黑龙江省东部跃进山群中绿片岩的地球化学特征及地质意义

跃进山群出露位于佳木斯地块和那丹哈达地体之间，是完达山造山带的组成部分。它由大陆斜坡相沉积物、大洋中脊型玄武岩和洋岛型玄武岩组成，其中有镁铁－超镁铁质岩块体。它不是一个地层单位，而是与活动大陆边缘板块俯冲作用有关的蛇绿混杂岩     

论江西双桥山群的底界问题

１∶５万庐山地区区域地质调查和专题研究，在星子县黄岭一带发现一套巨厚层状复成分的变质砾岩。根据该变质砾岩的砾石成分、变形组构及区域分布特点，以及上部（双桥山群）与下部（星子岩群）地层在变质与变形方面存在明显差别，认为变质砾岩应属于双桥山群的底部层位，是中元古界双桥山群与下伏下元古界星子岩群不整合关系的佐证。由于受后期构造叠加改造的影响，现今二者呈断层或隐蔽不整合接触关系。     

早元古代滹沱群玄武岩Rb-Sr、Sm-Nd同位素体系初论

本文给出的滹沱群下亚群青石村组玄武岩Ｒｂ－Ｓｒ、Ｓｍ－Ｎｄ全岩等时线年龄为２０４５．８±１７和２３６９±３０Ｍａ（Ｚ），角门石４０Ａｒ－３９Ａｒ坪年龄和最高视年龄为１３６４±１９和１９３２±１９Ｍａ（１）；中亚群河边村组玄武岩Ｒｂ－Ｓｒ全岩等时线年龄图的投点呈完全离散状，Ｓｍ－Ｎｄ全岩等时线年龄为２３２２±３１Ｍａ（２），角门石４０Ａｒ－３９Ａｒ坪年龄和最高视年龄为１３６０和１７４２±１７Ｍａ（１）。根据上述Ｒｂ－Ｓｒ、Ｓｍ－Ｎｄ数据与已知青石村组、河边村组单颗粒锆石Ｕ－Ｐｂ法确定的成岩年龄２４５０±１０和２４００±２０Ｍａ（２）的明显差别，４０Ａｒ－３９Ａｒ均揭示为较典型受扰动的年龄谱和较发育的透人性构造、晚期岩脉等地质证据，认为Ｒｂ－Ｓｒ、Ｓｍ－Ｎｄ是重设的同位素体系。     

内蒙古渣尔泰山群和白云鄂博群中Pt、Pd地球化学特征及找矿建议

内蒙古渣尔泰山群和白云鄂博群是一套陆源碎屑岩、泥页岩、碳酸盐岩，地层中Pt、Pd的含量与原岩中泥质、有机碳、有机质的含量有关。其中渣尔泰山群中的阿古鲁沟组炭质板岩、增隆昌组硅质炭质板岩为含Pt、Pd最佳层位(岩性)，白云鄂博群中的比鲁特组干枚状板岩也为含Pt、Pd的最佳层位(岩性)。通过研究Pt、Pd的富集状况、存在形式、矿物学特征等，可查明渣尔泰山群、白云鄂博群中的含矿层位，以达到寻找铂、钯矿床的目的。     

柴达木盆地北缘"沙柳河岩群"的重新启用

柴北缘变质基底岩系中的表壳岩包含了岩石组合、沉积建造、变质程度和地质时代不同的两套岩石组合。其中，分布在柴达木地块的沙柳河、鱼卡河等地的以大理岩、石英岩和含石榴石英片岩为主含榴辉岩透镜体的表壳岩系，时代限定在1．0～1．3Ga，与分布在欧龙布鲁克微陆块的全吉山、德令哈等地形成时代大约2.3～2.4Ga的达肯大坂岩群有着明显的不同，后者以斜长角闪岩、石榴石英片岩和黑云变粒岩为主，并具有较强的钾质混合岩化。由于前者岩石组合清楚，沉积建造特征明显，构造意义独特，且有一定的区域分布性和可比性，所以具备建立新的岩群的条件。根据定名优先的原则，决定重新启用沙柳河岩群。     

北秦岭二郎坪群低压变质作用研究

在对二郎坪群低压变质带进行相图分析后发现，二郎坪群低压变质带是叠加变质带，低压变质作用是在早期中压变质的抬升过程中发生的，中压变质的温压条件为0．5-0．6GPa、560～580℃，低压变质的压力为0．3-0．45GPa，红柱石-十字石带的温度为510～580℃，堇青石带为590-620℃。pT视剖面图在区分岩石中不同条件和期次的矿物组合及分析岩石温压演化历史和温压条件时显得更行之有效。     

内蒙古"宝音图隆起"的归属讨论

对比研究表明，内蒙古“宝音图隆起”和狼山地区的古元古代宝音图岩群与新太古代色尔腾山岩群都是由中低级变质的各种片岩、大理岩组成，一致的岩石组合和变质相暗示二者可能是等同物而不是两个岩群。以物探资料为据的构造研究也证实，“宝音图隆起”与狼山地区之间并无槽一台级的大型断裂构造分开，二者实为统一的构造整体而不是分属槽台，只因两侧被两条近于平行的NE向断裂围限，使其总构造线方向呈NE或NNE向而与色尔腾山的构造线不同。结论认为，“宝音图隆起”仍是华北陆块的一部分，不属于内蒙古一大兴安蛉地槽褶皱系。     

冀中坳陷-黄骅坳陷馆陶组热储发育差异性及成井条件

本文论述了冀中坳陷-黄骅坳陷馆陶组热储砂岩、底部砾岩、砂砾岩的发育、孔隙度及热水水质的差异性,对热储出水特征进行了探讨,提出了馆陶组热储成井的基本条件,对冀中坳陷-黄骅坳陷馆陶组热储成井具有一定的指导意义。     

Geochemical Correlation Between Metasediments of the Mfongosi Group of the Natal Sector of the Namaqua-Natal Metamorphic Province, South Africa and the Ahlmannryggen Group of the Grunehogna Province, Antarctica

The whole-rock geochemistry of metamorphosed greywackes, arenites and arkoses within the Mesoproterozoic Namaqua-Natal-Maudheim Province is interpreted with the aim of establishing geochemical correlations and defining common sediment source terrains. Metasediments of the Mfongosi Group of the Natal Sector of the Namaqua-Natal Metamorphic Province were sampled from their type area in the Mfongosi Valley. Metagreywackes from the northern limits of the Mfongosi Valley, directly adjacent to the Kaapvaal Craton, show ocean island arc signatures while metagreywackes from the southern limits of the Mfongosi Valley, near the contact with the Madidima Thrust of the Natal nappe zone, show mainly active continental margin signatures. Interleaved, geochemically distinct low-Ca+Na, high-K metamorphosed arkoses to lithic arkoses indicate a minor passive margin sediment component. Geochemical classification of low-grade Ahlmannryggen Group greywackes, arenites and arkoses of the Grunehogna Province, Antarctica, indicates both active and passive continental margin sediment sources. An oceanic island arc signature is not evident in Ahlmannryggen Group data. The active continental margin signature in both Natal Sector and Grunehogna Province metasediments potentially provides for a common link between these terranes. Discriminant Function Analysis, using three pre-defined provenance sub-sets within the Mfongosi Group and two pre-defined provenance sub-sets within the Ahlmannryggen Group, indicate that metasediments with active continental margin signatures from both groups are geochemically identical, implying that the active continental margin of the Grunehogna Province shed immature sediments westwards (African azimuths) into the developing, narrow or restricted Mesoproterozoic ‘Mfongosi Basin.’ This was accompanied by minor sediment influx from a stable continental platform, potentially the Kaapvaal Craton. Oblique and diachronous collision, initiated in the southwestern portions of the combined Natal Sector/Grunehogna Province system produced a laterally variable Mfongosi Group, which formed in the ‘Mfongosi Basin’. Coarse-grained sediments dominated in its eastern portions while basalts with thin sapropelite units dominated in its western portions.     

Temnospondyls from the Beaufort Group (Karoo Basin) of South Africa and Their Biostratigraphy

The Permo-Triassic Beaufort Group (Karoo Basin) of South Africa is biostratigraphically subdivided into eight, temporally successive assemblage zones based on therapsids (‘mammal-like reptiles’). The Temnospondyli, fossil tetrapods usually regarded as extinct amphibians, are second only to therapsids in terms of diversity and abundance in these strata, with nine higher-level taxa (‘families’) known. Temnospondyls are also playing an increasingly important role in biostratigraphy and correlation of the Beaufort strata. The lower Beaufort Group (Late Permian) contains six of the eight biozones, but only one temnospondyl ‘family’, the Rhinesuchidae, whose record in the Karoo is the richest in the world. However, rhinesuchid taxonomy remains in flux and the group is thus of limited biostratigraphic utility. The Early Triassic Lystrosaurus Assemblage Zone (middle Beaufort Group) contains the Rhinesuchidae, Amphibamidae, Lydekkerinidae, Tupilakosauridae, Rhytidosteidae, Mastodonsauridae and Trematosauridae, although the biostratigraphy of temnospondyls within this biozone is poorly constrained. The uppermost reaches of the Lystrosaurus biozone contain a paucity of fossils but includes ‘Kestrosaurus’ (Mastodonsauridae) and ?Trematosuchus (Trematosauridae), taxa previously thought to pertain to the lower part of the overlying Cynognathus biozone. The late Early to Middle Triassic Cynognathus Assemblage Zone (upper Beaufort Group) hosts the Mastodonsauridae, Trematosauridae, Brachyopidae, Laidleriidae and, possibly, the Rhytidosteidae. Based largely on the spatial and temporal distribution of mastodonsaurids, this biozone has been biostratigraphically subdivided into a lower A, middle B and upper C subzones, characterised by differing ages and faunas.