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| | part = Predicting the occurrence of oil and gas traps | | | part = Predicting the occurrence of oil and gas traps |
| | chapter = Applied paleontology | | | chapter = Applied paleontology |
− | | frompg = 17-1 | + | | frompg = 17-31 |
− | | topg = 17-65 | + | | topg = 17-35 |
| | author = Robert L. Fleisher, H. Richard Lane | | | author = Robert L. Fleisher, H. Richard Lane |
| | link = http://archives.datapages.com/data/specpubs/beaumont/ch17/ch17.htm | | | link = http://archives.datapages.com/data/specpubs/beaumont/ch17/ch17.htm |
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| ==Examples of data interpretation== | | ==Examples of data interpretation== |
− | Traverse<ref name=ch17r87>Traverse, A., 1988, Palaeopalynology: London, Unwin Hyman, 600 p.</ref> provides a general review of the methods of palynological paleoenvironmental analysis. He discusses the use of palynomorphs as paleoclimate indicators and the methods by which sedimentation of palynomorph assemblages help infer depositional environments in both marine and nonmarine settings. Additionally, Lipps<ref name=ch17r57>Lipps, J., H., ed., 1993, Fossil Prokaryotes and Protists: London, Blackwell Scientific, 342 p.</ref> provides a similar general review of paleoenvironmental approaches for micro[[paleontology]]. Following are three examples of paleoenvironmental information deduced from micropaleontology.
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| [[file:applied-paleontology_fig17-17.png|left|300px|thumb|{{figure number|1}}Biofacies associations reflect different and distinctive populations liv- ing in different paleoenvironments. Copyright: Lagoe;<ref name=ch17r54 /> courtesy Palaios.]] | | [[file:applied-paleontology_fig17-17.png|left|300px|thumb|{{figure number|1}}Biofacies associations reflect different and distinctive populations liv- ing in different paleoenvironments. Copyright: Lagoe;<ref name=ch17r54 /> courtesy Palaios.]] |
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| + | Traverse<ref name=ch17r87>Traverse, A., 1988, Palaeopalynology: London, Unwin Hyman, 600 p.</ref> provides a general review of the methods of palynological paleoenvironmental analysis. He discusses the use of palynomorphs as paleoclimate indicators and the methods by which sedimentation of palynomorph assemblages help infer depositional environments in both marine and nonmarine settings. Additionally, Lipps<ref name=ch17r57>Lipps, J. H., ed., 1993, Fossil Prokaryotes and Protists: London, Blackwell Scientific, 342 p.</ref> provides a similar general review of paleoenvironmental approaches for micro[[paleontology]]. Following are three examples of paleoenvironmental information deduced from micropaleontology. |
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| ==Species distribution and oxygen concentration== | | ==Species distribution and oxygen concentration== |
− | Lagoe<ref name=ch17r54>Lagoe, M. B., 1987, The stratigraphic record of sea-level and climatic fluctuations in an active-margin basin: the Stevens Sandstone, Coles Levee area, California: Palaios, vol. 2, no. 1, p. 48–68., 10., 2307/3514572</ref> recognizes four [[Fossil assemblage|biofacies]] of benthic foraminiferal species in the upper Miocene [[Stevens Sandstone]] of the southern [[San Joaquin Valley]]. He demonstrates that the biofacies distribution was largely controlled by changes in oxygen concentration caused by fluctuations in the position and intensity of low-oxygen water within the oxygen minimum zone. | + | Lagoe<ref name=ch17r54>Lagoe, M. B., 1987, The stratigraphic record of sea-level and climatic fluctuations in an active-margin basin: the Stevens Sandstone, Coles Levee area, California: Palaios, vol. 2, no. 1, p. 48–68., 10., 2307/3514572</ref> recognizes four [[Fossil assemblage|biofacies]] of [[benthic]] foraminiferal species in the upper Miocene [[Stevens Sandstone]] of the southern [[San Joaquin Valley]]. He demonstrates that the biofacies distribution was largely controlled by changes in oxygen concentration caused by fluctuations in the position and intensity of low-oxygen water within the oxygen minimum zone. |
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| In [[:file:applied-paleontology_fig17-17.png|Figure 1]], biofacies associations reflect different and distinctive populations living in different paleoenvironments. Biofacies are arranged from left to right in order of inferred increasing oxygen concentration. The stratigraphic distribution strongly suggests systematic shifts in oxygen concentration. | | In [[:file:applied-paleontology_fig17-17.png|Figure 1]], biofacies associations reflect different and distinctive populations living in different paleoenvironments. Biofacies are arranged from left to right in order of inferred increasing oxygen concentration. The stratigraphic distribution strongly suggests systematic shifts in oxygen concentration. |
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| [[file:applied-paleontology_fig17-18.png|300px|thumb|{{figure number|2}}Species inhabiting high-oxygen environments (e.g., shelf depth) are small, prolate forms; those in low-oxygen environments (e.g., basin depths) are large, lanceolate forms. Copyright: Douglas;<ref name=ch17r33 /> courtesy SEPM.]] | | [[file:applied-paleontology_fig17-18.png|300px|thumb|{{figure number|2}}Species inhabiting high-oxygen environments (e.g., shelf depth) are small, prolate forms; those in low-oxygen environments (e.g., basin depths) are large, lanceolate forms. Copyright: Douglas;<ref name=ch17r33 /> courtesy SEPM.]] |
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− | Test morphologies of some closely related species of the foraminiferal genus ''Bolivina'' differ in patterns apparently related to oxygen concentration<ref name=ch17r33>Douglas, R., G., 1979, Benthic foraminiferal ecology and paleoecology: a review of concepts and methods, in Lipps, J., H., ed., Foraminiferal Ecology and Paleoecology: SEPM Short Course 6, p. 21–53.</ref><ref name=ch17r34>Douglas, R., G., 1981, Paleoecology of continental margin basins: a modern case history from the borderland of southern California, in Depositional Systems of Active Continental Margin Basins: Pacific Section of Society of Economic Paleontologists and Mineralogists Short Course Notes, p. 121–156.</ref> in modern environments along the California continental margin. Compressed, relatively large species (''B. argentea'') are typical of low-oxygen environments. | + | Test morphologies of some closely related species of the foraminiferal genus ''Bolivina'' differ in patterns apparently related to oxygen concentration<ref name=ch17r33>Douglas, R., G., 1979, Benthic foraminiferal ecology and paleoecology: a review of concepts and methods, in Lipps, J., H., ed., Foraminiferal Ecology and Paleoecology: SEPM Short Course 6, p. 21–53.</ref><ref name=ch17r34>Douglas, R., G., 1981, Paleoecology of continental margin basins: a modern case history from the borderland of southern California, in Depositional Systems of Active Continental Margin Basins: Pacific Section of Society of Economic Paleontologists and Mineralogists Short Course Notes, p. 121–156.</ref> in modern environments along the California [[continental margin]]. Compressed, relatively large species (''B. argentea'') are typical of low-oxygen environments. |
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| In [[:file:applied-paleontology_fig17-18.png|Figure 2]], species inhabiting high-oxygen environments (e.g., shelf depth) are small, prolate forms; those in low-oxygen environments (e.g., basin depths) are large, lanceolate forms. | | In [[:file:applied-paleontology_fig17-18.png|Figure 2]], species inhabiting high-oxygen environments (e.g., shelf depth) are small, prolate forms; those in low-oxygen environments (e.g., basin depths) are large, lanceolate forms. |
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| Whittaker et al.<ref name=ch17r95>Whittaker, M. F., Giles, M. R., Cannon, S. J. C., 1992, Palynological review of the Brent Group, UK sector, North Sea, in Morton, A., C., Haszeldine, R., S., Giles, M., R., Brown, S., eds., Geology of the Brent Group: Geological Society Special Publication 61, p. 169–202.</ref> provide an industrial example in the [[Brent Group]] (Jurassic), [[North Sea]], in which the distribution of palynomorph types is used to infer the depositional environments and extent of delta [[Depocenter#Sediment_supply_rate_and_facies_patterns|progradation]] during brief intervals of the Jurassic. [[:file:applied-paleontology_fig17-19.png|Figure 3]] illustrates the nonmarine (fluvial and marsh), lagoon, barrier, and marine environments and the interpreted sediment transport direction (large arrow) during one time interval. This information can help identify regions of greater potential for fluvial reservoir sands. | | Whittaker et al.<ref name=ch17r95>Whittaker, M. F., Giles, M. R., Cannon, S. J. C., 1992, Palynological review of the Brent Group, UK sector, North Sea, in Morton, A., C., Haszeldine, R., S., Giles, M., R., Brown, S., eds., Geology of the Brent Group: Geological Society Special Publication 61, p. 169–202.</ref> provide an industrial example in the [[Brent Group]] (Jurassic), [[North Sea]], in which the distribution of palynomorph types is used to infer the depositional environments and extent of delta [[Depocenter#Sediment_supply_rate_and_facies_patterns|progradation]] during brief intervals of the Jurassic. [[:file:applied-paleontology_fig17-19.png|Figure 3]] illustrates the nonmarine (fluvial and marsh), lagoon, barrier, and marine environments and the interpreted sediment transport direction (large arrow) during one time interval. This information can help identify regions of greater potential for fluvial reservoir sands. |
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− | Oboh<ref name=ch17r67>Oboh, F. E., 1992, Multivariate statistical analysis of palyno debris from the Middle Miocene of the Niger Delta and their environmental significance: Palaios, vol. 7, p. 559–573., 10., 2307/3514869</ref> develops a paleoenvironmental model of Middle Miocene reservoir units from the Niger Delta, which uses palynomorphs and organic matter to interpret more precisely the depositional environments. This improves the understanding of the lateral continuity of the reservoir and its susceptibility to diagenetic changes. | + | Oboh<ref name=ch17r67>Oboh, F. E., 1992, Multivariate statistical analysis of palyno debris from the Middle Miocene of the Niger Delta and their environmental significance: Palaios, vol. 7, p. 559–573., 10., 2307/3514869</ref> develops a paleoenvironmental model of Middle Miocene reservoir units from the Niger Delta, which uses palynomorphs and organic matter to interpret more precisely the depositional environments. This improves the understanding of the [[lateral]] continuity of the reservoir and its susceptibility to diagenetic changes. |
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| ==Integrated paleoenvironmental interpretation== | | ==Integrated paleoenvironmental interpretation== |
− | [[:file:applied-paleontology_fig17-20.png|Figure 4]] shows an integrated paleoenvironmental interpretation of the E2.0 reservoir (Middle Miocene, [[Niger Delta]]). Lithofacies range from pebbly sandstones (S1) to mudstones (M2). The palynofacies are composed of the following substances: | + | [[:file:applied-paleontology_fig17-20.png|Figure 4]] shows an integrated paleoenvironmental interpretation of the E2.0 reservoir (Middle Miocene, [[Niger Delta]]). [[Lithofacies]] range from pebbly sandstones (S1) to mudstones (M2). The palynofacies are composed of the following substances: |
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| [[file:applied-paleontology_fig17-20.png|thumb|300px|{{figure number|4}}Integrated paleoenvironmental interpretation of the E2.0 reser- voir (Middle Miocene, Niger Delta). Copyright: Oboh;<ref name=ch17r67 /> courtesy Palaios.]] | | [[file:applied-paleontology_fig17-20.png|thumb|300px|{{figure number|4}}Integrated paleoenvironmental interpretation of the E2.0 reser- voir (Middle Miocene, Niger Delta). Copyright: Oboh;<ref name=ch17r67 /> courtesy Palaios.]] |
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| [[Category:Predicting the occurrence of oil and gas traps]] | | [[Category:Predicting the occurrence of oil and gas traps]] |
| [[Category:Applied paleontology]] | | [[Category:Applied paleontology]] |
| + | [[Category:Treatise Handbook 3]] |