Oversized Figure: Expedition 368X Methods Supplement, Figure

Total Page:16

File Type:pdf, Size:1020Kb

Oversized Figure: Expedition 368X Methods Supplement, Figure Proceedings of the International Ocean Discovery Program, Volume 367/368 Expedition 368X methods supplement, Figure F5. Calcareous nannofossil and planktonic foraminiferal events and scaled ages used during Expedition 368X (Gradstein et al., 2012). https://doi.org/10.14379/iodp.proc.368X.102.2020 Planktonic Calcareous foraminifers nannofossils Radiolarians Blow (1969) and Kennett Okada Sanfilippo Age Berggren and and and et al. Srinivasan Martini Bukry Nigrini (1995) (1983) (1971) (1981) (1998) Datum/Event (Ma) Secondary datum/event (Ma) (Ma) Period Epoch Age/Stage Polarity Chron 0 Hol. RN17 T Globorotalia flexuosa (0.07) Taran- NN21 CN15 B Buccinosphaera invaginata (0.18) T Globigerinoides ruber rosa (0.12) tian B Emiliania huxleyi (0.29) B Globigerinella calida (0.22) b b RN16 T Pseudoemiliania lacunosa (0.44) C1n NN20 T Stylatractus universus (0.44) B Globorotalia flexuosa (0.40) 0.5 RN15 B Collosphaera tuberosa (0.59) B Globorotalia hirsuta (0.45) CN14 T Globorotalia tosaensis (0.61) T Gephyrocapsa sp. 3 (0.61) Ionian a B Globorotalia hessi (0.75) Pt1 Tc Reticulofenestra asanoi (0.91) 1 N22 RN14 B Gephyrocapsa sp. 3 (1.02) 1 B Gephyrocapsa spp. >4 µm reentrance (1.04) Ta Gephyrocapsa spp. small (1.02) a NN19 T Anthocyrtidium angulare (1.21) Bc Reticulofenestra asanoi (1.14) C1r T Gephyrocapsa spp. >5.5 µm (1.24) Ba Gephyrocapsa spp. small (1.24) 2 b T Calcidiscus macintyrei (1.60) B Lamprocyrtis nigriniae (1.26) 1.5 CN13 B Gephyrocapsa spp. >5.5 µm (1.62) T Helicosphaera sellii (1.26) Calabrian RN13 B Gephyrocapsa spp. >4 µm (1.73) T Lamprocyrtis neoheteroporos (1.28) T Globigerinoides fistulosus (1.88) B Anthocyrtidium angulare (1.81) a T Discoaster brouweri (1.93) T Discoaster triradiatus (1.95) Pleistocene C2n Quaternary B Globorotalia truncatulinoides (1.93) T Globigerinoides extremus (1.98) 2 1 T Pterocanium prismatium (2.04) PL6 NN18 d T Theocorythium vetulum (2.04) C2r T Discoaster pentaradiatus (2.39) Ba Discoaster triradiatus (2.22) 2 b T Globorotalia pseudomiocenica (2.39) T Globorotalia pertenuis (2.30) NN17 c T Globoturborotalita woodi (2.30) Gelasian T Discoaster surculus (2.49) 2.5 RN12 B Lamprocyrtis neoheteroporus (2.65) b T Anthocyrtidium jenghisi (2.74) T Globoturborotalita decoraperta (2.75) CN12 a T Discoaster tamalis (2.80) T Globorotalia multicamerata (2.98) 1 T Stichocorys peregrina (2.87) T Didymocyrtis avita (3.18) 3 C2An PL5 N20/ B Globigerinoides fistulosus (3.33) NN16 B Globorotalia tosaensis (3.35) 2 N21 a b T Anthocyrtidium pliocenica (3.40) B Globorotalia pertenuis (3.52) RN11 T Phormostichoartus fistula (3.49) T Sphenolithus spp. (3.54) 3.5 Piacenzian 3 PL4 T Dentoglobigerina altispira (3.47) T Lychnodictyum audax (3.60) T Sphaeroidinellopsis seminulina (3.59) T Pulleniatina primalis (3.66) PL3 a T Reticulofenestra pseudoumbilicus (3.70) B Amphirhopalum ypsilon (4.01) C2Ar NN15 T Globorotalia margaritae (3.85) b T Phormostichoartus doliolum (3.89) T Spongaster pentas (4.13) 4 NN14 RN10 T Amaurolithus tricorniculatus (3.92) B Spongaster tetras tetras, S. pentas (4.13) PL2 CN11 Bc Discoaster asymmetricus (4.13) T Pulleniatina spectabilis (4.21) T Didymocyrtis penultima (4.24) T Spongaster berminghami (4.22) 1 a T Globoturborotalita nepenthes (4.37) T Spongaster klingi (4.22) Pliocene T Amaurolithus primus (4.50) B Globorotalia crassaformis s.l. (4.31) 4.5 T Globorotalia cibaoensis (4.60) 2 C3n NN13 Zanclean c 3 N18/ 5 PL1 CN10 T Ceratolithus acutus (5.04) 4 N19 B Ceratolithus rugosus (5.12) T Triquetrorhabdulus rugosus (5.28) b T Solenosphaera omnitubus procera (5.31) NN12 B Ceratolithus acutus (5.35) T Solenosphaera omnitubus omnitubus (5.31) a 5.5 B Globorotalia tumida [Pacific] (5.57) B Sphaeroidinellopsis dehiscens s.l. (5.53) C3r T Discoaster quinqueramus (5.59) B Pterocorys campanula (5.67) d B Turborotalita humilis (5.81) M14 T Globoquadrina dehiscens (5.92) 6 RN9 T Nicklithus amplificus (5.94) B Globorotalia margaritae (6.08) b T Globorotalia lenguaensis (6.14) B Globigerinoides conglobatus (6.20) 1 C3An c B Pulleniatina primalis (6.60) 6.5 2 Messinian B Globorotalia nicolae (6.83) B Nicklithus amplificus (6.91) 7 C3Ar NN11 CN9 B Neogloboquadrina atlantica (dex. -> sin.) (6.99) N17 b 1 C3Bn b B Solenosphaera omnitubus procera (7.41) 2 C3Br B Amaurolithus primus/Amaurolithus spp. (7.42) B Solenosphaera omnitubus omnitubus (7.41) 7.5 T Discoaster loeblichii (7.53) 1 a C4n B Stichocorys peregrina, T Stichocorys delmontensis (7.78) Bc Discoaster surculus (7.79) a B Globorotalia miotumida-conomiozea (7.89) 8 2 M13 RN8 B Discoaster quinqueramus (8.12) 1 B Didymocyrtis penultima (8.39) B Discoaster berggrenii (8.29) T Didymocyrtis antepenultima (8.39) C4r T Diartus hughesi (8.39) B Neogloboquadrina humerosa (8.56) 8.5 2 B Globorotalia plesiotumida (8.58) T Minylitha convallis (8.68) RN7 B Discoaster loeblichii (8.77) Bc Reticulofenestera pseudoumbilicus (8.79) NN10 CN8 B Diartus hughesi, T Diartus petterssoni (8.84) 9 C4An B Globigerinoides extremus (8.93) N16 T Discoaster bollii (9.21) 1 a Bc Discoaster pentaradiatus (9.37) C4Ar B Globorotalia cibaoensis (9.44) 9.5 T Discoaster hamatus (9.53) 2 T Catinaster calyculus (9.67) T Catinaster coalitus (9.69) B Neogloboquadrina acostaensis (9.83) B Globorotalia juanai (9.69) Tortonian 1 B Minylitha convallis (9.75) 10 NN9 CN7 X Discoaster hamatus -> D. neohamatus (9.76) M12 N15 T Globorotalia challengeri (9.99) B Discoaster bellus (10.40) C5n T Paragloborotalia mayeri (10.46) B Discoaster neohamatus (10.55) 10.5 2 B Discoaster hamatus (10.55) Bc Helicosphaera stalis (10.71) B Neogloboquadrina acostaensis [temperate] (10.57) Tc Helicosphaera walbersdorfensis (10.74) NN8 CN6 RN6 B Discoaster brouweri (10.76) B Catinaster coalitus (10.89) B Catinaster calyculus (10.79) 11 M11 N14 T Coccolithus miopelagicus (10.97) 1 B Globoturborotalita apertura (11.18) T Calcidiscus premacintyrei (11.21) Tr Globigerinoides obliquus (11.25) 2 NN7 b T Paragloborotalia mayeri [temperate] (11.40) B Globoturborotalita decoraperta (11.49) 11.5 C5r T Globigerinoides subquadratus (11.54) B Globoturborotalita nepenthes (11.63) Tc Discoaster kugleri (11.58) M10 N13 T Fohsella fohsi (11.79) 3 Bc Discoaster kugleri (11.90) T Cyclicargolithus floridanus (11.85) 12 T Clavatorella bermudezi (12.00) 1 T Coronocyclus nitescens (12.12) C5An CN5 2 b Tc Calcidiscus premacintyrei (12.38) 12.5 Bc Calcidiscus macintyrei (12.46) 1 M9 N12 NN6 a B Reticulofenestra pseudoumbilicus (12.83) Neogene 2 C5Ar B Globorotalia lenguanensis (12.84) 3 B Sphaeroidinellopsis subdehiscens (13.02) 13 B Fohsella robusta (13.13) C5AAn B Fohsella robusta (13.13) B Triquetrorhabdulus rugosus (13.27) Serravallian C5AAr a T Cassigerinella martinezpicoi (13.27) B Fohsella fohsi (13.41) Tc Cyclicargolithus floridanus (13.28) C5ABn B Calcidiscus macintyrei (13.36) 13.5 M8 N11 T Sphenolithus heteromorphus (13.53) C5ABr T Fohsella peripheroronda (13.80) RN5 B Fohsella praefohsi (13.77) Tr Clavatorella bermudezi (13.82) C5ACn T Globorotalia archeomenardii (13.87) Miocene M7 N10 14 C5ACr NN5 CN4 B Fohsella peripheroacuta (14.24) C5ADn B Globorotalia praemenardii (14.38) 14.5 T Praeorbulina sicana (14.53) T Praeorbulina sicana (14.53) M6 N9 T Globigeriantella insueta (14.66) C5ADr T Praeorbulina glomerosa s.s. (14.78) 1 T Helicosphaera ampliaperta (14.91) T Praeorbulina circularis (14.89) 15 C5Bn B Dorcadospyris alata, Dorcadospyris dentata (15.03) 2 B Orbulina suturalis (15.10) Langhian 15.5 C5Br B Clavatorella bermudezi (15.73) M5 b N8 Ta Discoaster deflandrei group (15.80) B Discoaster signus (15.85) B Praeorbulina circularis (15.96) 16 B Globigerinoides diminutus (16.06) 1 a RN4 B Praeorbulina glomerosa s.s. (16.27) B Globorotalia archeomenardii (16.26) 2 C5Cn NN4 CN3 B Praeorbulina sicana (16.38) B Praeorbulina curva (16.28) 16.5 b T Globorotalia incognita (16.39) 3 B Globorotalia birnageae (16.69) B Globorotalia miozea (16.70) M4 N7 17 C5Cr a B Globorotalia zealandica (17.26) C5Dn B Globorotalia semivera (17.26) 17.5 N6 T Catapsydrax dissimilis (17.54) 1 B Globigeriantella insueta s.s. (17.59) C5Dr B Calocycletta (Calocyclissima) costata (17.59) B Sphenolithus heteromorphus (17.71) 2 18 T Sphenolithus belemnos (17.95) NN3 RN3 T Triquetrorhabdulus carinatus (18.28) B Globorotalia praescitula (18.26) C5En M3 18.5 CN2 C5Er B Stichocorys wolffii (18.64) Burdigalian B Sphenolithus belemnos (19.03) 19 T Globiquadrina binaiensis (19.09) C6n B Globigerinatella sp. (19.30) N5 RN2 B Globiquadrina binaiensis (19.30) 19.5 C6r 20 T Theocyrtis annosa (20.05) B Globigerinoides altiaperturus (20.03) M2 1 C6An B Helicosphaera ampliaperta (20.43) 20.5 2 NN2 T Tenuitella munda (20.78) C6Ar c RN1 X Helicosphaera euphratis -> H. carteri (20.92) 21 CN1 B Globorotalia incognita (20.93) C6AAn T Paragloborotalia kugleri (21.12) T Globoturborotalita angulisuturalis (20.94) 1 T Paragloborotalia pseudokugleri (21.31) C6AAr B Globoquadrina dehiscens forma spinosa (21.44) 21.5 2 3 b B Cyrtocapsella tetrapera (21.82) 1 T Dentoglobigerina globularis (21.98) 22 C6Bn M1 Bc Helicosphaera carteri (22.03) Aquitanian 2 N4 C6Br B Globoquadrina dehiscens (22.44) T Orthorhabdus serratus (22.42) 22.5 a B Sphenolithus disbelemnos (22.76) 1 B Discoaster druggi s.s. (22.82) T Globigerina ciperoensis (22.90) C6Cn B Paragloborotalia kugleri (22.96) B Globigerinoides trilobus s.l. (22.96) 23 2 NN1 a/b RP22 T Sphenolithus capricornutus (22.97) T Reticulofenestra bisecta >10 µm (23.13) T Globigerina euapertura (23.03) T Sphenolithus delphix (23.11) 3 B Sphenolithus delphix (23.21) Bc Globigerinoides primordius (23.50) 23.5 C6Cr T Tenuitella gemma (23.50) T Zygrhablithus bijugatus (23.76) 24 1 O7 B Lychnocanoma elongata (24.18) 2 C7n 24.5 T Sphenolithus ciperoensis (24.43) C7r X Triquetrorhabdulus longus ->T.
Recommended publications
  • 14. Neogene and Quaternary Calcareous Nannofossil Biostratigraphy of the Walvis Ridge1
    14. NEOGENE AND QUATERNARY CALCAREOUS NANNOFOSSIL BIOSTRATIGRAPHY OF THE WALVIS RIDGE1 Ming-Jung Jiang, Robertson Research (U.S.) Inc., Houston, Texas and Stefan Gartner, Department of Oceanography, Texas A&M University, College Station, Texas ABSTRACT During DSDP Leg 74 in the South Atlantic, 11 holes were drilled at 5 sites (525-529) on the eastern end of Walvis Ridge. The sediments recovered range in age from late Campanian or early Maestrichtian to Holocene. This chapter deals only with the Neogene to Holocene interval. The calcareous nannofossils over this interval have been corroded as well as overgrown, but a precise biostratigraphy is possible at all sites because most of the key index species are present. INTRODUCTION CALCAREOUS NANNOFOSSIL ZONATION During DSDP Leg 74, 11 holes were drilled at 5 sites Martini's standard Tertiary and Quaternary zonation (525-529) on Walvis Ridge in the South Atlantic near (1971), which is widely used elsewhere, was the starting South Africa (Fig. 1). Sediments ranging in age from basis for the zonation described here. Because of the late Campanian or early Maestrichtian to Holocene scarcity or apparent lack of some of Martini's index fos- were recovered. This chapter deals with the calcareous sils, possibly owing to environmental exclusion of the nannofossils found in the Neogene to Holocene sedi- parent organism or to poor preservation, other species ment from these five sites. The calcareous nannofossils were selected to determine zones. Deviations from Mar- from the Paleogene and the Upper Cretaceous are docu- tinis zonation, necessary for the studied area, are dis- mented by Hélène Manivit in this same volume.
    [Show full text]
  • 33. Neogene and Quaternary Calcareous Nannofossils from the Blake Ridge, Sites 994, 995, and 9971
    Paull, C.K., Matsumoto, R., Wallace, P.J., and Dillon, W.P. (Eds.), 2000 Proceedings of the Ocean Drilling Program, Scientific Results, Vol. 164 33. NEOGENE AND QUATERNARY CALCAREOUS NANNOFOSSILS FROM THE BLAKE RIDGE, SITES 994, 995, AND 9971 Hisatake Okada2 ABSTRACT Twenty routinely used nannofossil datums in the late Neogene and Quaternary were identified at three Blake Ridge sites drilled during Leg 164. The quantitative investigation of the nannofossil assemblages in 236 samples selected from Hole 994C provide new biostratigraphic and paleoceanographic information. Although mostly overlooked previously, Umbilicosphaera aequiscutum is an abundant component of the late Neogene flora, and its last occurrence at ~2.3 Ma is a useful new biostrati- graphic event. Small Gephyrocapsa evolved within the upper part of Subzone CN11a (~4.3 Ma), and after an initial acme, it temporarily disappeared for 400 k.y., between 2.9 and 2.5 Ma. Medium-sized Gephyrocapsa evolved in the latest Pliocene ~2.2 Ma), and after two short temporary disappearances, common specimens occurred continuously just above the Pliocene/Pleis- tocene boundary. The base of Subzone CN13b should be recognized as the beginning of the continuous occurrence of medium- sized (>4 µm) Gephyrocapsa. Stratigraphic variation in abundance of the very small placoliths and Florisphaera profunda alter- nated, indicating potential of the former as a proxy for the paleoproductivity. At this site, it is likely that upwelling took place during three time periods in the late Neogene (6.0–4.6 Ma, 2.3–2.1 Ma, and 2.0–1.8 Ma) and also in the early Pleistocene (1.4– 0.9 Ma).
    [Show full text]
  • Biostratigraphy and Evolution of Miocene Discoaster Spp. from IODP Site U1338 in the Equatorial Pacific Ocean
    Research article Journal of Micropalaeontology Published online December 7, 2016 https://doi.org/10.1144/jmpaleo2015-034 | Vol. 36 | 2017 | pp. 137–152 Biostratigraphy and evolution of Miocene Discoaster spp. from IODP Site U1338 in the equatorial Pacific Ocean Marina Ciummelli1*, Isabella Raffi2 & Jan Backman3 1 PetroStrat Ltd, Tan-y-Graig, Parc Caer Seion, Conwy LL32 8FA, UK 2 Dipartimento di Ingegneria e Geologia, Università ‘G. d’Annunzio’ di Chieti-Pescara, I-66013 Chieti Scalo, Italy 3 Department of Geological Sciences, Stockholm University, SE-106 91 Stockholm, Sweden * Correspondence: [email protected] Abstract: Assemblages of upper lower through upper Miocene Discoaster spp. have been quantified from Integrated Ocean Drilling Program (IODP) Site U1338 in the eastern equatorial Pacific Ocean. These assemblages can be grouped into five broad morphological categories: six-rayed with bifurcated ray tips, six-rayed with large central areas, six-rayed with pointed ray tips, five-rayed with bifurcated ray tips and five-rayed with pointed ray tips. Discoaster deflandrei dominates the assemblages prior to 15.8 Ma. The decline in abundance of D. deflandrei close to the early–middle Miocene boundary occurs together with the evolution of the D. variabilis group, including D. signus and D. exilis. Six-rayed discoasters having large central areas become a prominent member of the assemblages for a 400 ka interval in the late middle Miocene. Five- and six-rayed forms having pointed tips become prominent in the early late Miocene and show a strong antiphasing relationship with the D. variabilis group. Discoaster bellus completely dominates the Discoaster assemblages for a 400 ka interval in the middle late Miocene.
    [Show full text]
  • Quaternary Calcareous Nannofossil Datums and Biochronology in the North Atlantic Ocean, IODP Site U13081 Tokiyuki Sato,2 Shun Chiyonobu,3 and David A
    Channell, J.E.T., Kanamatsu, T., Sato, T., Stein, R., Alvarez Zarikian, C.A., Malone, M.J., and the Expedition 303/306 Scientists Proceedings of the Integrated Ocean Drilling Program, Volume 303/306 Data report: Quaternary calcareous nannofossil datums and biochronology in the North Atlantic Ocean, IODP Site U13081 Tokiyuki Sato,2 Shun Chiyonobu,3 and David A. Hodell4 Chapter contents Abstract Abstract . 1 We studied high-resolution Quaternary calcareous nannofossil Introduction . 1 biostratigraphy to clarify the relationship between nannofossil events and oxygen isotope stratigraphy using the continuous sed- Samples and methods. 1 iment sequence from Integrated Ocean Drilling Program Site Results . 2 U1308 in the North Atlantic Ocean. Results indicate that some Remarks on stratigraphic position of datums . 2 nannofossil events found in the section, such as the last occur- Conclusion . 3 rences of Reticulofenestra asanoi and Gephyrocapsa spp. (large), are Acknowledgments. 3 located in a different stratigraphic position compared to previous References . 3 studies. We also clarify the critical stratigraphic positions of both Figures . 5 the first occurrence of Emiliania huxleyi and the last occurrence of Table . 9 Pseudoemiliania lacunosa, which occur just below the highest peaks of each marine isotope Stage 8 and 12. Introduction Quaternary calcareous nannofossil datums and their chronostrati- graphic framework have been discussed over the last 20 y mainly based on their correlation to magnetostratigraphy (Raffi and Rio, 1979; Rio, 1982; Takayama and Sato, 1987) or to oxygen isotope stages (Thierstein et al., 1977; Wei, 1993; Raffi et al., 1993; Raffi, 2002). These studies indicate that Quaternary nannofossil datums show a small diachroneity between different latitudes.
    [Show full text]
  • Applications of Calcareous Nannofossils and Stable Isotopes To
    Florida State University Libraries Electronic Theses, Treatises and Dissertations The Graduate School 2007 Applications of Calcareous Nannofossils and Stable Isotopes to Cenozoic Paleoceanography: Examples from the Eastern Equatorial Pacific, Western Equatorial Atlantic and Southern Indian Oceans Shijun Jiang Follow this and additional works at the FSU Digital Library. For more information, please contact [email protected] THE FLORIDA STATE UNIVERSITY COLLEGE OF ARTS AND SCIENCES APPLICATIONS OF CALCAREOUS NANNOFOSSILS AND STABLE ISOTOPES TO CENOZOIC PALEOCEANOGRAPHY: EXAMPLES FROM THE EASTERN EQUATORIAL PACIFIC, WESTERN EQUATORIAL ATLANTIC AND SOUTHERN INDIAN OCEANS By SHIJUN JIANG A dissertation submitted to the Department of Geological Sciences in partial fulfillment of the requirements for the degree of Doctor of Philosophy Degree Awarded: Fall Semester, 2007 The members of the Committee approve the Dissertation of Shijun Jiang defended on July 13, 2007. ____________________________________ Sherwood W. Wise, Jr. Professor Directing Dissertation ____________________________________ Richard L. Iverson Outside Committee Member ____________________________________ Anthony J. Arnold Committee Member ____________________________________ Joseph F. Donoghue Committee Member ____________________________________ Yang Wang Committee Member The Office of Graduate Studies has verified and approved the above named committee members. ii To Shuiqing and Jenny iii ACKNOWLEDGEMENTS First of all, I would like to thank my mentor Dr. Sherwood W. Wise, Jr., who constantly encouraged and supported me with his enthusiasm, reliance, guidance and, most of all, patience throughout my Ph.D adventure. He also opened a door into my knowledge of the paleo world, generously shared his time and his wealth of knowledge, patiently guided me through a western educational system totally different from my own background, and has successfully fostered my interest and enthusiasm in teaching.
    [Show full text]
  • The Gelasian Stage (Upper Pliocene): a New Unit of the Global Standard Chronostratigraphic Scale
    82 by D. Rio1, R. Sprovieri2, D. Castradori3, and E. Di Stefano2 The Gelasian Stage (Upper Pliocene): A new unit of the global standard chronostratigraphic scale 1 Department of Geology, Paleontology and Geophysics , University of Padova, Italy 2 Department of Geology and Geodesy, University of Palermo, Italy 3 AGIP, Laboratori Bolgiano, via Maritano 26, 20097 San Donato M., Italy The Gelasian has been formally accepted as third (and Of course, this consideration alone does not imply that a new uppermost) subdivision of the Pliocene Series, thus rep- stage should be defined to represent the discovered gap. However, the top of the Piacenzian stratotype falls in a critical point of the evo- resenting the Upper Pliocene. The Global Standard lution of Earth climatic system (i.e. close to the final build-up of the Stratotype-section and Point for the Gelasian is located Northern Hemisphere Glaciation), which is characterized by plenty in the Monte S. Nicola section (near Gela, Sicily, Italy). of signals (magnetostratigraphic, biostratigraphic, etc; see further on) with a worldwide correlation potential. Therefore, Rio et al. (1991, 1994) argued against the practice of extending the Piacenzian Stage up to the Pliocene-Pleistocene boundary and proposed the Introduction introduction of a new stage (initially “unnamed” in Rio et al., 1991), the Gelasian, in the Global Standard Chronostratigraphic Scale. This short report announces the formal ratification of the Gelasian Stage as the uppermost subdivision of the Pliocene Series, which is now subdivided into three stages (Lower, Middle, and Upper). Fur- The Gelasian Stage thermore, the Global Standard Stratotype-section and Point (GSSP) of the Gelasian is briefly presented and discussed.
    [Show full text]
  • Integrated Stratigraphy and Astronomical Calibration of the Serravallian=Tortonian Boundary Section at Monte Gibliscemi (Sicily, Italy)
    ELSEVIER Marine Micropaleontology 38 (2000) 181±211 www.elsevier.com/locate/marmicro Integrated stratigraphy and astronomical calibration of the Serravallian=Tortonian boundary section at Monte Gibliscemi (Sicily, Italy) F.J. Hilgen a,Ł, W. Krijgsman b,I.Raf®c,E.Turcoa, W.J. Zachariasse a a Department of Geology, Utrecht University, Budapestlaan 4, 3584 CD Utrecht, The Netherlands b Paleomagnetic Laboratory, Fort Hoofddijk, Budapestlaan 17, 3584 CD Utrecht, The Netherlands c Dip. di Scienze della Terra, Univ. G. D'Annunzio, via dei Vestini 31, 66013 Chieti Scalo, Italy Received 12 May 1999; revised version received 20 December 1999; accepted 26 December 1999 Abstract Results are presented of an integrated stratigraphic (calcareous plankton biostratigraphy, cyclostratigraphy and magne- tostratigraphy) study of the Serravallian=Tortonian (S=T) boundary section of Monte Gibliscemi (Sicily, Italy). Astronomi- cal calibration of the sedimentary cycles provides absolute ages for calcareous plankton bio-events in the interval between 9.8 and 12.1 Ma. The ®rst occurrence (FO) of Neogloboquadrina acostaensis, usually taken to delimit the S=T boundary, is dated astronomically at 11.781 Ma, pre-dating the migratory arrival of the species at low latitudes in the Atlantic by almost 2 million years. In contrast to delayed low-latitude arrival of N. acostaensis, Paragloborotalia mayeri shows a delayed low-latitude extinction of slightly more than 0.7 million years with respect to the Mediterranean (last occurrence (LO) at 10.49 Ma at Ceara Rise; LO at 11.205 Ma in the Mediterranean). The Discoaster hamatus FO, dated at 10.150 Ma, is clearly delayed with respect to the open ocean.
    [Show full text]
  • Pleistocene Calcareous Nannofossil Biostratigraphy and Gephyrocapsid Occurrence in Site U1431D, IODP 349, South China Sea
    geosciences Article Pleistocene Calcareous Nannofossil Biostratigraphy and Gephyrocapsid Occurrence in Site U1431D, IODP 349, South China Sea , Jose Dominick S. Guballa * y and Alyssa M. Peleo-Alampay Nannoworks Laboratory, National Institute of Geological Sciences, College of Science, University of the Philippines, Diliman, Quezon City 1101, Philippines; [email protected] * Correspondence: [email protected]; Tel.: +1-28-9707-5905 Current address: Department of Earth Sciences, University of Toronto, 22 Russell Street, Toronto, y ON M5S 3B1, Canada. Received: 25 August 2020; Accepted: 23 September 2020; Published: 28 September 2020 Abstract: We reinvestigated the Pleistocene calcareous nannofossil biostratigraphy of Site U1431D (International Ocean Discovery Program (IODP) Expedition 349) in the South China Sea (SCS). Twelve calcareous nannofossil Pleistocene datums are identified in the site. The analysis confirms that the last occurrence (LO) of Calcidiscus macintyrei is below the first occurrence (FO) of large Gephyrocapsa spp. (>5.5 µm). The FO of medium Gephyrocapsa spp. (4–5.5 µm) is also identified in the samples through morphometric measurements, which was unreported in shipboard results. Magnetobiochronologic calibrations of the numerical ages of LO of Pseudoemiliania lacunosa and FO of Emiliania huxleyi are underestimated and need reassessment. Other potential markers such as a morphological turnover of circular to elliptical variants of Pseudoemiliania lacunosa and a small Gephyrocapsa acme almost synchronous with the FO of Emiliania huxleyi may offer biostratigraphic significance in the SCS. The morphologic changes in Gephyrocapsa coccoliths are also examined for the first time in Site U1431D. Placolith length and bridge angle changes are comparable with other ocean basins, suggesting that morphologic changes are most likely evolutionary novelties rather than being caused by local climate anomalies.
    [Show full text]
  • Ocean Drilling Program Scientific Results Volume
    Ruddiman, W., Sarnthein M., et al., 1989 Proceedings of the Ocean Drilling Program, Scientific Results, Vol. 108 8. COMPARISON OF UPPER PLIOCENE DISCOASTER ABUNDANCE VARIATIONS FROM NORTH ATLANTIC SITES 552, 607, 658, 659, AND 662: FURTHER EVIDENCE FOR MARINE PLANKTON RESPONDING TO ORBITAL FORCING1 Alex Chepstow-Lusty,2 Jan Backman,3 and Nicholas J. Shackleton2 ABSTRACT Abundance variations of six Pliocene species of discoasters have been analyzed over the time interval from 1.89 to 2.95 Ma at five contrasting sites in the North Atlantic: Deep Sea Drilling Project Sites 552 (56°N) and 607 (41°N) and Ocean Drilling Program 658 (20°N), 659 (18°N), and 662 (1°S). A sampling interval equivalent to approximately 3 k.y. was used. Total Discoaster abundance showed a reduction with increasing latitude and from the effects of upwelling. This phenomenon is most obvious in Discoaster brouweri, the only species that survived over the entire time interval studied. Prior to 2.38 Ma, Discoaster pentaradiatus and Discoaster surculus are important components of the Discoaster assemblage: Discoaster pentaradiatus increases slightly with latitude up to 41°N, and its abundance relative to D. brouweri increases up to 56°N; D. surculus increases in abundance with latitude and with upwelling conditions relative to both D. brouweri and D. pentaradiatus and is dominant to the latter species at upwelling Site 658 and at the highest latitude sites. Discoaster asymmetricus and Discoaster tamalis appear to increase in abundance with latitude relative to D. brouweri. Many of the abundance changes observed appear to be connected with the initiation of glaciation in the North Atlantic at 2.4 Ma.
    [Show full text]
  • Discoaster Zonation of the Miocene of the Kutei Basin, East Kalimantan, Indonesia (Mahakam Delta Offshore) Bernard Lambert, Cécile Laporte-Galaa
    Discoaster zonation of the Miocene of the Kutei Basin, East Kalimantan, Indonesia (Mahakam Delta Offshore) Bernard Lambert, Cécile Laporte-Galaa To cite this version: Bernard Lambert, Cécile Laporte-Galaa. Discoaster zonation of the Miocene of the Kutei Basin, East Kalimantan, Indonesia (Mahakam Delta Offshore). Carnets de Geologie, Carnets de Geologie, 2005, CG2005 (M01), pp.1-63. hal-00167085 HAL Id: hal-00167085 https://hal.archives-ouvertes.fr/hal-00167085 Submitted on 14 Aug 2007 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. Carnets de Géologie / Notebooks on Geology - Memoir 2005/01 (CG2005_M01) Discoaster zonation of the Miocene of the Kutei Basin, East Kalimantan, Indonesia (Mahakam Delta Offshore). Bernard LAMBERT1 Cécile LAPORTE-GALAA2 Abstract: Thirteen time-stratigraphic associations of the nannofossil Discoaster have been defined and used in the Miocene Kutei Basin of eastern Borneo to establish a regional stratigraphic framework. The methodology used is discussed and the fossils employed are figured and annotated. Their aid in resolving the timing, stages and details of delta construction is presented graphically. Key Words: Borneo; delta; Discoaster; Kutei; Mahakam; Miocene; nannoflora; nannofossil; Neogene; stratigraphy; zonation. Citation: LAMBERT B., LAPORTE-GALAA C.
    [Show full text]
  • Deep Sea Drilling Project Initial Reports Volume 94
    26. PLIOCENE DISCOASTER ABUNDANCE VARIATIONS, DEEP SEA DRILLING PROJECT SITE 606: BIOCHRONOLOGY AND PALEOENVIRONMENTAL IMPLICATIONS1 Jan Backman, Department of Geology, University of Stockholm and Pierre Pestiaux, Institut d'Astronomie et de Géophysique Georges Lemaitre, Université Catholique de Louvain2 ABSTRACT Abundance variations of six Pliocene species of the calcareous nannofossil genus Discoaster have been determined for the time interval between 1.9 and 3.6 Ma at DSDP Site 606, using a sample interval of 30 cm (<9 kyr.). These quan- titative data contain information which can be interpreted in terms of both biochronology and paleoclimatic develop- ment. The following datums have been examined: D. brouweri (extinction at 1.89 Ma), D. triradiatus (extinction at 1.89 Ma), D. triradiatus (peak abundance begins at 2.07 Ma), D. pentaradiatus (extinction between 2.33 and 2.43 Ma), D. surcu- lus (extinction between 2.42 and 2.46 Ma), D. asymmetricus (sharp decline in abundance at 2.65 Ma), and D. tamalis (extinction at 2.65 Ma). The age of the peak abundance of D. triradiatus is accurately determined for the first time. The remaining estimates agree with those previously obtained from the northern North Atlantic and Pacific oceans. Plots of changes in total Discoaster accumulation rate indicate a long-term trend of progressive cooling of sea-sur- face temperatures during preglacial times in the area of Site 606. This trend is overprinted by short-term abundance os- cillations. The orbital forcing of paleoclimatic change is strongly imprinted on these short-term variations, as indicated by spectral analysis. The 413-kyr. eccentricity period, the 41-kyr.
    [Show full text]
  • Monte Dei Corvi (Middle^Upper Miocene, Northern Italy)
    Palaeogeography, Palaeoclimatology, Palaeoecology 199 (2003) 229^264 www.elsevier.com/locate/palaeo Integrated stratigraphy and astronomical tuning of the Serravallian and lower Tortonian at Monte dei Corvi (Middle^Upper Miocene, northern Italy) F.J. Hilgen a;Ã, H.Abdul Aziz b, W.Krijgsman b, I.Ra⁄ c, E.Turco d a IPPU, Utrecht University, Budapestlaan 4, 3584 CD Utrecht, The Netherlands b Paleomagnetic Laboratory, Fort Hoofddijk, Budapestlaan 17, 3584 CD Utrecht, The Netherlands c Dip. di Scienze della Terra, Univ. ‘G. D’Annunzio’, via dei Vestini 31, 66013 Chieti Scalo, Italy d Dip. di Scienze della Terra, Universita' di Parma, Parco Area delle Scienze 157/A, 43100 Parma, Italy Received 3 October 2002; accepted 13 June 2003 Abstract An integrated stratigraphy (calcareous plankton biostratigraphy, magnetostratigraphy and cyclostratigraphy) is presented for the Serravallian and lower Tortonian part (Middle^Upper Miocene) of the Monte dei Corvi section located in northern Italy.The detailed biostratigraphic analysis showed that both the Discoaster kugleri acme and the first influx of Neogloboquadrina acostaensis are recorded at Monte dei Corvi; these events, which passed unobserved in previous studies, play an important role in delineating the Serravallian^Tortonian boundary.Thermal and alternating field demagnetization revealed a characteristic low-temperature component marked by dual polarities.The resultant magnetostratigraphy for the upper part of the section can be unambiguously calibrated to the GPTS ranging from C5n.2n up to C4r.2r.
    [Show full text]