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 />
Orbigny), Bulim<strong>in</strong>a ovulum Reuss, Ool<strong>in</strong>a apiculata Reuss, Globorotalites<br />
michel<strong>in</strong>ianus (d , Orbigny), Ammodiscus <strong>cretaceous</strong> (Reuss), A. pruvianus,<br />
Marsonella oxycona (Reuss), Dorothia smokynensis Wall, D. retusa, D.<br />
rosetta, Textularia astutia. Lalicker, Spiroplectam<strong>in</strong>a israelskyi Hillebr<strong>and</strong>t, S.<br />
laevis. (Roemer), Gyroid<strong>in</strong>a girardana (Reuss), Gyroid<strong>in</strong>oides globosus.<br />
(Hagenow), Gaudryna pyramidata. Cushman, Clavul<strong>in</strong>oides globulifera.Ten Dam<br />
&Sigal, Conicospiril<strong>in</strong>a sp. Rotalia sp. Valvulamm<strong>in</strong>a sp. Omphalocyclus<br />
macroporus (Lamark), Orbitoides medius (d Archiac), O. tissoti Shlumberger, O.<br />
apiculatus Shlumberger, Lepidorbitioides socialis (Leymerie), Siderolites sp.<br />
L<strong>of</strong>tusia elongata Brady, L. morgani Douville, L. persica Brady, L. m<strong>in</strong>or Cox , L.<br />
coxi Henson, L. sp.These assemblages <strong>of</strong> benthonic foram<strong>in</strong>ifera <strong>in</strong> addition to<br />
macr<strong>of</strong>ossils like ech<strong>in</strong>oides, gastropods, cephalopods, brachiopods, corals <strong>and</strong><br />
pelecypods (coral like rudistids ),<strong>in</strong>dicate the fundamental variation <strong>in</strong> lithology<br />
<strong>and</strong> Faunal assemblages from Tanjero clastics to the <strong>in</strong>terf<strong>in</strong>ger<strong>in</strong>g <strong>in</strong>terval <strong>of</strong><br />
Aqra Limestone represents quite graditional change to reefal facies, probably<br />
formed due to the presence <strong>of</strong> submerged high with<strong>in</strong> the Tanjero forel<strong>and</strong><br />
bas<strong>in</strong> at the end <strong>of</strong> the Maastrichtian resulted from the term<strong>in</strong>ation <strong>of</strong><br />
Paraxysmal phases <strong>of</strong> Laramide orogeny. ( Lawa et al.,1998, Al Omari et al.,<br />
1989, Al Mutwali <strong>and</strong> Abawi, 2005)<br />
The age estimation <strong>of</strong> this biozone by (Li <strong>and</strong> Keller, 1998a), records the<br />
time span between (68.33 Ma) to (66.83 Ma) (1500 KY) estimat<strong>in</strong>g absolute<br />
ages based on magnetochron ages with (62 ky/m) low rate <strong>of</strong> deposition <strong>in</strong> Gali<br />
section, (13, 5 ky/m) high rate sedimentation <strong>in</strong> Sirwan area. (18 ky/m) high rate<br />
<strong>of</strong> deposition <strong>in</strong> Qulka section Dokan area. (Figs. 3.10 -3.11).<br />
Age: Early Late Maastrichtian.<br />
3.2.1.6- Pseudoguembel<strong>in</strong>a hariaensis Interval Zone (CF3)<br />
The Pseudoguembel<strong>in</strong>a hariaensis zone was def<strong>in</strong>ed by Li <strong>and</strong> Killer, (1998a)<br />
as a partial range <strong>of</strong> the nom<strong>in</strong>ate species between the FAD <strong>of</strong><br />
Pseudoguembel<strong>in</strong>a hariaensis Nederbragt <strong>and</strong> the LAD <strong>of</strong> Gansser<strong>in</strong>a gansseri<br />
(Bolli). In the studied area this zone also marked by the FAD <strong>of</strong> the nom<strong>in</strong>ate<br />
species to the last occurrence <strong>of</strong> Gansser<strong>in</strong>a gansseri (Bolli). (Plate 16; Fig. 6).It<br />
is covers the <strong>in</strong>tervals <strong>of</strong> (21)meter <strong>in</strong> Gali section, (23) meters <strong>in</strong> Qulka section<br />
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