A multi-elemental study of plant surface particles in relation to geochemistry and biogeochemistry

Surface particulate material was collected in dry weather from the foliage of gorse bushes (Ulex europaeus L.) at twenty background and mineralised sites in southwest England, together with soil and herbage samples. The foliar dusts were separated in the laboratory into four size fractions, and all the samples were analysed for sixteen elements by inductively coupled plasma (I.C.P.) emission spectrometry. Regression analysis of the data showed that the analytical values determined for foliar surface particles were correlated (P > 95%) in at least one particulate fraction with soil concentrations for the following elements: Cu, Pb, Mn, Zn, Al, Ca, Cr, Fe, Be, Sr, Ba, P and Cd. The multi-elemental data, supported by electron microprobe analysis and visual and microscopic examination of the particles, showed that plant material, as well as soil dust, contributed substantially to the chemistry of plant surface particles. Factors influencing the trace element chemistry of plant surfaces are discussed and should be appreciated if particle collection methods are to be applied as a routine geochemical/biogeochemical technique.     

The effect of cobalt ion on nucleation of calcium-carbonate polymorphs

Cobalt, like Mg, may cause the precipitation of aragonite rather than calcite in aqueous solutions due to the adsorption and crystal poisoning of calcite by a hydrated ion. Solutions containing NaCl and CaCl₂, having the ionic strength and Ca content of seawater (35‰ salinity), were spiked with known amounts of CoCl₂. Calcium carbonate was precipitated by the addition of 0.7 ml of 1 M Na₂CO₃. All experimental runs were made at 25°C, and all products were examined by X-ray diffraction. At low concentrations of Co (< 5·^?4M) calcite and vaterite formed. At concentrations from 5·10^?4 M to 2·10^?3M, the products consisted of combinations of calcite and vaterite; aragonite and calcite; aragonite and vaterite; calcite, vaterite and aragonite. In solutions of 3·10^?3M CoCl₂, most precipitates were aragonite with only one sample containing a small amount of calcite. All precipitates from 5·10^?3M CoCl₂ solutions either contained aragonite or were amorphous. Solutions with concentrations of 1 · 10^?2M CoCl₂ produced only amorphous precipitates. All precipitates contained an amorphous violet phase, assumed to be basic cobaltous carbonate (2CoCO₃·Co(OH)₂·H₂O).     

Geometric assessment of the kodak DCS Pro back

This paper reports on an investigation into the suitability of the Kodak DCS Pro Back for use in close range photogrammetric measurement. The camera back, being used in conjunction with a medium-format non-metric camera, has been assessed with a view to using it for low- to medium-order photogrammetric work in architectural recording. Examinations centred upon the stability of the camera back with respect to the camera body and the effects of the removable infrared filter that is present immediately above the camera's focal plane. Ultimately the camera combination was deemed suitable for application in recording of this kind and is now in active use by the Metric Survey Team at English Heritage.     

Reconstruction of Summer Temperatures in Interior Alaska from Tree-Ring Proxies: Evidence for Changing Synoptic Climate Regimes

Maximum latewood density and δ ¹³C discrimination of Interior Alaska white spruce were used to reconstruct summer (May through August) temperature at Fairbanks for the period 1800–1996, one of the first high-resolution reconstructions for this region. This combination of latewood density and δ ¹³C discrimination explains 59.9% of the variance in summer temperature during the period of record 1906–1996. The 200-yr. reconstruction is characterized by 7 decadal-scale regimes. Regime changes are indicated at 1816, 1834, 1879, 1916, 1937, and 1974, are abrupt, and appear to be the result of synoptic scale climate changes. The mean of summer temperature for the period of reconstruction (1800–1996) was 13.49 °C. During the period of instrument record (1903–1996) the mean of summer temperature was 13.31 °C for both the reconstruction and the recorded data. The coldest interval was 1916–1937 (12.62 ° C) and the warmest was 1974–1996 (14.23 °C) for the recorded data. The reconstruction differs from records of northern hemisphere temperatures over this period, especially because of Interior Alaska warm periods reconstructed from 1834 to 1851 (14.24 °C) and from 1862 to 1879 (14.19 °C) and because of the cool period in the early part of the 20th century (1917–1974). We show additional tree ring data that support our reconstruction of these warm periods. Alternate hypotheses involving autogenic effect of tree growth on the site, altered tree sensitivity, or novel combinations of temperature and precipitation were explored and while they cannot be ruled out as contributors to the anomalously warm 19th century reconstruction, they were not supported by available data. White spruce radial growth is highly correlated with reconstructed summer temperature, and temperature appears to be a reliable index of carbon uptake in this system.     

Regional-scale analysis of karst underground flow deduced from tracing experiments: examples from carbonate aquifers in Malaga province,southern Spain

Tracer concentration data from field experiments conducted in several carbonate aquifers (Malaga province, southern Spain) were analyzed following a dual approach based on the graphical evaluation method (GEM) and solute transport modeling to decipher flow mechanisms in karst systems at regional scale. The results show that conduit system geometry and flow conditions are the principal factors influencing tracer migration through the examined karst flow routes. Solute transport is mainly controlled by longitudinal advection and dispersion throughout the conduit length, but also by flow partitioning between mobile and immobile fluid phases, while the matrix diffusion process appears to be less relevant. The simulation of tracer breakthrough curves (BTCs) suggests that diffuse and concentrated flow through the unsaturated zone can have equivalent transport properties under extreme recharge, with high flow velocities and efficient mixing due to the high hydraulic gradients generated. Tracer mobilization within the saturated zone under low flow conditions mainly depends on the hydrodynamics (rather than on the karst conduit development), which promote a lower longitudinal advection and retardation in the tracer migration, resulting in a marked tailing effect of BTCs. The analytical advection-dispersion equation better approximates the effective flow velocity and longitudinal dispersion estimations provided by the GEM, while the non-equilibrium transport model achieves a better adjustment of most asymmetric and long-tailed BTCs. The assessment of karst underground flow properties from tracing tests at regional scale can aid design of groundwater management and protection strategies, particularly in large hydrogeological systems (i.e. transboundary carbonate aquifers) and/or in poorly investigated ones.     

A multi-method approach for groundwater resource assessment in coastal carbonate (karst) aquifers: the case study of Sierra Almijara (southern Spain)

Understanding the transference of water resources within hydrogeological systems, particularly in coastal aquifers, in which groundwater discharge may occur through multiple pathways (through springs, into rivers and streams, towards the sea, etc.), is crucial for sustainable groundwater use. This research aims to demonstrate the usefulness of the application of conventional recharge assessment methods coupled to isotopic techniques for accurately quantifying the hydrogeological balance and submarine groundwater discharge (SGD) from coastal carbonate aquifers. Sierra Almijara (Southern Spain), a carbonate aquifer formed of Triassic marbles, is considered as representative of Mediterranean coastal karst formations. The use of a multi-method approach has permitted the computation of a wide range of groundwater infiltration rates (17–60%) by means of direct application of hydrometeorological methods (Thornthwaite and Kessler) and spatially distributed information (modified APLIS method). A spatially weighted recharge rate of 42% results from the most coherent information on physiographic and hydrogeological characteristics of the studied system. Natural aquifer discharge and groundwater abstraction have been volumetrically quantified, based on flow and water-level data, while the relevance of SGD was estimated from the spatial analysis of salinity, ²²²Rn and the short-lived radium isotope ²²⁴Ra in coastal seawater. The total mean aquifer discharge (44.9–45.9 hm³ year^?1) is in agreement with the average recharged groundwater (44.7 hm³ year^?1), given that the system is volumetrically equilibrated during the study period. Besides the groundwater resources assessment, the methodological aspects of this research may be interesting for groundwater management and protection strategies in coastal areas, particularly karst environments.     

Estimation of Biodegradation Rates Using Respiration Tests During In Situ Bioremediation of Weathered Diesel NAPL

Respiration tests were carried out during a seven month bioremediation field trial to monitor biodegradation rates of weathered diesel non-aqueous phase liquid (NAPL) contaminating a shallow sand aquifer. Multiple depth monitoring of oxygen concentrations and air-filled porosity were carried out in nutrient amended and nonamended locations to assess the variability of degradation rate estimates calculated from respiration tests.
The field trial consisted of periodic addition of nutrients (nitrogen and phosphorus) and aeration of a 100 m² trial plot. During the bioremediation trial, aeration was stopped periodically, and decreases in gaseous oxygen concentrations were logged semi-continuously using data loggers attached to recently developed in situ oxygen probes placed at multiple depths above and within a thin NAPL-contaminated zone. Oxygen usage rate coefficients were determined by fitting zero-and first-order rate equations to the oxygen concentration reduction curves, although only zero-order rates were used to calculate biodegradation rates. Air-filled porosity estimates were found to vary by up to a factor of two between sites and at different times.
NAPL degradation rates calculated from measured air-filled porosity and oxygen usage rate coefficients ranged up to 69 mg kg^-1 day^-1. These rates are comparable to and higher than rates quoted in other studies, despite the high concentrations and weathered state of the NAPL at this test site. For nutrient-amended sites within the trial plot, estimates of NAPL degradation rates were two to three times higher than estimates from nonamended sites. Rates also increased with depth.