On the use of horizontal acoustic Doppler profilers for continuous bed shear stress monitoring

Continuous monitoring of bed shear stress in large river systems may serve to better estimate alluvial sediment transport to the coastal ocean.Here we explore the possibility of using a horizontally deployed acoustic Doppler current profiler(ADCP) to monitor bed shear stress,applying a prescribed boundary layer model,previously used for discharge estimation.The model parameters include the local roughness length and a dip correction factor to account for sidewall effects.Both these parameters depend on river stage and on the position in the cross-section, and were estimated from shipborne ADCP data.We applied the calibrated boundary layer model to obtain bed shear stress estimates over the measuring range of the HADCP.To validate the results,co-located coupled ADCPs were used to infer bed shear stress,both from Reynolds stress profiles and from mean velocity profiles. From HADCP data collected over a period of 1.5 years,a time series of width profiles of bed shear stress was obtained for a tidal reach of the Mahakam River,East Kalimantan,Indonesia.A smaller dataset covering 25 hours was used for comparison with results from the coupled ADCPs.The bed shear stress estimates derived from Reynolds stress profiles appeared to be strongly affected by local effects causing upflow and downflow,which are not included in the boundary layer model used to derive bed shear stress with the horizontal ADCP.Bed shear stresses from the coupled ADCP are representative of a much more localized flow,while those derived with the horizontal ADCP resemble the net effect of the flow over larger scales.Bed shear stresses obtained from mean velocity profiles from the coupled ADCPs show a good agreement between the two methods,and highlight the robustness of the method to uncertainty in the estimates of the roughness length.     

The distribution and population dynamics of O-group plaice (Pleuronectes platessa L.) on nursery grounds in the Firth of Forth

Midsummer (1 August) population estimates of about 2 million O-group plaice (Pleuronectes platessa L.) were derived for sandy bays around the Firth of Forth in 1979–1980. This is an order of magnitude less than similar estimates made for the Clyde Sea Area in 1973–1974. Autumn population estimates of 0·4–1·0 million fish were comparable to estimates by the Ministry of Agriculture, Fisheries and Food for the area between the Scottish border and Flamborough Head (2·3 million for 1970 and 1973) which represented 4·8% (1973) to 5·3% (1970) of the total number of O-group fish on the English east coast.Largo Bay was the most important nursery area holding 25% of the total population. It is particularly well situated to receive newly metamorphosed plaice carried in water currents along the north side of the Forth from the spawning ground off Fife Ness. Plaice in the Forth are mainly distributed on fine to medium sandy beaches (186–480 μm), the mean number per haul in midsummer (D) being correlated with the median diameter (m.d. in μm) of the low water sediments by the equation: D=−45·7666+0·2327 m.d. (n=11,r=0·68,P<0·02 but>0·01).The shallow inshore water in sandy bays in the outer Firth was well mixed and more marine than estuarine (27·7–35·0‰). The correlation coefficient between fish density and water temperature was low, while that with salinity (S‰) was: D=6·1618+0·2238S (n=23,r=0·62,P<0·005).Regression analysis demonstrated that the relationship between the instantaneous mortality rate (Z) and the initial population density (D_p) was: Z×100=0·7480+0·0546d_p (n=12,r=0·87,P<0·001).The mean mortality rate for the O-group plaice in the Forth nursery areas was 53% month⁻¹.     

华北北部古生代大陆地壳增生过程中的岩浆作用与成矿效应

包括前寒武纪克拉通与显生宙造山带两大构造单元的华北北部,古生代时期板块构造体制下古亚洲洋的裂解-扩展-消亡与汇聚大陆边缘的俯冲-碰撞-伸展循环构成了其大陆地壳增生与再造演化的基本图景,并形成了一系列记录这些因果演变连续过程的岩浆侵入与喷发事件。这些物质记录无疑是研究汇聚大陆边缘壳-幔作用和物质交换、大陆地壳演化与大规模成矿作用耦合关系的绝佳窗口。本文在系统总结最近几年积累的年代学和岩石地球化学资料的基础上,以一些带有特定过程印记的标志性岩浆事件为纲领,表征这些古生代岩浆作用形成过程中的地球动力学演变,揭示其所记录的华北北部大陆地壳的多阶段增生与再造演化机制,并初步探讨了有利地球动力学过程制约下的岩浆行为引起的成矿物质聚集效应。     

内蒙古白云鄂博地区基底岩石锆石年代学及对构造背景的指示

白云鄂博地区的克拉通基底岩石主要由糜棱岩化花岗片麻岩(2588±15Ma),正长岩、花岗闪长岩(2018±15Ma)和黑云母花岗片麻岩、含石榴石蓝晶石花岗片麻岩(～1890Ma)等组成,白云鄂博超大型稀土矿床就位于华北克拉通太古代基底之上。太古代克拉通基底在早元古代中晚期(2.0Ga)又经历了一次强烈的碰撞造山运动,造成了闪长质与花岗质岩浆侵位,以及1.9Ga片麻岩相变质事件。     

The food and growth of 0-group flatfish on nursery grounds in the Clyde Sea Area

In early summer plaice (Pleuronectes platessa L.) in the Clyde Sea Area eat Tellina siphons and spionid palps. As they grow, they take progressively larger siphons, fragments of spionids and some crustaceans. In late summer they eat entire spionids and other sedentary polychaetes. There is no significant predation on fish. The common dab [Limanda limanda (L.)] took a wider range of prey species than the plaice, but also depended mainly on polychaetes, crustaceans and bivalves. Depth distribution may limit both intra- and interspecific competition between these fish and also influence the choice of prey. The results from the main nursery areas of Irvine and Ayr Bays were similar to those from the other bays throughout the Clyde Sea Area and support earlier work at Firemore Bay in north-west Scotland and in the Dutch Wadden Sea.The growth rate of the fish increases during the early summer and may be related to increasing food availability, feeding experience of the fish and longer day length. Growth rate between areas appeared to be correlated with benthic productivity. 0-group plaice in Irvine, Ayr and Firemore Bays grew to different mean lengths by the end of the summer growth season, being 82 mm, 73 mm and 61 mm, respectively, for the period 1972–1974. This agrees with the known differences in standing stocks of intertidal macrobenthos in these bays (17·0, 11·1 and 1·3 g m^?2 dry weight, respectively). The significance of this in relation to survival is discussed. Offshore migration of the larger fish in the autumn may result in apparent slowing of growth rates prematurely in inshore areas. The year-class strength depends more on the food availability in the nursery areas than on the number of plaice that settle on the bottom.     

Contrasting patterns in the abundance of fish communities targeted by fishers on two coral reefs in southern Mozambique

Coastal populations of maritime countries in eastern Africa rely on fish as a primary source of protein, but baseline information on the abundance of fish communities on these coastlines is often lacking. We used baited remote underwater video stations to compare the abundance and diversity of reef fishes targeted by fishing at two sites in southern Mozambique, one at Lighthouse Reef within the Bazaruto Archipelago National Park and the other to the south at San Sebastian Reef on the San Sebastian Peninsula. Fish that are known targets of fisheries (mostly small-scale and artisanal) had an abundance that was almost three-times greater at San Sebastian Reef (80.22 ind. h^–1 [SE 18.00]) than at Lighthouse Reef (29.70 ind. h^–1 [SE 8.91]). Similarly, there was greater mean species richness at San Sebastian Reef (38.74 species h^–1 [SE 2.79]) than at Lighthouse Reef (25.37 species h^–1 [SE 3.66]). The main drivers of targeted fish abundance were habitat and depth, with shallow (<15 m) and mixed reef areas having the greatest abundance and richness. More sampling was done over sand habitat at Lighthouse Reef, which likely led to the lower abundance and species richness observed at this site; however, that finding could also be attributable to the fact that protection is provided to only a section of available coral reef habitat in a small area. Nevertheless, fish community structure was comparable between the sites, with similar proportions of carnivores (78–81%), herbivores (12–14%) and omnivores (7–8%). Our findings highlight the variation in species abundance and assemblages of coral-reef fish targeted by fishing in Mozambique and emphasise the importance of localised environmental variables as a driver of these patterns. To ensure maximum protection of Lighthouse Reef fish communities, we recommend an extension of the no-take zone to include the entire reef complex.