evidence of ancient vertebrate life because of the mineralized nature of tissues. Tere are numerous possibilities for chemical alteration during the transition from the bio- to the lithosphere of which bacterial catabolysis of these tissues and organic matter within the carcass is an important example 1,2.
    [Show full text]
  • A Monograph of the British Palaeozoic Asterozoa
    PAL.EONTOGRAPHICAL society. VOL. LXXI THE WEALDEN AND PURBECK FISHES. Part III. Pages i— viii, 105—148; Plates XXI—XXVI. Title-page and Index. THE PLIOCENE MOLLUSCA. Part IV. Pages i — xii, 463—483. Title-page and Index to Vol. I. THE PALEOZOIC ASTEROZOA. Part IV. Pages 169—196. THE CAMBRrAN TRILOBITES. Part V. Pages 89—120; Plates XI- XIV. Issued for 1917. (jftfiJoKnia ^fcaf/emu oJ cfcieneed RECEIVED BY PURCHASE 2. I go 9- Digitized by the Internet Archive in 2011 with funding from California Academy of Sciences Library http://www.archive.org/details/monographofbriti04spen PALEONTOGMPHICAL SOCIETY. VOLUME LXXI. CONTAINING 1. THE WEALDEN AND PURBECK FISHES. Part III. By Dr. A. S. Woodward. Six Plates. 2. THE PLIOCENE MOLLUSCA. Part IV. By Mr. F. W. Harmer. Title-page and Index to Vol. I. 3. THE PALAEOZOIC ASTEROZOA. Part IV. By Dr. W. K. Spencer. Twenty-six Text-figures. 4. THE CAMBRIAN TRILOBITES. Part V. By Mr. P. Lake. Four Plates. ISSUED FOR 1917. ^ •> LONDON: PRINTED FOR THE PAL^EONTOGRAPHICAL SOCIETY. AGENTS FOR THE SOCIETY DULAU AND CO., LTD., 34-36, MARGARET STREET, W. 1. APRIL, 1919. THE PAL^EONTOGRAPHICAL SOCIETY was established in the year L847, for the purpose of figuring and describing British Fossils. Each person subscribing One Guinea is considered a Member of the Society, and is entitled to lite Volume issued for the Year to which the Subscription relates. The price of the Volume to Non-subscribers is Twenty-five Shillings net. Subscriptions are considered to be due on the 1st of January in each year.
    [Show full text]
  • Biostratigraphy of Devonian-Carboniferous Boundary in Tuyeh-Darvar Section, North of Iran
    Iranian Journal of Earth Sciences IJES Vol. 12, No. 2, 2020, 98-123. Biostratigraphy of Devonian-Carboniferous boundary in Tuyeh-Darvar section, north of Iran Mohammad Taghi Najjarzadeh1, Ali Reaza Ashouri*2, Mehdi Yazdi3, Ali Bahrami3 1. Department of Geology, Science and Research Branch, Islamic Azad University, Tehran, Iran 2. Department of Geology, Faculty of Science, Ferdowsi University of Mashhad, Mashhad, Iran 3. Department of Geology, Faculty of Science, University of Isfahan, Isfahan, Iran Received 4 June 2019; accepted 17 December 2019 Abstract Devonian-Carboniferous boundary is not clear in the Eastern Alborz Mountains. In the current study Tuyeh-Darvar section with about 170 m, thickness is selected. In this investigation, the primary goal is revision of Devonian/Carboniferous Boundary (known as DCB) and the other goal is the redefinition of the DCB as a famous necessity (based on ICS program in 2008 for defining the boundary and to find a new GSSP). According to Conodont data from acid-leaching 53 carbonate samples(by acid acetic) that obtained from Late Devonian and Early Carboniferous deposits in this section, and based on standard conodont Zonation 6 Zone are recognized; 1. Bi.ultimus/or Si.praesulcata Zone, 2. Pr.kockeli /or Si.sulcata Zone, 3. Si.duplicata to Si.sandbergi bio interval, 4. Si.crenulata Zone, 5.Gnathodus-P.inornatus Zone, and 6.Ps.multistriatus Zone. Considering to the Conodont Zones above mentioned, Conodont faunas and other evidences, in the Tuyeh-Darvare section the DCB, is located within cream to grey silt stone beds, which are lies between K6 limestone and K8 dark carbonate beds (about 7.10 m above the base of recent studied section).
    [Show full text]
  • Adec Preview Generated PDF File
    Records of the Western Australian Museum 21: 235-267 (2002). A systematic revision of the family Harpetidae (Trilobita) Malte C. Ebach 1 and Kenneth J. McNamara 2 1 School of Botany, The University of Melbourne, Victoria 3010, Australia. 2 Department of Earth and Planetary Sciences, Western Australian Museum, Francis Street, Perth, Western Austaralia, 6000, Australia. Abstract - The systematics of the ten valid harpetid trilobite genera are reviewed. Seven are revised, using standard parsimony and three-item analysis. The monophyly of the Harpetidae is confirmed, and all ingroup genera can be defended as monophyletic groups except for the non­ monophyletic ScotolJarpes group. Emended diagnoses are provided for all the genera within the family. The three subfamilies Dolichoharpinae, Eoharpetinae and Harpetinae are supressed within the Harpetidae. The genera AlIstraloharpes and Sinoharpes are placed in synonymy with DlIbhglasina. Thorslundops and Wegeiinia are placed in synonymy with Hibbertia, and the subgenus FritclJaspis placed in synonymy with LiolJarpes. Reticuloharpes and HelioJwrpes are placed in synonymy with Harpes. The Harpetidae, along with the Entomaspididae and Harpididae, is considered to belong in the Harpetida, which is herein raised to ordinal rank within the subclass Libristoma. INTRODUCTION Woodward, 1898, Lioharpes Whittington, 1950a and The trilobite family Harpetidae Hawle and Corda, Scotoharpes Lamont, 1948a. Not included within this 1847 has been revised twice since its erection over analysis were Brachyhipposiderus Jell, 1985 and 150 years ago, firstly by Whittington (1950a) and Dolic1lOharpes Whittington, 1949, because each secondly by Pribyl and Vanek (1986). Subsequently, contain too few species to enable a cladistic analysis numerous authors (Prantl and Phbyl, 1954, Vanek, to be carried out.
    [Show full text]
  • 32. Palynological Study of Upper Jurassic and Lower Cretaceous Sediments, Site 511, Deep Sea Drilling Project Leg 71 (Falkland Plateau)1
    32. PALYNOLOGICAL STUDY OF UPPER JURASSIC AND LOWER CRETACEOUS SEDIMENTS, SITE 511, DEEP SEA DRILLING PROJECT LEG 71 (FALKLAND PLATEAU)1 Ida Z. Kotova, Geological Institute of the U.S.S.R. Academy of Sciences, Moscow, U.S.S.R. ABSTRACT Samples from Upper Jurassic and Lower Cretaceous sediments at Site 511 were analyzed for palynomorphs. Three palynological assemblages were identified: Upper Jurassic (presumably Tithonian), Neocomian-Aptian, and lower Al- bian. These were correlated to synchronous assemblages in Argentina, South Africa, and Australia and were compared with Jurassic palynoassemblages from Hole 330, Leg 36. INTRODUCTION this interval (Cores 63, 61, 59), amorphous detritus is coagulated into rounded yellow brown aggregates with At Site 511, on the Falkland Plateau (western part of an admixture of pyrite. Traces of pyrite are seen on the the Maurice Ewing Bank), Upper Jurassic and Lower surfaces of spores and pollen. Cretaceous sediments were penetrated by Hole 511, The available sapropelic material enables us to assume drilled to a depth of 632 meters some 10 km from Site that black shales in this interval were formed under an- 330 (Leg 36). Within the Jurassic-Lower Cretaceous in- aerobic conditions. The uneven distribution of pollen terval, two lithological units (Units 5 and Unit 6) were and spores suggests an alternation of anaerobic condi- identified. The upper unit (Unit 5) is composed of cal- tions with slightly oxidizing environments. However, careous claystones. Their oxidation state did not favor low abundances of spores can be due to unfavorable cli- the preservation of organic matter: the sediments con- matic conditions for ferns on the nearby land.
    [Show full text]
  • Late Cretaceous Palynofloras (Sporomorphs and Dinocysts) from the Kerguelen Plateau, Southern Indian Ocean (Sites 748 and 750)1
    Wise, S. W., Jr., Schlich, R., et al., 1992 Proceedings of the Ocean Drilling Program, Scientific Results, Vol. 120 19. LATE CRETACEOUS PALYNOFLORAS (SPOROMORPHS AND DINOCYSTS) FROM THE KERGUELEN PLATEAU, SOUTHERN INDIAN OCEAN (SITES 748 AND 750)1 Barbara A.R. Mohr2 and Carole T. Gee23 ABSTRACT Pollen, spore, and dinoflagellate cyst floras of Late Cretaceous age were found at Sites 748 (120-748C-62R through -79R) and 750 (120-750B-11W) of Ocean Drilling Program Leg 120 to the Kerguelen Plateau area in the Southern Indian Ocean. The ranges of dinocyst and sporomorph species indicate ages between the Cenomanian and Coniacian (to possibly the early Santonian). The ratio of marine/terrestrial flora elements is extremely variable, showing a trend from highly terrestrial (up to —70%) in the late Cenomanian to highly marine (up to 90%) in the Coniacian/early Santonian. Low sedimentation rates of about 3-5 cm/1000 yr were calculated for the glauconitic sediments of Turonian and Coniacian age at Site 748 (lithologic Subunit IIIB). INTRODUCTION Another important aspect of paleobotanical studies on Kerguelen Plateau floras is a historical one. As early as 1857, The objective of the drilling operations of Leg 120 of the Hooker mentioned the discovery of fossil wood in a letter to Ocean Drilling Program was to recover expanded Paleogene Darwin (Holdgate, 1960). More recently, Cookson (1946, and Cretaceous sections to document the early sedimentation 1947) described the first in situ palynofloras from southern and tectonic history of the Southern Kerguelen Plateau. This high latitudes, which were found in early Tertiary lignites on southern part lies at a depth of 1000-3000 m.
    [Show full text]
  • Godavari Basin (East Coast of India): Taxonomic, Taphonomic and Palaeoecological Considerations
    Acta Palaeobotanica 57(1): 13–32, 2017 e-ISSN 2082-0259 DOI: 10.1515/acpa-2017-0005 ISSN 0001-6594 Early Cretaceous flora from the Pranhita- Godavari Basin (east coast of India): taxonomic, taphonomic and palaeoecological considerations CHOPPARAPU CHINNAPPA* and ANNAMRAJU RAJANIKANTH Birbal Sahni Institute of Palaeobotany, 53, University Road, Lucknow 226007, Uttar Pradesh, India; e-mail: [email protected] Received 18 November 2016; accepted for publication 18 February 2017 ABSTRACT. The Early Cretaceous flora from the Gangapur Formation (Pranhita-Godavari Basin, east coast of India) was studied. Its plant diversity and abundance patterns were examined, and its palaeoecology and environment were interpreted, based on the micro- and macrofloras and sedimentological inputs. The flora is rich and diverse, and consists of bryophytes, pteridophytes, pteridosperms, gymnosperms and angiosperms. The microflora shows higher taxonomic diversity and abundance than the macroflora. Overall, the study indicated an abundance of conifers, particularly Podocarpaceae. The taphocoenosis of the flora comprises local to regional elements derived from riverbank, floodplain, backswamp and valley settings. Taken together, the data on the flora and sedimentology suggest that warm and humid environments prevailed. KEYWORDS: microflora, macroflora, taphonomy, palaeoecology, Early Cretaceous, Gangapur Formation, Pranhita-Godavari Basin INTRODUCTION The Pranhita-Godavari Basin, named after from north of Nowgaon (19°20′N, 79°24′E) to two well known rivers of Peninsular India west of Gangapur village (19°16′N, 79°26′E) (Pranhita, Godavari), is an intracratonic and to Dharmaram and Paikasigudem in the Gondwanic rift basin trending NW-SE. The east (Kutty 1969). basin extends to the east coast and plunges The Early Cretaceous Pranhita-Godavari into a pericratonic rift basin, the Krishna- flora is known from micro- and macrofos- Godavari Basin (Lakshminarayana 1996).
    [Show full text]
  • EARLY CRETACEOUS DINOCYST ZONATION NWS AUSTRALIA Robin Helby, Roger Morgan, and Alan D
    UPDATED JURASSIC – EARLY CRETACEOUS DINOCYST ZONATION NWS AUSTRALIA Robin Helby, Roger Morgan, and Alan D. Partridge Geoscience Australia publication ISBN: 1 920871 01 2 © Commonwealth of Australia 2004 This update of the dinocyst zonation used throughout the greater North West This will precipitate future revision of the age dictionaries in the latter database. approximate average subzone duration of less than 250,000 years. A Shelf (NWS) of Australia is an initiative of the Virtual Centre of Economic Finally, the two far right columns provide a selection of key taxa and the significant misalignment of the D. jurassicum/P. iehiense Zone boundary has Micropalaeontology and Palynology (VCEMP) in collaboration withstratigraphic positions of the regional NWS Event Markers. The other charts been caused by the extreme scarcity and often absence of Pseudoceratium biostratigraphers from Santos Ltd and Woodside Energy Ltd, and the principal (Figs 2 to 4) provide expanded versions of intervals that could not be iehiense towards the base of its range. A younger pick for the zone boundary consultants. In the last decade and half there has been wide acceptance within adequately illustrated on the main chart. On Fig. 2 the various subdivisions of has therefore been widely used in unpublished reports by Morgan Palaeo the petroleum exploration industry of the microplankton (herein dinocyst) the Cribroperidinium perforans to Pseudoceratium iehiense Zones are shown Associates, and in the high resolution palynostratigraphy study of the Wanaea zonation described in 1987 by Helby, Morgan & Partridge as the standard in more detail, and comparison is also made with the high resolution and Cossack fields by Bint & Marshall (1994).
    [Show full text]
  • High-Resolution Variation of Ostracod Assemblages from Microbialites Near the Permian-Triassic Boundary at Zuodeng, Guangxi, South China Junyu Wan, Aihua Yuan, S
    High-resolution variation of ostracod assemblages from microbialites near the Permian-Triassic boundary at Zuodeng, Guangxi, South China Junyu Wan, Aihua Yuan, S. Crasquin, Haishui Jiang, Hao Yang, Xia Hu To cite this version: Junyu Wan, Aihua Yuan, S. Crasquin, Haishui Jiang, Hao Yang, et al.. High-resolution variation of ostracod assemblages from microbialites near the Permian-Triassic boundary at Zuodeng, Guangxi, South China. Palaeogeography, Palaeoclimatology, Palaeoecology, Elsevier, 2019, 535, pp.109349. 10.1016/j.palaeo.2019.109349. hal-02613951 HAL Id: hal-02613951 https://hal.archives-ouvertes.fr/hal-02613951 Submitted on 20 May 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. 1 High-resolution variation of ostracod assemblages from microbialites near 2 the Permian-Triassic boundary at Zuodeng, Guangxi, South China 3 Junyu Wana, Aihua Yuana,*, Sylvie Crasquinb, Haishui Jianga,c, Hao Yangc, Xia Hua 4 a. School of Earth Sciences, China University of Geosciences, Wuhan, 430074, China 5 b. CR2P, MNHN, Sorbonne Université, CNRS, Campus Pierre et Marie Curie, 4 Place 6 Jussieu, 75252, Paris Cedex 05, France 7 c. State Key Laboratory of Biogeology and Environmental Geology, China University of 8 Geosciences, Wuhan, 430074, China 9 10 * Corresponding author at: School of Earth Sciences, China University of Geosciences, Wuhan, 11 430074, China.
    [Show full text]
  • Paleozoic Species of Bairata and Related Genera
    Paleozoic Species of BairataD ' 7* andJ Related Genera GEOLOGICAL SURVEY PROFESSIONAL PAPER 330-A Paleozoic Species of natrdiaD 7* andJ Related Genera By I. G. SOHN REVISION OF SOME PALEOZOIC OSTRACODE GENERA GEOLOGICAL SURVEY PROFESSIONAL PAPER 3 3 0-A A monographic subjective revision of genera and species, including identification keys and stratigraphic ranges UNITED STATES GOVERNMENT PRINTING OFFICE, WASHINGTON : 1960 UNITED STATES DEPARTMENT OF THE INTERIOR FRED A. SEATON, Secretary GEOLOGICAL SURVEY Thomas B. Nolan, Director For sale by the Superintendent of Documents, U.S. Government Printing Office Washington 25, D.C. - Price $1 (paper cover) CONTENTS Page Abstract ______ _ _ ____ 1 Introduction. ._ _________ __ 1 Page Acknowledgments _______ _____ _ __ 1 57 Methods of study _ _ _ _ _ ___ 2 60 Punched cards __ _ _ _ _ ______ 3 Orthobairdia n. gen _ ___ ________ 65 Definition of terms ______ 6 69 Internal casts ___________ _____ 7 69 Discrimination of species _ ___ ___ __ 7 69 Individual variation ._ __ __ _ __ _ ____ _ 7 72 Muscle scars. _ _ ____ _ __ __ ____ 8 72 Surface texture _________ 8 74 Paleontological nomenclature _ _ _ 8 74 8 76 Homonymy ______ q 76 10 76 Homonyms not renamed. 10 Rishona n. gen. ._ __ __ ______ 79 Collection localities. ... _ _ _ 11 80 Systematic descriptions _______ 11 81 Key to genera ______ 11 81 Family Bairdiidae _ _ 12 81 12 83 Stratigraphic range 12 Species assigned to genera not described in this paper 84 17 84 Key to Bairdia s.s 1Q 84 Assigned species ..
    [Show full text]