Ankylosaur Remains from the Early Cretaceous (Valanginian) of Northwestern Germany

A fragmentary cervico-pectoral lateral spine and partial humerus of an ankylosaur from the Early Cretaceous (early Valanginian) of Gronau in Westfalen, northwestern Germany, are described. The spine shows closest morphological similarities to the characteristic cervical and pectoral spines of Hylaeosaurus armatus from the late Valanginian of England. An extensive comparison of distal humeri among thyreophoran dinosaurs supports systematic differences in the morphology of the distal condyli between Ankylosauria and Stegosauria and a referral of the Gronau specimen to the former. The humerus fragment indicates a rather small individual, probably in the size range of H. armatus, and both specimens are determined herein as ?Hylaeosaurus sp.. A short overview of other purported ankylosaur material from the Berriasian-Valanginian of northwest Germany shows that, aside from the material described herein, only tracks can be attributed to this clade with confidence at present.     

Diversity patterns amongst herbivorous dinosaurs and plants during the Cretaceous: implications for hypotheses of dinosaur/angiosperm co‐evolution

Abstract Palaeobiologists frequently attempt to identify examples of co‐evolutionary interactions over extended geological timescales. These hypotheses are often intuitively appealing, as co‐evolution is so prevalent in extant ecosystems, and are easy to formulate; however, they are much more difficult to test than their modern analogues. Among the more intriguing deep time co‐evolutionary scenarios are those that relate changes in Cretaceous dinosaur faunas to the primary radiation of flowering plants. Demonstration of temporal congruence between the diversifications of co‐evolving groups is necessary to establish whether co‐evolution could have occurred in such cases, but is insufficient to prove whether it actually did take place. Diversity patterns do, however, provide a means for falsifying such hypotheses. We have compiled a new database of Cretaceous dinosaur and plant distributions from information in the primary literature. This is used as the basis for plotting taxonomic diversity and occurrence curves for herbivorous dinosaurs (Sauropodomorpha, Stegosauria, Ankylosauria, Ornithopoda, Ceratopsia, Pachycephalosauria and herbivorous theropods) and major groups of plants (angiosperms, Bennettitales, cycads, cycadophytes, conifers, Filicales and Ginkgoales) that co‐occur in dinosaur‐bearing formations. Pairwise statistical comparisons were made between various floral and faunal groups to test for any significant similarities in the shapes of their diversity curves through time. We show that, with one possible exception, diversity patterns for major groups of herbivorous dinosaurs are not positively correlated with angiosperm diversity. In other words, at the level of major clades, there is no support for any diffuse co‐evolutionary relationship between herbivorous dinosaurs and flowering plants. The diversification of Late Cretaceous pachycephalosaurs (excluding the problematic taxon Stenopelix) shows a positive correlation, but this might be spuriously related to poor sampling in the Turonian–Santonian interval. Stegosauria shows a significant negative correlation with flowering plants and a significant positive correlation with the nonflowering cycadophytes (cycads, Bennettitales). This interesting pattern is worthy of further investigation, and it reflects the decline of both stegosaurs and cycadophytes during the Early Cretaceous.     

中国鲤形目鱼类的中轴骨骼数及其生态适应性

为探讨中国鲤形目鱼类中轴骨骼数及其与系统发育和生态习性的相关性,采用X光透视照相法对157种鲤科(Cyprinidae)、鳅科(Cobitidae)、平鳍鳅科(Balitoridae)鱼类的脊椎骨数、肋骨数、尾椎数进行了比较分析。结果显示,中国鲤形目鱼类的脊椎骨数在30-52枚之间,均值39.45?4.44;肋骨数在8-28对之间,均值15.27?3.08;尾椎数在14-34枚之间,均值21.08?2.89。依据脊椎骨数、肋骨数、尾椎数对鲤科各亚科进行聚类,显示鲤科12个亚科分为2大类：雅罗鱼类,包括雅罗鱼亚科、鲌亚科、鲴亚科、裂腹鱼亚科等4亚科;鲃类,包括鲢亚科、鮈亚科、鱼丹亚科、鲃亚科、野鲮亚科、鳅鮀亚科、鲤亚科、鱊亚科等8亚科。单因素方差分析显示,鲤科肉食性鱼类的肋骨数与脊椎骨数的比值显著少于植食性鱼类(P＜0.05),而脊椎骨数、尾椎数则显著多于植食性鱼类(P＜0.05)。中上层鱼类的脊椎骨数、尾椎数显著多于下层鱼类(P＜0.05)。极小型鱼类的脊椎骨数、肋骨数,以及肋骨数与脊椎骨数之比显著少于大型鱼类(P＜0.05)。表明鲤科鱼类的中轴骨骼数与其系统发育和生态习性及体型具有明显的相关性。     

Disparity vs. diversity in Stegosauria (Dinosauria,Ornithischia): cranial and post-cranial sub-dataset provide different signals

The Stegosauria represents an iconic group of ornithischian dinosaurs, with a fossil record spanning the Middle Jurassic to the Late Cretaceous. In this contribution I present the first detailed analysis of the relationship between disparity and diversity through the evolutionary history of the group. The analysis has been performed on a recently published cladistic dataset, allowing the separate study of the signals deriving from discrete characters and from continuous morphometric characters. Whereas the disparity as sum of variance is decoupled with respect to diversity, the sum of ranges provides a signal fairly consistent with the trend in the number of taxa. Both sub-data sets show that evolution of stegosaurs can be considered essentially as symmetrical, i.e. the maximum exploration of the possible morphospace takes place about half way through the history of the group, with subsequent significant decline until extinction in the Upper Cretaceous. An interesting result is a decoupling of the tempo and mode of evolution of the cranium and postcranium in stegosaurs. Specifically, the evolutionary radiation with maximum saturation of morphospace is anticipated in the cranial skeleton, with maximum peak in the Oxfordian; in contrast, the postcranium explores the largest number of morphotypes subsequently during the Kimmeridgian.     

Using creation science to demonstrate evolution 2: morphological continuity within Dinosauria

Creationist literature claims that sufficient gaps in morphological continuity exist to classify dinosaurs into several distinct baramins (‘created kinds’). Here, I apply the baraminological method called taxon correlation to test for morphological continuity within and between dinosaurian taxa. The results show enough morphological continuity within Dinosauria to consider most dinosaurs genetically related, even by this creationist standard. A continuous morphological spectrum unites the basal members of Saurischia, Theropoda, Sauropodomorpha, Ornithischia, Thyreophora, Marginocephalia, and Ornithopoda with Nodosauridae and Pachycephalosauria and with the basal ornithodirans Silesaurus and Marasuchus. Morphological gaps in the known fossil record separate only seven groups from the rest of Dinosauria. Those groups are Therizinosauroidea + Oviraptorosauria + Paraves, Tazoudasaurus + Eusauropoda, Ankylosauridae, Stegosauria, Neoceratopsia, basal Hadrosauriformes and Hadrosauridae. Each of these seven groups exhibits within‐group morphological continuity, indicating common descent for all the group’s members, even according to this creationist standard.     

Numerical variation of the presacral vertebral column in three population groups in North America

A total of 1,239 skeletons from among Mongoloid, Caucasoid and Negroid population groups in North America was examined for variations in the number of presacral vertebrae. The overall incidence of variation was 11%; 6% with 23 and 5% with 25 presacral vertebrae. Differences in total variation among the three groups were not significant, but differences in the incidence of 23 and 25 presacral vertebrae among the groups were highly significant. Numerical vertebral variation occurred in 11% of both sexes, but with males having a higher frequency of 25 presacral vertebrae and females having a higher frequency of 23 presacral vertebrae. The incidence of the specific variation of 23 or 25 presacral vertebrae was not significantly different among the males of the three groups studied, whereas 23 presacral vertebrae were found significantly more often in the Negroid females. Numerical variation of vertebrae was not associated with age. The data strongly support the conclusion that the total frequency of variation in the number of presacral vertebrae is a specific characteristic of any particular population group and that there is a tendency in all population groups toward an increase in number in males and a decrease in number in females.     

Trunk elongation and ontogenetic changes in the axial skeleton of Triturus newts

Body elongation in vertebrates can be achieved by lengthening of the vertebrae or by an increase in their number. In salamanders, longer bodies are mostly associated with greater numbers of vertebrae in the trunk or tail region. However, studies on the relative contribution of the length of single vertebra to body elongation are lacking. In this study, we focus on evolutionary and ontogenetic changes in differentiation of the trunk vertebrae and the relative contribution of individual vertebrae to trunk lengthening in Triturus newts, a monophyletic group of salamanders that shows remarkable disparity in body shape. We compared juveniles and adults of the most elongated T. dobrogicus , which has 17 trunk vertebrae, with juveniles and adults of two closely related species (T. ivanbureschi and T. anatolicus belonging to the T. karelinii species complex) representing a stout and robust morphotype with thirteen trunk vertebrae. We show that trunk vertebrae are uniform in size at the juvenile stage of both analyzed morphotypes. In adults, the trunk vertebrae of the elongated T. dobrogicus are largely uniform, while in those of T. anatolicus , the first two vertebrae differ from the remaining trunk vertebrae. There was no difference in the relative contribution of individual vertebrae to body lengthening between species or stages. We conclude that body elongation in Triturus newts is achieved by increasing the number of vertebrae but not their length.     

Heritability and genetic correlation of abdominal and caudal vertebral numbers in latitudinal populations of the medaka <Emphasis Type="Italic">Oryzias latipes</Emphasis>

Body axes of fishes consist of two anatomically distinct types of vertebrae: abdominal and caudal. In the medaka Oryzias latipes, the number of abdominal vertebrae increases with increasing latitudes, whereas caudal vertebrae do not vary systematically across latitudes, suggesting local adaptation in abdominal vertebral numbers. However, because heritable variation in abdominal and caudal vertebral numbers has not been examined within each latitudinal population, it is not clear whether abdominal and caudal vertebrae can evolve independently. Offspring-midparent regression demonstrated substantial heritability of abdominal vertebral numbers in each of two latitudinal populations whereas the heritability of caudal vertebral numbers was not significant. Full-sib analyses revealed that intra-family variation was larger in caudal vertebrae than in abdominal vertebrae, indicating larger non-additive genetic variation and/or larger errors of development in the former. Moreover, the genetic correlation between abdominal and caudal vertebral numbers was very weak. These results suggest that abdominal and caudal vertebrae are controlled by separate developmental modules, which supports their independent evolution with local adaptation of abdominal vertebral numbers in this fish. On the other hand, the weak heritability of caudal vertebrae suggests that the evolution of caudal vertebrae may be restricted, causing unequal evolutionary lability between abdominal and caudal regions.     

DR全脊柱成像技术应用探讨

目的探讨DR全脊柱成像技术在脊柱侧弯畸形诊断及测量中的价值,研究不同检查方法对成像质量及测量精度的影响。方法利用PHIIAPS公司Digital Diagnost DR系统和具有全脊柱拼接功能的SUN后处理工作站,对分次所摄的脊柱正位、侧位、左、右侧屈位影像进行拼接处理后作必要的测量,并打印成像。结果经上述处理后的全脊柱正位、侧位及左、右侧屈位均能将颈、胸、腰、骶椎完整联接,显示在1张14＋17的X光片上,其测量的数据真实可靠。结论DR全脊柱成像技术克服了以往颈、胸、腰、骶椎单独成像后测量上的误差,为临床手术提供了更精确的数据。     

Mechanical implications of pneumatic neck vertebrae in sauropod dinosaurs

The pre-sacral vertebrae of most sauropod dinosaurs were surrounded by interconnected, air-filled diverticula, penetrating into the bones and creating an intricate internal cavity system within the vertebrae. Computational finite-element models of two sauropod cervical vertebrae now demonstrate the mechanical reason for vertebral pneumaticity. The analyses show that the structure of the cervical vertebrae leads to an even distribution of all occurring stress fields along the vertebrae, concentrated mainly on their external surface and the vertebral laminae. The regions between vertebral laminae and the interior part of the vertebral body including thin bony struts and septa are mostly unloaded and pneumatic structures are positioned in these regions of minimal stress. The morphology of sauropod cervical vertebrae was influenced by strongly segmented axial neck muscles, which require only small attachment areas on each vertebra, and pneumatic epithelia that are able to resorb bone that is not mechanically loaded. The interaction of these soft tissues with the bony tissue of the vertebrae produced lightweight, air-filled vertebrae in which most stresses were borne by the external cortical bone. Cervical pneumaticity was therefore an important prerequisite for neck enlargement in sauropods. Thus, we expect that vertebral pneumaticity in other parts of the body to have a similar role in enabling gigantism.     

Remodelling of the vertebral axis during metamorphic shrinkage in the pearlfish

Body shortening was observed in the pearlfish Carapus homei during metamorphosis. The tenuis larva at first possessed a suite of osseous vertebral bodies of similar length. The reduction in both the number and size of vertebrae followed increasing decalcification, degeneration of organic tissue and shortening. This involved a complete degradation and disappearance of the caudal tip vertebrae, and there was a reduction in the size of most of the remaining vertebrae. The further development of the vertebrae began with ossification of the neural and haemal arches before that of the vertebral body. This second part of the development followed a gradient: a gradual decreases towards the caudal tip in the size of the vertebrae and their completeness.     

Assessing the accuracy of using whole and sectioned vertebrae to determine the age of an endemic sisorid catfish, <Emphasis Type="Italic">Glyptosternon maculatum</Emphasis>, in Tibet,China

The purpose of this study was to develop a reliable method of age estimation for Glyptosternon maculatum (Sisoridae, Siluriformes) in the Yarlung Tsangpo River basin of Tibetan Plateau using whole and sectioned vertebrae. Sectioned vertebrae showed that translucent bands were separated by distinct opaque bands through the focus to the margin. Although whole vertebrae showed clear band patterns in the intermediate region, such band patterns are obscure around the region of the focus of the vertebrae in older fish. The whole and sectioned vertebrae methods produced consistent ages until age 6, but there was a trend towards greater differences between the two methods as age increased. These findings indicate that sectioned vertebrae are suitable for age estimation of this species.     

Accumulation of platinum in the intervertebral discs and vertebrae of ovarian tumor-bearing patients treated with cisplatin

Platinum was determined by the inductively coupled plasma mass spectrometry (ICP-MS) in the intervertebral discs and vertebrae of ovarian tumor bearing patients treated withcis-diamminedichloro-platinum (II) (cisplatin). Platinum was 0.05 ng/mL at the absolute detection limit, and platinum was undetectable in the intervertebral discs and vertebrae of human specimens without cisplatin treatments. On the other hand, platinum was detected in the intervertebral discs and vertebrae of patients administered cisplatin, and platinum concentration was at levels of 1.06–10.31 μg/g dry tissue in the intervertebral discs and 0.60–1.28 μg/g dry tissue in the vertebrae, respectively. The platinum level of intervertebral discs was 4.3-fold higher than that of the vertebrae. Thus, platinum accumulates greatly in the intervertebral discs and somewhat in the vertebrae after administering cisplatin to patients for therapy.     

Lordotic vertebrae in sea bass (Dicentrarchus labrax L.) are adapted to increased loads

Lordosis in fish is an abnormal ventral curvature of the vertebral column, accompanied by abnormal calcification of the afflicted vertebrae. Incidences of lordosis are a major problem in aquaculture and often correlate with increased swimming activity. To understand the biomechanical causes and consequences of lordosis, we mapped the morphological changes that occur in the vertebrae of European sea bass during their development from larva to juvenile. Our micro-CT analysis of lordotic and non-lordotic vertebrae revealed significant differences in their micro-architecture. Lordotic vertebrae have a larger bone volume, flattened dorsal zygapophyses and extra lateral ridges. They also have a larger second moment of area (both lateral and dorso-ventral) than non-lordotic vertebrae. This morphology suggests lordotic vertebrae to be adapted to an increased bending moment, caused by the axial musculature during increased swimming activity. We hypothesize the increase in swimming activity to have a two-fold effect in animals that become lordotic. The first effect is buckling failure of the axial skeleton due to an increased compressive load. The second effect is extra bone deposition as an adaptive response of the vertebrae at the cellular level, caused by an increased strain and strain rate in these vertebrae. Lordosis thus comprises both a buckling failure of the vertebral column and a molecular response that adapts the lordotic vertebrae to a new loading regime.     

Percutaneous vertebral augmentation (PVA) in osteoporosis of the vertebrae--an experimental study]

The present study was conducted with the aim of establishing whether minimally invasive percutaneous techniques used to stabilize osteoporotic vertebrae are technically feasible. Two different methods were investigated in human thoracolumbar cadaveric vertebrae. In the first technique, special titanium implants were placed via a postero-lateral approach. With the second method, the vertebrae were filled with different types of cement of different viscosities. After each procedure, the vertebrae were examined with conventional X-ray and CT scans. The first technique proved quite unsuccessful--the insertion of the titanium implants proving difficult despite the use of special instruments. The results achieved with the second method were much better. The use of low-viscosity bone cement produced the best results. Despite a single lateral point of entry, the vertebrae were almost completely filled right into the contralateral side. Lumbar vertebrae required an average volume of cement of 7 ml (range: 6.5-10 ml) and thoracic vertebrae 5.5 ml (range: 4-7 ml). Specially developed cement application devices made possible problem-free, controlled introduction of the cement.     

Vertebrae in compression: Mechanical behavior of arches and centra in the gray smooth‐hound shark (Mustelus californicus)

In swimming sharks, vertebrae are subjected, in part, to compressive loads as axial muscles contract. We currently have no information about which vertebral elements, centra, arch cartilages, or both, actually bear compressive loads in cartilaginous vertebrae. To address this issue, the goal of this experiment was to determine the load‐bearing ability of arch and centrum cartilages in compression, to determine the material properties of shark vertebrae, and to document fracture patterns in the centra with and without the arches. Intact vertebrae and vertebrae with the arch cartilages experimentally removed (centra alone) were subjected to compressive loading to failure at a single strain rate. The maximum compressive forces sustained by the vertebrae and the centra are statistically indistinguishable. Thus we conclude that under these testing conditions the arch does not bear appreciable loads. Independent evidence for this conclusion comes from the fact that vertebrae fail in compression at the centra, and not at the arches. Overall, the results of these mechanical tests suggest that the neural arches are not the primary load‐bearing structure during axial compression. J. Morphol. 2010. © 2009 Wiley‐Liss, Inc.     

Vertebral numbers in male and female snakes: the roles of natural,sexual and fecundity selection

The relative numbers of trunk (body) and caudal (tail) vertebrae in snakes might be influenced by at least four processes: (1) natural selection for crawling speed, (2) fecundity selection for larger trunk size in females, (3) sexual selection for longer bodies or tails in males and/or (4) developmental constraints (if an increase in the number of body vertebrae requires a decrease in the number of tail vertebrae, or vice versa). These four hypotheses generate different predictions about the relationship between sex differences in the numbers of body vertebrae vs. tail vertebrae. I collated published data to test these predictions, both with raw data and using phylogenetically independent contrasts. Some snake lineages show a negative correlation between the magnitude of sex disparities in trunk vs. caudal vertebrae whereas other lineages show the reverse pattern, or no correlation. Thus, different selective pressures seem to have been important in different lineages. Vertebral numbers in snakes may offer a useful model system in which to explore the conflicts between natural, fecundity and sexual selection.     

Latitudinal variation in axial patterning of the medaka (Actinopterygii: Adrianichthyidae): Jordan's rule is substantiated by genetic variation in abdominal vertebral number

Because the body axes of fish consist of two anatomically distinct vertebrae, abdominal and caudal, one type may be more variable in number than the other and thus contribute more to morphological diversification. Jordan's rule, a geographical tendency for fish from higher latitudes to have more vertebrae, has not been examined in terms of numbers of abdominal and/or caudal vertebrae, despite its prevalence. Vertebral observations of wild populations of the medaka ( Oryzias latipes ) revealed that the latitudinal increase in vertebral number is caused by an increase in abdominal vertebrae; caudal vertebrae did not vary systematically across latitudes. Laboratory experiments revealed that this latitudinal cline in abdominal vertebral number persists in a range of common environments, demonstrating a genetic basis. Phenotypic plasticity was also evident: lower developmental temperatures resulted in more abdominal vertebrae. This indicates that greater numbers of abdominal vertebrae in higher latitude individuals in the wild may be caused not only by genetic factors but by lower habitat temperatures, although the contribution of the former to Jordan's rule is assessed to be much greater. The genetic basis of the latitudinal variation in abdominal vertebral number suggests that selection on functions associated with abdominal regions is the probable explanation for Jordan's rule in this fish.  © 2009 The Linnean Society of London, Biological Journal of the Linnean Society , 2009, 96 , 856–866.     

四川自贡中侏罗世峨眉龙—新种

记述了产自四川自贡大山铺中侏罗世峨眉龙属一新种——焦氏峨眉龙(Omeisaurus jiaoisp.nov.)。新种为大型蜥脚类恐龙,以如下特征区别于其他蜥脚类:前、中部背椎为典型的后凹型,后部背椎为双平型,背椎神经棘呈高大棒状,不分叉;尾椎为弱双凹型,第一尾椎不具扇形尾肋;第一脉弧短小且与第一尾椎关联;锁骨长大;肱骨和股骨细长而圆实;肱骨与股骨长度之比为0.83,尺骨与肱骨长度之比为0.72,胫骨与股骨长度之比为0.63。     

Vertebral age changes in Japanese macaques

This study deals with maturation and aging of the vertebrae in Japanese macaques (Macaca fuscata fuscata) of known chronological age. The samples used were 103 skeletons of captive raised Japanese macaques varying in age from 6-23 years. Epiphyseal union between the vertebral body and the epiphyseal disk (epiphyseal ring, annular epiphysis) and degenerative changes of the vertebrae were macroscopically examined. It was revealed that vertebral epiphyseal union develops comparatively rapidly in the sacral and cervical vertebrae, moderately in the lumbar vertebrae, and slowly in the thoracic vertebrae. It was found that, as a central tendency, the vertebral epiphyseal union begins at about 6 years of age, progresses lineally in proportion to age, and completes at about 23 years of age. However, considerable variation in developmental states of union was observed among individuals of the same age. Concerning vertebral degenerative changes, few were observed among the present samples. Compared with the other primates with regard to the timing of vertebral maturation, shortening of duration of maturation was found among humans. Human vertebrae may have become an early-maturing organ in order to sustain the increased loading that is accompanied by the adoption of habitual erect posture and bipedal locomotion.