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101.
贵州贵阳地区下三叠统凝缩段的遗迹化石特征   总被引:2,自引:0,他引:2  
贵阳地区下三叠统是一个完整的碳酸盐岩层序(相当于三级旋回层序).该层序中的凝缩段由深色薄层(单层厚0.5cm~1cm)的泥晶灰岩和泥质条带灰岩组成.凝缩段中产丰富的遗迹化右.该遗迹群落为:Cochlichnus,Cosmorhaphe,Chondrites,Gordia,Huaxich-nus,Oldhamia,Phycosiphon.Protopaleodictyon,Pinnatpedus,Mammillichnus,Neonerites和生物扰动构造.遗迹化石组合与Nereites遗迹相相似。此外,文本还讨论了此遗迹群落的形成原因。  相似文献   
102.
刘金辉  李学礼 《矿床地质》2001,20(3):259-264
形成于古水热系统排泄区(减压区)的下庄花岗岩型铀矿床是地下热水与岩石相互作用的产物。矿物流体包裹体水文地球化学分析表明,成矿期铀成矿古热水溶液气体成分主要为CO2,水化学类型为HCO3-Ca.Na型,F-Ca型和HCO3.F-K型。地球化学模式和热力学计算证明,热水溶液中铀的存在形式为UO2(CO3)2^2-,UO2F3^-和UO2F4^2-。热水溶液深循环过程中CO2的加入可使溶液铀沉淀临界电位值(EhC,U)明显降低,从而保持水-铀比电位值(ΔEhW,U)为正值(ΔEhW,U=EhW-EhC,U)使铀在深部相对还原的条件下仍能稳定迁移。当富铀成矿热液进入减压排泄区时,由于溶液物理-化学条件的改变,发生CO2脱气作用和中和还原作用,导致ΔEhW,U小于零,使铀沉淀、富集,最终形成花岗岩型铀矿床。  相似文献   
103.
古炭屑与古森林火?   总被引:9,自引:1,他引:9       下载免费PDF全文
森林火普遍发生在地质历史时期中,它对自然植被系统的演替起着重要作用。不同强度和频率的森林火培育出不同类型的植被:频繁的森林火导致草甸的形成,而热带雨林形成的原因之一是森林火的缺乏。古炭屑作为古森林火的遗迹,具有分布广泛、细胞结构保存完好以及原地埋藏等特点,为研究古森林火发生的强度和频率提供了宝贵的材料。古炭屑的出现与当时的气候因素、植被类型和地理状况有密切关系:干旱、少雨的气候常常伴随高频率森林火的发生,表现出古炭屑的数量增多;易燃物种组成的植被易发生森林火,古炭屑的出现也会增多,而耐火树种会降低森林火的强度,古炭屑则出现少。因此,从古炭屑的数量和种类的变化,可探讨古森林火的发生规律,进而推断长期地质历史时期的气候、植被、地理状况的演变。  相似文献   
104.
贵州关岭生物群中植物化石的发现及其意义   总被引:4,自引:1,他引:4  
关岭生物群是近年来在我国贵州关岭地区瓦窑组中发现的一个十分重要的生物群 ,其中的植物化石经研究计有 Equisetites cf.arenaceus(Jaeger) Bronn.、Ctenozamitessarrani Zeiller。依据植物化石 C.sarrani常见于晚三叠世和 E.cf.arenaceus系似木贼属中较古老的类型 ,指出含植物化石的地层时代为晚三叠世卡尼期。瓦窑组系海相沉积 ,其中的植物化石无疑为异地埋藏 ,但从化石通常保存尚好来看 ,估计搬运的距离不会很远 ,它们可能是从距海岸不远的陆地被河流带到较平静的海湾或海槽而沉积下来的。此外 ,从该组植物茎干化石具清楚的年轮分析 ,推测卡尼期时 ,贵州关岭一带为非热带雨林地区 ,一年中气候不是四季如一 ,而是有明显的季节变化  相似文献   
105.
论卡以头组的时代   总被引:2,自引:2,他引:2  
中国科学院南京地质古生物研究所的有关人员 (1980 )曾做过大量地层古生物工作 ,证实卡以头砂页岩层或卡以头组的时代为三叠纪最早期 ,是飞仙关组底部地层的相变。“论卡以头组”一文认为该组下部的时代为二叠纪 ,上部则属三叠纪。对该文提供的地层古生物资料进行分析后 ,本文作者认为该论点缺乏证据 ,不能成立 ;将陆相的威宁哲觉剖面代替标准地点宣威羊场的过渡相剖面作为卡以头组的标准剖面 ,也是不合适的  相似文献   
106.
新疆乌什—阿克苏地区下寒武统玉尔吐斯组的小壳化石丰富,已描述了近50属90种,包括1个新属,15个新种。计有软舌螺类、似软舌螺类、单板类、腹足类、骨针类及分类位置未定的化石,还有节肢动物门的高肌虫类。按小壳化石在地层纵向出现的次序及其代表性,可将玉尔吐斯组小壳动物群的比石划分为3个带,即1.Anabarites trisulcatus带;2.Cambroclavus-Aurisella带;3.Adyshevitheca-Xinjiangella带。其中1带可与梅树村阶I.Anabarites-Protohertzina带对比;2—3带大致可与梅树村阶Ⅱ.Paragloborilus-Siphogonuchites带—Ⅲ.Sinosachites-Lapworthella带对比。因Aanbarites trisulcatus的发现,证实玉尔吐斯组的下界可与梅树阶的底界对比;玉尔吐斯组顶部发现的高肌虫有别于筇竹寺阶的高肌虫。前者与大量梅树村期小壳动物共生,可以认为梅树村期已经出现高肌虫的先遣分子。  相似文献   
107.
淮北煤田早二叠世化石植物丰富,其形成于炎热多雨的热带滨海三角洲沉积体系中。下三角洲平原是该区化石植物最宜生长的地方。早二叠世该区化石植物常形成四类植物群落:森林沼泽植物群落、沿岸水生植物群落、高地植物群落、三角洲平原真蕨及种子蕨混生植物群落(早期)、树蕨-大羽羊齿类雨林植物群落(晚期)。随着时间的推移,这四类植物群落的结构及面貌发生着不断的变化;其演替显示,早二叠世晚期该区气侯更加湿热,雨林气侯更为普遍。  相似文献   
108.
Palaeozoic and early Mesozoic fish faunas of the Japanese Islands   总被引:2,自引:0,他引:2  
MASATOSHI GOTO 《Island Arc》1994,3(4):247-254
Abstract In recent years, many fish teeth and scales have been found from the Palaeozoic and Mesozoic age strata of the Japanese Islands. This study is a compilation of the Japanese fish record from the Palaeozoic and early Mesozoic age deposits. Based on the published and unpublished data, the fossil fishes from the Palaeozoic and Early Mesozoic of Japan can be classified into 27 genera and 33 species, that is, one species of Devonian placoderms, 19 species of Permian to Jurassic elasmobranchs, three species of Permian cochliodonts, seven species of Carboniferous to Permian petalodonts, and three species of Triassic to Jurassic osteichthyans.  相似文献   
109.
Hideo  Horikawa 《Island Arc》1994,3(4):309-328
Abstract The well preserved cranium of Protodobenus japonicus, a new genus and species of odobenine walrus, is from the lower part of the Tamugigawa Formation at Ooshima-mura, Higashi Kubiki-gun, Niigata Prefecture, central Japan. The lower part of the formation that yielded P. japonicus is Early Pliocene, dating approximately from 5.0 to 4.9 Ma. The skull of P. japonicus is generally shaped like that of the modern walrus, Odobenus rosmarus (Linnaeus, 1758), but is much more primitive, especially in the dentition. Protodobenus japonicus is derived from the Imagotariinae. It is similar to such primitive fossil walruses as Prorosmarus alleni from the Western Atlantic and Aivukus cedrosensis from Baja California, and has some similarities as well as significant differences from them. Protodobenus japonicus could have evolved directly into Odobenus in the North Pacific Ocean, and could have dispersed directly to the Arctic Ocean. This is contrary to the scenario proposed by Repenning and Tedford, in which primitive odobenids, like Aivukus cedrosensis, migrated to the Atlantic Ocean through the Central American Seaway and returned to the North Pacific Ocean as O rosmarus via the Arctic about 0.6 Ma. Regarding the first lower premolar of the living walrus, Fay concluded after studying fetal O. rosmarus that the first premolar (P1) of the mandible is absent, and that the lower tooth row consists of: C1 P2, P3, P4. Protodobenus japonicus has in its mandible I 1-2 C1 P2, P3, P4, and this is the primitive pinniped formula. Pinnipeds typically lose the molars, not the anterior premolars, and the present author believes that the correct tooth formula for O rosmarus is C1 P1, P2, P3. Its skull, palate, and mandible suggest that P. japonicus had morphology pre-adapted to an early stage of benthic suction feeding, but it probably was unable to rely on that method of feeding. The discovery of P. japonicus demonstrates that the odobenine lineage (true walruses) goes back in time at least 5 Ma. Other more aberrant odobenine walruses, such as Aivukus and Prorosmarus, and pseudo-walruses of the subfamily Dusignathinae, are more distantly removed from the lineage leading to living walruses than has previously been suspected.  相似文献   
110.
Abstract Fossil pinnipeds in the extinct otariid subfamily Allodesminae are large, relatively highly evolved marine carnivores that became abundant and diverse in Middle Miocene time and were restricted to the North Pacific Ocean. Their record extends from early Middle Miocene through Late Miocene, with records from California, Oregon, Washington, Baja California and Japan. Allodesmines are characterized by extreme sexual dimorphism, a large orbit, retracted orbital margin of the zygomatic arch, a deeply mortised jugal-squamosal junction, wide palate, bulbous cheek tooth crowns, nearly flat tympanic bulla with wrinkled ventral surface, a large tympanohyal fossa, large ear ossicles and deep mandible. Eleven allodesmine species are known (eight of which are named), in at least four genera, and most belong to the typical genus Allodesmus Kellogg, 1922. The earliest and most generalized allodesmine known is from the early Middle Miocene (ca 16 Ma) Astoria Formation in coastal Oregon. The last known records are from Late Miocene rocks (ca 10 Ma) in California and Washington. New taxa proposed here are: the genus Brachyallodesmus Barnes and Hirota, to contain Allodesmus packardi Barnes, 1972; the genus Megagomphos Hirota and Barnes, to contain Allodesmus sinanoensis (Nagao, 1941); the species Allodesmus sadoensis Hirota, (Middle Miocene, Japan); the species Allodesmus megallos Hirota (Middle Miocene, Japan); and the species Allodesmus gracilis Barnes (Middle Miocene, California). Additionally, the genus Atopotarus Downs, 1956, and the species Allodesmus kelloggi Mitchell, 1966, are resurrected. Allodesmines were apparently a rapidly evolving group, and most appear to have been adapted to roles later filled by otariine, dusignathine and imagotariine otariids, and the Phocidae (true seals). They became extinct in Late Miocene time and left no living descendants. Although some of their characters evolved convergently with various living species of the pinniped family Phocidae, Allodesminae are an otariid group and not part of the evolutionary history of Phocidae.  相似文献   
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