Chemical alteration of tephra in the depositional environment: theoretical stability modelling

The study of the chemical stability of vitreous material in aqueous media is well‐established. There has to date been little consideration of the implications of variations in the chemical durability of tephra in Quaternary tephrochronology. Chemical alteration can take the form of cationic leaching from the matrix, or complete destruction of the silica network, either of which could constrain the ability to chemically identify distal tephra. Here we apply established models of vitreous durability to the published chemical analyses of a large number of Icelandic tephras in order to predict their relative durabilities under equivalent conditions. This suggests that some important tephras have relatively poor chemical stability, and that rhyolitic tephras are, in general, more stable than basaltic. We conclude that tephras should be expected to show predictable differential chemical stability in the post‐depositional environment. Copyright © 2003 John Wiley & Sons, Ltd.     

Variations in the natural abundance of 15N in estuarine suspended particulate matter: A specific indicator of biological processing

In this study, the ¹⁴N:¹⁵N ratio of suspended particulate material collected from the Tamar river estuary, south-west England, is described. Three populations of particles, distinguishable by their ¹⁵N content, were observed. This investigation has shown that populations of estuarine particles are generated by biological transformations in situ and that the ¹⁵N content of estuarine particles does not merely reflect hydrodynamic mixing of the freshwater and seawater source particulate material.     

The exchange of organic carbon in basin mangrove forests in a southwest Florida estuary

The magnitude and seasonality of organic carbon exchange was estimated for two basin mangrove forests in Rookery Bay, Florida. Runoff and tidal inundation in the forests were seasonal with half the annual total of each occurring from August to October. In each forest there were 152 tides yr^?1 with a cumulative depth of about 12 m. Total organic carbon increased in bay waters exporting from the mangroves following a flood tide and peak concentrations were associated with export due to rainfall. The amount of net export from each basin forest was similar, although the concentration of organic carbon in each were different. Monthly net organic carbon export was proportional to the cumulative tidal amplitude within the forest. Total organic carbon export was 64 gC m^?2 yr^?1 and DOC was 75% of the total. A comparison of organic carbon export among riverine, fringe and basin mangroves suggests that tidal hydrology influences the proportion of litter fall that is exported from mangroves; and the magnitude of this organic carbon export from mangroves is related to the cumulative tidal amplitude within the forests.     

Dissolved organic carbon dynamics in two streams draining forested catchments at loch ard,Scotland

Dissolved organic carbon (DOC) was measured at four or eight hour intervals between mid-1989 and mid-1991 in two catchments in west central Scotland. The experimental catchment had been recently clear-felled and the control remained under forest. The amount of DOC varied during individual storm events following the stream hydro-graph. Maximum variations were found in the summer half-year and in the clear-felled catchment. There was also evidence of the exhaustion of DOC in the later events of a sequence. Differences between the catchments were related to catchment characteristics and to land-use change. The reduced magnitude of variation in DOC with discharge in the control stream was due to the influence of a wetland area through which the stream flowed. The mean DOC concentrations were similar in the two streams and annual exports were 15 g m^?2 from the control and 16g m^?2 from the felled catchment. The stream draining the clear-felled catchment had greater high flow DOC concentrations in the summer half-year, probably due to the effect of greater mean summer temperatures on DOC release and of the greater supply of organic debris in the stream channel.     

鲁苏榴辉岩的地球化学

以微量元素、稀土元素、Ｓｒ和Ｎｄ同位素变异特征为依据，确定鲁苏榴辉岩为多成因、多来源和多阶段，指出主要是在印支期扬子陆块与华北陆块碰撞造山作用过程中，挤入的上地幔碎片以及不同原岩类型的壳内高压变质岩碎块。燕山晚期的区域构造热事件使得某些榴辉岩的同位素体系再平衡。     

南海南部约30 ka来沉积有机质的生物输入特征

对位于南沙海区的1962柱状样中的有机质进行了热解色谱分析，估算了沉积有机质中水生生物输入和陆源生物输入的变化情况，得出了两种输入的高分辨率的堆积速率曲线，并依此探讨了有关的古海洋事件。发现Younger Dryas、Heinrich及Bond周期事件在本海区皆有表现，说明“西太平洋暖池”在末次冰期是不稳定的。     

Ratios of stable carbon isotopes in some High Arctic plants and lake sediments

¹³C/¹²C ratios for a number of High Arctic vascular plants (51 determinations), mosses (11), and freshwater algae (11) show considerable variation, particularly among the freshwater algae (range from-6.9 to -36.3). In some cases the stable carbon ratios on modern and fossil materials provide guidance as to whether marine waters formerly occupied a given pond or lake basin. In other cases the ¹³C values for algae collected along the present-day shore of a pond or lake bear no relation to the values obtained on constituents preserved within the bottom sediments, suggesting that major changes have occurred in the last few thousand years.Geological Survey of Canada Contribution No. 17291. Contribution No. 41 from the Cape Herschel Project.     

An electrochemical study of pyrite oxidation in the presence of carbon coatings in cyanide medium

The anodic and cathodic behaviour of pyrite with clay and different carbon coatings of activated carbon, graphite and carbonaceous matter in cyanide medium was investigated using the potentiodynamic method. The presence of clay coating did not change the polarisation curve appearance for either the anodic oxidation of pyrite or the cathodic reduction of oxygen or the potential of the current plateau, but only decreased the plateau current especially at a higher coating thickness. The presence of the carbon coatings marginally shifted the rest potential for pyrite to a more anodic position and slightly changed the polarisation curve appearance for pyrite oxidation. The current density for pyrite oxidation largely increased in the presence of the carbon coatings, the potential at the plateau shifted to more cathodic positions, and the plateau width became smaller. These effects became more noticeable at a higher coating thickness. The activated carbon, graphite and carbonaceous matter coatings performed similarly in affecting pyrite oxidation at a similar thickness. The carbon coatings significantly increased the limiting current densities for oxygen reduction on pyrite, and the limiting current plateau became steeper at a higher coating thickness. The carbon coatings increased the limiting current density for oxygen reduction to a similar extent at a low coating thickness, but increased to varied extents at a higher coating thickness. The carbon coatings also greatly increased the cathodic current density for gold reduction on pyrite. The enhancement of pyrite oxidation and oxygen or gold reduction on pyrite by the carbon coatings was likely attributed to the electrochemical interaction between pyrite and the carbon materials with electron-rich surfaces and high conductivity. The presence of the carbon coatings significantly increased the oxidation of pyrite in aerated cyanide solutions and the preg-robbing of pyrite especially at a higher coating thickness.