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Author de Jong, I.J.H.; Arif, S.S.; Gollapalli, P.K.R.; Neelam, P.; Nofal, E.R.; Reddy, K.Y.; Röttcher, K.; Zohrabi, N. url  openurl
  Title Improving agricultural water productivity with a focus on rural transformation* Type Journal Article
  Year 2021 Publication (up) Irrigation and Drainage Abbreviated Journal  
  Volume 70 Issue 3 Pages 458-469  
  Keywords irrigation efficiency, water productivity, rural transformation, efficacité de l’irrigation, productivité de l’eau, transformation rurale  
  Abstract ABSTRACT As a result of population growth, economic development and climate change, feeding the world and providing water security will require important changes in the technologies, institutions, policies and incentives that drive present-day water management, as captured in Goal 6.4 of the Millennium Development Goals. Irrigation is the largest and most inefficient water user, and there is an expectation that even small improvements in agricultural water productivity will improve water security. This paper argues that improvements in irrigation water productivity involves a complex and comprehensive rural transformation that goes beyond mere promotion of water saving technologies. Many of the measures to improve water productivity require significant changes in the production systems of farmers and in the support provided to them. Looking forward, water use and competition over water are expected to further increase. By 2025, about 1.8 billion people will be living in regions or countries with absolute water scarcity. Demand for water will rise exponentially, while supply becomes more erratic and uncertain, prompting the need for significant shifts of inter-sectoral water allocation to support continued economic growth. Advances in the use of remote sensing technologies will make it increasingly possible to cost-effectively and accurately estimate crop evapotranspiration from farmers’ fields.  
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  Call Number THL @ christoph.kuells @ https://doi.org/10.1002/ird.2451 Serial 89  
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Author Milena-Pérez, A.; Piñero-García, F.; Benavente, J.; Expósito-Suárez, V.M.; Vacas-Arquero, P.; Ferro-García, M.A. url  openurl
  Title Uranium content and uranium isotopic disequilibria as a tool to identify hydrogeochemical processes Type Journal Article
  Year 2021 Publication (up) Journal of Environmental Radioactivity Abbreviated Journal  
  Volume 227 Issue Pages 106503  
  Keywords 234U/238U, Betic cordillera, Groundwater, Hydrogeochemistry, Uranium natural isotopes  
  Abstract This paper studies the uranium content and uranium isotopic disequilibria as a tool to identify hydrogeochemical processes from 52 groundwater samples in the province of Granada (Betic Cordillera, southeastern Spain). According to the geological complexity of the zone, three groups of samples have been considered. In Group 1 (thermal waters; longest residence time), the average uranium content was 2.63 ± 0.16 μg/L, and 234U/238U activity ratios (AR) were the highest of all samples, averaging 1.92 ± 0.30. In Group 2 (mainly springs from carbonate aquifers; intermediate residence time), dissolved uranium presented an average value of 1.34 ± 0.13 μg/L, while AR average value was 1.38 ± 0.25. Group 3 comes from pumping wells in a highly anthropized alluvial aquifer. In this group, where the residence time of the groundwater is the shortest of the three, average uranium content was 5.28 ± 0.26 μg/L, and average AR is the lowest (1.17 ± 0.12). In addition, the high dissolved uranium value and the low AR brought to light the contribution of fertilizers (Group 3). In the three groups, 235U/238U activity ratios were similar to the natural value of 0.046. Therefore, 235U detected in the samples comes from natural sources. This study is completed with the determination of major ions and physicochemical parameters in the groundwater samples and the statistical analysis of the data by using the Principal Component Analysis. This calculation indicates the correlation between uranium isotopes and bicarbonate and nitrate anions.  
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  Call Number THL @ christoph.kuells @ milena-perez_uranium_2021 Serial 112  
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Author Musy, S.; Meyzonnat, G.; Barbecot, F.; Hunkeler, D.; Sültenfuss, J.; Solomon, D.K.; Purtschert, R. url  openurl
  Title In-situ sampling for krypton-85 groundwater dating Type Journal Article
  Year 2021 Publication (up) Journal of Hydrology X Abbreviated Journal  
  Volume 11 Issue Pages 100075  
  Keywords Noble gases, Tracers, Groundwater, Dating, Sampling Methodology  
  Abstract Krypton-85 and other radioactive noble gases are widely used for groundwater dating purposes. 85Kr analysis require large volumes of water to reach the analytical requirements. Conventionally, this water is pumped to the surface to be degassed with a gas extraction system. The large pumping rate may disturb the natural flow field and requires substantial field logistics. Hence, we propose a new in-situ degassing method, in which membrane contactors are used to degas the groundwater directly in the well and gas is collected at the surface. This way, field work is facilitated, groundwater system disturbance is minimized, and the gas sample is collected at a specific depth. We demonstrate the tightness of the system regarding atmospheric air contamination for a collection times of 24 h, which is sufficient for both low-level counting and laser-based counting methods for 85Kr. The minimal borehole diameter is 7.5 cm for the prototype presented in this research but can easily be reduced to smaller diameters. In a case study, we compare the results obtained with the new passive method with those from a conventional packer setup sampling. Additionally, 3H/3He samples were collected for both sampling regimes and the dating results were compared with those from 85Kr. A good agreement between tracer ages is demonstrated and the age stratigraphy is consistent with the expected age distribution for a porous unconfined aquifer. In addition, our study emphasizes the differences between the age information sampled with various methods. In conclusion, we demonstrate that the new in situ quasi-passive method provides a more representative age stratigraphy with depth in most cases.  
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  ISSN 2589-9155 ISBN Medium  
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  Call Number THL @ christoph.kuells @ Musy2021100075 Serial 215  
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Author Zeng, S.; Shen, Y.; Sun, B.; Zhang, N.; Zhang, S.; Feng, S. url  openurl
  Title Pore structure evolution characteristics of sandstone uranium ore during acid leaching Type Journal Article
  Year 2021 Publication (up) Nuclear Engineering and Technology Abbreviated Journal  
  Volume 53 Issue 12 Pages 4033-4041  
  Keywords Acid method, In situ leaching, Nuclear magnetic resonance, Pore characteristic, Sandstone uranium ore  
  Abstract To better understand the permeability of uranium sandstone, improve the leaching rate of uranium, and explore the change law of pore structure characteristics and blocking mechanism during leaching, we systematically analyzed the microstructure of acid-leaching uranium sandstone. We investigated the variable rules of pore structure characteristics based on nuclear magnetic resonance (NMR). The results showed the following: (1) The uranium concentration change followed the exponential law during uranium deposits acid leaching. After 24 h, the uranium leaching rate reached 50%. The uranium leaching slowed gradually over the next 4 days. (2) Combined with the regularity of porosity variation, Stages I and II included chemical plugging controlled by surface reaction. Stage I was the major completion phase of uranium displacement with saturation precipitation of calcium sulfate. Stage II mainly precipitated iron (III) oxide-hydroxide and aluminum hydroxide. Stage III involved physical clogging controlled by diffusion. (3) In the three stages of leaching, the permeability of the leaching solution changed with the pore structure, which first decreased, then increased, and then decreased.  
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  ISSN 1738-5733 ISBN Medium  
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  Call Number THL @ christoph.kuells @ zeng_pore_2021 Serial 199  
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Author Rallakis, D.; Michels, R.; Cathelineau, M.; Parize, O.; Brouand, M. url  openurl
  Title Conditions for uranium biomineralization during the formation of the Zoovch Ovoo roll-front-type uranium deposit in East Gobi Basin, Mongolia Type Journal Article
  Year 2021 Publication (up) Ore Geology Reviews Abbreviated Journal  
  Volume 138 Issue Pages 104351  
  Keywords Bioreduction, East Gobi Basin, Mongolia, Organic matter, Roll-front, Sulfur isotopes, Uranium  
  Abstract The Zoovch Ovoo uranium roll-front-type deposit is hosted in the Sainshand Formation, a Late Cretaceous siliciclastic reservoir, which constitutes the upper part of the post-rift infilling of the Mesozoic East Gobi Basin in SE Mongolia. The Sainshand Formation consists of unconsolidated medium-grained sand, silt and clay intervals deposited in fluvial-lacustrine settings. The uranium deposit is confined within a 60–80 m thick siliciclastic sequence inside aquifer-driven systems. The overall system experienced shallow burial and was never subjected to temperatures higher than 40 °C. This study proposes a comprehensive metallogenic model for this uranium deposit. Sedimentological and mineralogical observations from drill core samples to the microscopic scale (optical and Scanning Electron Microscopy) together with in situ geochemistry of late-formed phases (Laser Ablation–Inductively Coupled Plasma Mass Spectrometry, Electron Probe Microanalysis, Fourier Transform–Infrared Spectroscopy) were considered for the reconstruction of the main stages of U trapping. In the mineralized zone, the uranium ore is expressed as Ca–enriched uraninite (UO2) and less commonly as Ca–enriched phospho-coffinite (U, P)SiO4. Trapping mechanisms include i) complexation (i.e. uranyl-carboxyl complexes), ii) adsorption on organic or clay particles) and iii) reduction by pyrite and by bacterial activity to amorphous uraninite. In all cases, the organic matter plays either the role of trap for uranium or nutrient for bacteria that can trap uranium through their metabolism. The shallow burial diagenesis conditions do not allow direct reduction of U(VI) by organic carbon. The δ34S values of the iron disulfide are very diverse, fluctuating in extreme cases between −50 to + 50‰, with an average δ34S value for framboidal pyrite at 2‰, and −20‰ for euhedral pyrite. The positive and negative values reflect close versus open fractionation systems, while bacterial sulphate reduction (BSR) is active during the whole diagenetic history of the deposit as an essential source of reduced sulfur. Therefore, using detrital organic matter as a carbon source, microorganisms play a significant role in uranium trapping, either as a direct reducing agent for uranium or pyrite formation, which will trap uranium through redox driven epigenetic processes.  
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  Call Number THL @ christoph.kuells @ rallakis_conditions_2021 Serial 176  
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