三峡水库地震孕震机理及蓄水地震活动分析

本文从三峡库区区域地质构造、活动断裂及库区水文地质特点建立三峡库区区域地震模型;根据蓄水后岩石的库水与地质相互作用对该区水文地质及构造影响,对该区水库诱发地震进行理论分析,浅释了三峡库区水库地震孕震机理;以三峡遥测台网测震资料及宜昌台地壳形变手段在蓄水前后的监测的地壳动态变化特征为基础,对三峡水库诱发地震作了初步探讨及趋势分析.     

华东地区前寒武纪主要地质事件及构造演化

通过对地层分区与板块构造关系的分析,依据华东地区前寒武纪地质事件主要特点及划分原则．在充分了解现代构造观和基本地质事实基础上,建议将华东地区“晋宁运动二幕”改为“休宁上升‘”;“栏杆运动”和“霍丘运动”改为“栏杆上升”和“霍丘上升”．因为它们不具备造山运动性质。通过对新太古代末蚌埠运动、古元古代末龙川运动、迪口运动,中元古代末凤阳运动、青白田纪内部神功运动的特点分析,认为区内经历了新太古代陆核的生成;占元占代褶皱变质和混合岩化;凤阳运动和神功运动造成了华北古板块、扬子古板块和华夏古板块的拼合等演化阶段;并发生了四次造山运动和三次裂陷运动。     

南美地台地质构造演化与主要金属矿产成矿作用

南美地台区矿产资源丰富,从太古代到新生代不同阶段的地质构造演化为其奠定了优越的成矿地质条件。地质构造演化与矿产资源的形成关系密切,不同地质构造演化阶段形成不同的矿产资源。本文总结了南美地台的构造演化及其成矿作用,指出不同阶段构造演化对区内成矿作用控制的不同特点,总结区内主要矿产空间分布规律。     

长江口湿地景观镶嵌结构演变的数量特征与分形分析

鉴于国内湿地研究对象大多为块状湿地。而对狭长形湿地鲜有研究，本文利用1990年和2003年遥感影像作为基本信息源。在GIS技术支持下。选取长江口狭长湿地，建立长江口湿地植被空间数据库。选取斑块大小、分维数、景观破碎度、景观多样性和优势度等指标，研究区域景观的数量特征动态变化；运用分形理论建立各种景观类型形态的分形结构模型，以分维数为依据分析各种景观形态的复杂性；探讨控制和影响区域景观格局的主要因素。结果显示，1990—2003年期间，在自然与人为双重因素作用下该地区的湿地景观发生了显著变化，景观趋于破碎化。植物群落的演替由于人为的原因加速，一些地区景观呈自然变化趋势。一些地区由于围垦的原因。人为扰动大。呈现衰退趋势。     

Eocene bunoselenodont Artiodactyla from southern Thailand and the early evolution of Ruminantia in South Asia

Although Asia is thought to have played a critical role in the basal radiation of Ruminantia, the fossil record of early selenodont artiodactyls remains poorly documented in this region. Dental remains of a new bunoselenodont artiodactyl are described from the late Eocene of Krabi, southern Thailand. This new form, Krabitherium waileki gen. et sp. nov, is tentatively referred to the Tragulidae (Ruminantia) on the basis of several dental features, including a weak Tragulus fold and the presence of a deep groove on the anterior face of the entoconid. Although this new form is suggestive of the enigmatic ?Gelocus gajensis Pilgrim 1912 from the “base of the Gaj” (lower Chitarwata Formation) of the Bugti Hills (Central Pakistan), K. waileki most likely represents an early representative of a relatively bunodont group of tragulids that includes the genus Dorcabune, known from the Miocene of south Asia. This addition to the Eocene record of early ruminants attests to the antiquity of the group in Southeast Asia and lends support to the hypothesis that the Tragulidae represents one of the first offshoots in the evolutionary history of Ruminantia.     

Clockwork blue: on the evolution of non-image-forming retinal photoreceptors in marine and terrestrial vertebrates

This paper presents a hypothesis that could explain why blue light appears to dominate non-image-forming (NIF) ocular photoreception in marine as well as terrestrial vertebrates. Indeed, there is more and more evidence suggesting that 'novel' retinal photoreceptors, which are sensitive to blue light and were only discovered in the 1990s, could be a feature shared by all vertebrates. In our view, blue light photoreception evolved and persisted as NIF photoreception because it has been useful in the colonisation of extensive photo-dependent oceanic habitats and facilitated the move of vertebrates from an aquatic to a terrestrial environment. Because the available scattered evidence is compatible with the validity of our hypothesis, we hope that our rationale will be followed up. Indeed, it (1) involves testable predictions, (2) provides plausible explanations for previous observations, (3) unites phenomena not previously considered related to one another and (4) suggests tests that have not been carried out before. Overall, our approach not only embraces cross-disciplinary links; it, moreover, serves as a reminder of an all-embracing evolutionary history, especially with regard to a ubiquitous photoreceptive 'clockwork-blue' in marine and terrestrial vertebrates.     

Amniocentesis rate and the detection of down syndrome and other chromosomal anomalies in Israel

We investigated the contribution of different screening criteria to the prenatal detection of Down syndrome (DS) as well as other chromosomal anomalies in the Jewish population in Israel during 1990 and 1992. There was a significant decrease (P<0·03) in the incidence of DS live-births during 1992 (40:78 442) compared with 1990 (69:73 751) which paralleled a marked increase in total prenatal testing and in DS cases detected prenatally. Private laboratories, which perform amniocenteses mostly for women with a low risk of DS and without genetic counselling, had a significantly lower detection rate (1:917) compared with that of the genetic institutes, which following genetic counselling test both women ≥ 37 years of age (1:91) and women younger than 37 years (1:113). The detection of chromosomal anomalies other than DS was less affected by the reason for amniocentesis. Amniocentesis indicated by maternal serum marker screening of women younger than 37 years identified a greater number of chromosomal anomalies other than DS than amniocentesis based on age (≥37 years) alone (111:9604 versus 94:9810; P<0·06). Prenatal detection of DS is most effective when the indication for amniocentesis follows genetic counselling. The increasing use of maternal serum marker screening leads to a significant improvement in the positive detection rate of chromosomal anomalies other than DS in young women.     

Present status and changes of the phytoplankton community after invasion of Neosalanx taihuensis since 1982 in a deep oligotrophic plateau lake, Lake Fuxian in the subtropical China

Introduction Introduction of exotic fish from the Yangtze River tolakes of Yunnan Guizhou Plateau has led to significantecological consequences of the lake ecosystem. So far, mostconcerns have been on the extinction of endemic fish species(Y…     

Potter's syndrome in the second trimester—prenatal screening and pathological findings in 60 cases of oligohydramnios sequence

Fifty-two second-trimester and eight third-trimester (>28/40) autopsies with clinical or pathological evidence of oligohydramnios sequence (“Potter's syndrome”) were reviewed. Twenty-eight cases had renal anomalies (71 per cent in terminations following prenatal ultrasound), 27 had no renal malformation (35 per cent with chorioamnionitis), and five had external assessments only. In 15 cases, the renal lesion was part of a multiple malformation syndrome. Seven cases had a lesion which either recurred in a sibling in the same family or was a recognized autosomal recessive syndrome. Three cases had an abnormal karyotype, two of which had renal anomalies. Maternal serum alpha-fetoprotein (AFP) did not discriminate between cases with renal malformations and those without. Pulmonary hypoplasia was commoner in third-trimester than in second-trimester cases. External appearance and absent umbilical artery were not reliable predictors of underlying internal anomalies. These findings reflect the shift from postnatal to prenatal diagnosis in modern practice. In this series, mainly second-trimester cases, 50 per cent of cases had no malformations, in a condition which is traditionally associated with renal disease. The high incidence of chorioamnionitis suggests that the mechanism of oligohydramnios is occult amniotic fluid leakage. Prenatal diagnosis of oligohydramnios in the second trimester is dependent on ultrasound scanning and a full post-mortem examination is necessary to identify any underlying fetal cause.     

Prenatal diagnosis of Opitz (BBB) syndrome in the second trimester by ultrasound detection of hypospadias and hypertelorism

Prenatal diagnosis in a kindred with the Opitz (BBB) syndrome is presented. The inheritance is consistent with either autosomal dominant inheritance with sex limited expression or X-linked inheritance. The abnormalities in the kindred consist of hypertelorism, hypospadias, ambiguous genitalia, urocolic fistula, imperforate anus, mental retardation, diaphragmatic hernia, and malrotation with volvulus. A male fetus at 19 weeks was found by ultrasound to have hypertelorism and hypospadias with a small phallus consistent with the syndrome. The diagnosis was confirmed by pathologic examination after pregnancy termination. This is the first report of prenatal diagnosis of Opitz syndrome by ultrasonographic demonstration of hypertelorism and hypospadias in the second trimester.     

Revised estimates and projections of down syndrome births in the United States,and the effects of prenatal diagnosis utilization, 1970–2002

The objectives of this study were to: (1) calculate revised estimates and projections of United States annual Down syndrome (DS) births for 1970–2002, and (2) estimate the effects of amniocentesis on these baseline DS birth projections. Three models of amniocentesis utilization among 30–34 and ≧ 35-year-old women were considered. The recently revised Census Bureau birth projections, and new single year maternal age DS risk rates estimated from a 1970–1983 Ohio data set, were used. Data from all three Census Bureau projection series were analysed; series II was considered in depth since it is consistent with recent fertility levels. Assuming no use of amniocentesis, total estimated DS births dropped from about 4770 in 1970 to 4120 in 1980 (a 14 per cent decline), but are projected to a plateau of about 5100 by the year 1990 (a 24 per cent increase). DS births to women ≧ 35 would increase dramatically from about 1050 in 1980 to 1900 in 2000 (an 81 per cent increase). Assuming 1983 Ohio prenatal diagnosis ratios for women aged 30–34 (1.7 per cent) and ≧ 35 (23.4 per cent) are used nationally, an annual reduction of about 7 per cent of DS births in 1986 and 9 per cent in 2002 would result. Fifty and 70 per cent utilization among women 30–34 and 235, respectively, would reduce DS births by about 33 per cent in 1986 and 38 per cent in 2002. Therefore, if the projected increase in DS births is to be averted, utilization of prenatal diagnosis by ≧ 30-year-old women must increase substantially.     

Pregnancy-associated plasma protein A: A possible marker in the classification and prenatal diagnosis of Cornelia de Lange syndrome

The concentration of human placental lactogen (hPL), pregnancy specific beta-1 glycoprotein (SP-1) and pregnancy-associated plasma protein A (PAPP-A) were analysed in consecutive serum samples from a patient who gave birth to a child with Cornelia de Lange syndrome. HPL and SP-1 were present in normal concentrations from week 20 to week 35 of gestation whereas PAPP-A could not be detected in any of the samples examined. Immunohisto-chemical examination of two placentae from Cornelia de Lange syndrome revealed normal localization of hPL and SP-1 but the absence of PAPP-A from the syncytiotrophoblast. The significance of association between Cornelia de Lange syndrome and compromised synthesis of PAPP-A is discussed.     

hCG,AFP, and uE3 patterns in the 14–20th weeks of Down's syndrome pregnancies

A marked gestational-age-dependent variation in the 15-20th week pattern of human chorionic gonadotropin concentrations in Down's syndrome (DS) pregnancies is described and its weight in DS screening is discussed.     

Roles of serum uric acid on the association between arsenic exposure and incident metabolic syndrome in an older Chinese population

Growing evidences showed that heavy metals exposure may be associated with metabolic diseases.Nevertheless,the mechanism underlying arsenic(As)exposure and metabolic syn-drome(MetS)risk has not been fully elucidated.So we aimed to prospectively investigate the role of serum uric acid(SUA)on the association between blood As exposure and incident MetS.A sample of 1045 older participants in a community in China was analyzed.We deter-mined As at baseline and SUA concentration at follow-up in the Yiwu Elderly Cohort.MetS events were defined according to the criteria of the International Diabetes Federation(IDF).Generalized linear model with log-binominal regression model was applied to estimate the association of As with incident MetS.To investigate the role of SUA in the association be-tween As and MetS,a mediation analysis was conducted.In the fully adjusted log-binominal model,per interquartile range increment of As,the risk of MetS increased 1.25-fold.Com-pared with the lowest quartile of As,the adjusted relative risk(RR)of MetS in the highest quartile was 1.42(95％confidence interval,CI:1.03,2.00).Additionally,blood As was posi-tively associated with SUA,while SUA had significant association with MetS risk.Further mediation analysis demonstrated that the association of As and MetS risk was mediated by SUA,with the proportion of 15.7％.Our study found higher As was remarkably associated with the elevated risk of MetS in the Chinese older adults population.Mediation analysis indicated that SUA might be a mediator in the association between As exposure and MetS.     

Analysis of maternal serum alpha-fetoprotein and free beta human chorionic gonadotrophin in the first trimester: Implications for down's syndrome screening

The aim of this study was to determine the maternal population, pregnancy, serum alpha-fetoprotein (AFP) and free β subunit of human chorionic gonadotrophin (FβhCG) parameters in a large series of women attending prenatal clinics before 15 weeks' gestation and to assess the practical problems of population screening for Down's syndrome in the first trimester using these markers. Serum samples were collected from 8600 women attending prenatal clinic booking visits. Maternal serum AFP and FβhCG medians were calculated for each day of gestation (49–104 days), using both dates and ultrasound estimates of gestation. The effects of maternal weight, twin pregnancies, and threatened abortion on AFP and FβhCG levels were analysed. The median age of the population was 27.1 years and the median weight 62.1 kg. Twenty-six per cent of samples were collected before 70 days and 50 per cent before 78 days' gestation. Eighty-nine per cent of all samples had gestational estimates by dates, 60 per cent by ultrasound and 52 per cent by both dates and ultrasound. The AFP median was 5 kU/1 at 49 days, 5.9 kU/1 at 70 days, and 17.9 kU/1 at 100 days. The peak median FβhCG level was 66.4 ng/ml at 64 days, falling to 20.6 ng/ml at 100 days' gestation. Both AFP and FβhCG levels showed log Gaussian distributions but the standard deviation for AFP was 20 per cent greater than that found in the second trimester. AFP and FβhCG levels showed an inverse relationship with maternal weight and were increased in twin pregnancies (1.68 and 1.97 multiples of the median, respectively). AFP and FβhCG can be readily measured in a large screening population in the first trimester. Down's syndrome screening protocols based on these markers could be refined by the use of gestations in individual days but AFP is likely to be a less effective marker and detection rates are likely to be lower than in the second trimester. To realize the potential of first-trimester screening, more women should be encouraged to attend the prenatal clinic in early pregnancy and ultrasound dating should be carried out for all pregnancies at this stage.     

Convergent evolution in the antennae of a cerambycid beetle, <Emphasis Type="Italic">Onychocerus albitarsis,</Emphasis> and the sting of a scorpion

Venom-injecting structures have arisen independently in unrelated arthropods including scorpions, spiders, centipedes, larval owlflies and antlions, and Hymenoptera (wasps, ants, and bees). Most arthropods use venom primarily as an offensive weapon to subdue prey, and only secondarily in defense against enemies. Venom is injected by biting with fangs or stinging with a specialized hypodermic structure used exclusively for the delivery of venom (usually modified terminal abdominal segments). A true sting apparatus, previously known only in scorpions and aculeate wasps, is now known in a third group. We here report the first known case of a cerambycid beetle using its antennae to inject a secretion that causes cutaneous and subcutaneous inflammation in humans. Scanning electron microscopy revealed that the terminal antennal segment of Onychocerus albitarsis (Pascoe) has two pores opening into channels leading to the tip through which the secretion is delivered. This is a novel case of convergent evolution: The delivery system is almost identical to that found in the stinger of a deadly buthid scorpion.     

A review of early gadiform evolution and diversification: first record of a rattail fish skull (Gadiformes, Macrouridae) from the Eocene of Antarctica, with otoliths preserved in situ

Codfishes, the Gadiformes, are quite abundant in modern temperate and polar waters with a fossil record ranging back into the Palaeogene. The oldest records are from the Danian and Selandian of Europe and South Australia. The bipolar distribution early in their evolutionary history implies that their origin must have occurred quite early in the Palaeocene, or even in the Late Cretaceous with subsequent rapid diversification. By the Eocene, gadiforms were highly abundant and widespread. With the exception of gadiforms, no Eocene Antarctic teleostean group is present in the modern Antarctic fauna. Here, we review the early evolution and diversification of gadiforms in general and of macrouroids in particular. We also describe the undoubtedly oldest skeletal macrourid specimen with otoliths preserved in situ. It is the first definitive record of this group from the Eocene of Antarctica filling a gap in its stratigraphic distribution. The fossil record of gadiforms in general and macrouroids in particular indicates that the origin of both was in shallow shelf environments but with adaptations to deep-water settings early in their evolution. While gadoids seemingly originated in the earliest Palaeogene and rapidly experienced a first major radiation event in the eastern North Atlantic and/or North Sea Basin, macrouroids evolved in the Southern Ocean and migrated northwards into the South Atlantic before the establishment of the circum-Antarctic current and subsequent isolation of the Antarctic fish fauna. These two timely and regional separated adaptive radiation events in the Palaeogene gave rise to their modern taxonomic diversity and global distribution.