Applications of the random model of drainage basin composition

The random model of drainage basin composition is founded on the assumptions that (a) natural channels are topologically random in the absence of geological controls and (b) for channel networks developed in similar environments, the exterior and interior link lengths are independent random variables with a common distribution for each type. The effectiveness of this model in estimating the values of geomorphic variables and in explaining and predicting geomorphic relationships is illustrated by several examples. The data required for these examples were obtained from map studies of 30 channel networks, comprising a total of about 8700 links, in eastern Kentucky. A common factor in the success of all three applications of the model is the way in which the planimetric features of drainage basins are determined by their underlying topologic structure.     

Relative influence of vegetation on urban energy budgets and surface temperatures

Two deterministic models were combined: one for canopy leaf energy budgets and one for street canyon energy budgets. The effects of street parks and roof gardens in contrast to non-vegetated city blocks were examined by the use of four typical urban morphologies, which were exposed latitudinally to summer and winter simulations. A variety of increases and decreases in shortwave radiation, net radiation, sensible heat flux, and system reradiation resulted. These changes appear to represent the generalized limits of the possible responses to the addition of vegetation to non-vegetated city blocks.     

用电子束CT作冠状动脉血管造影

本文介绍用电子束ＣＴ作冠状动脉可视化造影的方法,说明本项成就的特征和在应用这项技术的局限性,并指出这种技术在临床上,可能成为新无创伤性的诊断工具。     

Functioning of intertidal flats inferred from temporal and spatial dynamics of O<Subscript>2</Subscript>, H<Subscript>2</Subscript>S and pH in their surface sediment

In this article, we describe the dynamics of pH, O₂ and H₂S in the top 5–10 cm of an intertidal flat consisting of permeable sand. These dynamics were measured at the low water line and higher up the flat and during several seasons. Together with pore water nutrient data, the dynamics confirm that two types of transport act as driving forces for the cycling of elements (Billerbeck et al. 2006b): Fast surface dynamics of pore water chemistry occur only during inundation. Thus, they must be driven by hydraulics (tidal and wave action) and are highly dependent on weather conditions. This was demonstrated clearly by quick variation in oxygen penetration depth: Seeps are active at low tide only, indicating that the pore water flow in them is driven by a pressure head developing at low tide. The seeps are fed by slow transport of pore water over long distances in the deeper sediment. In the seeps, high concentrations of degradation products such as nutrients and sulphide were found, showing them to be the outlets of deep-seated degradation processes. The degradation products appear toxic for bioturbating/bioirrigating organisms, as a consequence of which, these were absent in the wider seep areas. These two mechanisms driving advection determine oxygen dynamics in these flats, whereas bioirrigation plays a minor role. The deep circulation causes a characteristic distribution of strongly reduced pore water near the low water line and rather more oxidised sediments in the centre of the flats. The two combined transport phenomena determine the fluxes of solutes and gases from the sediment to the surface water and in this way create specific niches for various types of microorganisms.     

Impact of precipitation seasonality changes on isotopic signals in polar ice cores: a multi-model analysis

For Central Greenland, water isotope analysis indicates a temperature difference of about 10°C since the Last Glacial Maximum (LGM). However, borehole thermometry and gas diffusion thermometry indicate that LGM surface temperatures were about 20°C colder than today. Two general circulation model studies have shown that changes in the seasonal precipitation timing in Central Greenland might have caused a warm bias in the LGM water isotope proxy temperatures, and that this bias could explain the difference in the estimated paleotemperatures. Here we present an analysis of a number of atmospheric general circulation model simulations mostly done within the framework of the Paleoclimate Modeling Intercomparison Project. The models suggest that the seasonal cycle of precipitation and surface mass balance over Central Greenland at the LGM might have been very different from today. This supports the idea that the accuracy of the water isotope thermometry at the LGM in Greenland might be compromised as a result of a modified surface mass balance seasonality. However, the models disagree on the amplitude and sign of the bias. For Central East Antarctica, a strong seasonality effect on the LGM isotopic signal is not simulated by any of the analyzed models. For the mid-Holocene (6 kyr BP) the models suggest relatively weak isotope paleothermometry biases linked to changes in the surface mass balance seasonality over both ice sheets.     

Kinetics of redox cycling of iron coupled with fulvic acid

The kinetics of conversion of iron(III) (hydr)oxides to ferrous iron mediated by fulvic acid have been investigated in order to improve the understanding of the redox cycling of iron at the oxic-anoxic boundary in natural waters. Under the conditions similar to natural waters, fulvic acid is able to reduce the iron(III) (hydr)oxide. The kinetics of the reaction depend on the reactivity of iron(III) (hydr)oxides and the reducing power of the fulvic acid. The rate of reaction is 60 nm/h obtained under following conditions: total concentration of Fe(III) 1.0 × 10^–4 M, pH 7.5, fulvic acid 5 mg/L. The rate is considered as a net result of reduction and oxidation in the > Fe^III-OH/Fe(II) wheel coupled with fulvic acid. In a real natural water system, reductants other than fulvic acid may be of importance. The results obtained in the laboratory, however, provide evidence that the Fe(OH)₃(s)/Fe(II) redox couple is able to act as an electron-transfer mediator for the oxidation of natural organic substances, such as fulvic acid by molecular oxygen either in the absence of microorganisms or as a supplement to microbial activity.     

Isotope hydrological study of mean transit times in an alpine basin (Wimbachtal, Germany)

Measurements of tritium and ¹⁸O concentrations in precipitation and runoff were used to provide further insight into the groundwater storage properties of the Wimbachtal Valley, a catchment area of 33.4 km², extending between 636 and 2713 m a.s.l. in the Berchtesgaden Alps. The catchment includes three aquifer types: a dominant porous aquifer; a fractured dolomite; a karstic limestone aquifer. Employing a simple hydrological model, information about mean transit times of environmental tracers is derived for the groundwater runoff component and several karst springs from the application of the exponential and dispersion flow models to the isotopic input and output data. The mean transit times calculated from a dispersion model with transit times of 4.1 years for ¹⁸O and 4.2 years for tritium, which agree well, allow calculation of total (mobile + stagnant) groundwater storage volume, which is equivalent to 6.6 m of water depth. Direct runoff appears negligible as in many other cases.     

The effect of rock moisture on Schmidt hammer rebound: tests on rock samples from Marion Island and South Africa

In an assessment of the influence of internal rock moisture content on Schmidt hammer readings, rebound (R) values are found to decrease with increasing moisture content. For samples of basalt, sandstone and dolerite the maximum decrease in R‐values is found between oven dry values and saturated rock rebound values, the magnitude of which varies from 2 to 10 points on the R‐scale. A quartzite block has the greatest decline of 6 points at 60 per cent saturation. For certain rock types under differing site‐to‐site field moisture conditions the moisture effect can be a significant factor in the interpretation of the relative state of weathering from rebound values. Copyright © 2002 John Wiley & Sons, Ltd.