Channel precipitation dynamics in a forested Pennsylvania headwater catchment (USA)

Seasonal and event variations in stream channel area and the contributions of channel precipitation to stream flow were studied on a 106‐ha forested headwater catchment in central Pennsylvania. Variations in stream velocity, flowing stream surface width and widths of near‐stream saturated areas were periodically monitored at 61 channel transects over a two‐year period. The area of flowing stream surface and near‐stream saturated zones combined, ranged from 0·07% of basin area during summer low flows to 0·60% of total basin area during peak storm flows. Near‐stream saturated zones generally represented about half of the total channel area available to intercept throughfall and generate channel precipitation. Contributions of routed channel precipitation from the flowing stream surface and near‐stream zones, calculated using the Penn State Runoff Model (PSRM, v. 95), represented from 1·1 to 6·4% of total stream flow and 2·5–29% of total storm flow (stream flow–antecedent baseflow) during the six events. Areas of near‐stream saturated zones contributed 35–52% of the computed channel precipitation during the six events. Channel precipitation contributed a higher percentage of stream flow for events with low antecedent baseflow when storm flow generated by subsurface sources was relatively low. Expansion of channel area and consequent increases in volumes of channel precipitation with flow increases during events was non‐linear, with greater rates of change occurring at lower than at higher discharge rates. Copyright © 1999 John Wiley & Sons, Ltd.     

Recent shifts in coastline change and shoreline stabilization linked to storm climate change

Since cuspate coastlines are especially sensitive to changes in wave climate, they serve as potential indicators of initial responses to changing wave conditions. Previous work demonstrates that Cape Hatteras and Cape Lookout, North Carolina, which are largely unaffected by shoreline stabilization efforts, have become increasingly asymmetric over the past 30 years, consistent with model predictions for coastline response to increases in Atlantic Ocean summer wave heights and resulting changes in the distribution of wave‐approach angles. Historic and recent shoreline change observations for Cape Fear, North Carolina, and model simulations of coastline response to an increasingly asymmetric wave climate in the presence of beach nourishment, produce comparable differences in shoreline change rates in response to changes in wave climate. Results suggest that the effect of beach nourishment is to compensate for – and therefore to mask – natural responses to wave climate change that might otherwise be discernible in patterns of shoreline change alone. Therefore, this case study suggests that the effects of wave climate change on human‐modified coastlines may be detectable in the spatial and temporal patterns of shoreline stabilization activities. Similar analyses of cuspate features in areas where the change in wave climate is less pronounced (i.e. Fishing Point, Maryland/Virginia) and where local geology appears to exert control on coastline shape (i.e. Cape Canaveral, Florida), suggest that changes in shoreline configuration that may be arising from shifting wave climate are currently limited to sandy wave‐dominated coastlines where the change in wave climate has been most pronounced. However, if hurricane‐generated wave heights continue to increase, large‐scale shifts in patterns of erosion and accretion will likely extend beyond sensitive cuspate features as the larger‐scale coastline shape comes into equilibrium with changing wave conditions. Copyright © 2014 John Wiley & Sons, Ltd.     

Quantifying the rate and depth dependence of bioturbation based on optically‐stimulated luminescence (OSL) dates and meteoric 10Be

Both the rate and the vertical distribution of soil disturbance modify soil properties such as porosity, particle size, chemical composition and age structure; all of which play an important role in a soil's biogeochemical functioning. Whereas rates of mixing have been previously quantified, the nature of bioturbation's depth dependence remains poorly constrained. Here we constrain, for the first time, the relationship between mixing rate and depth in a bioturbated soil in northeast Queensland, Australia using a novel method combining OSL (optically‐stimulated luminescence) ages and meteoric beryllium‐10 (¹⁰Be) inventories. We find that the best fit mixing rate decreases non‐linearly with increasing soil depth in this soil and the characteristic length scale of 0.28 m over which the mixing coefficient decays is comparable to reported rooting depth coefficients. In addition we show that estimates of surface mixing rates from OSL data are highly dependent on erosion rate and that erosion rate must be constrained if accurate mixing rates are to be quantified. We calculate surface diffusion‐like mixing coefficients of 1.8 × 10^?4 and 2.1 × 10^?4 m² yr^?1 for the studied soil for two different estimates of soil erosion. © 2014 The Authors. Earth Surface Processes and Landforms Published by John Wiley & Sons Ltd.     

Power law relating 10.7 cm flux to sunspot number

To investigate the relation between observations of the 10.7 cm flux and the international sunspot number so that a physical unit may be ascribed to historical records, both polynomial and power law models are developed giving the radio flux as a function of sunspot number and vice versa. Bayesian data analysis is used to estimate the model parameters and to discriminate between the models. The effect on the parameter uncertainty and on the relative evidence of normalizing the measure of fit is investigated. The power law giving flux as a function of sunspot number is found to be the most plausible model and may be used to estimate the radio flux from historical sunspot observations.     

A high-amplitude thermal inertia anomaly of probable magnetospheric origin on Saturn’s moon Mimas

Spectral maps of Mimas’ daytime thermal emission show a previously unobserved thermal anomaly on Mimas’ surface. A sharp V-shaped boundary, centered at 0°N and 180°W, separates relatively warm daytime temperatures from a cooler anomalous region occupying low- to mid-latitudes on the leading hemisphere. Subsequent observations show the anomalous region is also warmer than its surroundings at night, indicating high thermal inertia. Thermal inertia in the anomalous region is , compared to < outside the anomaly. Bolometric Bond albedos are similar between the two regions, in the range 0.49-0.70. The mapped portion of the thermally anomalous region coincides in shape and location to a region of high-energy electron deposition from Saturn’s magnetosphere, which also has unusually high near-UV reflectance. It is therefore likely that high-energy electrons, which penetrate Mimas’ surface to the centimeter depths probed by diurnal temperature variations, also alter the surface texture, dramatically increasing its thermal inertia.     

Small-scale, high-precision and high-accuracy determination of Poisson’s ratios in cohesive marine sediments

Poisson’s ratio (static) appears as a parameter in models of soft-sediment geomechanical processes such as gas bubble formation and bioturbation, and in a number of practical applications, including acoustic imaging, but is rarely measured in soft near-surface (upper 20 cm) marine sediments. A new uniaxial apparatus was developed to assess Poisson’s ratios of cylindrical samples of soft cohesive sediments under finite-strain, unconfined, undrained conditions. No constraining membrane around the sample is necessary in the instrument. By monitoring the fluid level in a capillary, changes in sample volume can be determined to high precision (reproducibility). Measurements on reference materials, i.e., gelatine and polyurethane, also indicate high accuracy (veracity). For natural sediments from Nova Scotia, Canada, Poisson’s ratios range from 0.4951 to 0.5 with no indication of anisotropy; therefore, such sediments act as incompressible solids to short-term/small-magnitude stresses, as occur during bubble formation and infaunal movement.     

Hydrothermal Metalliferous Sediments and Waters Off the Lesser Antilles

Abstract

Considerable metal enrichments have been found in hydrothermal fluids and metalliferous sediments off the central Lesser Antilles Volcanic Arc. The elements variably enriched in the fluids as a result of the hydrothermal activity are Fe, Mn, As, Si, B, Li and in the sediments, Fe, P, Mo, As, Sb, Hg, Cu and Pb. Variations in the concentrations of these elements in both fluids and sediments along the arc result from a number of factors, the most important of which is the stage that each island's volcano has reached in its eruptive cycle. Although hydrothermal mineralization on the sea floor off the islands is only low grade, phase separation in the hydrothermal fluids at depth could be leading to higher grade stockwork mineralization below the vent fields or the discharge of metal rich brines on the lower flanks of the volcanic islands.     

Binary Mixtures of Permanganate and Chlorinated Volatile Organic Compounds in Groundwater Samples: Sample Preservation and Analysis

Groundwater samples collected at sites where in situ chemical oxidation (ISCO) has been deployed may contain binary mixtures of groundwater contaminants and permanganate (MnO₄^–), an oxidant injected into the subsurface to destroy the contaminant. Commingling of the oxidant and contaminant in aqueous samples may negatively impact the quality of the sample as well as the analytical instruments used to quantify contaminant concentrations. In this study, binary mixtures comprised of (1) a multicomponent standard with permanganate and (2) groundwater samples collected at two ISCO field sites were preserved with ascorbic acid. Ascorbic acid reacts rapidly with the MnO₄^– and limits the reaction between MnO₄^– and the organic compounds in the mixture. Consequently, most of the compounds in the multicomponent standard were within the control limit for quality assurance. However, despite timely efforts to preserve the samples, the rapid reaction between permanganate and contaminant caused the concentration of several sensitive compounds to fall significantly below the lower control limit. Concentrations of volatile organic compounds in the field‐preserved binary mixture groundwater samples were greater than in samples refrigerated in the field and preserved upon arrival at the laboratory, indicating the time‐dependency and benefit of field preservation. The molar ratio of ascorbic acid required to neutralize KMnO₄ was 1.64 (mol ascorbic acid/mol KMnO₄); this provided a baseline to estimate the volume of ascorbic acid stock solution and/or the weight of crystalline ascorbic acid required to neutralize MnO₄^–. Excess ascorbic acid did not negatively impact the quality of the aqueous samples, or analytical instruments, used in the analyses.