Abstract
"Calcareous nannofossils" form a heterogeneous group of minute calcareous
objects that range in size from 1 to 30 microns. The majority of the fossils
resemble the coccoliths of the exterior calcareous cover (coccosphere) of the
Haptophyceae and therefore it is generally accepted that these fossils are remains
of such unicellular algae.
Reviews of basic information
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about the calcareous nannofossils have been
published by Hay (1977), Gartner (1977), Haq (1978), Tappan (1980) and
Lord and Taylor (1982).
The recognition of the calcareous nannofossils as a worthwhile tool for
biostratigraphic correlations is generally credited to Bramlette and his coworkers
Riedel, Sullivan, Martini and Wilcoxon (1954-1967). Following
these pioneering efforts, intensive taxonomic and biostratigraphic studies of
calcareous nannofossils have been carried out, and these have formed the
basis for several biozonal schemes of the Mesozoic and the Cenozoic Systems.
The Cenozoic zonations are far more refined than the Mesozoic ones,
mainly owing to the great number of Cenozoic sections with well-preserved
nannofossil content obtained by the coring of deep ocean sediments. The
two comprehensive zonations of the Cenozoic most frequently used are the
compilations of Martini (1971) and of Bukry (1971,1975). Although both
zonal schemes have so far provided a good working basis for biostratigraphic
correlations, they are not applicable everywhere. The Neogene of the Mediterranean
area has proved especially hard to calibrate with the standard
Zonations of the open oceans.
Our biostratigraphic investigation was concentrated on Miocene Mediterranean
sections, firstly because numerous land sections and cores of this interval
were either available in the Utrecht collections or easily accessible, and
secondly because the "standard" Miocene zonations were inadequate for
biostratigraphic correlations in the Mediterranean region.
As most of the Mediterranean sections were fragmentary, a large number
of sections were studied in order to cover the Miocene interval completely
and to check the reproducibility of our initial biostratigraphic results. This study led to the composition of a new "Mediterranean Miocene Zonation"
(fig. 44).
The applicability of our biostratigraphic data from the Mediterranean sections
was checked on some DSDP cores and land sections in extra-Mediterranean
areas. The use of our new markers in combination with the conventional
ones that we found in these sections resulted in a more refined general
biozonal scheme: the "Integrated Miocene Zonation" (fig. 45).
A large amount of taxonomic information was gathered during the progress
of our investigation. of all the taxa encountered we chose to make a
thorough revision of the taxonomy of two major groups, namely the helicoliths
and the discoasters. As a basis for this revision we used our new findings
concerning the ultrastructure of the nannoliths of these groups (chapters
4 and 5). Both groups were chosen because of their rich and diverse representation
in our Miocene samples. In order to complete our knowledge about
these nannofossil groups and to reconstruct "evolutional patterns" we expanded
our study by incorporating data from several pre-Miocene and postMiocene
sections and samples (fig. 2).
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