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Kaminski, Michael Anthony; Gradstein, Felix M; Berggren, William A (1989): Estimated chronologic ages of benthic microfossil events in ODP Site 105-647 (Table 1) [dataset]. PANGAEA, https://doi.org/10.1594/PANGAEA.745254, Supplement to: Kaminski, MA et al. (1989): Paleogene benthic foraminifer biostratigraphy and paleoecology at Site 647, southern Labrador Sea. In: Srivastava, SP; Arthur, M; Clement, B; et al. (eds.), Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 105, 705-730, https://doi.org/10.2973/odp.proc.sr.105.124.1989

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Abstract:
Benthic foraminifers were examined from the Paleogene of Ocean Drilling Program (ODP) Site 647 and Deep Sea Drilling Program (DSDP) Site 112 in the southern Labrador Sea. The Paleogene sequence of the deep Labrador Sea can be subdivided into seven assemblages, based on the ranges and relative abundance of characteristic taxa. The first occurrences (FOs) and last occurrences (LOs) of important benthic taxa are calibrated to a standard biochronology, by interpolating from our age model for Site 647. The biostratigraphy of Site 647 is used to improve the age estimates of Site112 cores. Fifteen microfossil events in Site 647 also are found in the sedimentary wedge along the Labrador Margin. A comparison of the probabilistic microfossil sequence from the Labrador Margin with that at Site 647 yields four isochronous benthic foraminifer LOs. Two new species are described from Sites 647 and 112: Hyperammina kenmilleri, Kaminski n.sp., and Ammodiscus nagyi Kaminski n.sp.
Significant faunal turnovers are observed at the Ypresian/Lutetian and Eocene/Oligocene boundaries. The Ypresian/Lutetian boundary is characterized by a Glomospira-facies and is attributed to a rise in the CCD (carbonate compensation depth) associated with the NP14 lowstand in sea level. The Eocene/Oligocene boundary is delimited by the LO of Spiroplectammina spectabilis and Reticulophragmium amplectens. The change from an Eocene agglutinated assemblageto a predominantly calcareous assemblage in the early Oligocene took place gradually, over a period of about 4 Ma, but the rate of change accelerated near the boundary. This faunal turnover is attributed to changes in the preservationof agglutinated foraminifers, as delicate species disappeared first. Increasingly poorer preservation of agglutinated foraminifers in the late Eocene to earliest Oligocene reflects the first appearance of cool, nutrient-poor deep water in the southern Labrador Sea. The approximately coeval disappearance of agglutinated assemblages along the Labrador Margin was caused by a regional trend from slope to shelf environments, accentuated by the 'mid'-Oligocene lowstand in sea level.
Project(s):
Coverage:
Latitude: 53.331300 * Longitude: -45.262000
Date/Time Start: 1985-10-15T00:00:00 * Date/Time End: 1985-10-25T00:00:00
Minimum DEPTH, sediment/rock: 155.9 m * Maximum DEPTH, sediment/rock: 657.5 m
Event(s):
105-647 * Latitude: 53.331300 * Longitude: -45.262000 * Date/Time Start: 1985-10-15T00:00:00 * Date/Time End: 1985-10-25T00:00:00 * Elevation: -3870.0 m * Penetration: 839.3 m * Recovery: 537.8 m * Location: South Atlantic Ocean * Campaign: Leg105 * Basis: Joides Resolution * Method/Device: Composite Core (COMPCORE) * Comment: 86 cores; 819.9 m cored; 0 m drilled; 65.6% recovery
Comment:
Based on the age model used for the sedimentation-rate curve (Srivastava, Arthur, et al., 1987, doi:10.2973/odp.proc.ir.105.1987)
Parameter(s):
#NameShort NameUnitPrincipal InvestigatorMethod/DeviceComment
Ageprofile Datum DescriptionAgeprof dat desKaminski, Michael AnthonyFO = first occurrence, LO = last occurrence
DEPTH, sediment/rockDepth sedmGeocode
Age modelAge modelkaKaminski, Michael Anthony
Age, minimum/youngAge minkaKaminski, Michael Anthony
Age, maximum/oldAge maxkaKaminski, Michael Anthony
Size:
101 data points

Data

Download dataset as tab-delimited text — use the following character encoding:


Ageprof dat des

Depth sed [m]

Age model [ka]

Age min [ka]

Age max [ka]
LO Turrilina alsatica155.931000
LO Bathysiphon sp.251.235500
LO Glomospira charoides251.135500
LO Ammodiscus latus251.135500
LO Nuttallides umbonifera262.735800
LO Ammodiscus cretaceous280.536300
LO Osangularia mexicana280.536300
LO Gavelinella micra280.536300
LO Bolivina huneri281.436400
LO Glomospira irregularis285.036500
LO Recurvoides spp.290.336600
LO Reticulophragmium amplectens290.336600
LO Spiroplectammina spectabilis290.336600
LO Ammolagena clavata290.336600
LO Trochammina deformis290.336600
LO Ammobaculites aff. polythalamus290.336600
LO Subreophax scalaria290.336600
LO Saccammina complanata290.836600
LO Glomospira serpens290.836600
LO Trochamminoides irregularis290.836600
LO Rhizammina spp.300.336900
LO Haplophragmoides walteri300.336900
LO Reophax pilulifer318.037400
LO Gavelinella capitata318.037400
LO Cibicidoides grimsdalei328.437600
LO Hyperammina kenmilleri n.sp.329.937700
LO Bulimina macilenta329.937700
LO Karreriella coniformis331.437700
LO Bigenerina sp.331.437700
LO Reophax guttifer339.238000
LO Ammosphaeroidina sp.340.738000
LO Reticulophragmium placenta350.638300
LO Hormosina distans360.338600
LO Glomospira gordialis360.338600
LO Nuttallides truempyi386.039200
LO Karreriella con versa405.839800
FO Spiroplectammina cubensis408.839900
FO Spirosigmoilinella compressa425.840400
LO Spiroplectammina spectabilis perplexa434.440600
LO Spiroplectammina navarroana460.341300
FO Ammodiscus nagyi n.sp.498.342400
LO Aragonia spp.540.043500
LO Cibicidoides subspiratus569.144300
FO Ammodiscus latus578.844600
LO Verneuilinoides polystrophus578.844600
LO Dendrophrya ex gr. excelsa620.7488000526000
LO Hormosina ovulum627.2488000526000
LO Abyssammina spp.638.6526000536000
LO Quadrimorphina profunda657.554200