Separation of phytoplanktonic pigments by HPLC for the study of phyto-zooplankton trophic relationships

Phyto-zooplankton trophic relationships were studied using phytoplanktonic pigments (chlorophylls and carotenoids) as organic natural markers. Pigments were separated by high-pressure liquid chromatography (HPLC).Comparison of pigment profiles from monospecific cultures of various taxonomic groups (Chlorophyceae, Bacillariophyceae and Cyanobacteria) and from Cladocera crustaceans (Daphnia magna) fed with these cultures, showed that the characteristic pigment associations of the different taxa are conserved during their transfer from primary producers to secondary consumers.Chromatographic profiles of the Bacillariophyceae and Chlorophyceae type were obtained fromDaphnia respectively fed with mixtures of a Chlorophyceae and a diatom species and mixture of a Chlorophyceae and a Cyanobacterium. This showed the importance of this method in demonstrating a possible selective feeding by the herbivorous zooplankton.The observation of pigment profiles of the Dinophyceae type following feeding of a zooplankton assemblage from Lake Pavin within this natural medium (phytoplankton dominated by a Dinophyceae) and of a Chlorophyceae type profile as the same assemblage was fed in the laboratory on phytoplankton from Lake Villerest (composed of about 80% Cyanobacteria and 20% Chlorophyceae), suggested that this method could be applied to the natural environment.     

Trialling tools using hand-weeding,weed mat and artificial shading to control nuisance macrophyte growth at multiple scales in small agricultural waterways

ABSTRACT

Introduced aquatic macrophytes can dominate small agricultural waterways in summer and autumn becoming a significant management problem. Excessive growth can clog waterways, causing drainage issues and reducing agricultural productivity while in-stream velocities are reduced and sedimentation increased. Consequently, water managers remove them by mechanical clearance, chemical spray and cutting which can be costly and have negative impacts on in-stream habitat and ecological health. We trialled three tools to reduce macrophytes: hand-weeding, weed mat and artificial shading, at a reach-scale (50?m) and larger-scale (200–400?m). Hand-weeding reduced cover in the short-term, however macrophytes recovered to pre-treatment levels within one season. Weed mat along the banks was effective at reducing emergent macrophytes, particularly Erythranthe guttata (monkey musk) and Nasturtium microphyllum (watercress). Weed mat lasted for several growing seasons and continued to be effective. Shading over the waterway using polythene markedly reduced submerged macrophytes indicating that heavy shading by riparian plantings could reduce submerged macrophytes in the longer-term. These results indicate that in the short-term, weed mat could be used to limit sprawling emergent macrophytes. In the longer-term, weed mat used in conjunction with riparian planting could provide shading so that macrophyte cover in these small waterways could be reduced and controlled.     

Uncertainty of gas saturation estimates in a subbituminous coal seam

To assess the commercial viability of a coalbed methane prospect two of the key geological parameters measured are gas content (desorbed gas) and gas holding capacity (adsorption capacity). These two measures, together with reservoir pressure, give an estimate of the gas saturation of the reservoir. Typically gas saturation has been assessed by collecting one adsorption isotherm sample and assuming it is representative of the whole seam reservoir conditions. This study addresses that assumption.To understand the level of variation, and thus the inherent uncertainty in saturation, one core (Jasper-1) from the Huntly coalfield in New Zealand was analysed in detail. Ten samples (representing the whole coal seam) were placed into gas desorption canisters and desorbed for ten days and then analysed for adsorption capacity. Desorption analyses for total measured gas content (average in-situ basis) ranged from 2.32 to 2.89 m³/t (standard deviation (sd) = 0.18) and gas adsorptive capacity at 4 MPa (average in-situ basis) from 2.11 to 3.51 m³/t (sd = 0.38) resulting in saturations ranging from 66% to 120% (sd = 15).Determination of how many samples are required to make a realistic assessment of average reservoir properties requires a consideration of: (i) the level of accuracy desired, (ii) the limit of accuracy possible, which is governed by the magnitude of experimental error, and (iii) the innate variability of the seam. It was found that a minimum of five samples each for adsorption and desorption were required in order to significantly decrease the uncertainty in gas saturation estimates for a subbituminous coal.     

LIBS analysis of geomaterials: Geochemical fingerprinting for the rapid analysis and discrimination of minerals

Laser-induced breakdown spectroscopy (LIBS) is a simple atomic emission spectroscopy technique capable of real-time, essentially non-destructive determination of the elemental composition of any substance (solid, liquid, or gas). LIBS, which is presently undergoing rapid research and development as a technology for geochemical analysis, has attractive potential as a field tool for rapid man-portable and/or stand-off chemical analysis. In LIBS, a pulsed laser beam is focused such that energy absorption produces a high-temperature microplasma at the sample surface resulting in the dissociation and ionization of small amounts of material, with both continuum and atomic/ionic emission generated by the plasma during cooling. A broadband spectrometer-detector is used to spectrally and temporally resolve the light from the plasma and record the intensity of elemental emission lines. Because the technique is simultaneously sensitive to all elements, a single laser shot can be used to track the spectral intensity of specific elements or record the broadband LIBS emission spectra, which are unique chemical ‘fingerprints’ of a material. In this study, a broad spectrum of geological materials was analyzed using a commercial bench-top LIBS system with broadband detection from ∼200 to 965 nm, with multiple single-shot spectra acquired. The subsequent use of statistical signal processing approaches to rapidly identify and classify samples highlights the potential of LIBS for ‘geochemical fingerprinting’ in a variety of geochemical, mineralogical, and environmental applications that would benefit from either real-time or in-field chemical analysis.     

New Olivine Reference Material for In Situ Microanalysis

A new olivine reference material – MongOL Sh11‐2 – for in situ analysis has been prepared from the central portion of a large (20 × 20 × 10 cm) mantle peridotite xenolith from a ~ 0.5 My old basaltic breccia at Shavaryn‐Tsaram, Tariat region, central Mongolia. The xenolith is a fertile mantle lherzolite with minimal signs of alteration. Approximately 10 g of 0.5–2 mm gem quality olivine fragments were separated under binocular microscope and analysed by EPMA, LA‐ICP‐MS, SIMS and bulk analytical methods (ID‐ICP‐MS for Mg and Fe, XRF, ICP‐MS) for major, minor and trace elements at six institutions world‐wide. The results show that the olivine fragments are sufficiently homogeneous with respect to major (Mg, Fe, Si), minor and trace elements. Significant inhomogeneity was revealed only for phosphorus (homogeneity index of 12.4), whereas Li, Na, Al, Sc, Ti and Cr show minor inhomogeneity (homogeneity index of 1–2). The presence of some mineral and fluid‐melt micro‐inclusions may be responsible for the inconsistency in mass fractions obtained by in situ and bulk analytical methods for Al, Cu, Sr, Zr, Ga, Dy and Ho. Here we report reference and information values for twenty‐seven major, minor and trace elements.     

Effect of anorthite on granite phase relations: Experimental data and models

New experimental data on the effect of anorthite (An) on liquidus phase equilibria in the system Qz–Ab–Or are presented. The data were obtained for 5 wt% An added to variable Qz/Ab/Or compositions at 300 MPa and under H₂O-saturated conditions. Crystal–liquid equilibria were determined for 13 synthetic glass compositions made from gels in experiments performed between 660 and 750 °C in cold-seal pressure vessels. Forward and reversal experiments were systematically conducted on each composition to demonstrate equilibrium. A total of 51 charges was examined. Three crystalline phases, quartz, alkali feldspar and plagioclase appear on the H₂O-saturated liquidus surface. The determined minimum liquidus 5 wt% An “piercing” point (39% Qz, 33% Ab, 28% Or) is shifted away from the Ab apex toward the Qz–Or sideline when compared with the An-free 300 MPa H₂O-saturated minimum. This shift is of the same type as that observed at 100 MPa in the same system and at 200 MPa in a rhyolitic system. The new experimental results are used to test both empirical and thermodynamic models for silicic magmas. Empirical models reproduce reasonably well the new experimental data, although more sophisticated calculations schemes appear to be required to improve their accuracy. The new experimental results in the haplogranodiorite system are not well reproduced with the model of Holland and Powell (2001), mainly because plagioclase stability appears greatly enhanced in the model. Rhyolite-MELTS satisfactorily reproduces the Qz-, Pl- and Af-liquid phase equilibria, but model H₂O solubilities are significantly lower and crystallization temperatures higher than in experiments.     

Large and growing environmental reservoirs of Deca-BDE present an emerging health risk for fish and marine mammals

Polybrominated diphenyl ethers (PBDEs) have been the subject of intense scientific and regulatory scrutiny during recent years. Of the three commercial forms (Penta, Octa and Deca) of PBDEs that have been widely used as flame retardants in textiles, furniture upholstery, plastics, and electronics, only Deca-BDE remains on the general market in North America, while a recent ruling of the European Court spells an impending end to its use in Europe. We review here highlights of aquatic research documenting the rapid emergence of PBDEs as a high priority environmental concern in Canada. PBDEs are being introduced in large quantities to the aquatic environment through sewage discharge and atmospheric deposition. In certain environmental compartments, the single congener BDE-209, the main ingredient in the Deca-BDE formulation, has surpassed the legacy PCBs and DDT as the top contaminant by concentration. Limited biomagnification of BDE-209 in aquatic food webs reflects its high log K_ow and preferential partitioning into the particle phase. As a result, large environmental reservoirs of BDE-209 are being created in sediments, and these may present a long-term threat to biota: BDE-209 breaks down into more persistent, more bioaccumulative, more toxic, and more mobile PBDE congeners in the environment.     

Variability in the annual cycle of vertical particulate organic carbon export on Arctic shelves: Contrasting the Laptev Sea,Northern Baffin Bay and the Beaufort Sea

The ongoing regression of sea ice cover is expected to significantly affect the fate of organic carbon over the Arctic continental shelves. Long-term moored sediment traps were deployed in 2005–2006 in the Beaufort Sea, Northern Baffin Bay and the Laptev Sea to compare the annual variability of POC fluxes and to evaluate the factors regulating the annual cycle of carbon export over these continental shelves. Annual POC fluxes at 200 m ranged from 1.6 to 5.9 g C m⁻² yr⁻¹ with the highest export in Northern Baffin Bay and the lowest export over the Mackenzie Shelf in the Beaufort Sea. Each annual cycle exhibited an increase in POC export a few weeks before, during, or immediately following sea ice melt, but showed different patterns over the remainder of the cycle. Enhanced primary production, discharge of the Lena River, and resuspension events contributed to periods of elevated POC export over the Laptev Sea slope. High POC fluxes in Northern Baffin Bay reflected periods of elevated primary production in the North Water polynya. In the Beaufort Sea sediment resuspension contributed to most of the large export events. Our results suggest that the outer shelf of the Laptev Sea will likely sustain the largest increase in POC export in the next few years due to the large reduction in ice cover and the possible increase in the Lena River discharge. The large differences in forcing among the regions investigated reinforce the importance of monitoring POC fluxes in the different oceanographic regimes that characterize the Arctic shelves to assess the response of the Arctic Ocean carbon cycle to interannual variability and climate change.     

Pb–Nd isotopic constraints on sedimentary input into the Lesser Antilles arc system

The Lesser Antilles arc is a particularly interesting island arc because it is presently very active, it is located perpendicular to the South American continent and its chemical and isotopic compositions display a strong north–south gradient. While the presence in the south of a thick pile of sedimentary material coming from the old South American continent has long been suspected to explain the geochemical gradient, previous studies failed to demonstrate unambiguously a direct link between the arc lava compositions and the subducted sediment compositions.Here, we present new Nd, Sm, Th, U and Pb concentrations and Nd–Pb isotopic data for over 60 sediments from three sites located in the fore arc region of the Lesser Antilles arc. New data for DSDP Site 543 drill core located east of Dominica Island complement the data published by White et al. [White, W.M., Dupré, B. and Vidal, P., 1985. Isotope and trace element geochemistry of sediments from the Barbados Ridge–Demerara Plain region, Atlantic Ocean. Geochimica et Cosmochimica Acta, 49: 1875–1886.] and confirm their relatively uniform isotopic compositions (i.e., ²⁰⁶Pb/²⁰⁴Pb between 19.13 and 19.53). In contrast, data obtained on DSDP Site 144 located further south, on the edge of the South American Rise and on sediments from Barbados Island are much more variable (²⁰⁶Pb/²⁰⁴Pb ranges from 18.81 to 27.69). The very radiogenic Pb isotopic compositions are found in a 60 m thick black shale unit, which has no age equivalent in the Site 543 drill core. We interpret the peculiar composition of the southern sediments as being due to two factors, (a) the proximity of the South American craton, which contributes coarse grain old detrital material that does not travel far from the continental shelf, and (b) the presence of older sediments including the thick black shale unit formed during Oceanic Anoxic events 2 and 3.The north–south isotopic change known along the Lesser Antilles arc can be explained by the observed geographical changes in the composition of the subducted sediments. About 1% contamination of the mantle wedge by Site 543 sediments explains the composition of the northern islands while up to 10% sediments like those of Site 144 is required in the source of the southern island lavas. The presence of black shales in the subducted pile provides a satisfactory explanation for the very low Δ8/4 values that characterize the Lesser Antilles arc.     

An alternative measure of discharge effectiveness

Since 1960, geomorphic effectiveness has been quantified by analytically combining measures of the frequency and the magnitude of geomorphic processes, most often for the case of sediment yield in rivers via the calculation of effective discharge, Q_eff. Here we leverage the Q_eff analysis approach to develop an alternative metric, the functional‐equivalent discharge Q_fed, which is the discharge that will reproduce the magnitude of the sediment load generated by the full hydrologic distribution. Q_fed is intended to be a more representative metric of hydrologic variability than Q_eff: whereas Q_eff provides a measure of the effectiveness of individual flow rates, Q_fed incorporates a measure of the average effectiveness of the entire flow distribution. We develop an analytical approximation of Q_fed based on relatively few parameters, apply the approach to a set of suspended sediment load data and describe how Q_fed varies broadly with sediment and hydrologic conditions. Copyright © 2007 John Wiley & Sons, Ltd.