首页> 外文期刊>Journal of African Earth Sciences >Integrated biostratigraphy, stage boundaries and Paleoclimatology of the Upper Cretaceous-Lower Eocene successions in Kharga and Dakhala Oases, Western Desert, Egypt
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Integrated biostratigraphy, stage boundaries and Paleoclimatology of the Upper Cretaceous-Lower Eocene successions in Kharga and Dakhala Oases, Western Desert, Egypt

机译:埃及西部沙漠喀尔加河和达哈拉绿洲上白垩统-下新世始新统统的生物地层学,阶段边界和古气候学

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摘要

The Upper Cretaceous-Lower Eocene succession in the studied sections is divided into four rock units that arranged from base to top: the Dakhla, Tarawan, Esna and the Thebes formations. Detailed study of the foraminifera and calcareous nannofossils has led to the recognition of 58 and 82 species, respectively. Based on planktonic foraminifera and calcareous nannofossils 8 planktonic foraminiferal biozones (CF4, P2, P3, P4, E1, E2, E3 and E4) have been recognized as well as 8 calcareous nannofossil biozones (CC25b, NP3, NP4, NP5, NP6, NP7/8, NP9, and NP10). At Gabal Teir/Tarawan section, Kharga Oasis, the Paleocene can be divided into three stages; Danian, Selandian and Thanetian. The Danian/Selandian boundary is placed at P3a/P3b zonal boundary (LO of Igo-rina albeari) which corresponds to the level of LO of Lithoptychius ulii, Fasciculithus pileatus, Fasciculithus involutus and Lithoptychius janii (upper part of Zone NP4). The Selandian/Thanetian boundary, on the other hand, can be traced within the foraminiferal Zone P4 (Globanomalina pseudomenardii Zone) and between the nannofossil zones NP6 and NP7/8 (LO of Discoaster mohleri). At Gabal Ghanima section, the Paleocene/Eocene boundary is located within the lower part of the Esna Formation. It can be traced at the base of planktonic foraminiferal Zone El (Los of Acarinina africana, A sibaiyaensis and Morozovella allinsoensis), and at the NP9a/NP9b subzonal boundary (LO of Rhomboaster spp). However, the lower Eocene succession seems to be condensed and punctuated by minor hiatus (absence of Subzone NP10a). The dominance of cool water nannofossil species in the late Maastrichtian and early Danian interval suggests a gradual decrease in the surface water paleotemperature. However, a slight warming condition prevailed around the Danian/Selandian transition as evidenced by the warm water nannofossil species. At the P/E boundary interval, the high abundance of warm-water taxa (e.g. Discoaster, Sphenolithus, Rhnmboaster, Tribrachiatus and Pontosphaera species) indicates a warm-water paleotemperatures.
机译:研究区的上白垩统-下始新统被划分为四个岩石单元,从底部到顶部依次排列:达赫拉,塔拉旺,埃斯纳和底比斯地层。对有孔虫和钙质纳米化石的详细研究分别导致了58种和82种的识别。基于浮游有孔虫和钙质纳米化石,已识别出8个浮游有孔虫生物区(CF4,P2,P3,P4,E1,E2,E3和E4)以及8个钙化纳米化石生物区(CC25b,NP3,NP4,NP5,NP6 / 8,NP9和NP10)。在喀尔加绿洲的加巴尔泰尔河/塔拉旺河段,古新世可分为三个阶段。 Danian,Selandian和Thanetian。 Danian / Selandian边界位于P3a / P3b地带边界(Igo-rina albeari的LO),对应于Lithoptychius ulii,Fasciculithus Pileatus,Fasciculithus involutus和Lithoptychius janii(NP4上部)的LO水平。另一方面,Selandian / Thanetian边界可以追溯到有孔虫区P4(球藻拟假单胞菌区)内以及纳米化石区NP6和NP7 / 8(Discoaster mohleri的LO)之间。在Gabal Ghanima段,古新世/始新世边界位于埃斯纳组的下部。它可以追溯到浮游有孔虫区El(非洲car螨,西贝亚虫和莫罗佐夫拉藻)的底部,以及NP9a / NP9b次区域边界(Rhomboaster spp的LO)。然而,较低的始新世演替似乎被较小的裂隙(不存在子区域NP10a)所压缩和打断。在马斯特里赫特晚期和大年纪早期,冷水纳米化石种类占主导地位,表明地表水古温度逐渐降低。然而,温水的纳米化石物种表明,在大年期/塞拉第期过渡附近普遍存在轻微的变暖条件。在P / E边界区间,暖水类群(例如Discoaster,Sphenolithus,Rhnmboaster,Tribrachiatus和Pontosphaera物种)数量很多,表示暖水古温度。

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