doi:10.1016/j.palaeo.2007.02.043
Copyright © 2007 Published by Elsevier B.V.
The Manumiella seelandica global spike: Cooling during regression at the close of the Maastrichtian
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Daniel Habiba,
,
and Farnosh Saeedib
aSchool of Earth and Environmental Sciences, Queens College of the City University of New York, Flushing, NY 11367, USA
bBronx Community College, Bronx, New York, USA
Received 18 February 2005;
accepted 14 February 2007.
Available online 16 June 2007.
Abstract
Manumiella seelandica (Lange 1969) Bujak and Davies 1983, emend. Firth 1987 occurs in great abundance, together with a closely related and possibly conspecific form, Isabelidinium? sp., virtually at the end of the Maastrichtian. The abundance of M. seelandica immediately adjacent the Cretaceous/Paleogene (KPg) boundary, and its global distribution, serve as an excellent biostratigraphic marker for dating it. The abundance spike is widely distributed in both Northern and Southern hemispheres, and ranges from locations as far south as Seymour Island, Antarctica to as far north as West Greenland. The global distribution of the M. seelandica spike in such widely separated areas, and the ease with which it is recognized in closely sampled sections, underscores its value in dating.
Until recently, this short-lived event was correlated within an interval of global sea level fall and regression which extended from the latest Maastrichtian into the earliest Danian; that is, that the species became numerically abundant as the shoreline approached. However, based on our study of the boundary interval at Bass River in southern New Jersey USA, we propose that an additional factor may have contributed to its origin. Our investigation of this section shows that there is a prominent abundance spike in the 20 cm (7.8 in.)-interval immediately beneath the boundary, and that this interval correlates precisely with the δ18O isotope evidence of cooling. At Bass River, the last 500 ky of the Maastrichtian was a period of global warmth, as revealed by geochemical evidence. However, based on the geochemical evidence, a mild cooling period began within tens of thousands of years of the close of the Cretaceous Period. Based on this correlation, we present the hypothesis that the cooling event played an important role in producing this global assemblage of dinoflagellates.
Study of a large number of fossils in the sample situated 15 cm (5.85 in.) beneath the boundary shows that there is considerable variation in overall form and archeopyle excystment in Manumiella seelandica. The same degree of variation was not observed in the samples with fewer specimens.
Keywords: Global distribution of Manumiella seelandica; Cretaceous-Paleocene boundary; Oxygen isotopes; Paleoclimate; Bass River spherule layer; Morphological variation in M. seelandica
Fig. 1. Location map of Bass River site in southern New Jersey, USA.
Fig. 2. Stratigraphic occurrences of Isabelidinium? sp. and Manumiella seelandica in the interval from 1275 ft to 1259.5 ft, compared with the δ18O distribution in the planktonic foraminifera Rugoglobigerina. Geochemical data after Olsson et al., 2002.
Fig. 3. Percentage (solid lines) and numerical abundance (dashed lines) of Manumiella seelandica, compared with the δ18O excursions and species index. Geochemical data after Olsson et al., 2002.
Fig. 4. Proportional distribution of terrigenous (inertinite) and marine (amorphous debris) detritus correlated against the dinoflagellate species index for the same interval.
Plate I.
- 1 Apparently excysted specimen. Pericystal 2a archeopyle and attached operculum bracketed by archeopyle sutures which extends down to the region of the cingulum. Plate 3a and attached precingular plate also extend downward. Apical series, containing the cylindrical horn, dehisces from intercalary series, exposing a relatively large archeopyle. Endocystal archeopyle evident. Six-sided endocystal Plate 2a in focus. Rectangle in lower right represents a length of 16 μm. Note the attached 2a operculum in the outermost periphragmal layer of the pericyst.
2 Specimen with standard pericystal 2a archeopyle and attached operculum. Pericystal apical series partially dehisced from intercalary series. Endocyst closed, and apparently not excysted. Rectangle 16 μm.
3 Scanning electron micrograph. Pericystal 2a archeopyle evident. Operculum attached to precingular plate and folded back. Endocystal archeopyle evident. Length of specimen (apex–antapex) 80 μm.
4 Scanning electron micrograph. Specimen with cylindrical apical horn and flattened antapex. Pericystal archeopyle evident and discrete intercalary endocystal plates. Length of specimen (apex–antapex) 93 μm.
Plate II.
- 1 Specimen with tapering apical horn, similar to the specimens illustrated by Firth (1987). Rectangle represents a length of 16 μm.
2 Isabelidinium ? sp. Specimen similar and possibly conspecific with M. seelandica, except that it possesses an elongate form in compression. The species ranges from the late Maastrichtian through the peak abundance of M. seelandica. It always occurs at less than 1% in the dinoflagellate assemblages. Rectangle 16 μm.
3 Scanning electron micrograph. Specimen with open pericystal 2a archeopyle exposing opercular pieces of open endocystal archeopyle. Length (apex–antapex) 90 μm.
4 Scanning electron micrograph. Folded specimen, but showing the tapering apical horn. Length (apex–antapex) 85 μm.
Table 1.
List of the samples that were studied in the interval from 1275 ft to 1255 ft in the Bass River stratigraphy

Table 2.
List of the five samples containing specimens of Manumiella seelandica


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