1,767 research outputs found
Nota sobre la captura d'Ocythoe tuberculata Rafinesque, 1814 (Cephalopoda: Ocytohoidae) en aigĂŒes de Menorca
Abstract not availabl
Dissolution experiments of commercial PWR (52 MWd/kgU) and BWR (53 MWd/kgU) spent nuclear fuel cladded segments in bicarbonate water under oxidizing conditions. Experimental determination of matrix and instant release fraction
The denominated instant release fraction (IRF) is considered in performance assessment (PA) exercises to govern the dose that could arise from the repository. A conservative definition of IRF comprises the total inventory of radionuclides located in the gap, fractures, and the grain boundaries and, if present, in the high burn-up structure (HBS). The values calculated from this theoretical approach correspond to an upper limit that likely does not correspond to what it will be expected to be instantaneously released in the real system. Trying to ascertain this IRF from an experimental point of view, static leaching experiments have been carried out with two commercial UO2 spent nuclear fuels (SNF): one from a pressurized water reactor (PWR), labelled PWR, with an average burn-up (BU) of 52 MWd/kgU and fission gas release (FGR) of 23.1%, and one from a boiling water reactor (BWR), labelled BWR, with an average BU of and 53 MWd/kgU and FGR of 3.9%.; One sample of each SNF, consisting of fuel and cladding, has been leached in bicarbonate water during one year under oxidizing conditions at room temperature (25 +/- 5) degrees C. The behaviour of the concentration measured in solution can be divided in two according to the release rate. All radionuclides presented an initial release rate that after some days levels down to a slower second one, which remains constant until the end of the experiment. Cumulative fraction of inventory in aqueous phase (FIAPc) values has been calculated. Results show faster release in the case of the PWR SNF. In both cases Np, Pu, Am, Cm, Y, Tc, La and Nd dissolve congruently with U, while dissolution of Zr, Ru and Rh is slower. Rb, Sr, Cs and Mo, dissolve faster than U. The IRF of Cs at 10 and 200 days has been calculated, being (3.10 +/- 0.62) and (3.66 +/- 0.73) for PWR fuel, and (035 +/- 0.07) and (0.51 +/- 0.10) for BWR fuel. (C) 2015 Elsevier B.V. All rights reserved.Peer ReviewedPostprint (author's final draft
Fiscal policy shocks in the euro area and the US: an empirical assessment
We analyse the impact of fiscal policy shocks in the euro area as a whole, using a newly available quarterly dataset of fiscal variables for the period 1981-2007. To allow for comparability with previous results on euro area countries and the US, we use a standard structural VAR framework, and study the impact of aggregated and disaggregated government spending and net taxes shocks. In addition, to frame euro area results, we apply the same methodology for the same sample period to US data. We also explore the sensitivity of the provided results to the inclusion of variables aiming at measuring âfinancial stressâ (increases in risk) and âfiscal stressâ (sustainability concerns). Analysing US and euro area data with a common methodology provides some interesting insights on the interpretation of fiscal policy shocks. JEL Classification: E62, H30euro area, Fiscal multipliers, Fiscal shocks, SVAR
Microclimate, an important part of ecology and biogeography
Brief introduction: What are microclimates and why are they important?Microclimate science has developed into a global discipline. Microclimate science is increasingly used to understand and mitigate climate and biodiversity shifts. Here, we provide an overview of the current status of microclimate ecology and biogeography in terrestrial ecosystems, and where this field is heading next.Microclimate investigations in ecology and biogeography: We highlight the latest research on interactions between microclimates and organisms, including how microclimates influence individuals, and through them populations, communities and entire ecosystems and their processes. We also briefly discuss recent research on how organisms shape microclimates from the tropics to the poles.Microclimate applications in ecosystem management: Microclimates are also important in ecosystem management under climate change. We showcase new research in microclimate management with examples from biodiversity conservation, forestry and urban ecology. We discuss the importance of microrefugia in conservation and how to promote microclimate heterogeneity.Methods for microclimate science: We showcase the recent advances in data acquisition, such as novel field sensors and remote sensing methods. We discuss microclimate modelling, mapping and data processing, including accessibility of modelling tools, advantages of mechanistic and statistical modelling and solutions for computational challenges that have pushed the state-of-the-art of the field.What's next?We identify major knowledge gaps that need to be filled for further advancing microclimate investigations, applications and methods. These gaps include spatiotemporal scaling of microclimate data, mismatches between macroclimate and microclimate in predicting responses of organisms to climate change, and the need for more evidence on the outcomes of microclimate management
UO2 surface oxidation by mixtures of water vapor and hydrogen as a function of temperature
In the present work, X-Ray Photoelectron Spectroscopy (XPS) was used to study the effect of water vapor on the UO2 surface as a function of temperature. The experiments were performed in situ inside a high pressure chamber attached to the XPS instrument. UO2 samples were put in contact with either hydrogen or argon streams, saturated with water at room temperature, and the sample surface evolution was analyzed by XPS. In the case of the water vapor/argon experiments, one experiment at 350°C was performed and, in the case of the water vapor/hydrogen experiments, the temperatures used inside the reactor were 60, 120, 200 and 350°C. On one hand, in presence of argon, the results obtained showed that the water vapor in the argon stream oxidized 93% of the U(IV) in the sample surface. On the other hand, the degree of UO2 surface oxidation showed a different dependence on the temperature in the experiments performed in the presence of hydrogen: the maximum surface oxidation occurred at 120°C, where 65.4% of U(IV) in the sample surface was oxidized, while at higher temperatures, the surface oxidation decreased. This observation is attributed to the increase of hydrogen reducing effect when temperature increases which prevents part of the oxidation of the UO2 surface by the water vapor.Peer ReviewedPostprint (author's final draft
Exploring alternative practices in urban water management through the lens of circular economy: a case study in the Barcelona metropolitan area
Urban water management has recently been questioned because of the fragmented nature of the urban water system and its linear model. The integration and management of water systems are currently recognized as a socio-technical challenge that must be addressed for a more sustainable urban water management. In the short term, a key factor for its transition will be integration of alternative practices that allow for experimentation, learning, and scaling up. This study aims to identify potential shifts supported by two alternative practices for water reuse: nature-based solutions and water reuse technologies, using circular economy principles as analytical categories. The research uses a case study, the BesĂČs river of the Barcelona metropolitan area, to show that: i) improving biodiversity and water quality helps to regenerate natural capital; ii) water reuse for streamflow augmentation keeps resources in use and promotes synergies, which benefits social livability; and iii) risk management and a potential fit-to-purpose strategy can marginally help to avoid waste externalities. This research has shown that the CE principles are applicable as a framework for identifying the interconnected shifts promoted by water systems. A reflexive understanding of the alternative practices provides deeper insight into the experiences, barriers, and shifts that allow innovative interactions in specific urban contexts and can deliver additional benefits for society. This knowledge can be useful for integrated urban management; however, further integration of cross-sectoral collaboration and flexibility are required.Peer ReviewedPostprint (published version
Monopoles in arbitrary dimension
"Vegeu el resum a l'inici del document del fitxer adjunt"
Unraveling the active microbial populations involved in nitrogen utilization in a vertical subsurface flow constructed wetland treating urban wastewater
The dynamics of the active microbial populations involved in nitrogen transformation in a vertical subsurface flow constructed wetland (VF) treating urban wastewater was assessed. The wetland (1.5 m2) operated under average loads of 130 g COD m- 2 d- 1 and 17 g TN m- 2 d- 1 in Period I, and 80 g COD m- 2 d- 1 and 19 g TN m- 2 d- 1 in Period II. The hydraulic loading rate (HLR) was 375 mm d- 1 and C/N ratio was 2 in both periods. Samples for microbial characterization were collected from the filter medium (top and bottom layers) of the wetland, water influent and effluent at the end of Periods I (JunâOct) and II (NovâJan). The combination of qPCR and high-throughput sequencing (NGS, MiSeq) assessment at DNA and RNA level of 16S rRNA genes and nitrogen-based functional genes (amoA and nosZ-clade I) revealed that nitrification was associated both with ammonia-oxidizing bacteria (AOB) (Nitrosospira) and ammonia-oxidizing archaea (AOA) (Nitrososphaeraceae), and nitrite-oxidizing bacteria (NOB) such as Nitrobacter. Considering the active abundance (based in amoA transcripts), the AOA population revealed to be more stable than AOB in both periods and depths of the wetland, being less affected by the organic loading rate (OLR). Although denitrifying bacteria (nosZ copies and transcripts) were actively detected in all depths, the denitrification process was low (removal of 2 g TN m- 2 d- 1 for both periods) concomitant with NOx-N accumulation in the effluent. Overall, AOA, AOB and denitrifying bacteria (nosZ) were observed to be more active in bottom than in top layer at lower OLR (Period II). A proper design of OLR and HLR seems to be crucial to control the activity of microbial biofilms in VF wetlands on the basis of oxygen, organic-carbon and NOx-N forms, to improve their capacity for total nitrogen removal.Peer ReviewedPostprint (author's final draft
Immobilization of selenite onto natural siderite (FeCO3)
The sorption processes of metals and semimetals on siderite are being studied because of the potential adequacy of the mineral for removing contaminants from natural waters and because of its formation during the reduction of iron(III) (hydr)oxides under anaerobic conditions in the presence of organic matter or bacteria. This transformation could involve the release of contaminants previously sorbed on the iron(III) (hydr)oxides.
In this work, the sorption of selenite on natural siderite (Bordes de Conflent, Lleida, Spain) is experimentally studied and the results obtained are compared to the previous results on selenite sorption on magnetite, hematite and goethite.Results indicate that the process of sorption was very fast; the equilibrium was reached in less than 1 hour, which indicates that sorption will not be kinetically controlled. The experimental data were fitted with a non-competitive Langmuir isotherm, which would indicate that the main process for the decrease of selenite in solution would be its sorption on siderite via monolayer coverage of the solid surface. The values of maximum sorption capacity of siderite obtained at pH 7,1 and 8,0 were 6,9 10-7 and 6,4 10-7 mol g-1, respectively and the same value of Langmuir constant was obtained for both pH values, 4,7 104 L mol-1.Postprint (published version
Water-air volatilization factors to determine volatile organic compound (VOC) reference levels in water
The goal of this work is the modeling and calculation of
volatilization factors
(VFs) from water to air for
volatile organic compounds
(VOCs) in order to perform
human
health risk
-
base
d reference levels
(RLs) for the safe use of water. The VF models have
been developed starting from
the
overall mass
-
transfer coefficients (
K
overall
) concept from
air to water for two interaction geometries (flat surface and spherical droplets) in indoor
a
nd outdoor scenarios
.
For
a case study with
five groups of risk scenarios
and thirty VOCs
,
theoretical VFs have been calculated
by using
the developed models.
Results showed that
K
overall
values
for flat and spherical
surface
geometries
were
close to
the
m
ass transfer
coefficient for water
(
K
L
)
when
Henry
âs law
constant (
K
H
)
was high. I
n the case of
s
pherical drop geometry
,
the
fraction of volatilization
(
f
V
)
was asymptotical
when
increasing
K
H
with
f
V
values also
limited
due to
K
overall
.
VFs for flat surfa
ces were
calculated from the emission flux of VOCs
,
and results showed values close to
1000
K
H
for
the most conservative indoor scenarios and almost constant values for outdoor scenarios.
VFs for spherical geometry
in indoor scenarios
followed
also constant
VFs and
were
far
from
1000
K
H
.
The highest calculated VF values corresponded to
the
E2A, E2B, E3A and
E5A scenarios and were compared with experimental
and real
results in order to check the
goodness of
flat and sphere geometry models. Results showed an ov
erestimation of
OPEN ACCESS
Toxics
2014
,
2
277
calculated values for
the
E2A
and
E2B scenarios and an underestimation for
the
E3A and
E5A scenarios. In both cases
,
most of the calculated VFs were from 0.1
-
to 10
-
times higher
than experimental
/real
valuesPeer ReviewedPostprint (published version
- âŠ