Potassium‐argon dates from the Arltunga Nappe complex,northern territory

Twenty‐four mineral separates from the Arunta Complex, four from the metamorphosed Heavitree Quartzite (White Range Quartzite), and one whole rock sample of metamorphosed Bitter Springs Formation, all from the western part of the White Range Nappe of the Arltunga Nappe Complex, and two samples from the autochthonous basement west of the nappe have been dated by the K‐Ar method. The samples from the basement rocks form two groups. Those in the southern or frontal part of the nappe are of Middle Proterozoic (Carpentarian) age (1660–1368 m.y.), determined on hornblende, biotite, and muscovite. In the northern or rear part of the nappe, all but one of the muscovite samples and two biotites are of Middle Silurian to Early Carboniferous age (431–345 m.y.); the remainder of the biotite dates range from 1775 to 548 m.y. (including the two samples from the autochthon), and two hornblendes gave dates of 1639 and 2132 m.y. respectively. All the muscovite samples from the Heavitree Quartzite, and the whole rock sample from the Bitter Springs Formation gave Early to Middle Carboniferous dates (358–322 m.y.). The findings support the identification of the White Range Quartzite as the metamorphosed part of the Heavitree Quartzite, which in turn supports the interpretation of the structure of the area as a large, basement‐cored fold nappe. In addition, they date the time of the Alice Springs Orogeny as pre‐Late Carboniferous, which agrees with fossil evidence from elsewhere in the area. The Alice Springs Orogeny was accompanied by widespread greenschist facies meta‐morphism that progressively metamorphosed the Heavitree Quartzite and Bitter Springs Formation, and retrogressively metamorphosed the Arunta Complex. However, the basement rocks in the southern part of the nappe escaped this metamorphism and retain a Middle Proterozoic age, thus dating the time of the Arunta Orogeny in this region as Carpentarian or older.     

郑西高铁地面振动实测分析及隔振沟效果研究

高铁列车动载会引起环境振动问题。为研究高速列车运行在高架段和路堤段引起的环境振动差异,文章对郑西线高速铁路展开现场测试,对比分析高架段和路堤段地面振动特征及其衰减规律。测试结果表明,路基段的振动响应大于高架段,高架段近场区衰减作用高于路堤段近场区域。振动传播过程中存在多次反弹增大现象,路堤段地面振动反弹增大位置滞后于高架段。高架段和路堤段的二次反弹增大率均明显大于一次反弹增大率。Z振级随距离的衰减符合对数衰减规律,拟合得到黄土地区Z振级衰减公式,最大偏差均出现在反弹增大区。引入无限元-黏弹性耦合边界条件,建立路堤段三维轨道-土体-隔振沟数值模型分析高速铁路隔振沟对减隔振的影响。研究发现空沟对中高频（30~60 Hz）振动波的隔振效果较低频（1~20 Hz）振动波明显,其具有低通滤波作用。空沟比填充沟隔振效果好,但是考虑到沟壁的稳定性,可在空沟中填入软质材料。研究成果可为高速铁路的设计及其环境振动的评价和控制提供参考。     

Preliminary results of measuring the crustal deformation in Qinghai-Xizang area using GPS technique

GPS repetition measurement tbta in Qinghai-Xizatlg (Tibetan) area in 1992 and 1994 have been used to determine the change rates of seven bascline vectors of Lhasa-Wenquan, etc. It is the first time to obtain the direct observation results of the large-scale crustal horizontal motions in this area. Thesc preliminary results also for the first time provide the direct observation evidence for some important geophysical and geological viewpoints, such as the northward gradual reduce of the effect of the northward push-pressing to Eurasian continent by Indian Plate in the Qinghai-Xizang area, having a southward strike slip movement of the Chuan-Dian diamond block, etc.     

青黄公路交通调查及交通量预测

通过对1998年2月青黄公路的交通调查,分析了青黄公路的交通现状,根据青岛市的国民经济增长速度、交通运输发展及城市出入口资料,利用弹性系数法预测了2000年和2010年青黄公路的城市交通量。     

A multi‐stock,length‐based assessment model for New Zealand rock lobster (Jasus Edwardsii)

We describe a multi‐stock, length‐based Bayesian assessment model for New Zealand spiny lobster (Jasus edwardsii) fisheries. This model allows simultaneous modelling of two or more stocks with a mixture of common and stock‐specific parameters: recruitment is always stock‐specific, but any other parameter can be specified as either common or stock‐specific. Common parameters are estimated from a wider base than they would be in a single‐stock model. The model's time step is flexible and can be changed during the period being modelled to accommodate better data quality in recent data. Other options include the capacity to estimate movements among stocks, allow density‐dependent growth, and choose among likelihood functions for the various data sets, between finite and instantaneous fishing dynamics and between two forms of selectivity curve.     

高速公路软土地基沉降变形监测分析与预报

通过对高速公路软土地基沉降变形监测的非等步长观测序列进行数据处理后,变成等步长的数据序列,运用GM(1,1)模型进行变形分析与预报,得出了有益的结论。     

Depth of settlement of two mussel species on suspended collectors in Marlborough Sounds,New Zealand (Note)

The preferred depth of settlement and settlement period of two species of mussel spat were monitored at Yncyca Bay (NZMS1 S15 220460) and Wet Inlet (NZMS1 S16 265432) in the Marlborough Sounds on collectors suspended in 0–4 m of water between 20 October 1975 and 4 April 1976. Peak settlement of Mytilus edulis aoteanus was between 20 October 1975 and 4 January 1976, and decreased with increasing depth. Peak settlement of Perna canaliculus was between 16 February 1976 and 12 April 1976, and showed no preferred depth of settlement.

Capture of wild stocks of Mytilus edulis aoteanus and Perna canaliculus spat for use in aquaculture has become more reliable through accurate forecasting of peak settlement periods, and knowledge of preferred depth of settlement of the two species.

Preferred depth of settlement of spat may affect the shore zonation of mussels.     

Burrowing behaviour of the paddle crab Ovalipes catharus (White, 1843) (Brachyura: Portunidae)

The burrowing behaviour of Ovalipes catharus (White, 1843) is described and compared with that of some other burrowing crabs. O. catharus is a fast, back burrowing crab which makes temporary burrows in soft sand. The average time from initiation of burrowing to complete submergence was 6.5 s, there was no difference between males and females but burrowing time increased significantly with crab size. Similar morphological adaptations are required for burrowing and swimming: streamlined body shape, smooth lightly constructed exoskeleton, and flattened legs. O. catharus has a reversed respiratory current like O. guadulpensis but it differs in its burrowing behaviour. Compared to some other crabs, burrowing in O. catharus is rapid.     

Insights into zooplankton‐cyanobacteria interactions derived from enclosure studies

Few workers have used enclosures specifically to study interactions between zoo‐plankton and cyanobacteria. Differences among studies in enclosure size, nutrient level, plankton abundance and species composition, presence or absence of fish, and length of experiments make generalisations difficult. Zooplankton had no direct effect on the growth of ungrazed cyanobacteria (Anabaena flos‐aquae, Aphanizomenon flos‐aquae, large Microcystis colonies) in short‐term (<5 days) and long‐term (> 1 month) enclosure studies. When large cyanobacteria were abundant, some Daphnia spp. snowed reduced reproduction and development. When large grazers were abundant they suppressed the growth of edible, colonial cyanobacteria (Aphanizomenon elenkinii, small Microcystis colonies). By altering the ambient light and nutrient environment, large zooplankton may suppress cyanobacteria; evidence for the importance of grazers in promoting cyanobacterial dominance by removing competing phytoplankton species is equivocal. Zooplankton may suppress nitrogen fixation by cyanobacteria through ammonia excretion and may promote a change in dominance from diatoms to cyanobacteria through recycling phosphorus but not silicon.     

Biochemical‐genetic and meristic evidence that blue and copper moki (Teleostei: Latridae: Latridopsis) are discrete species

Specimens of blue moki Latridopsis ciliaris (Forster in Bloch & Schneider, 1801) from New Zealand were shown to differ from specimens of copper moki Latridopsis forsteri (Castelnau, 1872) using two genetic methods—allozymes and muscle proteins. Allozyme techniques revealed fixed differences between blue and copper moki at 4 out of 15 loci. There was a genetic distance of 0.31–0.34 between population samples of the two colour morphs. The two morphs were also distinguished by iso‐electric focusing of muscle proteins. Meristic characters, counted in the specimens studied with genetic markers, revealed diagnostic markers in tubed lateral line scales and scales in the lower transverse series. It is concluded that specimens of blue moki from New Zealand and copper moki from New Zealand and Tasmania are valid species.