西藏南部晚白垩世-古新世大洋红层的分布与时代

特提斯—喜马拉雅北沉积亚带沉积有一套大洋红色岩层,由东往西在羊卓雍错、江孜、萨迦、萨嘎、札达一带断续出露,并与宗卓组上部地层相关。这套海相红层,根据岩性特征和浮游有孔虫可以直接进行区域对比。其时代在江孜地区为Santonian晚期—Campanian中期,包括Dicarinella asymetrica, Globotruncanitaelevata,Globotruncana ventricosa 和Globotruncanita calcarata 浮游有孔虫带;在萨迦地区限于Campanian期,鉴定有Globotruncanita elevata, Globotruncana ventricosa 和G. linneiana等具时代意义的浮游有孔虫;在萨嘎—吉隆地区为Maastrichtian期,识别出Gansserina gansseri 和Abthomphalus mayaroensis 浮游有孔虫带;在札达地区为古新世早期,以Glibigerina eugubina G. fringa化石带为代表。海相红层在西藏南部由东往西其时代逐渐变新,主要沉积时代分布在Santonian晚期—古新世早期。其总体时间跨度较大,大约长达20Ma。而事件在各个地点的延续时间有限,基本在3~8 Ma之内。根据对海相红层和沉积基质中浮游有孔虫的研究,该沉积带宗卓组的顶界时代已超出白垩纪,进入了古新世。     

世界一流的有孔虫标本模型在中国地质科学院地质研究所装架展示

正世界一流的有孔虫标本模型在中国地质科学院地质所区域地质与编图研究室完成装架并长期展示。这架有孔虫标本模型(图1,见第139页)系由郑守仪院士亲自雕制并监督制作,一共有120个属种,每个种都是标准的环境指相种。标准有孔虫是地层时代的定年器(世界性浮游有孔虫化石带)、古海洋的温度计、盐度计和深度计(浮游与底栖有孔虫),对它的鉴定必须准确无误。如果误定,对年代和环境信息的解译将会发生错误。因为有孔虫是小如灰尘的微体动物,一般小于1.0毫米,只能借助高倍实体显微镜才能看到其     

长江三角洲南通NB5孔有孔虫分布特征及环境指示意义

南通NB5孔位于长江三角洲北翼,受太平洋和长江双重沉积作用影响,第四纪时期海陆变化频繁,沉积物复杂。对NB5孔岩芯进行有孔虫鉴定,根据钻孔中底栖有孔虫和浮游有孔虫种类及分布特征,总结其赋存规律和反映的环境信息。结果显示有孔虫在地层中分布极不均匀,40 m以上含较多有孔虫,40 m之下几乎不含有孔虫,仅在128 m处见少量有孔虫;0～40 m之间存在3个层段有孔虫富集。认为40 m以上的全新世地层受海侵影响而赋存较多的有孔虫,且能分出明显的3个海侵加强阶段;40 m之下的地层有孔虫缺乏或少有,一是因为海侵地层缺失,二是因为研究区是河流的主河道区,淘洗作用强烈,有孔虫不易保存。全新世镇江海侵应该是研究区最强的一次海侵。     

莺歌海盆地DF1-1-11井有孔虫生物地层与沉积环境研究

结合ODP184航次及2008年"国际地层表"等研究成果,对莺歌海盆地基准井DF1-1-11井岩屑地层(630～3508 m)的有孔虫定量分析资料进行研究,建立可靠的生物地层及年代地层格架,并通过对钻井中有孔虫丰度、分异度、浮游比例、组合特征及古水深估算分析,讨论了DF1-1一11井中中新世以来的沉积环境演化.研究结果...     

南海北部大陆架莺琼盆地新生代海平面变化

南海北部大陆架莺琼盆地是建立西太平洋新生代海平面变化的关键地区之一。基于有孔虫和钙质超微化石资料所建立的莺歌海盆地和琼东南盆地新生代相对分辨率较高的年代地层格架,通过南海海域表层建立的浮游有孔虫含量与水深的定量关系,辅以古生态、成因相及特征沉积构造分析和反射地震剖面的海岸上超分析,编制了海平面变化曲线。识别出包含三个完整二级海平面变化旋回和半周期的海平面上升旋回。海平面变化幅度在0～200 m之间。海水最深的时期在早中新世晚期至中中新世早期以及上新世早期,与Haq曲线较为吻合。     

河北邢台地区晚古生代有孔虫动物群研究

通过对邢台沙巴沟太原组实测剖面有孔虫动物群进行研究,在太原组灰岩地层中鉴定出有孔虫11科15属23种,建立了Nodosaria-Multidiscus-Glomospira组合带。与国内不同地区晚古生代的有孔虫动物群进行对比后,确定有孔虫动物群的时代为晚石炭世晚期。     

赤道东经90°海岭3.5Ma以来远洋记录反映的重大环境事件

通过对东经90°海岭ODP758钻孔岩心3.5Ma以来的浮游有孔虫远洋记录的研究,结合岩性地层、稳定同位素地层、碳酸盐地层等资料,探讨了喜马拉雅山加速隆升、"中更新世气候转型"、"中布容溶解"事件等重大构造、环境事件在研究区的表现及相关机制。通过对各项指标的分析和对比,根据ODP758岩心的有孔虫组合面貌、古温度、古盐度和古温跃层的变化情况,推断研究区在1.4～0.7Ma期间的气候变化可能是在"中更新世气候转型"条件下发生的。碳酸钙、碳酸钙沉积通量和非碳酸钙沉积通量曲线在1.7Ma时快速增长,与现有资料显示的青藏高原的隆升历史相符,分别与青藏高原隆升过程中的青藏运动A幕、B幕、C幕(1.7Ma)和昆仑-黄河运动(1.2～0.6Ma)相当。碳酸钙含量、大于150μm的粗组分含量、浮游有孔虫沉积通量和浮游有孔虫生物地层揭示出在0.5～0.4Ma期间研究区深海碳酸盐遭受了强烈溶解。此事件与大西洋、太平洋、印度洋及南沙海区沉积记录中的"中布容溶解"事件一致。     

河北邢台地区晚古生代有孔虫动物群研究

通过对邢台沙巴沟太原组实测剖面有孔虫动物群进行研究,在太原组灰岩地层中鉴定出有孔虫11科15属23种,建立了Nodosaria-Multidiscus-Glomospira组合带。与国内不同地区晚古生代的有孔虫动物群进行对比后,确定有孔虫动物群的时代为晚石炭世晚期。     

有孔虫动物群的特征及其地层学意义

塔里木盆地西部是我国中新生代有孔虫比较发育的一个地区。中生代后期特提斯海水自西侵入本区,在晚白垩世到第三纪一段较长的时间内保持了海盆的性质,这为本区有孔虫的发育提供了有利的条件。本区有孔虫比较丰富,自上白垩统到中新统各层段均有分布。经笔者鉴定各种类型的有孔虫共计76属278种。其中胶结壳有孔虫69种,占24.82％;似瓷质壳有孔虫9种,占3.24％;钙质微孔壳有孔虫200种,占71.94％,其中浮游有孔虫16种,占总种数的5.76％。     

微体古生物微型计算机辅助研究系统

微体古生物微型计算机辅助研究系统是一个包括古生物化石属种数据厍、图象库、图象处理和数据采集系统以及定量分析系统在内的综合性古生物数据处理系统。其中,数据库和图象库的主要作用在于辅助化石鉴定。目前数据库和图象库包括了新生代浮游有孔虫1036个种的文字和图象资料。数据库和定量分析系统之间的数据传送非常方便,实现了对大批量古生物数据的定量分析,包括聚类分析、因子分析、瓦格纳网络分析、个体发育分析以及各种统计方法,这些分析程序都配制了相应的绘图功能,使分析结果能以直观的形式输出。定量分析有助于我们对一些“同物异名”和“异物同名”问题的厘定,并由此产生对分类问题的一些新认识。同时,定量分析有助于从定量的角度考查新生代浮游有孔虫的整体变化。     

Lithostratigraphy and planktonic foraminiferal biostratigraphy of the late Eocene-Middle Miocene sequence in the area between Wadi Al Zeitun and Wadi Al Rahib,Al Bardia area,northeast Libya

The present study deals with the lithostratigraphy and planktonic foraminiferal biostratigraphy of the Late Eocene-Middle Miocene sequence in the Al Bardia area, northeast Libya. The lithostratigraphical studies carried out on three stratigraphical surface sections, namely Wade Al Rahib, Wadi Al Hash and Wadi Al Zeitun, led to the recognition of three rock units from base to top: (1) the Al Khowaymat Formation (Late Eocene-Early Oligocene); (2) the Al Faidiyah Formation (Late Oligocene-Early Miocene); and (3) the Al Jaghboub Formation (Early-Middle Miocene). The planktonic foraminiferal biostratigraphical analysis led also to the recognition of nine planktonic foraminiferal zones ranged in age from Late Eocene to Early Miocene with one larger foraminiferal zone of Middle Miocene age. These are, from base to top, as follows: Truncorotaloides rohri Zone (Late-Middle Eocene, Lutetian), Globigerinatheka semiinvoluta and Turborotalia cerroazulensis s.l. Zones (Late Eocene, Priaborian), Cassigerinella chipolensis/Pseudohasitgerina micra Zone (Early Oligocene, Rupelian), Globigerina ciperoensis ciperoensis, Globorotalia kugleri Zones (Late Oligocene, Chattian), Globigerinoides primordius Zone (Early Miocene, Aquitanian), Globigerinoides altiaperturus/Catapsydrax dissimilis and Globigerinoides trilobus Zones (Early Miocene, Burdigalian), and the larger benthonic foraminiferal zone, Borelis melo melo Zone (Middle Miocene, Langhian to Serravallian). The study of planktonic foraminifera proved the existence of a regional unconformity between the Early and Late Oligocene, with the Middle Oligocene deposits being absent (absence of Globigerina ampliapertura and Globorotalia opima opima Zones), and another, smaller unconformity located between the Late Eocene and Early Oligocene, in which the uppermost part of the Late Eocene is missing.     

Revision of the planktonic foraminiferal biostratigraphy of the Voirons Flysch (Chablais Prealps,Haute-Savoie,France)

The ages obtained from planktonic foraminiferal assemblages retrieved from two exposures in the Gurnigel Flysch and from the re-examination of similar material gathered by previous researchers from the Voirons Flysch reveal only minor discrepancies with previous studies based on nannofossil biostratigraphy. In contrast, major divergences between this work and previous studies on the Voirons Flysch also based on planktonic foraminifera have been identified. They are generally related to distinct approaches in species classification and the use of different zonal schemes. Based on our data, the age of the Voirons Flysch extends from the Early Eocene (planktonic foraminiferal zone P7) to the Middle Eocene (planktonic foraminiferal zone P12). Contrasting with claims made in earlier studies, no specimen of Late Eocene or Early Oligocene age has been observed in the revised material. However, we cannot exclude a younger age (possibly Late Eocene) for the upper portion of this flysch from which we did not revise any sample. Thus, more research and sampling are needed to resolve this question. The palaeogeographic origin of the Voirons-Wägital complex as well as the sedimentation history of these flyschs need now to be re-evaluated in light of this revised biostratigraphic data.     

Variation on Foraminiferal Composition in Cretaceous Black-Gray-Red Bed Sequence of Southern Tibet, China

An Upper Cretaceous black-gray-red bed sequence was deposited in the Tethys-Himalayan Sea where abundant foraminifera, especially planktons, were yielded. In the shallow shelf to the upper slope on the north margin of Indian plate was recorded an extinction-recovery-radiation cycle of foraminiferal fauna highly sensitive to paleoceanographical changes. The black unit, consisting of the Late Cenomanian-earliest Turonian beds, displays a major extinction, with keeled planktonic and many benthic species as the principal victims at the end of the Cenomanian when existed only low diversity, sin-face water-dwelling foraminifera. The gray unit spans a long-term recovery interval from the Turonian to the early Santonian with keeled planktonic foraminifera returning stepwise to the water colunm. The planktonic biota in the red unit, extremely abundant, indicate a biotic radiation during the Late Santonian and the Early Campanian, implying that the high oxygen levels had returned to all the oceanic depth levels,and that the water stratification disappeared, followed by the radiation of all depth-dwellers. The variation on foraminiferal faunas from the whole sequence refers to the extreme warm climate that appeared in the Middle Cretaceous and to the declined temperature toward the late epoch. Substantial deposits for this warming and cooling zones represent the black shales in the Middle Cretaceous and the red beds in the later period of the southern Tibet. The change in the foraminiferal composition corresponded to the formation of dysaerobic facies and to the development of high-oxidized circumstances.     

西太平洋782A钻孔新生代的有孔虫

大洋钻探工程” 1 2 5航次的 782 A钻孔位于西太平洋菲律宾海东北部 ,井深 4 76.8m。基底为安山岩 ,上覆盖层为中始新统—更新统的沉积层 ,其中保存有低丰度的有孔虫。自下而上可划分出 8个浮游有孔虫带。由于出现 Catapsydrax dissimilis,C.stainforthi为 N5 、N6 带的带化石 ,表明本钻孔存在早中新世的地层。同时由于缺失浮游有孔虫带 P1 5 — P1 6 下部 ,N3上部—N4,N7—N1 1 带的带化石 ,说明在中始新世与晚始新世之间、晚渐新世与早中新世之间、早中新世与中中新世之间存在 3个沉积间断。钻孔中的有孔虫标志本区当时处于温暖亚热带环境。根据不同时期温度的变化 ,可划分出 5个阶段 ,包括 3个偏暖时期和 2个温凉时期。     

Tertiary stratigraphy of Western Australia

This paper is a summary of the present knowledge of the Tertiary stratigraphy of Western Australia. Also included is new information on the Cainozoic of the Carnarvon Basin, a result of petroleum exploration in the area.

Tertiary rocks formed during more than one cycle of deposition in three basins (Eucla, Perth, and Carnarvon), and also as thin units deposited in a single transgression along the south coast. The Tertiary stratigraphy of the Bonaparte Gulf Basin is not well known.

Drilling in the Eucla Basin has encountered up to 400 m of Tertiary in the south central part, with uniform thinning towards the margins. The section begins with a middle‐upper Eocene carbonate unit which represents the dominant event in the Tertiary sedimentation in this basin. More carbonates were deposited in the late Oligocene‐early Miocene and middle Miocene.

Along the south coast, the so‐called Bremer Basin, the Plantagenet Group (up to 100 m) of siltstone, sandstone, spongolite, and minor limestone, was deposited during the late Eocene.

The Perth Basin contains up to 700 m of Tertiary sediment, formed during at least two phases of sedimentation. The upper Paleocene‐lower Eocene Kings Park Formation consists of marine shale, sandstone, and minor limestone, with a thickness of up to 450 m. The Stark Bay Formation (200 m) includes limestone, dolomite, and chert formed during the early and middle Miocene. Events after deposition of the Stark Bay Formation are not well known.

The northern Carnarvon Basin and Northwest Shelf contain by far the most voluminous Tertiary sediment known from Western Australia: 3500 m is known from BOCAL's Scott Reef No. 1. A more usual maximum thickness is 2500 m. Most sediments were laid down in four episodes, separated by unconformities: late Paleocene‐early Eocene; middle‐late Eocene; late Oligocene‐middle Miocene; and late Miocene to Recent.

The Paleocene‐early Eocene cycle consists of about 100–200 m (up to 450 m in the north) of carbonate, shale, and marl of the Cardabia Group containing rich faunas of planktonic foraminifera.

The middle‐late Eocene sediments include diverse rock types. Marine and nonmarine sandstone formed in the Merlinleigh Trough. At the same time, the Giralia Calcarenite (fauna dominated by the large foraminifer Discocyclina) and unnamed, deeper water shale, marl, and carbonate (with rich planktonic foraminiferal faunas) formed in the ocean outside the embayment. Thickness is usually of the order of 100–200 m.

The main cycle of sedimentation is the late Oligocene‐middle Miocene, during which time the Cape Range Group of carbonates formed. This contains dominantly large foraminiferal faunas, of a wide variety of shallow‐water microfacies, but recent oil exploration farther offshore has recovered outer continental shelf facies with abundant planktonic foraminifera. A minor disconformity representing N7 and perhaps parts of N6 and N8 is now thought to be widespread within the Cape Range Group. The last part of this cycle resulted in sedimentation mainly of coarse calcareous marine sandstone (unnamed), and, in the Cape Range area, of the sandstone and calcareous conglomerate of the Pilgramunna Formation. Maximum thickness encountered in WAPET wells is 900 m.

After an unconformity representing almost all the late Miocene, sedimentation began again, forming an upper Miocene‐Recent carbonate unit which includes some excellent planktonic faunas. Thickness is up to 1100 m.

Thin marine sediments of the White Mountain Formation outcrop in the Bonaparte Gulf Basin. They contain some foraminifera and a Miocene age has been suggested.     

Biostratigraphy of a Paleocene-Eocene Foreland Basin boundary in southern Tibet

<正>This study of the Paleocene—Eocene boundary within a foreland basin of southern Tibet, which was dominated by a carbonate ramp depositional environment,documents more complex environmental conditions than can be derived from studies of the deep oceanic environment.Extinction rates for larger foraminiferal species in the Zongpu-1 Section apply to up to 46%of the larger foraminiferal taxa. The extinction rate in southern Tibet is similar to rates elsewhere in the world,but it shows that the Paleocene fauna disappeared stepwise through the Late Paleocene,with Eocene taxa appearing abruptly above the boundary.A foraminifera turnover was identified between Members 3 and 4 of the Zongpu Formation—from the Miscellanea—Daviesina assemblage to an Orbitolites—Alveolina assemblage.The Paleocene and Eocene boundary is between the SBZ 4 and SBZ 5,where it is marked by the extinction of Miscellanea miscella and the first appearance of Alveolina ellipsodalis and a large number of Orbitolites. Chemostratigraphically,theδ~(13)C values from both the Zongpu-1 and Zongpu-2 Sections show three negative excursions in the transitional strata,one in Late Paleocene,one at the boundary,and one in the early Eocene.The second negative excursion ofδ~(13),which is located at the P—E boundary,coincides with larger foraminifera overturn.These faunal changes and the observedδ~(13)C negative excursions provide new evidence on environmental changes across the Paleocene—Eocene boundary in Tibet.     

"Biostratigraphy and Paleoecology of Paleocene/Eocene (P/E) interval of some geological sections in Central Egypt"

The Paleocene/Eocene boundary intervals were studied in three outcrops along the Nile Valley: Gabal Taramsa, Gabal Qreiya, and Gabal Nag El Quda in Qena and Esna regions. The planktonic and benthic foraminifera have been examined. The qualitative study of planktonic foraminifera distinguishes eight planktonic biozones from (P4 and P5) Paleocene age to (E1, E2, E3, E4, E5, and E6) Early Eocene age. The analysis of quantitative distribution patterns of benthic foraminifera allows the reconstruction of the paleoenvironmental settings in the studied area. The disappearance or scarce appearance of deeper-water benthic foraminifera (Angulogavelinella avnimelechi and Gavelinella rubiginosus) and increasing dominance of shallow-marine taxa (Buliminides, Loxostomoides applinae) indicate deposition in shallow water environments. The benthic foraminiferal assemblages which dominated by Loxostomoides applinae, Buliminids, and Lenticulina indicate Dysoxic conditions and maximum food levels. The species of mid-way type fauna dominate the assemblages of the studied area; the species of Velasco-type fauna are very rare.     

塔里木盆地新生代海相沉积问题

基于前人文献,对塔里木盆地新生代海相沉积问题进行梳理,进而探讨该盆地新生代海侵的次数和范围以及海退的时限、原因。研究表明,新生代,塔里木盆地至少经历古近纪的阿尔塔什晚期至齐姆根早期(古新世早期至古新世晚期)、卡拉塔尔期—乌拉根期(始新世中期)、巴什布拉克中期(始新世晚期至早渐新世)等三期海侵;塔里木盆地中新世仍有海相地层这一认识获得广泛认可仍需更多的地质证据来支持。塔里木盆地海侵范围在卡拉塔尔—乌拉根组沉积时期达到最大,向东可达玛扎塔格地区,在盆地北缘和南缘分别可以到达库尔勒以东地区和洛浦县阿其克以东地区。由于受到全球海平面变化和构造运动的共同影响,副特提斯海新生代从塔里木盆地退却的沉积记录包括齐姆根组顶部、乌拉根组顶部、巴什布拉克组第四段和第五段,时间上分别对应于古新世晚期、始新世中晚期和早渐新世。     

Biostratigraphic Study of the Paleocene–Eocene Boundary in Northern Tunisia, North Africa

A new section at Jebel Gorraa,in northern Tunisia,contains the Paleocene-Eocene transition interval.Sample analysis of the section delivers abundant and diverse microfauna of planktonic and benthic foraminifera.Biostratigraphically,the Acarinina sibaiyaensis index-species is identified for the first time in this region,which allows us to specify the location of the Paleocene-Eocene boundary as well as the first E1 biozone of the lower Eocene.Samples from this biozone contain calcitic tests poorly preserved with an enrichment of iron oxide signifying a period of upheaval in local marine environments linked to the global warming of the Paleocene-Eocene Thermal Maximum （PETM）,the marker for the P/E boundary.     

Stages in the Magura Basin: a case study of the Polish sector (Western Carpathians)

The Magura Basin domain developed in its initial stage as a Jurassic-Early Cretaceous rifted passive margin that faced the eastern parts of the oceanic Alpine Tethys. In the pre- and syn-orogenic evolution of the Magura Basin the following prominent periods can be distinguished: Middle Jurassic-Early Cretaceous syn-rift opening of basins (1) followed by Early Cretaceous post-rift thermal subsidence (2), latest Cretaceous–Paleocene syn-collisional inversion (3), Late Paleocene to Middle Eocene flexural subsidence (4) and Late Eocene - Early Miocene synorogenic closing of the basin (5). The driving forces of tectonic subsidence of the basin were syn-rift and thermal post-rift processes, as well as tectonic loads related to the emplacement of accretionary wedge. This process was initiated at the end of the Paleocene at the Pieniny Klippen Belt (PKB)/Magura Basin boundary and was completed during Late Oligocene in the northern part of the Magura Basin. During Early Miocene the Magura Basin was finally folded, thrusted and uplifted as the Magura Nappe.