Research paper
A magnetostratigraphic calibration of Middle Miocene through Pliocene dinoflagellate cyst and acritarch events in the Iceland Sea (Ocean Drilling Program Hole 907A)

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Abstract

A detailed dinoflagellate cyst investigation of the almost continuous Middle Miocene through Pliocene of Ocean Drilling Program Hole 907A in the Iceland Sea has been conducted at 100-kyr resolution. The investigated section is well constrained by magnetostratigraphy, providing for the first time an independent temporal control on a succession of northern high-latitude dinoflagellate cyst bioevents.

Based on the highest/lowest occurrences (HO/LO) and highest common occurrence (HCO) of 20 dinoflagellate cyst taxa and one acritarch species, 26 bioevents have been defined and compared with those recorded at selected DSDP, ODP, and IODP sites from the North Atlantic and contiguous seas, and in outcrops and boreholes from the onshore and offshore eastern U.S.A., and the North Sea and Mediterranean basins.

Comparisons reveal near-synchronous HOs of the dinoflagellate cysts Batiacasphaera micropapillata (3.8–3.4 Ma, mid-Pliocene) and Reticulatosphaera actinocoronata (4.8–4.2 Ma, Lower Pliocene) across the Nordic Seas and North Atlantic, highlighting their value on a supraregional scale. This probably applies also to Hystrichosphaeropsis obscura (upper Tortonian), when excluding ODP Hole 907A where its sporadic upper stratigraphic range presumably relates to cooling in the early Tortonian. Over a broader time span within the upper Tortonian, the HO of Operculodinium piaseckii likely also permits correlation across the Nordic Seas and North Atlantic, and the HO of Labyrinthodinium truncatum appears useful in the Labrador and Nordic Seas. Biostratigraphic markers useful for regional rather than supraregional correlation are the HOs of Batiacasphaera hirsuta (c. 8.4 Ma, upper Tortonian) and Unipontidinium aquaeductus (c. 13.6–13.9 Ma, upper Langhian), the HCO of the acritarch Decahedrella martinheadii (c. 6.7–6.3 Ma, Messinian), and possibly the LO of Cerebrocysta irregulare sp. nov. (c. 13.8 Ma, uppermost Langhian) across the Nordic Seas. Since Habibacysta tectata, B. micropapillata, R. actinocoronata and D. martinheadii have been observed in the Arctic Ocean, they are potentially useful for high latitude correlations in the polar domain.

The LOs of Habibacysta tectata and Unipontidinium aquaeductus suggest a mid- to late Langhian age (15.1–13.7 Ma) for deposits at the base of Hole 907A, thus providing new constraints on the age of basalts at the base of ODP Hole 907A.

The stratigraphically important dinoflagellate cysts Cerebrocysta irregulare sp. nov., and Impagidinium elongatum sp. nov. are formally described.

Highlights

► A continuous Neogene high-latitude sequence was palynologically investigated. ► 26 dinocyst and acritarch events are defined and calibrated vs magnetostratigraphy. ► We provide first-time independent age control on high-latitude dinocyst events. ► Their stratigraphic utility is evaluated by comparison across the North Atlantic. ► Impagidinium elongatum and Cerebrocysta irregulare are formally described.

Introduction

Following the first published Neogene dinoflagellate cyst (dinocyst) biozonation by Williams (1975) on drill holes from offshore eastern Canada, assemblages of Miocene through Pliocene age have been reported frequently from the Northern Hemisphere, and our knowledge of their (paleo)ecology and stratigraphy has improved significantly (e.g. Williams and Bujak, 1985, Stover et al., 1996). It soon became evident that dinocysts are the only microfossil group with a continuous Neogene record in the high northern latitudes, and their relatively high diversity predisposes them to detailed and reliable biostratigraphic correlations in a region critical for understanding the development of Northern Hemisphere climate (De Schepper and Head, 2008). Despite their biostratigraphic potential, and although Miocene and Pliocene sequences have been drilled successfully in the subpolar/polar North Atlantic and Arctic Ocean (Deep Sea Drilling Project [DSDP] Leg 38, Ocean Drilling Program [ODP] Legs 104, 105, 151, 162, and Integrated Ocean Drilling Program [IODP] Expedition 302), a consistent dinocyst biozonation for the Neogene is still not available.

The independent age calibration of dinocyst events is hampered partly by an incomplete chronostratigraphic framework of DSDP/ODP sites, as few holes have robust age control. First-order absolute age determinations using magnetic polarity reversals are often fragmentary due to incomplete core recovery and drilling disturbances caused by the technical difficulties of drilling at high latitudes. Where available, magnetostratigraphy is primarily supported by calcareous microfossil datums, but the paucity of biogenic carbonate in the high northern latitudes restricts their use and has relegated stable oxygen and carbon isotope stratigraphy to a subordinate role (Fronval and Jansen, 1996, Matthiessen et al., 2009a). In addition, the low evolutionary turnover of these calcareous microfossil groups at high latitudes reduces the number of bioevents, which themselves are not necessarily synchronous between high and low latitudes (Backman et al., 1984). These deficiencies are compounded by the susceptibility of foraminiferal tests and calcareous placoliths to dissolution in the colder waters of high northern latitude sites (e.g. Spiegler and Jansen, 1989).

Dinocysts are therefore crucial for high-latitude biostratigraphy, but to further enhance their utility it is necessary to study those sites with robust chronostratigraphy as a means of independently calibrating the dinocyst datums (De Schepper and Head, 2008). ODP Hole 907A in the Iceland Sea (Fig. 1) is at one of few high northern latitude sites featuring a comparatively well-constrained magnetic polarity stratigraphy for the Middle and Upper Miocene (Channell et al., 1999a), in this case supported independently by silicoflagellate biostratigraphy (Amigo, 1999). Located today under the influence of cold water-masses exported from the Arctic Ocean, Hole 907A serves as a reference section for biostratigraphic correlation in the polar environments.

For these reasons the Middle Miocene to Pliocene interval of Hole 907A has been selected for a detailed palynostratigraphic study. We present a suite of biostratigraphically useful dinocyst and acritarch bioevents that are correlated for the first time in the Nordic Seas to the astronomically-tuned Neogene time scale (ATNTS 2004, Lourens et al., 2005), by using a revised magnetostratigraphy for Hole 907A (Channell et al., 1999a).

To identify those bioevents in Hole 907A that potentially extend biostratigraphic correlation into the high northern latitudes, we have compared the timing of our events with the published records of lower-latitude sites having independent age control. The most important of these sites are in the North Atlantic region, but we also compare our data with records from the North Sea and Mediterranean Sea basins and the on- and offshore eastern U.S.A. to evaluate possible ecologically- or climatically-induced asynchronies.

Section snippets

Materials and methods

ODP Leg 151 Hole 907A was drilled in the southwestern part of the Norwegian–Greenland Sea, on the eastern Iceland Plateau (69°14.989′ N, 12°41.894′ W; 2035.7 m water depth; Fig. 1), which is a flat-topped platform defined by the 1800-m contour. The drill hole penetrated a horizontal, undisturbed, pelagic sequence and reached a total depth of 224.1 meters below sea floor (mbsf). The lithology consists of 216.3 m of sediment (recovery 102.6%) underlain by 8.7 m of basalts (recovery 60.2%) at the base

Chronostratigraphic summary of sites used for comparison

To test the biostratigraphic utility of bioevents calibrated in Hole 907A on a regional and supraregional scale, comparisons are made with the few relatively high-resolution Neogene palynostratigraphic studies from the North Atlantic region that have detailed and reliable magnetostratigraphy and/or independent biostratigraphy (Fig. 1). The age assignments of bioevents in the older literature have been revised where new chronostratigraphic control is available, and all datums are calibrated to

Discussion

The appearance and disappearance datums of dinocyst species are rarely precisely synchronous worldwide (e.g. Williams et al., 2004), especially in the late Cenozoic owing to increasing latitudinal temperature gradients. Nonetheless, De Schepper and Head (2008) recently compared mid-Pliocene through Pleistocene dinocyst events across the North Atlantic and, despite evident latitudinal control on the stratigraphic ranges of many species, they identified several bioevents suitable for

Conclusions

Based on the palynological analyses of 120 samples spanning the interval c. 14.5–2.5 Ma in ODP Hole 907A at c. 100 kyr temporal resolution, a magnetostratigraphic calibration of 26 potentially useful dinocyst and acritarch bioevents has been conducted for the first time in the Miocene and Pliocene of the high northern latitudes. Most events are last appearances and reflect a progressive extinction of species in response to long-term cooling from the Middle Miocene towards the intensification of

Systematic paleontology

Division DINOFLAGELLATA (Butschli, 1885) Fensome et al., 1993

Subdivision DINOKARYOTA Fensome et al., 1993

Class DINOPHYCEAE Pascher, 1914

Subclass PERIDINIPHYCIDAE Fensome et al., 1993

Order GONYAULACALES Taylor, 1980

Suborder GONYAULACINEAE (Autonym)

Family GONYAULACACEAE Lindemann, 1928

Subfamily GONYAULACOIDEAE (Autonym)

Genus IMPAGIDINIUM Stover and Evitt, 1978

Type: Impagidinium dispertitum (Cookson and Eisenack, 1965) Stover and Evitt, 1978

Impagidinium elongatum sp. nov. (Plate II, 6–20; Fig. 6,

Acknowledgments

This research uses samples and data provided by DSDP and ODP and we thank Walter Hale and Alex Wülbers for technical support while sampling at the IODP Core Repository, Bremen. We are grateful to Morten Smelror who shared unpublished data, and Stijn De Schepper for comments on an earlier draft of this manuscript. Support was provided by the German Research Foundation (DFG MA 3913/2) to J.M. and M.S., and a Natural Sciences and Engineering Research Council of Canada Discovery Grant to M.J.H.

References (128)

  • S. Piasecki et al.

    Lower Pliocene dinoflagellate cysts from cored Utsira Formation in the Viking Graben, northern North Sea

    Marine and Petroleum Geology

    (2002)
  • H.A. Abels et al.

    Long-period orbital control on middle Miocene global cooling: integrated stratigraphy and astronomical tuning of the Blue Clay Formation on Malta

    Paleoceanography

    (2005)
  • G. Alberti

    Zur Kenntnis mesozoischer and alttertiärer Dinoflagellaten und Hystrichosphaerideen von Nord- und Mitteldeutschland sowie einigen anderen europäischen Gebieten

    Palaeontographica Abteilung A

    (1961)
  • A.E. Amigo

    Miocene silicoflagellate stratigraphy: Iceland and Rockall Plateaus

    Proceedings of the Ocean Drilling Program, Scientific Results

    (1999)
  • Anstey, C.E., 1992. Biostratigraphic and paleoenvironmental interpretation of upper middle Miocene through lower...
  • M.P. Aubry

    Neogene allostratigraphy and depositional history of the De Soto Canyon area, northern Gulf of Mexico

    Micropaleontology

    (1993)
  • J. Backman

    Cenozoic calcareous nannofossil biostratigraphy from the north-eastern Atlantic Ocean - Deep Sea Drilling Project Leg 81

  • J. Backman et al.

    Biostratigraphy of Leg 81 sediments—a high latitude record

  • P.N. Benedek et al.

    Dinoflagellate cysts from the middle and upper Oligocene of Tönisberg (Niederrheingebiet): a morphological and taxonomical restudy

    Nova Hedwigia

    (1981)
  • U. Bleil

    Magnetostratigraphy of Neogene and Quaternary sediment series from the Norwegian Sea: Ocean Drilling Program, Leg 104

    Proceedings of the Ocean Drilling Program, Scientific Results

    (1989)
  • S. Brown et al.

    Dinoflagellate cyst stratigraphy of Paleocene to Miocene sediments from the Goban Spur (Sites 548–550, Leg 80)

  • J.P. Bujak et al.

    Neogene dinoflagellate cysts from the Hunt Dome KOPANOAR M-13 Well, Beaufort Sea, Canada

    Bulletin of Canadian Petroleum Geology

    (1981)
  • J.P. Bujak et al.

    Late Cenozoic dinoflagellate cyst zonation in the western and northern Pacific

  • G. Canninga et al.

    Late Cenozoic magnetostratigraphy of Deep Sea Drilling Project Hole 603C, Leg 93, on the North American continental rise off Cape Hatteras

  • J.E.T. Channell et al.

    Magnetic stratigraphy at Sites 907 and 985 in the Norwegian–Greenland Sea and a revision of the Site 907 composite section

    Proceedings of the Ocean Drilling Program, Scientific Results

    (1999)
  • J.E.T. Channell et al.

    Age models for glacial fan deposits off East Greenland and Svalbard (Sites 986 and 987)

    Proceedings of the Ocean Drilling Program, Scientific Results

    (1999)
  • B. Clement et al.

    Magnetostratigraphy of Leg 94 sediments

  • L.I. Costa et al.

    Cenozoic dinocyst stratigraphy of Sites 403 to 406 (Rockall Plateau) IPOD, Leg 48

  • L.L. Davis et al.

    The petrology and 40Ar/39Ar age of tholeiitic basalt recovered from Hole 907A, Iceland Plateau

    Proceedings of the Ocean Drilling Program, Scientific Results

    (1996)
  • E. de Kaenel et al.

    Oligocene–Miocene calcareous nannofossil biostratigraphy and paleoecology from the Iberia Abyssal Plain

    Proceedings of the Ocean Drilling Program, Scientific Results

    (1996)
  • S. De Schepper et al.

    Age calibration of dinoflagellate cyst and acritarch events in the Pliocene–Pleistocene of the eastern North Atlantic (DSDP Hole 610A)

    Stratigraphy

    (2008)
  • S. De Schepper et al.

    Pliocene dinoflagellate cyst stratigraphy, palaeoecology and sequence stratigraphy of the Tunnel-Canal Dock, Belgium

    Geological Magazine

    (2008)
  • A. de Vernal et al.

    Pliocene and Pleistocene palynostratigraphy at ODP Sites 646 and 647, eastern and southern Labrador Sea

    Proceedings of the Ocean Drilling Program, Scientific Results

    (1989)
  • L. de Verteuil

    Data report: Upper Cenozoic dinoflagellate cysts from the continental slope and rise off New Jersey

    Proceedings of the Ocean Drilling Program, Scientific Results

    (1996)
  • L. de Verteuil

    Palynological delineation and regional correlation of Lower through Upper Miocene sequences in the Cape May and Atlantic City boreholes, New Jersey coastal plain

    Proceedings of the Ocean Drilling Program, Scientific Results

    (1997)
  • L. de Verteuil et al.

    Miocene dinoflagellate stratigraphy and systematics of Maryland and Virginia

    Micropaleontology

    (1996)
  • G.P. Eberli et al.

    A synopsis of the Bahamas Drilling Project: results from two deep core borings drilled on the Great Bahamas Bank

    Proceedings of the Ocean Drilling Program, Initial Reports

    (1997)
  • L.E. Edwards

    Miocene dinocysts from Deep Sea Drilling Project Leg 81, Rockall Plateau, eastern North Atlantic

  • M. Ellegaard et al.

    Cyst–theca relationship, life cycle, and effects of temperature and salinity on the cyst morphology of Gonyaulax baltica sp. nov. (Dinophyceae) from the Baltic Sea area

    Journal of Phycology

    (2002)
  • E.R. Engel

    Palynologische Evidenz klimarelevanter Ereignisse in miozänen Sedimenten des Nordatlantiks

    Geologisches Jahrbuch A

    (1992)
  • Expedition 302 Scientists

    Sites M0001–M0004

    Proceedings of the Integrated Ocean Drilling Program

    (2006)
  • R.A. Fensome et al.

    The Lentin and Williams index of fossil dinoflagellates

    (2004)
  • M. Frank et al.

    Beryllium isotopes in central Arctic Ocean sediments over the past 12.3 million years: stratigraphic and paleoclimatic implications

    Paleoceanography

    (2008)
  • T. Fronval et al.

    Late Neogene paleoclimates and paleoceanography in the Iceland–Norwegian Sea: evidence from the Iceland and Vøring Plateaus

    Proceedings of the Ocean Drilling Program, Scientific Results

    (1996)
  • S. Gartner et al.

    Aspects of calcareous nannofossil biostratigraphy and abundance in the Pliocene and Late Miocene of Site 905

    Proceedings of the Ocean Drilling Program, Scientific Results

    (1996)
  • R.M. Goll

    A synthesis of Norwegian Sea biostratigraphies: ODP Leg 104 on the Vøring Plateau

    Proceedings of the Ocean Drilling Program, Scientific Results

    (1989)
  • R.M. Goll et al.

    A new radiolarian biostratigraphy for the Neogene of the Norwegian Sea: ODP Leg 104

    Proceedings of the Ocean Drilling Program, Scientific Results

    (1989)
  • E.A. Hailwood

    Paleomagnetism of late Mesozoic to Holocene sediments from the Bay of Biscay and Rockall Plateau, drilled on IPOD Leg 48

  • R. Harland

    Dinoflagellate biostratigraphy of Neogene and Quaternary sediments at Holes 400/400A in the Bay of Biscay (Deep Sea Drilling Project Leg 48)

  • M.J. Head

    Dinoflagellates, sporomorphs, and other palynomorphs from the Upper Pliocene St. Erth Beds of Cornwall, southwestern England

    Journal of Paleontology

    (1993)
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