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Christopher J. Daughney Matthias Raiber Magali Moreau-Fournier Uwe Morgenstern Rob van der Raaij 《Hydrogeology Journal》2012,20(1):185-200
Baseline monitoring of groundwater quality aims to characterize the ambient condition of the resource and identify spatial or temporal trends. Sites comprising any baseline monitoring network must be selected to provide a representative perspective of groundwater quality across the aquifer(s) of interest. Hierarchical cluster analysis (HCA) has been used as a means of assessing the representativeness of a groundwater quality monitoring network, using example datasets from New Zealand. HCA allows New Zealand??s national and regional monitoring networks to be compared in terms of the number of water-quality categories identified in each network, the hydrochemistry at the centroids of these water-quality categories, the proportions of monitoring sites assigned to each water-quality category, and the range of concentrations for each analyte within each water-quality category. Through the HCA approach, the National Groundwater Monitoring Programme (117 sites) is shown to provide a highly representative perspective of groundwater quality across New Zealand, relative to the amalgamated regional monitoring networks operated by 15 different regional authorities (680 sites have sufficient data for inclusion in HCA). This methodology can be applied to evaluate the representativeness of any subset of monitoring sites taken from a larger network. 相似文献
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The activities of particulate and soluble phosphatase were analyzed monthly for 1 year in the coastal ecosystems of the NW Mediterranean Sea. The mean contribution of the particulate activity increased from 56% at an MUF-P concentration of 30 μM to 77% at 0.04 μM. This particulate activity was negatively correlated with the DIP, DOP and TDP concentrations when the activities were related to the seawater volume, chlorophyll a or the protein concentration. The TDP correlations were highly significant (p: 0.001). The DOP correlations were significant (p: 0.04) and became highly significant (p: 0.009) at low DIP concentrations (<0.13 μM). The DIP correlations were significant (p: 0.04) only at low DOP concentrations (<0.18 μM). Thus, the effects of seawater DIP and DOP were found to be linked. The soluble activity exhibited distinct phosphatase fractions with high (0.5–29.5 μM) and low (0.02–2 μM) Km values, but none exhibited significant correlations with phosphorus compounds. 相似文献
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Denis Wirrmann Anne-Marie Sémah Jean-Pierre Debenay Magali Chacornac-Rault 《Quaternary Research》2011,76(2):229-242
Multiproxy analysis of three littoral cores from western New Caledonia supports the hypothesis that the main controlling factors of environmental changes are sea-level change, ENSO variability and extra-tropical phenomena, such as the Medieval Warm Period (MWP) marked by a tendency for La Niña-like conditions in the tropical Pacific. The record starts during the late Holocene sea-level rise when the terrestrial vegetation indicated wet and cool conditions. The site was a coastal bay definitely transformed into a freshwater swamp at around 3400 cal yr BP, after the rapid drawdown of sea level to its current level. Sediments and foraminiferal assemblages indicated subsequent episodes of freshwater infillings, emersion or very high-energy conditions, likely related to climatic changes and mostly controlled by ENSO variability. Between 2750 and 2000 cal yr BP, relatively dry and cool climate prevailed, while wetter conditions predominated between ca. 1800 and 900 cal yr BP. The Rhizophoraceae peak between ca. 1080 and 750 cal yr BP, coeval with the MWP, may indicate a global phenomenon. Microcharcoal particles present throughout the record increased after 1500 cal yr BP, suggesting an anthropogenic source. From ca. 750 cal yr BP the appearance of current type of vegetation marks the human impact. 相似文献
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Jaume Bech Magali Suarez Ferran Reverter Pedro Tume Pedro Sánchez Joan Bech Alejandro Lansac 《Journal of Geochemical Exploration》2010
Selenium is an essential trace element in regard to human and other animals' health, but it presents a narrow range of dietary deficiency and toxic excess. Some phosphate rocks are rich in selenium. Furthermore it is necessary to control selenium's and other trace elements’ compositions in the phosphate rocks, because phosphorite ores of different geographical sites are varied, and even ores from the same outcrop can vary substantially in trace element levels. 相似文献
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Rainer Dähn André M ScheideggerAlain Manceau Michel L Schlegel Bart BaeyensMichael H Bradbury Magali Morales 《Geochimica et cosmochimica acta》2002,66(13):2335-2347
Wet chemistry kinetics and powder and polarized extended X-ray absorption fine structure (EXAFS and P-EXAFS) spectroscopy were combined to investigate the mechanism of Ni uptake on montmorillonite, at pH 8, high ionic strength (0.2 M Ca(NO3)2), initial Ni concentration of 660 μM, and solid concentration of 5.3 g/L. Approximately 20% of Ni sorbed within the first 24 h; thereafter, the Ni uptake rate slowed, and 12% of the initial Ni concentration remained in solution after 206 d of reaction time. Powder EXAFS spectra collected on wet pastes at 1, 14, 90, and 206 d showed the presence of Ni-Ni pairs at ∼3.08 Å in an amount that gradually increased with time. Results were interpreted by the nucleation of a Ni phase having either an α-Ni-hydroxide- or a Ni-phyllosilicate-like local structure. The latter possibility was confirmed by recording P-EXAFS spectra of a highly textured, self-supporting montmorillonite film prepared in the same conditions as the wet samples and equilibrated for 14 d. The orientation distribution of the c*-axes of individual clay particles off the film plane, as measured by quantitative texture analysis, was 32.8° full width at half maximum, and this value was used to correct from texture effect the effective numbers of Ni and Si nearest neighbors determined by P-EXAFS. Ni atoms were found to be surrounded by 2.6 ± 0.5 Ni atoms at 3.08 Å in the in-plane direction and by 4.2 ± 0.5 Si atoms at 3.26 Å in the out-of-plane direction. These structural parameters, but also the orientation and angular dependence of the Ni and Si shells, strongly support the formation of a Ni phyllosilicate having its layers parallel to the montmorillonite layers. The neoformation of a phyllosilicate on metal uptake on montmorillonite, documented herein for the first time, has important geochemical implications because this dioctahedral smectite is overwhelmingly present in the environment. The resulting sequestration of sorbed trace metals in sparingly soluble phyllosilicate structure may durably decrease their migration and bioavailability at the Earth’s surface and near surface. 相似文献
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Thomas Franck Rizza Magali Bellier Olivier Billant Jérémy Dussouillez Philippe Fleury Jules Delanghe Doriane Ollivier Vincent Godard Vincent Talon Brigitte 《Natural Hazards》2021,105(2):1453-1490
Natural Hazards - The Provence region, located in the south-east of France, has experienced a few destructive earthquakes during the last centuries, such as the 1909 Lambesc earthquake or the 1509... 相似文献
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Paolo Benettin Magali F. Nehemy Lucas A. Cernusak Ansgar Kahmen Jeffrey J. McDonnell 《水文研究》2021,35(3):e14073
Source water apportionment studies using the dual isotopes of oxygen and hydrogen have revolutionized our understanding of ecohydrology. But despite these developments—mostly over the past decade—many technical problems still exist in terms of linking xylem water to its soil water and groundwater sources. This is mainly due to sampling issues and possible fractionation of xylem water. Here we explore whether or not leaf water alone can be used to quantify the blend of rainfall event inputs from which the leaf water originates. Leaf water has historically been avoided in plant water uptake studies due to the extreme fractionation processes at the leaf surface. In our proof of concept work we embrace those processes and use the well-known Craig and Gordon model to map leaf water back to its individual precipitation event water sources. We also employ a Bayesian uncertainty estimation approach to quantify source apportionment uncertainties. We show this using a controlled, vegetated lysimeter experiment where we were able to use leaf water to correctly identify the mean seasonal rainfall that was taken up by the plant, with an uncertainty typically within ± 1‰ for δ18O. While not appropriate for all source water studies, this work shows that leaf water isotope composition may provide a new, relatively un-intrusive method for addressing questions about the plant water source. 相似文献
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Ammonia (NH3) is the major intermediate phase in the pathway of nitrogen (N) transfer from the fixed N phases (e.g., in crustal material) to free N2 (e.g., in natural gas reservoirs and volcanic gases). Yet the N isotopic behavior during these N-cycling processes remains poorly known. In an attempt to contribute to the understanding of N cycling using N isotopes, we carried out laboratory experiments to investigate the N isotopic effect associated with thermal decomposition of ammonia (2NH3 → N2 + 3H2). Pure NH3 (with initial δ15NNH3 of ∼ −2‰, relative to air standard) was sealed into quartz tubes and thermally decomposed at 600, 700 or 800 °C from 2 hours to 500 days. With the progress of the reaction, the δ15N of the remaining NH3 and the accumulated N2 increased from −2 to +35‰ and from −20 to −2‰, respectively. The differences of the N-isotope fractionations at the three temperatures are not significant. Modeling using the Rayleigh distillation model yielded similar kinetic N-isotope fractionation factors (αN2-NH3) of 0.983 ± 0.002 for 600, 700 and 800 °C. Applied to geological settings, this significant isotope discrimination (∼17‰) associated with partial decomposition of NH3/NH4+ from crustal sources (δ15Naverage ∼ +6.3‰) can produce mantle-like (i.e. ∼ −5‰) or even lower δ15N values of N2. This may explain the large variation of δ15N (−20 to +30‰) of N2 in natural gas reservoirs. It can also possibly explain the extreme 15N-depletion of N2 in some volcanic gases. This possibility has to be carefully considered when using N isotopes to trace geological N cycling across subduction zones by analysis of volcanic N2. 相似文献