biostratigraphy and paleoecology of cretaceous/tertiary boundary in ...
biostratigraphy and paleoecology of cretaceous/tertiary boundary in ...
biostratigraphy and paleoecology of cretaceous/tertiary boundary in ...
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Chapter Three Biostratigraphy<br />
(kiko<strong>in</strong>e), Racemiguembel<strong>in</strong>a fructicosa (Egger), Pseudoguembel<strong>in</strong>a hariaensis<br />
Nederbragt, P. palpebra, P. excolata (Cushman), Hedbergella monmothensis<br />
(Olsson), H. holmdelensis Olsson, Gubler<strong>in</strong>a cuvillieri Kiko<strong>in</strong>e, Gumbelitria<br />
cretacea Cushman.<br />
As def<strong>in</strong>ed above, the present zone (CF2) <strong>of</strong> studied area is equivalent to the<br />
same zone <strong>of</strong> the P. palpebra Zone <strong>of</strong> South Atlantic DSDP Site 525A (Li &<br />
Keller, 1998a), (Abramovich et al.,2002); <strong>and</strong> Tunisia (Li & Keller, 1998b),<br />
(Arenillas et al.,2000); eastern Tethys (Keller, 2004), the present P. palpebra<br />
Zone is equivalent to the upper part <strong>of</strong> Abathomphalus mayaroensis Zone<br />
recorded from different parts <strong>of</strong> the world (Premoli Silva & Sliter, 1995 & 1999),<br />
(Mol<strong>in</strong>a et al., 1996) Canudo et al., 1991); from Spa<strong>in</strong>; Premoli Silva et al.,1998<br />
eastern Mediterranean; (Robaszynski et al., 1984; Caron, 1985), general;<br />
(Maestas et al., 2003), USA California; <strong>and</strong> Egypt (Obaidalla, 2005; Samir 2002;<br />
Elnady &Shah<strong>in</strong>, 2001; Lun<strong>in</strong>g et al.,1998). The present P. palpebra Zone is<br />
equivalent to the upper part <strong>of</strong> Abathomphalus mayaroensis Zone recorded from<br />
different localities from Iraq, (Al-Mutwali <strong>and</strong> Al Juboury, 2005; Al-Mutwali, 1996;<br />
Hammoudi, 2000; Abawi et al., 1982; Abdel-Kireem, 1986; Kassab, 1972, 1974,<br />
1975, 1976, 1979, <strong>and</strong> Kassab et al., 1986) (Figs 3.10 -12)<br />
The age estimation <strong>of</strong> this biozone by (Li <strong>and</strong> Keller, 1998a), records the<br />
Upper Late Maastrichtian, with the time span <strong>of</strong> (65.45Ma) to (65.30Ma)<br />
estimat<strong>in</strong>g absolute ages based on magnetochron ages. (150 Ky) estimat<strong>in</strong>g<br />
absolute ages based on magnetochron ages with (6 ky/m) high rate <strong>of</strong><br />
deposition <strong>in</strong> Gali section. (17 ky/m) high rate <strong>of</strong> deposition <strong>in</strong> Qulka section<br />
Dokan area.(6 ky/m) high rate <strong>of</strong> sedimentation <strong>in</strong> Sirwan valley. (Figs. 3.12 -14)<br />
Age: Upper Late Maastrichtian.<br />
3.2.1.8- Plummerita hantken<strong>in</strong>oides Total Range Zone (CF 1)<br />
The biostratigraphic <strong>in</strong>terval <strong>of</strong> this zone def<strong>in</strong>ed by the total range <strong>of</strong> the<br />
nom<strong>in</strong>ate taxon, Plummerita hantken<strong>in</strong>oides (Bronnimann). Pardo et al. (1996)<br />
<strong>in</strong>troduced the P. hantken<strong>in</strong>oides Zone for the latest Maastrichtian <strong>of</strong> Spa<strong>in</strong>. It<br />
marks the uppermost Cretaceous biozones. As its top marks the K/P <strong>boundary</strong>.<br />
The upper limit <strong>of</strong> this zone co<strong>in</strong>cides with the mass ext<strong>in</strong>ction <strong>of</strong> large tropical--<br />
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