陕西渭北奥陶系放射虫硅质岩与火山凝灰岩的成因环境

通过对层状放射虫硅质岩的岩石学和火山凝灰岩岩石类型的特征研究，认为渭北奥陶系的放射虫硅质岩是由远源的火山喷发物提供了ＳｉＯ２的来源，造成有利于硅质生物大量繁殖的条件，死后堆积海底，最终转变为层状放射虫硅质岩。从而进一步推断，本区中、上奥陶统的沉积形成于海平面大规模上升的远洋或半远洋的深水环境。火山凝灰岩则是岛弧火山喷发的产物，反映本区曾一度是华北板块活动大陆边缘弧后盆地北部边缘部分。     

陕西渭北奥陶系放射虫硅质岩与火山凝灰岩的成因环境

通过对层状放射虫硅质岩的岩石学和火山凝灰岩石学类型的特征研究，认为渭北奥陶系的放射虫硅质岩是上远源的火山喷发物提供了ＳｉＯ２的来源，造成有利于硅质生物大量繁殖的条件，死后堆积海底，最终转变为层状放射虫硅质岩，从而进一步推断，本区中，上奥陶统的沉积形成于海平面大规模上升的远洋或半远洋的深水环境，火山凝灰岩则是岛弧火山喷发的产物，反映本区曾一度是华北板块活动大陆边缘弧后盆地北部边缘部分。     

二叠-三叠纪转折期放射虫动物群的变化

综述了二叠 -三叠纪转折期放射虫动物群的研究进展 ,长兴阶晚期放射虫动物群 90 %以上的种在二叠纪末期灭绝 ,只有少数在浅海灰岩和远洋硅质岩中均能够发现的属种才成功残存到三叠纪 ;三叠纪放射虫的复苏和辐射经历了较长的过程 ,Griesbachian至 Smithian为放射虫残存期 ,Spathian 为放射虫的复苏期 ,Anisian是放射虫的辐射期。Anisian放射虫的辐射受到强缺氧事件的影响。     

老挝西北部琅勃拉邦构造带放射虫硅质岩及其构造意义

琅勃拉邦构造带内放射虫硅质岩含有放射虫Entactinia vulgaris Won, Entactinosphaera palimpola Foreman和Belowea variabilis (Ormiston et Lane),时代为早石炭世,为老挝境内首次报告。硅质岩样品具有很高的SiO2质量分数(95.29%~98.17%),大部分样品表现出相类似的稀土配分模式,部分样品配分模式图表现为上凸状,具有中稀土富集,均具有明显的Ce负异常,Ce/Ce*值为0.64~0.74,其中部分样品具有Eu的负异常,为0.58~0.68。Y/Ho比值为31.05~40.96,类似日本Sasayama中-晚二叠世的远洋硅质岩。地球化学显示其为含酸性火山碎屑非热液成因的远洋硅质岩。这些研究证实了在思茅板块和印支板块之间存在一个开阔的石炭纪时期弧后盆地。     

藏北双湖地区才多茶卡一带构造混杂岩中发现晚泥盆世和晚二叠世放射虫硅质岩

报道了在西藏北部双湖才多茶卡地区新发现的晚泥盆世和晚二叠世放射虫硅质岩,实测剖面的第9层硅质岩以产Neoalbaillella动物群为特征,其中N.ormithoformis,N.optima是晚二叠世长兴阶的2个带化石;第14层硅质岩以产Entactinids动物群为特征,其中Stigmosphaerostylusoumonhaoensis,Triloneheechinata,Archocyrtiumriedeli等主要见于晚泥盆世法门阶。上述2个动物群在西藏尚属首次发现。才多茶卡地区晚古生代放射虫硅质岩的发现为重新认识双湖构造混杂岩带的形成时代、构造环境、“构造带是否东延”等重大地质问题,提供了新的重要资料。     

放射虫硅质岩对华南古地理的启示

放射虫硅质岩在中国南方及邻区广泛分布,有重要的古地理意义。按其时空分布,可分为南区及北区和东带。南区包括滇西、滇东南、桂西和桂南,主要为晚古生代至中生代早期放射虫硅质岩。滇西硅质岩带南延至泰国和马来西亚,代表古特提斯主支。滇东南、桂西和桂南的硅质岩则指示古特提斯多岛洋的分支海盆。北区包括两广中北部、湘赣中南部和长江中下游一带,主要为二叠纪中晚期放射虫硅质岩,标志当时扬子台缘与古特提斯洋连通的深水盆地。东带沿南海和东海外侧的岛弧分布,从菲律宾北巴拉望经琉球到西南日本内带,主要为中二叠世至晚侏罗世放射虫硅质岩,与古地磁证据一起指示了该期间华南南方一个低纬度的远洋盆地,可称为“古南中国海”。它的张开可能是中晚二叠世云开地体和中国东南部其他地方造山事件的原因,它的随后发展对华南东部三叠纪和侏罗纪古地理演化也有重大影响。晚侏罗世太平洋伊泽奈崎板块的迅速北移,使“古南中国海"俯冲消减,导致东南沿海大规模的钙碱性岩浆活动。     

昌宁-孟连结合带弄巴地区泥盆系、石炭系的时代及沉积环境:放射虫、碎屑锆石U-Pb年龄和Hf同位素约束

造山带中远洋深水沉积物是恢复古大洋的重要依据之一,昌宁-孟连古特提斯结合带存在大量海相沉积物,但是否存在大洋盆地相的远洋沉积还不清楚.对弄巴地区被认为最可能是洋盆相沉积的石炭系岩片和海相泥盆系岩片进行了岩石学、放射虫时代、碎屑锆石U-Pb年龄和Hf同位素研究.石炭系岩片放射虫硅质岩中鉴定出放射虫6属8种,时代为早石炭世早-中期.LA-ICP-MS锆石U-Pb定年结果显示,泥盆系岩片岩屑石英杂砂岩碎屑锆石年龄范围为387~3 266 Ma,最年轻一组年龄为387~413 Ma;石炭系岩片中与放射虫硅质岩共生的基性凝灰岩碎屑锆石年龄为341~3 403 Ma,最年轻一组年龄为341~354 Ma.综合锆石年龄和化石资料,限定泥盆系岩片原始沉积时代为早-中泥盆世,石炭系岩片时代为早石炭世早-中期.碎屑锆石U-Pb年龄谱特征和Hf同位素组成指示泥盆系岩片和石炭系岩片具有相似的物质源区,主要来源于亲冈瓦纳的陆壳,少量来自于古生代特提斯域新生岛弧.早-中泥盆世地层岩片原始沉积于亲冈瓦纳的大陆斜坡环境;早石炭世地层岩片原始沉积于亲冈瓦纳的大陆斜坡至古特提斯洋盆边缘环境,不是远洋深水的大洋盆地环境.寻找以远洋深水沉积物为代表的大洋盆地相沉积并开展研究是当前昌宁-孟连古特提斯研究的重要方向之一.      

西藏班公湖-怒江缝合带中段塔仁本洋岛型玄武岩的发现及地质意义

塔仁本洋岛型玄武岩是中特提斯洋古洋壳的重要组成部分,是班公湖怒江缝合带内构造混杂岩中局部有序部分的特殊洋壳残片。它以具有海底爆发相与远洋放射虫硅质岩相整合和大洋板内碱性玄武岩的构造环境为主要特征。它的发现丰富了班怒带的研究内容,证明当时中特提斯洋曾经有发育完好的古洋壳存在     

思茅地块西缘大凹子组地层序列及地质时代

目前关于思茅地块西缘大凹子组的形成时代仍有分歧.在思茅地块西缘大中河剖面采集了硅质岩、砂岩、凝灰岩和玄武岩,通过放射虫组合和锆石U-Pb年龄方法,厘定其地质时代,并结合区域资料恢复地层序列.通过详细剖面实测,发现该剖面由6个地层断片组成:第一、四断片以含放射虫硅质岩为特征,放射虫组合指示其时代为晚泥盆世至早石炭世早期;第二、五断片以火山碎屑岩、具有鲍玛序列沉积特征的火山碎屑沉积岩为主,锆石U-Pb同位素年龄指示其时代为志留纪中期至早泥盆世;第三、六断片以火山岩沉积为特征,锆石U-Pb同位素年龄指示其时代为志留纪早期.结合前人资料认为思茅地块西缘分布的海相火山岩、碎屑岩和含放射虫硅质岩地层层序代表了志留纪到早石炭世早期的岛弧火山-沉积地层序列.      

西藏班公湖-怒江缝合带中段塔仁本洋岛型玄武岩的发现及地质意义

塔仁本洋岛型玄武岩是中特提斯洋古洋壳的重要组成部分,是班公湖-怒江缝合带内构造混杂岩中局部有序部分的特殊洋壳残片.它以具有海底爆发相与远洋放射虫硅质岩相整合和大洋板内碱性玄武岩的构造环境为主要特征.它的发现丰富了班-怒带的研究内容,证明当时中特提斯洋曾经有发育完好的古洋壳存在.     

Radiolarian-Based zonal scheme of the cretaceous (Albian–Santonain) of the Tethyan regions of Eurasia

A scheme of radiolarian zonal subdivision is proposed for the upper Albian–Santonian of the Tethyan regions of Eurasia. The upper Albian contains one zone: Crolanium triangulare; the Cenomanian contains three zones: Patellula spica (lower Cenomanian), Pseudoaulophacus lenticulatus (middle Cenomanian), and Triactoma parva (upper Cenomanian); the Turonian contains four zones: Acanthocircus tympanum (lower Turonian (with no upper part)), Patellula selbukhraensis (upper part of the lower Turonian), Phaseliforma turovi (middle Turonian (with no upper part)), and Actinomma (?) belbekense (upper part of the middle Turonian–upper Turonian); the Coniacian contains two zones: Alievium praegallowayi (lower part of the Coniacian) and Cyprodictyomitra longa (upper part of the Coniacian); the Santonian contains three zones: Theocampe urna (lower Santonian), Crucella robusta (middle Santonian–lower part of the upper(?) Santonian), and Afens perapediensis (upper part of the upper Santonian). The biostratigraphic subdivisions are correlated with biostrata in the schemes proposed previously for the Tethys and Pacific. A new species Patellula selbukhraensis Bragina sp. nov. is described.     

Turonian Radiolarians in the Section of Ak Mountain,Crimea

In the sections from the western and eastern peaks of Ak Mountain, the Patellula selbukhraensis Zone (upper part of the lower Turonian), which is established for the first time in the southwestern Mountainous Crimea, is traced. The first data on the radiolarian distribution in the section of the eastern peak of Ak Mountain, which is stratotypical of the Phaseliforma turovi (middle Turonian, without the upper part) and Actinomma (?) belbekense (upper part of the middle Turonian–upper Turonian) zones, are presented. These zones are also traced in the parallel section of the western peak of Ak Mountain.     

Turonian Radiolarians from Karnezeika,Argolis Peninsula,Peloponnesus (Greece)

Near Karnezeika a roughly 140 m thick Upper Cretaceous section consists of interbedded pelagic limestones, cherts and coarse polymict breccias including ophiolites and shallow water limestones. At the base, pink pelagic limestones rest on deeply altered and fractured Lower Jurassic Pantokrator Limestone. This first pelagic facies is dated as middle Turonian, based on planktonic Foraminifera. Over 100 m of coarse ophiolite-carbonate breccias, interpreted as a channel or canyon fill in a pelagic environment, document the erosion of the Late Jurassic nappe edifice along the Cretaceous Pelagonian margin. Above these breccias, we mesured 16 m of principally pink and red pelagic limestones and radiolarian cherts, in which we recovered well-preserved radiolarians discussed here. In this interval, the presence of planktonic Foraminfera allows to state a late Turonian to Coniacian age. More than 40 radiolarian species are described and figured in this work. The radiolarian chronostratigraphy established by 10 different authors in 11 publications was compared for this study and used to establish radiolarian ranges. This exercise shows major discrepancies between authors for the radiolarian ranges of the studied assemblage. Nevertheless, a Turonian age can be stated based on a synthesis of cited radiolarian ranges. This age is consistent with the age based on planktonic foraminifera. In combining the ages of both Radiolaria and planktonic Foraminifera, the studied samples can be restricted to the late Turonian. However, the discrepancies of published radiolarian ranges call for an urgent, major revision of the Late Cretaceous radiolarian biochronology. The integration of planktonic foraminifera with radiolarians may greatly enhance biochronologic resolution in sections where both groups occur.     

Biostratigraphy of the Çeşmeler and Elmalι Dere formations: First records of upper Cretaceous planktonic foraminifera and radiolarians from the Eastern Pontides (Maçka,Trabzon, Turkey)

Upper Cretaceous pelagic deposits outcropping in the Maçka (Trabzon) region include radiolarians and pelagic foraminifera. The Çatak Group represented by the volcano-sedimentary successions consists of three formations having different properties. Two sections, ÇTK1 and ÇTK2, are selected from the Çe meler and Elmalι Dere formations, respectively, establishing the biostratigraphy of outcropping sedimentary units. A total of 17 species of Whiteinella, Helvetoglobotruncana, Marginotruncana, Dicarinella, Praeglobotruncana, Archaeoglobigerina and Hedbergella demonstrating the early Turonian–Coniacian are established in the ÇTK1 stratigraphic section. The early Turonian radiolarian fauna consisting of Halesium sexangulum Pessagno, 1971, Crucella cachensis Pessagno, 1971, Stichomitra communis Squinabol, 1903 is also defined in the same section. A total of 30 species of Crucella, Halesium, Pessagnobrachia, Patulibracchium, Alievium, Archaeospongoprunum, Dicyomitra, Stichomitra, Diacanthocapsa, Dactiyliodiscus, Amphipydax, Pseudoaulophocus, Acaeniotyle, Archaeodictyomitra, Actinomma, Xitus, Neosciadocapsidae characterizing the early and late Turonian, as well as the Coniacian–early Santonian are recognized from red-coloured pelagic limestones of the ÇTK2 section. Also, planktonic foraminifera species of Marginotruncana, Hedbergella, Heterohelix, Globotruncana, Globotruncanita, Archaeoglobigerina, Dicarinella characterizing the Coniacian–Santonian are described in the thin sections of the same samples. The age of red-coloured limestones is identified as the Coniacian–Santonian benefit from radiolarians and pelagic foraminifera. Consequently, radiolarians and pelagic foraminifera within sedimentary successions of the investigation area are distributed in two intervals that coincide with the early Turonian–Coniacian and Coniacian–Santonian intervals.     

Evolution of radiolarians in the late Albian–Campanian

The dynamics of radiolarian evolution in the late Albian–Campanian is analyzed, and several stages are recognized. The first stage (late Albian–middle Cenomanian), related to the MCE regional anoxic event, showed low evolutionary tempos and hence lacked structural change in radiolarian communities. The second stage (late Cenomanian–early Turonian), corresponding to ОАЕ 2, which was a global anoxic event, is characterized by a decrease in the number of genera, while many genera showed increased diversification of species composition. At this stage, a considerable number of genera became extinct and appeared, suggesting an increased rate of the radiolarian evolution. The third stage (middle Turonian–early Coniacian), including the beginning of ОАЕ 3, is characterized by a stabilized number of genera. The fourth stage (late Coniacian–Santonian) completely encompasses ОАЕ 3 except for its very beginning. At this stage, the radiolarian communities underwent a significant structural change, while their rate of evolution increased considerably. Nevertheless, during the ОАЕ 3 stage, a distinct trend toward a decrease in generic diversity continued from the late Cenomanian to the middle Turonian. The fifth stage (Campanian) is characterized by quite significant changes in the assemblage composition, while the trend toward a gradual decrease in the number of genera steadily continued. At this stage, which coincided with a considerable cooling, twice as many genera became extinct as during ОАЕ 2. The analysis of the dynamics of radiolarian evolution showed that the anoxic MCE, ОАЕ 2, and ОАЕ 3 events did not result in degradation of radiolarian assemblages. This suggests that this group has significant stratigraphic potential. In general, the evolution of radiolarians in the Late Cretaceous was gradual. By the end of the Campanian, nearly half of the generic diversity was composed of genera which appeared at the beginning of the Cretaceous and earlier.     

The radiolarian assemblages of the Bonarelli Horizon in the Umbria-Marche Apennines and Southern Alps, Italy

The Bonarelli Horizon is an important regional marker level in the Umbria-Marche Apennines. It is characterized by consisting of black bituminous shales that yield a distinctive radiolarian fauna. Black shales referable to the Bonarelli Horizon are also present in the Southern Alps. The horizon is of uniform lithology and contains radiolarian assemblages of late Cenomanian-early Turonian age throughout both the Umbria-Marche Apennines and Southern Alps. Several new radiolarian taxa have been recognised and described from the Bonarelli Horizon of both areas. Two new species are defined in this paper, namelySethocapsa bossoensisandXitus picenus.     

Foraminifers and radiolarians across the Albian-Cenomanian and Cenomanian-Turonian Boundaries (Northern Peri-Tethys)

Changes in morphological diversity and taxonomic composition of late Albian-early Turonian foraminiferal and radiolarian assemblages from the northern Peri-Tethys are considered. Several stages are defined in evolution of planktonic foraminifers: polytaxic (Albian-Cenomanian), oligotaxic (Cenomanian-Turonian boundary period), and polytaxic (Turonian). The Albian-Cenomanian stage was characterized by intense development of rotaliporids representing an intricate group of planktonic foraminifers, which became extinct in the terminal Cenomanian. An intense speciation of the radiolarian genus Crolanium and last occurrences of its most species, the index species C. cuneatum included, was characteristic of the terminal Albian. Spheroid and discoid radiolarians were dominant in the Cenomanian, while the Turonian was marked by intense development of all the radiolarian morphotypes.     

New data on the Albian-Cenomanian radiolarians from the Karai Formation (South India)

Radiolarians from the lower part of the Karai Formation (upper Albian-middle Cenomanian) are studied in detail for the first time. Among over 50 radiolarian species identified in the formation, there are Acaeniotyle amplissima (Foreman), Savaryella novalensis (Squinabol), S. quadra (Foreman), Vitorfus campbelli Pessagno, Archaeodictyomitra montisserei (Squinabol), Holocryptocanium barbui Dumitrica, Pseudoeucyrtis sp. cf. Ps. spinosa (Squinabol), Stichomitra communis Squinabol, Tubilustrionella transmontanum (O’Dogherty), and others. The discovered radiolarians are divided into the Halesium triacanthum-Orbiculiforma nevadaenis (late Albian-early Cenomanian), Crucella latum-Cryptamphorella micropora (late Albian?-early Cenomanian), and Becus sp. B-Godia concava (terminal Albian-middle Cenomanian) assemblages. In general, the Albian-Cenomanian radiolarians of South India are comparatively less diverse than the concurrent assemblages of the Mediterranean region and California. In taxonomic composition and morphological peculiarities, they are comparable with the Aptian-Albian radiolarians of Western Australia (Ellis, 1993). Consequently it can be postulated that sea basins of South India were situated during the Albian-Cenomanian in the temperate latitudes of the Southern Hemisphere.     

藏北多格错仁红层及孢粉组合特征

青藏高原北部羌塘地块广泛出露第三纪陆相红层 ,确定这些红层及其变形的时代对认识青藏高原的形成演化过程具有非常重要的意义。 1998～ 1999年 ,INDEPTH III项目地质课题组人员 2次深入西藏可可西里地区进行科学考察 ,新发现藏北多格错仁红层 ,并在其中发现较多种属的孢粉化石。该孢粉组合反映以温带旱生草原为主体的古植被面貌。通过对青藏高原北部及邻区主要新生代盆地孢粉组合与古环境演化的对比分析 ,结合多格错仁红层上覆弱变形玄武岩 2 5～ 3 2Ma的40 Ar- 3 9Ar高精度测年资料 ,推断多格错仁红层的形成时代为晚中新世 ,多格错仁红层挤压变形所致的约 5 0 %的地壳缩短量发生在中新世末—上新世初。这些资料为建立青藏高原动力学模式提供了新的年代依据     

Displaced dolomites in radiolarian cherts of the Chichibu Belt on Shikoku Island,Southwest Japan

The northern tract of the Chichibu Belt on Shikoku Island, Southwest Japan, in places contains dolomites of Late Carboniferous age displaced into radiolarian cherts. The sections here examined are along the Niyodo gorge, central Shikoku. The sequence begins with thinly interbedded dolomitized radiolarian cherts and dolomites with a small amount of dolomitized radiolarian claystone and calcisiltite beds. These rocks, 5–10 m thick, are succeeded by a thick section of bedded and massive dolomites, commonly 40–50 m thick, which have thin intercalations of radiolarian claystone in the upper part. This dolomite sequence is depositionally overlain by a sequence, up to 50 m thick, comprising thinly interbedded radiolarian cherts and claystones, which, in turn, contain lenticular bodies of dolomite.Thin-section examination reveals that most of dolomites of the area have an arenitic or lithic texture, and should be termed doloarenite and dololithite. This means that dolomites are detrital. All lines of evidence suggest that the dolomites were not formed in the same depositional site in which the radiolarian cherts were being accumulated, but formed instead as allochthonous bodies which were displaced into a deep oceanic basin of chert deposition.The following sequence of events is postulated: (1) deposition of shallow-water calcareous sediments in a subtidal area; (2) dolomitization in a very shallow-water to supratidal environment; (3) displacement of dolomitized sediments, possibly mainly as debris flows into a deep-water, truely pelagic realm, in which siliceous radiolarian sediments were accumulating; (4) continued accumulation of siliceous sediments after the major influx of dolomitized sediments; and (5) minor influxes of dolomitized sediments during the continuous accumulation of siliceous sediments.