湖北三叠纪海生爬行动物的层位及时代

通过对化石点的实地调查证实 ,湖北南漳、远安发现的海生爬行类除孙氏南漳龙 (大冶组顶部或嘉陵江组底部 )外都产自嘉陵江组 ,它们的时代同为早三叠世奥伦尼克期。由孙氏南漳龙、南漳湖北鳄、湖北汉江蜥和远安贵州龙形成的这一海生爬行动物组合 ,是上扬子地区层位最低的 ,生存时代早于其他海生爬行动物组合。与产自欧洲的肿肋龙类有密切亲缘关系的贵州龙和汉江蜥 ,是该科最早的代表 ,也是鳍龙类最早的代表之一 ,为探讨鳍龙类和肿肋龙类的起源及传播提供了新的证据。     

关岭及相关生物群沉积与生态环境的探讨

根据近年来对黔东南至滇东关岭、兴义、贞丰和罗平等地中一晚三叠世含海生爬行动物骨架和(或)深水海百合黑色岩系(通常所称黑色页岩)化石库的研究,现将该区岩石地层单位划分.以及这些黑色岩系化石库生物组合特征、时代、分布、沉积和古地理环境概括如下:1)在关岭-兴义地区中-晚三叠世(安尼期、拉丁期和早卡尼期)地层中,至少夹有3层、甚至4层含海生爬行动物的黑色岩系化石库(或黑色"页岩"化石库),自下而上产盘县生物群、兴义生物群和关岭生物群.云南罗平地区中三叠统关岭组中新发现的"罗平生物群"与盘县生物群层位大致相当.贞丰龙场赖石科组上部新挖掘出的30m厚产创口海百合、双壳类及菊石的黑色岩系,应该是研究地区最高层位的海相三叠纪黑色岩系,时代似属晚三叠世早卡尼期晚期;2)推测这些含海生爬行动物骨架的黑色岩系化石库是在印支造山运动影响下,伴随南盘江前陆盆地隆升和闭合,在扬子克拉通台地边缘所形成的一个或几个边缘凹陷、或边缘盆地之中形成的,这些凹陷或盆地形成之初,表层水充氧,且具有很好的食物链结构,有利于各类海生生物生活;后来的海平面上升至最大海泛期,以及由此引起缺氧和含硫化氢水位的上升,导致这些凹陷逐渐变成安静、滞流的死亡之海和黑色岩系化石库;3)关岭生物群产于晚三叠世卡尼期早期小凹组下段上部黑色岩系之中,是一个典型的在滞流、缺氧且海底没有食腐动物边缘局限盆地中所形成的黑色页岩化石库,以产大量海生爬行动物和深水假浮游海百合为特征,此外还有个别的两栖类和原始龟类发现;4)产于竹杆坡组近底部黑色岩系中的兴义生物群,以产大量肿肋龙类为特点,尤以个体较小的贵州龙最为常见,共生的还有多种鱼类化石,在生物组合和产出层位上,可与阿尔卑斯南部Meride灰岩所夹黑色含沥青页岩化石库对比,时代似应归属拉丁期早或中期;大量米虾在竹杆坡组近底部含贵州龙层的发现.推测兴义生物群可能形成于台地边缘早期并不缺氧,且具有理想食物链结构的浅水、超盐的凹陷或盆地之中.由于存在浮游生物-虾-贵州龙-欧龙-虾-浮游生物所组成的生态组合和食物链结构,从而为解释以肿肋龙类为代表的兴义生物群的繁衍和多生提供了依据;接踵而来的沉积速率下降和缺氧水位的上升,以及间歇性火山作用,导致该特有生态体系的崩溃和化石库的形成.根据对贞丰挽澜竹杆坡组底部首次发现的棘皮动物的化石库的研究,指出该化石库系由海星、细小蛇尾、底栖海百合茎、海胆和海参等5类棘皮动物化石和含贵州龙骨架碎片组成,其下为8m厚夹有薄层的骨层的凝缩层沉积,后者位于硬底之上.此种沉积和埋藏模式与德国上壳灰岩早拉丁期的棘皮动物化石库类似,是在近岸海水不太浅的内陆棚的环境下,由于风暴潮作用所形成的化石库,他们与在滞流、缺氧海底、通过化石聚集所形成的化石库是不同的;5)产盘县生物群的黑色岩系化石库主要见于盘县羊件和普安青山中三叠世(安尼期)关岭组中,与云南罗平地区的"罗平生物群"在层位及生物组合上大致相当,均以含大量混鱼龙、幻龙和欧龙.以及鱼类为特点,共生的还有大量节肢动物.所不同的是后者由于靠近滨岸,故而出现大量幼年期的鱼类以及虾类和鲎类化石,推测他们形成于靠近古陆或滨岸的台缘浅水表层充氧的正常、且有时超盐的凹陷之中,时代上早于阿尔卑斯南部安尼期/拉丁期比塞娄组;其集群死亡除因后期盆地滞流、缺氧外,可能还与风暴和火山作用有关.     

贵州中三叠世长颈龙属(原龙目:长颈龙科)一幼年个体

记述了贵州兴义法郎组竹杆坡段（中三叠世拉丁期）长颈龙属未定种（Tanystropheus sp．）一幼年个体的不完整骨架。这是该属在欧洲和中东以外的首次发现。新材料仅保存部分颈椎、躯干和前肢。根据特殊的颈椎形态将该标本归入长颈龙属,而区别于另一种长颈的海生原龙类——东方恐头龙（Dinocephalosaurus orientalis）。新标本的腕骨形态简单,骨化程度弱,表明长颈龙是终生水生的动物。“长颈、长颈肋”见于多种不同海生爬行动物（如原龙类、初龙类）,它们很可能都以“吞吸”的方式捕食。长颈龙化石在我国的发现进一步验证了中国南方三叠纪海生爬行动物群与欧洲西特提斯动物群（western Tethyan fauna）之间的密切关系。     

中国三叠纪海生爬行类综述

三叠纪海生爬行类化石广泛分布于中国南方的安徽、湖北、贵州、云南、广西和西藏。它们不仅包括有世界性分布的鱼龙类、鳍龙类、海龙类、原龙类等,而且还有仅出现于扬子海区的湖北鳄类。简单回顾了中国三叠纪海生爬行类的研究历史。根据化石的地史分布确认了自早三叠世晚期至晚三叠世早期的7个海生爬行类组合带。它们是奥伦尼克期的 Chaohu- saurus-Keichousaurus-Hupehsuchus 组合带,安尼期的 Chinchenia-Sanchiaosaurus 组合带和 Dino- cephalosaurus-Mixosaurus 组合带,拉丁期的 Dingxiaosaurus 带和 Keichousaurus-Nothosaurus 组合带,卡尼期的 Anshunsaurus-Qianichthyosaurus-Sinocyamodus 组合带和诺利期的 Himalayasaurus 带。对化石的古地理环境分析表明,中国早三叠世晚期的海生爬行类主要分布于扬子海区东部(安徽、湖北)的浅海开阔台地和局限海台地。中三叠世由于东部地区的抬升,鱼龙类和鳍龙类向西扩散,在扬子区西部(贵州、云南)辐射发展,在拉丁期达到个体数量和种类的高峰。晚三叠世卡尼期动物的数量依然很多,个体有增大的趋向,但高级分类阶元的数量减少,它们埋藏于海水相对较深的浊积岩相中。晚三叠世诺利期的化石发现于西藏的定日和聂拉木,这是中国惟一属于冈瓦那特提斯区的三叠纪海生爬行类组合带,仅含大型的鱼龙类。受动物的生存环境和埋藏条件的影响,中国三叠纪海生爬行类化石记录并不完整。目前尚有相当数量的化石未经研究,已记述的化石也需要在研究程度上进一步深化。     

中国三叠纪海生爬行动物化石研究的回顾与进展

中国三叠纪海生爬行动物化石研究始于20世纪50年代，近10年来取得了重要的进展。此类化石在华南分布广泛，已见于多个省区的十余处地点，涉及自下三叠统奥伦尼克阶至上三叠统诺利阶的至少7个层位，并显示出由东向西产出层位逐渐升高的趋势。我国的三叠纪海生爬行动物化石门类齐全，属种丰富，已知类群包括鱼龙类、海龙类、檐齿龙类、始鳍龙类、原龙类、初龙类和湖北鳄类，显示出典型的西特提斯动物群特征，同时也体现了与东太平洋动物群的某些联系，以及一定的地方色彩。这些化石为研究三叠纪海生爬行动物各个类群的起源、演化和绝灭以及海洋环境的变迁提供了新的材料。     

论广西武鸣三叠纪海生爬行动物东方广西龙(鳍龙类)的时代

广西武鸣产出广西地区迄今唯一一件三叠纪海生爬行动物化石——东方广西龙(Kwangsisaurus orientalis)。受限于20世纪50年代研究条件,有关该化石产出地点、地层层位和时代信息一直比较模糊,对后人阐述中国三叠纪海生爬行动物演化过程及探究鳍龙类在华南的古地理迁移历史造成了一定阻碍。本文从岩石地层学和生物地层学入手,结合高精度同位素年代学定年结果,对武鸣地区早、中三叠世地层进行了综合分析,着重研究了含东方广西龙地层的岩性组合、生物群面貌及地层时代。东方广西龙产于板纳组薄层泥晶灰岩中,伴生有丰富的菊石化石,所属地层时代为中三叠世安尼期。对含东方广西龙地层上部层状凝灰岩中具有岩浆韵律的锆石进行了SIMS原位U-Pb年代学测试,获得了(244.2±0.7)Ma的绝对年龄值,时代相当于安尼期中晚期。东方广西龙时代的厘定排除了鳍龙类早三叠纪世晚期在下扬子区和右江盆地同时出现的原有结论,同时同位素年代学新证据证实广西武鸣海生爬行动物化石与贵州盘县海生爬行动物群基本同期,表明了鳍龙类在华南东部起源后在三叠纪中期向西南地区辐射扩散范围的广阔性和适应环境的多样性。     

云南中三叠世豆齿龙类（爬行纲：楯齿龙目）一新属

中国已知的檐齿龙目(Placodontia)化石仅见于贵州省西南部地区,其中豆齿龙亚目(Cya-modontoidea)产自关岭地区的法郎组瓦窑段,时代为晚三叠世卡尼期;楯齿龙亚目(Placodon-toidea)产自盘县的关岭组Ⅱ段,时代为中三叠世安尼期.本文记述的豆齿龙类新属种--康氏雕甲龟龙(Glyphoderma kangi gen.et sp.nov.)产于云南富源的法郎组竹杆坡段,属中三叠世拉丁期.正型标本保存于浙江自然博物馆(编号:M 8729),其头骨高度愈合,代表一个完全成年之个体,根据以下特征明显区别于我国的Psephochelys和欧洲的Psephoderma:1)头骨枕部具3枚大型的锥状鳞;2)背甲甲片结构更为复杂,具明显的放射状沟/脊结构.到目前为止,康氏雕甲龟龙是龟龙科(Placochelyidae)中惟一的中三叠世属种,该科的其他成员全部发现于上三叠统.     

贵州中三叠世长颈龙属(原龙目:长颈龙科)一幼年个体

记述了贵州兴义法郎组竹杆坡段(中三叠世拉丁期)长颈龙属未定种(Tanystropheus sp.)一幼年个体的不完整骨架。这是该属在欧洲和中东以外的首次发现。新材料仅保存部分颈椎、躯干和前肢。根据特殊的颈椎形态将该标本归入长颈龙属,而区别于另一种长颈的海生原龙类———东方恐头龙(Dinocephalosaurus orientalis)。新标本的腕骨形态简单,骨化程度弱,表明长颈龙是终生水生的动物。“长颈、长颈肋”见于多种不同海生爬行动物(如原龙类、初龙类),它们很可能都以“吞吸”的方式捕食。长颈龙化石在我国的发现进一步验证了中国南方三叠纪海生爬行动物群与欧洲西特提斯动物群(western Tethyan fauna)之间的密切关系。     

云南中三叠世豆齿龙类(爬行纲：楯齿龙目)—新属(英文)

中国已知的楯齿龙目(Placodontia)化石仅见于贵州省西南部地区,其中豆齿龙亚目(Cya- modontoidea)产自关岭地区的法郎组瓦窑段,时代为晚三叠世卡尼期;楯齿龙亚目(Placodon- toidea)产自盘县的关岭组Ⅱ段,时代为中三叠世安尼期。本文记述的豆齿龙类新属种——康氏雕甲龟龙(Clyphoderma kangi gen.et sp.nov.)产于云南富源的法郎组竹杆坡段,属中三叠世拉丁期。正型标本保存于浙江自然博物馆(编号:M 8729),其头骨高度愈合,代表一个完全成年之个体,根据以下特征明显区别于我国的Psephochelys和欧洲的Psephoderma:1)头骨枕部具3枚大型的锥状鳞;2)背甲甲片结构更为复杂,具明显的放射状沟/脊结构。到目前为止,康氏雕甲龟龙是龟龙科(Placochelyidae)中惟一的中三叠世属种,该科的其他成员全部发现于上三叠统。     

山西地质博物馆脊椎动物化石发掘研究的助推者

正如今一提到山西地质博物馆,在全国地质专业类博物馆界已小有名气。山西地质博物馆展陈的最大特色是古生物展厅,而古生物厅的突出亮点是早中三叠世的中国肯氏兽动物群。中国肯氏兽动物群是指中国北方早中三叠世以兽孔类和原始主龙类为主体的四足类动物群。为了融科学性、趣味性于一体,我们同时将我国南方中晚三叠世的关岭生物群以及相近的海生爬行动物作了"南海北陆"的对比展示,着实给观众提供了十分丰盛的文化大餐。     

The cranial anatomy of Chinese placodonts and the phylogeny of Placodontia (Diapsida: Sauropterygia)

Placodonts are Triassic marine reptiles that inhabited the eastern and western margins of the Tethys Ocean (modern South China and Europe/Middle East). Although the crania of European taxa are relatively well understood, those of Chinese taxa have not been extensively studied, and most of them have not been incorporated into a comprehensive phylogeny. Here we present the first reconstructions of all known Chinese placodont holotype skulls using micro‐computed tomographic (μCT) scanning and/or detailed anatomical study. We also present the first phylogenetic analyses that incorporate all placodont genera using a general diapsid matrix that includes postcranial characters, and a placodont‐only cranial matrix. Results vary between the matrices; however, both support a monophyletic Placodontia with eastern taxa interspaced throughout, indicating no major separation between the eastern and western Tethyan realms. Support is strong for a western Tethyan origin of Placodontia, although the highly nested Placochelyidae first appear in the upper Middle Triassic of the eastern Tethys. Thus, all placodont clades appear to have originated in a period of intense speciation during the Middle Triassic. © 2015 The Linnean Society of London     

川西,藏东晚三叠世有孔虫及海参骨片

金沙江上游两岸为川西、藏东地区。此区的四川省白玉县、西藏贡觉县及江达县的晚三叠世诺利期沉积中发现了有孔虫１８属２１种,海参骨片５属８种。三叠纪海参在中国为首次报道：白玉县及贡觉县的三叠世有孔虫也为首次发现。这一动物群在区域地质史及古地理研究上具有一定意义。     

贵州兴义中三叠统法郎组竹杆坡段Lariosaurus一新种

记述了贵州兴义法郎组竹杆坡段鸥龙的一新种──兴义鸥龙(Ｌａｒｉｏｓａｕｒｕｓ ｘｉｎｇｙｉｅｎｓｉｓ ｓｐ．ｎｏｖ．)。兴义鸥龙以其上颞孔是眼眶长度的两倍,顶骨平台细长而不收缩,肱骨缺失外髁沟和旋后肌突,及肱骨短于股骨而有别于鸥龙的其他种。兴义鸥龙与意大利拉丁晚期的Ｌａｒｉｏｓａｕｒｎｓｖａｌｃｅｒｅｓｉｉ最为相似。依据脊椎动物的对比,法郎组竹杆坡段的时代应为中三叠世晚期。     

Fossil reptiles from the Spanish Muschelkalk (mont‐ral and alcover,province Tarragona)

The marine tetrapods from the late Ladinian Spanish Muschelkalk deposits located between the towns of Mont‐ral and Alcover (province Tarragona) are reviewed. The fauna comprises an undetermined thalattosaur, a small cyamodontoid placodont probably referrable to Psephoderma, a possible pachypleurosaur with (if any) affinities to the Serpianosaurus‐Neusticosaurus clade, lariosaur specimens currently referred to Lariosaurus balsami, an incomplete specimen of Lariosaurus calcagnii, an endemic nothosaur (Nothosaurus cymatosauroides), and a possible pistosaur. Collectively, the faunal mix comprises endemic taxa as well as elements with affinities to the fauna of the Alpine and/or Germanic Triassic. The fauna suggests faunal interchange through the Burgundy Gate linking the southern branch of the developing Neotethys to the Germanic Basin.     

Paleobiogeography of Mesozoic brachiopod faunas from Andean–Patagonian areas in a global context

During the Mesozoic, the Andean region has played a hinging role between high- and low-latitude faunas, which are, respectively, characterized by stocks that display long-term fidelity. This paper is aimed at providing an updated review of Late Triassic to Late Cretaceous South American articulated brachiopods in the light of previous knowledge at worldwide scale. Late Triassic brachiopods from the Argentine–Chilean Andes show unmistakable Maorian (or Notal) faunal elements alongside some more cosmopolitan genera, with certain influence of Eastern Pacific taxa. By Early Jurassic times, differentiation of Tethyan and Boreal Realms became progressively evident in Europe. In South America, Hettangian–Sinemurian brachiopod faunules from the Argentinian Andes are somewhat impoverished, with mostly cosmopolitan genera showing certain affinities to Maorian species, and with the addition of some endemics later. Increasingly, diverse Pliensbachian Andean brachiopods denote close relationships to Celto-Swabian taxa, then by Domerian times, a certain degree of endemism was developed, though somewhat delayed Tethyan influences, and persistent links with New Zealand are subordinately recognizable, too; most Toarcian assemblages reveal basically Celto-Swabian and Iberian affinities as well. East-west austral links across the Pacific may have been favored by migratory routes fringing the Gondwana margin, whereas faunal exchange with the western end of the Tethys appears to reflect an intermittent shallow-marine connection through the Hispanic Corridor. During the Middle Jurassic, distinction of Tethyan and Boreal Realms was maintained in the northern Hemisphere, and the differentiation of an Ethiopian or Southern Tethyan fauna became better characterized. Aalenian and Bajocian brachiopods of the Andes display generic affinities mainly with those from western Europe, with some minor endemic developments; brachiopods recorded from the Bathonian–Callovian of Argentina (and Chile) also occur along the northern Tethyan margin, yet with some genera extending into Indo-Ethiopian areas. During the Late Jurassic, Boreal faunas from high-latitudes became even more strongly differentiated from low-latitude, Tethyan ones. Oxfordian and Tithonian brachiopods from the Andes apparently belong to genera of cosmopolitan or northern Tethyan affiliation, yet there are few elements in common with other eastern Pacific areas, such as Mexico. Early Cretaceous brachiopods, in addition to Andean basins of Chile and western Argentina, are known also from Patagonia and Tierra del Fuego. They belong mostly to widely distributed, mainly Tethyan genera, with some quasi-cosmopolitan and circum-Pacific components (some shared with Antarctica become noticeable). Late Cretaceous brachiopods from northern Patagonia show significant affinities to Maastrichtian ones of northwest Europe and central Asia, which calls for further assessing the potential role that may have played the trans-Saharan passageway in such dispersal. Broad aspects of Mesozoic brachiopod paleobiogeography are fairly well understood, yet details of ranking and naming of certain units are still in need of more agreement.     

A biogeographically mixed, Middle Permian brachiopod fauna from the Baoshan Block, western Yunnan, China

A small brachiopod fauna is described from the carbonate rocks of the basal Shazipo Formation of the Baoshan Block, western Yunnan, south-west China, including significant new ventral and dorsal internal morphological features of Cryptospirifer omeishanensis Huang. This fauna is regarded as Wordian (Middle Guadalupian, Middle Permian) because of the presence of Cryptospirifer omeishanensis Huang and associated fusulinids ( Neoschwagerina craticulifera Zone). Palaeobiogeographically, the brachiopod fauna is of considerable interest because of its admixed nature characterized by typical warm-water Cathaysian elements intermingled with temperate Peri-Gondwanan taxa. This in turn is interpreted to indicate that the Baoshan Block may have been situated in an intermediate palaeogeographical position between Gondwanaland to the south and Cathaysia to the north during the Mid Permian and, as such, it probably furnished an important 'stepping stone' for the dispersal of Mid Permian eastern Tethyan marine invertebrate taxa (e.g. Cryptospirifer ) to the western Tethys.