Factors affecting the distribution and abundance of Macrobrachium petersi (Hilgendorf) in the Keiskamma River and estuary,South Africa

A dry (1979–1980) and a wet (1980–1981) season had a marked effect on the freshwater inflow into the Keiskamma estuary. Under low inflow conditions, which results in elevated salinities in the upper reaches, an upstream migration of adult Macrobrachium petersi (Hilgendorf) to freshwater takes place. During periods of increased river inflow adult M. petersi move downstream to the more saline reaches of the estuary. These two migratory responses have been interpreted as (a) a breeding migration under high inflow conditions which ensures that larvae are in close proximity to salinities that favour growth and development, and (b) an adult upstream migration back to freshwater to escape elevated estuarine salinities as a result of the low freshwater inflow.     

全球Ms≥7￣3／4级地震的定向迁移

对全球尺度的６条大地震带内１９００～１９９０年中１８４次Ｍｓ≥７３／４级地震进行了沿地震带方向定向迁移的分析，获得了全球统一的地震定向迁移规律，总体是由西向东，迁移速度由７００ｋｍ／ａ变为１５０ｋｍ／ａ，此现象可以作多种暂态地球动力作用过程的推论，如以大西洋脊间歇式张裂引起上地幔软流物质自西向东运动，呈现纵波式的振荡传播；也可解释为非洲板块、阿拉伯板块和印度板块自西南向东北对欧亚地震带依次的推压引起向东的应变波的传播；太平洋脊两侧洋底板块向西北和东北两侧的斜向推压，可能是造成两侧地震带地震向北迁移的触发源     

Migration of the Ganga river and its implication on hydro-geological potential of Varanasi area, U.P., India

Borehole data reveals that during Late Quaternary, the Ganga river was non-existent in its present location near Varanasi. Instead, it was flowing further south towards peripheral craton. Himalayan derived grey micaceous sands were being carried by southward flowing rivers beyond the present day water divide of Ganga and mixed with pink arkosic sand brought by northward flowing peninsular rivers. Subsequently, the Ganga shifted to its present position and got incised. Near Varanasi, the Ganga river is flowing along a NW-SE tectonic lineament. The migration of Ganga river is believed to have been in response to basin expansion caused due to Himalayan tectonics during Middle Pleistocene times. Multi-storied sand bodies generated as a result of channel migration provide excellent aquifers confined by a thick zone of muddy sediments near the surface. Good quality potable water is available at various levels below about 70 m depth in sandy aquifers. Craton derived gravelly coarse-to-medium grained sand forms the main aquifer zones of tens of meter thickness with enormous yield. In contrast, the shallow aquifers made up of recycled interfluve silt and sandy silt occur under unconfined conditions and show water-level fluctuation of a few meters during pre-and post-monsoon periods.     

Fluid flow equations governing primary oil migration as a separate phase

A mathematical model of primary oil migration as a separate phase out of compacting shales is presented. During burial and oil generation, source rock porosity decreases and oil saturation increases until residual oil saturation is reached. At this stage oil is expelled out by capillary and excess fluid pressure gradients. The model is a system of differential equations which relate changes in oil and water saturation in time to water and oil flow out of the source rock during burial. An additional set of equations for periods of erosion of overburden are also provided. The equations can be numerically solved by finite difference method. If oil and water flow is to be simulated during oil generation, then at each time step, changes by oil generation in oil and water saturations and porosity must be calculated. The solution procedure is briefly outlined.     

Diet shifts of Caribbean grunts (Haemulidae) and snappers (Lutjanidae) and the relation with nursery-to-coral reef migrations

The spatial size distribution of grunts and snappers have previously indicated the separation of juveniles in nursery habitats from the adults on the coral reef. This implies life cycle migrations from nursery habitats (such as seagrass beds and mangroves) to the coral reef. If diet shifts are related to such migrations, then the diets of these fish must change before or around the fish size at which such migrations take place. A wide size range of juveniles of two grunt species (Haemulon sciurus and Haemulon flavolineatum) and of two snapper species (Lutjanus apodus and Ocyurus chrysurus) were caught in seagrass beds and mangroves, and their gut contents identified and quantified. Regression analysis between fish size and dietary importance of small crustaceans showed a negative relationship in all four species. Positive relations were found for H. sciurus, L. apodus and O. chrysurus between fish length and the dietary importance of decapods, and for L. apodusand O. chrysurus between fish length and prey fish importance. Critical changes in the fish diets with fish size were examined by application of a Canonical Correspondence Analysis (CCA). The CCA yielded three clusters of size-classes of fishes with similar diets, and application of a Mantel test showed that each of these clusters had significantly different diets, and that each cluster diet was significantly specialised. The size at which a fish species ‘switched’ from one cluster to another was compared with size-at-maturity data and with the typical size at which these species migrate from the nursery habitats to the coral reef. H. sciurus and H. flavolineatum may be prompted to migrate from the nursery habitats to coral reef habitats because of dietary changes, or because of the development of the gonads. For L. apodus and O. chrysurus, a dietary changeover forms a more likely explanation for nursery-to-reef migrations than does sexual maturation because these species reach maturity at sizes much larger than the maximum size of individuals found in nursery habitats. Although other factors may theoretically initiate or promote the migration patterns, the results of this study indicate that ontogenetic dietary changes may crucially influence the nursery-to-coral reef migrations of these reef fish species.