重新审视三叠纪的海平面上升变化

Q1 Earth and Planetary Sciences
GSA Today Pub Date : 2018-11-29 DOI:10.1130/GSATG381A.1
B. Haq
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The trend reverses again with a decline in the late Norian and the base level remaining close to the pdmsl, and then dipping further in the mid-Rhaetian to ~50 m below pdmsl into the latest Triassic and earliest Jurassic. Superimposed upon this long-term trend is the record of 22 widespread third-order sequence boundaries that have been identified, indicating sealevel falls of mostly minor (<25 m) to medium (25–75 m) amplitude. Only six of these falls are considered major, exceeding the amplitude of 75 m. The long interval of Triassic oceanic withdrawal is likely to have led to general scarcity of preserved marine record and large stratigraphic lacunae. Lacking evidence of continental ice sheets in the Triassic, glacio-eustasy as the driving mechanism for the third-order cyclicity can be ruled out. And even though transfer of water to and from land aquifers to the ocean as a potential cause is plausible for minor (a few tens of meters) sea-level falls, the process seems counter-intuitive for third-order events for much of the Triassic. Triassic paleoenvironmental scenarios demonstrate a close link between eustasy, climates, and biodiversity. INTRODUCTION The Triassic Period encompasses 50.5 m.y., spanning an interval from 251.9 to 201.4 Ma (Ogg et al., 2016). By this time, the megacontinent of Pangaea had already assembled, surrounded by the Panthalassa Ocean that covered >70% of Earth’s surface, and by the mid-Triassic the Pangaean landmass was almost evenly distributed in the two hemispheres around the paleo-equator (see Fig. S1 in the GSA Data Repository1). The interval from latest Permian through the earliest Jurassic, a time span of nearly 80 m.y., represents the longest spell of low seastands of the Phanerozoic. The Triassic is also bracketed by two major biotic extinctions near the Permian-Triassic (P-T) and Triassic-Jurassic boundaries, the one at P-T boundary being the most severe biotic turnover of the Phanerozoic (Raup and Sepkowski, 1982; Hallam and Wignall, 1997; McElwain et al., 1999). The Late Triassic experienced the beginning of the lithospheric swell, ushering the breakup of Pangaea and its eventual split into discrete continents in the later Mesozoic (see Fig. S1 [see footnote 1]). The definite signs of the beginning of Pangaean fragmentation were clearly manifest by the end of the Triassic with the basaltic outpouring of the massive Central Atlantic magmatic province (see, e.g., Marzoli et al., 1999, 2004; Davies et al., 2017). In the past two decades substantial new stratigraphic data from Triassic sections has come to light, and there have been significant refinements in time scales, making a review and revision of the Triassic sealevel variations timely. The documentation for the revised Triassic sea-level curve, though still largely from northwestern and central Europe (western Tethys), now also includes sections further east from other parts of the Tethys, such as the Arabian Platform, Pakistan, India, China, and Australia. From the boreal latitudes documentation includes sections from the Sverdrup Basin, Svalbard, and the Barents Sea. This paper serves to complete a review of the entire Mesozoic as both Cretaceous and Jurassic sea-level variations have already been reappraised (Haq, 2014, 2017). For a background of the paleoenvironmental conditions (oceans and climates) in the Triassic see the GSA data repository (see footnote 1). TRIASSIC TIME SCALE UPDATES A succinct discussion of the methodological advancements and modifications to the Triassic time scale can be found in Preto et al. (2010), and a detailed discussion of Triassic stratigraphy has been presented by Ogg et al. (2014). Since the last update of the Triassic third-order sea-level variations (Haq and Al-Qahtani, 2005) that was calibrated to an earlier version of the time scale, there have been several refinements to the Triassic chronostratigraphy. The latest version of the time scale (Ogg et al., 2016) modifies the boundaries of Triassic standard stages (ages) by anywhere between <1 m.y. to almost 6 m.y. Like earlier versions, the new time scale is mainly based on biostratigraphy, anchored by selected radiometric dates, with some intervals refined by astronomical and cyclostratigraphical fine-tuning, and others aided by magnetostratigraphy. Conodonts and ammonoids constitute the mainstay of the Triassic biostratigraphic correlations. Special problems concerning wider correlations using these fossil groups in the Triassic include taxonomic standardization, rarity of markers, potential diachroniety in conodontsʼ first and last appearance, and provinciality among ammonoids. Since much of the Pangaean landscape was dominated by terrestrial sediments, regional correlations often rely on palynology, ostracods and tetrapods that do not lend themselves to wider correlations with marine records. Ogg et al. (2016) ascribe a Bilal U. Haq, Smithsonian Institution, Washington, D.C., USA, and Sorbonne University, Paris, France composite error of between 0.2 and 0.59 m.y. for the stage boundaries in the Triassic depending on the type of data (see also the GSA data repository for further discussion of time scales [see footnote 1]). LARGE TIME GAPS IN THE RECORD OF THE MIDDLE AND LATE TRIASSIC? Even a cursory look at the most recent update of the Triassic time scale (Ogg et al., 2016) reveals its extreme lopsidedness: while the Early Triassic spans only 5.1 m.y. and the Middle Triassic increases to 9.1 m.y., the Late Triassic jumps to a substantial span of 35.6 m.y. Some unevenness is to be expected, but this extreme asymmetry is also witnessed in the time spans of the stages (ages) and biostratigraphic zones within the stages, as well the lengths of the sequence cycles and corresponding sealevel events that all increase in duration in the Middle to Late Triassic. If the above apparent chronostratigraphic asymmetry is real, then the large differences in the duration of fossil zones imply that evolutionary rates (as measured by appearance of new species/m.y.) were relatively rapid in the Early Triassic (thus the availability of a high-resolution biozonal subdivision), declining somewhat in the Middle Triassic, and slowing down to an extreme thereafter (characterized by a few long-duration biozones), especially in the later Late Triassic. However, the temporal lengths of sequence cycles (based on sedimentary facies shifts) do not have to follow the biotic evolutionary trends, and yet they do. Their long time spans (average of ~5 m.y./cycle in the Middle and Late Triassic) would imply a built-in bias in the record expressed as a lack of preserved marine stratigraphic record. This seems plausible in a scenario where the long-term trend of low seastands for the period means fewer marine records in favor of more terrestrial sedimentary records. This is exacerbated by mostly type-1 sequence boundaries (when the base line withdraws beyond the shelf edges) that may incorporate large erosional time gaps. Large temporal lacunae in the stratigraphic record could explain the potentially specious signal that comes across as slowdown in the biotic evolutionary rates, as well as the dearth of sequence cycles for the interval in question (i.e., Middle and Late Triassic). An oxygenisotopic record of the Triassic derived from Tethyan conodont apatite shows trends that duration = 0.77 m.y.), and expand for the remainder of the Carnian through Rhaetian interval (average ammonoid zonal duration = 2.43 m.y.). Using multiple overlapping criteria (i.e., several fossil groups), these uncertainties can sometimes be narrowed. The long-term sea-level envelope for the Triassic is similar to those shown in Haq et al. (1987, 1988) and Hardenbol et al. (1998). The original long-term curve for the Triassic was based on continental flooding data and this is still the case, because other constraints for this envelope, such as mean age of oceanic crust, are not available since almost all of the Triassic age oceanic crust has since been subducted, with the exception of a limited area of the seafloor on Exmouth Plateau west of Australia (von Rad et al., 1989). Recently van der Meer et al. (2017) have produced independent estimates of the long-term sea level based on Sr-isotope data, which show close similarities to the continental flooding curves and to the long-term Triassic curve presented here, although the interpreted amplitudes differ. The documentation for the short-term (third-order) sea-level events is based on sequence-stratigraphic information pieced together from several available longer duration sections and augmented by some shorter-duration records. In addition to sequence-stratigraphic interpretive criteria that are now well established and do not require repetition, other features that were particularly helpful in stratigraphic interpretations (originally listed in Haq and Schutter, 2008) in the Triassic include forced-regressive facies, organic-rich facies of the condensed sections, transgressive coals, evaporites, exposure-related deposits (including incised valley fills, autochthonous coals, eolian sandstones, and karst), and laterite/bauxite deposits. These features can often aid in the identification of depositional surfaces and system tract bou","PeriodicalId":35784,"journal":{"name":"GSA Today","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2018-11-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"90","resultStr":"{\"title\":\"Triassic Eustatic Variations Reexamined\",\"authors\":\"B. 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The trend reverses again with a decline in the late Norian and the base level remaining close to the pdmsl, and then dipping further in the mid-Rhaetian to ~50 m below pdmsl into the latest Triassic and earliest Jurassic. Superimposed upon this long-term trend is the record of 22 widespread third-order sequence boundaries that have been identified, indicating sealevel falls of mostly minor (<25 m) to medium (25–75 m) amplitude. Only six of these falls are considered major, exceeding the amplitude of 75 m. The long interval of Triassic oceanic withdrawal is likely to have led to general scarcity of preserved marine record and large stratigraphic lacunae. Lacking evidence of continental ice sheets in the Triassic, glacio-eustasy as the driving mechanism for the third-order cyclicity can be ruled out. And even though transfer of water to and from land aquifers to the ocean as a potential cause is plausible for minor (a few tens of meters) sea-level falls, the process seems counter-intuitive for third-order events for much of the Triassic. Triassic paleoenvironmental scenarios demonstrate a close link between eustasy, climates, and biodiversity. INTRODUCTION The Triassic Period encompasses 50.5 m.y., spanning an interval from 251.9 to 201.4 Ma (Ogg et al., 2016). By this time, the megacontinent of Pangaea had already assembled, surrounded by the Panthalassa Ocean that covered >70% of Earth’s surface, and by the mid-Triassic the Pangaean landmass was almost evenly distributed in the two hemispheres around the paleo-equator (see Fig. S1 in the GSA Data Repository1). The interval from latest Permian through the earliest Jurassic, a time span of nearly 80 m.y., represents the longest spell of low seastands of the Phanerozoic. The Triassic is also bracketed by two major biotic extinctions near the Permian-Triassic (P-T) and Triassic-Jurassic boundaries, the one at P-T boundary being the most severe biotic turnover of the Phanerozoic (Raup and Sepkowski, 1982; Hallam and Wignall, 1997; McElwain et al., 1999). The Late Triassic experienced the beginning of the lithospheric swell, ushering the breakup of Pangaea and its eventual split into discrete continents in the later Mesozoic (see Fig. S1 [see footnote 1]). The definite signs of the beginning of Pangaean fragmentation were clearly manifest by the end of the Triassic with the basaltic outpouring of the massive Central Atlantic magmatic province (see, e.g., Marzoli et al., 1999, 2004; Davies et al., 2017). In the past two decades substantial new stratigraphic data from Triassic sections has come to light, and there have been significant refinements in time scales, making a review and revision of the Triassic sealevel variations timely. The documentation for the revised Triassic sea-level curve, though still largely from northwestern and central Europe (western Tethys), now also includes sections further east from other parts of the Tethys, such as the Arabian Platform, Pakistan, India, China, and Australia. From the boreal latitudes documentation includes sections from the Sverdrup Basin, Svalbard, and the Barents Sea. This paper serves to complete a review of the entire Mesozoic as both Cretaceous and Jurassic sea-level variations have already been reappraised (Haq, 2014, 2017). For a background of the paleoenvironmental conditions (oceans and climates) in the Triassic see the GSA data repository (see footnote 1). TRIASSIC TIME SCALE UPDATES A succinct discussion of the methodological advancements and modifications to the Triassic time scale can be found in Preto et al. (2010), and a detailed discussion of Triassic stratigraphy has been presented by Ogg et al. (2014). Since the last update of the Triassic third-order sea-level variations (Haq and Al-Qahtani, 2005) that was calibrated to an earlier version of the time scale, there have been several refinements to the Triassic chronostratigraphy. The latest version of the time scale (Ogg et al., 2016) modifies the boundaries of Triassic standard stages (ages) by anywhere between <1 m.y. to almost 6 m.y. Like earlier versions, the new time scale is mainly based on biostratigraphy, anchored by selected radiometric dates, with some intervals refined by astronomical and cyclostratigraphical fine-tuning, and others aided by magnetostratigraphy. Conodonts and ammonoids constitute the mainstay of the Triassic biostratigraphic correlations. Special problems concerning wider correlations using these fossil groups in the Triassic include taxonomic standardization, rarity of markers, potential diachroniety in conodontsʼ first and last appearance, and provinciality among ammonoids. Since much of the Pangaean landscape was dominated by terrestrial sediments, regional correlations often rely on palynology, ostracods and tetrapods that do not lend themselves to wider correlations with marine records. Ogg et al. (2016) ascribe a Bilal U. Haq, Smithsonian Institution, Washington, D.C., USA, and Sorbonne University, Paris, France composite error of between 0.2 and 0.59 m.y. for the stage boundaries in the Triassic depending on the type of data (see also the GSA data repository for further discussion of time scales [see footnote 1]). LARGE TIME GAPS IN THE RECORD OF THE MIDDLE AND LATE TRIASSIC? Even a cursory look at the most recent update of the Triassic time scale (Ogg et al., 2016) reveals its extreme lopsidedness: while the Early Triassic spans only 5.1 m.y. and the Middle Triassic increases to 9.1 m.y., the Late Triassic jumps to a substantial span of 35.6 m.y. Some unevenness is to be expected, but this extreme asymmetry is also witnessed in the time spans of the stages (ages) and biostratigraphic zones within the stages, as well the lengths of the sequence cycles and corresponding sealevel events that all increase in duration in the Middle to Late Triassic. If the above apparent chronostratigraphic asymmetry is real, then the large differences in the duration of fossil zones imply that evolutionary rates (as measured by appearance of new species/m.y.) were relatively rapid in the Early Triassic (thus the availability of a high-resolution biozonal subdivision), declining somewhat in the Middle Triassic, and slowing down to an extreme thereafter (characterized by a few long-duration biozones), especially in the later Late Triassic. However, the temporal lengths of sequence cycles (based on sedimentary facies shifts) do not have to follow the biotic evolutionary trends, and yet they do. Their long time spans (average of ~5 m.y./cycle in the Middle and Late Triassic) would imply a built-in bias in the record expressed as a lack of preserved marine stratigraphic record. This seems plausible in a scenario where the long-term trend of low seastands for the period means fewer marine records in favor of more terrestrial sedimentary records. This is exacerbated by mostly type-1 sequence boundaries (when the base line withdraws beyond the shelf edges) that may incorporate large erosional time gaps. Large temporal lacunae in the stratigraphic record could explain the potentially specious signal that comes across as slowdown in the biotic evolutionary rates, as well as the dearth of sequence cycles for the interval in question (i.e., Middle and Late Triassic). An oxygenisotopic record of the Triassic derived from Tethyan conodont apatite shows trends that duration = 0.77 m.y.), and expand for the remainder of the Carnian through Rhaetian interval (average ammonoid zonal duration = 2.43 m.y.). Using multiple overlapping criteria (i.e., several fossil groups), these uncertainties can sometimes be narrowed. The long-term sea-level envelope for the Triassic is similar to those shown in Haq et al. (1987, 1988) and Hardenbol et al. (1998). The original long-term curve for the Triassic was based on continental flooding data and this is still the case, because other constraints for this envelope, such as mean age of oceanic crust, are not available since almost all of the Triassic age oceanic crust has since been subducted, with the exception of a limited area of the seafloor on Exmouth Plateau west of Australia (von Rad et al., 1989). Recently van der Meer et al. (2017) have produced independent estimates of the long-term sea level based on Sr-isotope data, which show close similarities to the continental flooding curves and to the long-term Triassic curve presented here, although the interpreted amplitudes differ. The documentation for the short-term (third-order) sea-level events is based on sequence-stratigraphic information pieced together from several available longer duration sections and augmented by some shorter-duration records. In addition to sequence-stratigraphic interpretive criteria that are now well established and do not require repetition, other features that were particularly helpful in stratigraphic interpretations (originally listed in Haq and Schutter, 2008) in the Triassic include forced-regressive facies, organic-rich facies of the condensed sections, transgressive coals, evaporites, exposure-related deposits (including incised valley fills, autochthonous coals, eolian sandstones, and karst), and laterite/bauxite deposits. 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引用次数: 90

摘要

由于缺乏保存的海洋地层记录,三叠纪海平面变化的文献受到限制,这些记录主要局限于特提斯洋的低纬度和中纬度地区。根据对全球地层数据的重新评估,修订后的海平面曲线显示,从二叠纪晚期到侏罗纪早期,在近80万年的长时间内,海平面呈明显的低海平面趋势。在三叠纪早期和中期,长期海平面与现今平均海平面(pdmsl)相似或高出10-20米。这一趋势在拉丁尼亚晚期发生了逆转,其特征是稳步上升,并在卡尼亚晚期达到三叠纪的海平面峰值(pdmsl以上约50米)。这一趋势再次逆转,在诺里阶晚期下降,基准面保持在pdmsl附近,然后在雷蒂阶中期进一步下降至pdmsl下方约50m,进入三叠纪晚期和侏罗纪早期。叠加在这一长期趋势之上的是已经确定的22个广泛的三阶层序边界的记录,这表明海平面下降大多很小(占地球表面的70%),到三叠纪中期,Pangaean陆地几乎均匀分布在古赤道周围的两个半球(见图GSA数据库1中的S1)。从最晚的二叠纪到最早的侏罗纪,时间跨度近80 m.y.,代表了显生宙最长的低潮期。三叠纪还被二叠纪-三叠纪(P-T)和三叠纪-侏罗纪边界附近的两次主要生物灭绝所包围,P-T边界的一次是显生宙最严重的生物更替(Raup和Sepkowski,1982;Hallam和Wignall,1997;McElwain等人,1999)。晚三叠纪经历了岩石圈膨胀的开始,盘古大陆解体,并最终在中生代晚期分裂为离散的大陆(见图S1[见脚注1])。到三叠纪末,随着中大西洋大规模岩浆区的玄武岩喷出,Pangaean碎裂开始的确切迹象明显显现(例如,见Marzoli等人,19992004;Davies等人,2017)。在过去的二十年里,三叠纪剖面的大量新地层数据被发现,并且在时间尺度上有了显著的改进,这使得对三叠纪海平面变化的审查和修正变得及时。修订后的三叠纪海平面曲线的文件虽然主要来自欧洲西北部和中部(特提斯西部),但现在也包括特提斯其他地区向东的部分,如阿拉伯地台、巴基斯坦、印度、中国和澳大利亚。来自北纬度的文件包括斯维尔德鲁普盆地、斯瓦尔巴群岛和巴伦支海的部分。本文旨在完成对整个中生代的回顾,因为白垩纪和侏罗纪的海平面变化已经得到了重新评估(Haq,20142017)。有关三叠纪古环境条件(海洋和气候)的背景,请参阅GSA数据库(见脚注1)。三叠纪时间尺度更新Preto等人对三叠纪时间尺度的方法进步和修改进行了简要讨论。(2010),Ogg等人对三叠纪地层学进行了详细讨论。(2014)。自上一次更新三叠纪三阶海平面变化(Haq和Al-Qahtani,2005)以来,三叠纪时间地层学已经进行了几次改进。最新版本的时间尺度(Ogg et al.,2016)将三叠纪标准阶段(年龄)的边界修改了<1 m.y.到近6 m.y.。与早期版本一样,新的时间尺度主要基于生物地层学,由选定的辐射测量日期锚定,一些间隔通过天文和气旋地层学微调进行细化,以及其他借助磁地层学的研究。牙形石和菊石构成了三叠纪生物地层对比的主体。三叠纪使用这些化石群进行更广泛的相关性的特殊问题包括分类学标准化、标记物的稀有性、牙形石首次和最后出现的潜在历时性,以及菊石的地方性。由于Pangaean景观的大部分由陆地沉积物主导,区域相关性通常依赖于孢粉学、介形虫和四足动物,而这些与海洋记录的相关性并不广泛。Ogg等人(2016)根据数据类型,将Bilal U.Haq、美国华盛顿特区史密森学会和法国巴黎索邦大学的三叠世阶段边界的综合误差归为0.2至0.59 m.y.(关于时间尺度的进一步讨论,另见GSA数据库[见脚注1])。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Triassic Eustatic Variations Reexamined
Documentation of eustatic variations for the Triassic is limited by the paucity of the preserved marine stratigraphic record, which is confined mostly to the low and middle paleolatitudes of the Tethys Ocean. A revised sea-level curve based on reevaluation of global stratigraphic data shows a clear trend of low seastands for an extended period that spans almost 80 m.y., from the latest Permian to the earliest Jurassic. In the Early and Middle Triassic, the long-term sea levels were similar to or 10–20 m higher than the present-day mean sea level (pdmsl). This trend was reversed in the late Ladinian, marked by a steady rise and culminating in peak sea levels of the Triassic (~50 m above pdmsl) in the late Carnian. The trend reverses again with a decline in the late Norian and the base level remaining close to the pdmsl, and then dipping further in the mid-Rhaetian to ~50 m below pdmsl into the latest Triassic and earliest Jurassic. Superimposed upon this long-term trend is the record of 22 widespread third-order sequence boundaries that have been identified, indicating sealevel falls of mostly minor (<25 m) to medium (25–75 m) amplitude. Only six of these falls are considered major, exceeding the amplitude of 75 m. The long interval of Triassic oceanic withdrawal is likely to have led to general scarcity of preserved marine record and large stratigraphic lacunae. Lacking evidence of continental ice sheets in the Triassic, glacio-eustasy as the driving mechanism for the third-order cyclicity can be ruled out. And even though transfer of water to and from land aquifers to the ocean as a potential cause is plausible for minor (a few tens of meters) sea-level falls, the process seems counter-intuitive for third-order events for much of the Triassic. Triassic paleoenvironmental scenarios demonstrate a close link between eustasy, climates, and biodiversity. INTRODUCTION The Triassic Period encompasses 50.5 m.y., spanning an interval from 251.9 to 201.4 Ma (Ogg et al., 2016). By this time, the megacontinent of Pangaea had already assembled, surrounded by the Panthalassa Ocean that covered >70% of Earth’s surface, and by the mid-Triassic the Pangaean landmass was almost evenly distributed in the two hemispheres around the paleo-equator (see Fig. S1 in the GSA Data Repository1). The interval from latest Permian through the earliest Jurassic, a time span of nearly 80 m.y., represents the longest spell of low seastands of the Phanerozoic. The Triassic is also bracketed by two major biotic extinctions near the Permian-Triassic (P-T) and Triassic-Jurassic boundaries, the one at P-T boundary being the most severe biotic turnover of the Phanerozoic (Raup and Sepkowski, 1982; Hallam and Wignall, 1997; McElwain et al., 1999). The Late Triassic experienced the beginning of the lithospheric swell, ushering the breakup of Pangaea and its eventual split into discrete continents in the later Mesozoic (see Fig. S1 [see footnote 1]). The definite signs of the beginning of Pangaean fragmentation were clearly manifest by the end of the Triassic with the basaltic outpouring of the massive Central Atlantic magmatic province (see, e.g., Marzoli et al., 1999, 2004; Davies et al., 2017). In the past two decades substantial new stratigraphic data from Triassic sections has come to light, and there have been significant refinements in time scales, making a review and revision of the Triassic sealevel variations timely. The documentation for the revised Triassic sea-level curve, though still largely from northwestern and central Europe (western Tethys), now also includes sections further east from other parts of the Tethys, such as the Arabian Platform, Pakistan, India, China, and Australia. From the boreal latitudes documentation includes sections from the Sverdrup Basin, Svalbard, and the Barents Sea. This paper serves to complete a review of the entire Mesozoic as both Cretaceous and Jurassic sea-level variations have already been reappraised (Haq, 2014, 2017). For a background of the paleoenvironmental conditions (oceans and climates) in the Triassic see the GSA data repository (see footnote 1). TRIASSIC TIME SCALE UPDATES A succinct discussion of the methodological advancements and modifications to the Triassic time scale can be found in Preto et al. (2010), and a detailed discussion of Triassic stratigraphy has been presented by Ogg et al. (2014). Since the last update of the Triassic third-order sea-level variations (Haq and Al-Qahtani, 2005) that was calibrated to an earlier version of the time scale, there have been several refinements to the Triassic chronostratigraphy. The latest version of the time scale (Ogg et al., 2016) modifies the boundaries of Triassic standard stages (ages) by anywhere between <1 m.y. to almost 6 m.y. Like earlier versions, the new time scale is mainly based on biostratigraphy, anchored by selected radiometric dates, with some intervals refined by astronomical and cyclostratigraphical fine-tuning, and others aided by magnetostratigraphy. Conodonts and ammonoids constitute the mainstay of the Triassic biostratigraphic correlations. Special problems concerning wider correlations using these fossil groups in the Triassic include taxonomic standardization, rarity of markers, potential diachroniety in conodontsʼ first and last appearance, and provinciality among ammonoids. Since much of the Pangaean landscape was dominated by terrestrial sediments, regional correlations often rely on palynology, ostracods and tetrapods that do not lend themselves to wider correlations with marine records. Ogg et al. (2016) ascribe a Bilal U. Haq, Smithsonian Institution, Washington, D.C., USA, and Sorbonne University, Paris, France composite error of between 0.2 and 0.59 m.y. for the stage boundaries in the Triassic depending on the type of data (see also the GSA data repository for further discussion of time scales [see footnote 1]). LARGE TIME GAPS IN THE RECORD OF THE MIDDLE AND LATE TRIASSIC? Even a cursory look at the most recent update of the Triassic time scale (Ogg et al., 2016) reveals its extreme lopsidedness: while the Early Triassic spans only 5.1 m.y. and the Middle Triassic increases to 9.1 m.y., the Late Triassic jumps to a substantial span of 35.6 m.y. Some unevenness is to be expected, but this extreme asymmetry is also witnessed in the time spans of the stages (ages) and biostratigraphic zones within the stages, as well the lengths of the sequence cycles and corresponding sealevel events that all increase in duration in the Middle to Late Triassic. If the above apparent chronostratigraphic asymmetry is real, then the large differences in the duration of fossil zones imply that evolutionary rates (as measured by appearance of new species/m.y.) were relatively rapid in the Early Triassic (thus the availability of a high-resolution biozonal subdivision), declining somewhat in the Middle Triassic, and slowing down to an extreme thereafter (characterized by a few long-duration biozones), especially in the later Late Triassic. However, the temporal lengths of sequence cycles (based on sedimentary facies shifts) do not have to follow the biotic evolutionary trends, and yet they do. Their long time spans (average of ~5 m.y./cycle in the Middle and Late Triassic) would imply a built-in bias in the record expressed as a lack of preserved marine stratigraphic record. This seems plausible in a scenario where the long-term trend of low seastands for the period means fewer marine records in favor of more terrestrial sedimentary records. This is exacerbated by mostly type-1 sequence boundaries (when the base line withdraws beyond the shelf edges) that may incorporate large erosional time gaps. Large temporal lacunae in the stratigraphic record could explain the potentially specious signal that comes across as slowdown in the biotic evolutionary rates, as well as the dearth of sequence cycles for the interval in question (i.e., Middle and Late Triassic). An oxygenisotopic record of the Triassic derived from Tethyan conodont apatite shows trends that duration = 0.77 m.y.), and expand for the remainder of the Carnian through Rhaetian interval (average ammonoid zonal duration = 2.43 m.y.). Using multiple overlapping criteria (i.e., several fossil groups), these uncertainties can sometimes be narrowed. The long-term sea-level envelope for the Triassic is similar to those shown in Haq et al. (1987, 1988) and Hardenbol et al. (1998). The original long-term curve for the Triassic was based on continental flooding data and this is still the case, because other constraints for this envelope, such as mean age of oceanic crust, are not available since almost all of the Triassic age oceanic crust has since been subducted, with the exception of a limited area of the seafloor on Exmouth Plateau west of Australia (von Rad et al., 1989). Recently van der Meer et al. (2017) have produced independent estimates of the long-term sea level based on Sr-isotope data, which show close similarities to the continental flooding curves and to the long-term Triassic curve presented here, although the interpreted amplitudes differ. The documentation for the short-term (third-order) sea-level events is based on sequence-stratigraphic information pieced together from several available longer duration sections and augmented by some shorter-duration records. In addition to sequence-stratigraphic interpretive criteria that are now well established and do not require repetition, other features that were particularly helpful in stratigraphic interpretations (originally listed in Haq and Schutter, 2008) in the Triassic include forced-regressive facies, organic-rich facies of the condensed sections, transgressive coals, evaporites, exposure-related deposits (including incised valley fills, autochthonous coals, eolian sandstones, and karst), and laterite/bauxite deposits. These features can often aid in the identification of depositional surfaces and system tract bou
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GSA Today
GSA Today Earth and Planetary Sciences-Geology
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