Josep Mas-Pla

Prof. Dr. Josep Mas-Pla

Catalan Institute for Water Research & University of Girona, 17003 Girona, Spain

Research Focus & Metrics

Academic Career Length

35Years (1992-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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2 July 2019 in Hydrological Sciences Journal
Verified
Journal Article
Open access
Günter BlöschlGünter Blöschl
Günter Blöschl
MBMarc F.P. Bierkens
Marc F.P. Bierkens
ACAntonio Chambel
Antonio Chambel
CCChristophe Cudennec
Christophe Cudennec
Georgia  DestouniGeorgia Destouni
Georgia Destouni
Yongqiang ZhangYongqiang Zhang
Yongqiang Zhang
This paper is the outcome of a community initiative to identify major unsolved scientific problems in hydrology motivated by a need for stronger harmonisation of research efforts. The procedure involved a public consultation through on-line media, followed by two workshops through which a large number of potential science questions were collated, prioritised, and synthesised. In spite of the diversity of the participants (230 scientists in total), the process revealed much about community priorities and the state of our science: a preference for continuity in research questions rather than radical departures or redirections from past and current work. Questions remain focussed on process-based understanding of hydrological variability and causality at all space and time scales. Increased attention to environmental change drives a new emphasis on understanding how change propagates across interfaces within the hydrological system and across disciplinary boundaries. In particular, the expansion of the human footprint raises a new set of questions related to human interactions with nature and water cycle feedbacks in the context of complex water management problems. We hope that this reflection and synthesis of the 23 unsolved problems in hydrology will help guide research efforts for some years to come.

1 January 2016 in Science of The Total Environment
Verified
Journal Article
Open access
Anna MencióAnna Menció
Anna Menció
JMJosep Mas-Pla
Josep Mas-Pla
NONeus Otero
Neus Otero
OROriol Regàs
Oriol Regàs
MBMercè Boy-Roura
Mercè Boy-Roura
AFAlbert Folch
Albert Folch
Contamination from agricultural sources and, in particular, nitrate pollution, is one of the main concerns in groundwater management. However, this type of pollution entails the entrance of other substances into the aquifer, as well as it may promote other processes. In this study, we deal with hydrochemical and isotopic analysis of groundwater samples from four distinct zones in Catalonia (NE Spain), which include 5 different aquifer types, to investigate the influence of fertilization on the overall hydrochemical composition of groundwater. Results indicate that intense fertilizer application, causing high nitrate pollution in aquifers, also homogenize the contents of the major dissolved ions (i.e.; Cl(-), SO4(2-), Ca(2+), Na(+), K(+), and Mg(2+)). Thus, when groundwater in igneous and sedimentary aquifers is compared, significant differences are observed under natural conditions for Cl(-), Na(+) and Ca(2+) (with p-values ranging from <0.001 to 0.038), and when high nitrate concentrations occur, these differences are reduced (most p-values ranged between 0.054 and 0.978). Moreover, positive linear relationships between nitrate and some ions are found indicating the magnitude of the fertilization impact on groundwater hydrochemistry (with R(2) values of 0.490, 0.609 and 0.470, for SO4(2-), Ca(2+) and Cl(-), respectively). Nevertheless, the increasing concentration of specific ions is not only attributed to agricultural pollution, but to their enhancing effect upon the biogeochemical processes that control water-rock interactions. Such results raise awareness that these processes should be evaluated in advance in order to assess an adequate groundwater resources management.

1 January 2018 in Science of The Total Environment
Verified
Journal Article
Open access
MBM. Boy-Roura
M. Boy-Roura
JMJosep Mas-Pla
Josep Mas-Pla
MPM. Petrovic
M. Petrovic
Meritxell GrosMeritxell Gros
Meritxell Gros
DSD. Soler
D. Soler
Anna MencióAnna Menció
Anna Menció
Antibiotics are an increasing focus of interest due to their high detection frequency in the environment. However, their presence in water bodies is not regulated by environmental policies. This field study investigates, for the first time, the occurrence, behavior and fate of a selection of 53 antibiotics, including up to 10 chemical groups, in an alluvial aquifer originated from manure application in an agricultural region using hydrogeological, hydrochemical and isotopic approaches. Up to 11 antibiotics were found in groundwater corresponding to 4 different chemical groups: fluoroquinolones, macrolides, quinolones and sulfonamides. In surface water, only 5 different antibiotics from 2 chemical groups: fluoroquinolones and sulfonamides, were quantified. The most frequent antibiotics were sulfamethoxazole and ciprofloxacin. Concentrations of antibiotics were in the order of ng/L, with maximum concentrations of 300ng/L in groundwater. Hydrochemistry and isotopic data and geostatistics confirmed the spatial trend observed for nitrates, where nitrate concentrations tend to be higher in the margin areas of the study area, and lower concentrations are found nearby the river. On the other hand, no clear continuous spatial concentration trend of antibiotics was observed in the aquifer, supported by the short spatial correlation found in the variograms. This indicates that the physical-chemical properties and processes of each antibiotic (mainly, sorption and degradation), and other environmental issues, such as a patchy diffuse input and the manure antibiotic content itself, play an important role in their spatial distribution in groundwater. A discussion on the estimation of the antibiotic sorption parameter reveals the difficulties of describing such phenomena. Furthermore, retardation factors will extend over several orders of magnitude, which highly affects the movement of individual antibiotics within the aquifer. To summarize, this study points out the difficulties associated with antibiotic research in groundwater in order to define water resources quality management strategies and environmental regulations.

1 March 2019 in Science of The Total Environment
Verified
Journal Article
Closed access
Meritxell GrosMeritxell Gros
Meritxell Gros
JMJosep Mas-Pla
Josep Mas-Pla
MBMercè Boy-Roura
Mercè Boy-Roura
IGIrma Geli
Irma Geli
FDFrancesc Domingo
Francesc Domingo
MPMira Petrović
Mira Petrović

1 February 2009 in Journal of Hydrology
Verified
Journal Article
Closed access
ECEleonora S Carol
Eleonora S Carol
EKEduardo Kruse
Eduardo Kruse
JMJosep Mas-Pla
Josep Mas-Pla

1 September 2009 in Agriculture, Ecosystems & Environment
Verified
Journal Article
Open access
NON. Otero
N. Otero
CTC. Torrentó
C. Torrentó
Albert SolerAlbert Soler
Albert Soler
Anna MencióAnna Menció
Anna Menció
JMJosep Mas-Pla
Josep Mas-Pla
This paper describes an integrated application of classical hydrogeological methods and multi-isotopic methods (δ15N, δ 18ON O3, δ34S, δ 18OS O4, δ13C) to assess the fate of groundwater nitrate in the Osona area, declared vulnerable to nitrate pollution by the Catalan Government in 1998, where nitrate is derived from intensive pig farming activities. Previous studies, involving a small area, indicated the occurrence of denitrification processes and their relationship with pyrite oxidation [Vitòria, L., Soler, A., Canals, A., Otero, N., 2008. Environmental isotopes (N, S, C, O, D) to determine natural attenuation processes in nitrate contaminated waters: example of Osona (NE Spain). Appl. Geochem. 23, 3597-3611]. For the present study, groundwater samples were collected at 60 production wells at three different periods between April 2005 and May 2006 to confirm that denitrification takes place in a larger area than that studied by Vitòria et al. [Vitòria, L., Soler, A., Canals, A., Otero, N., 2008. Environmental isotopes (N, S, C, O, D) to determine natural attenuation processes in nitrate contaminated waters: example of Osona (NE Spain). Appl. Geochem. 23, 3597-3611]. The aim of the study was to characterize the denitrification processes that control natural attenuation and to study their spatial and temporal variations. Nitrate concentration ranged from 10 to 529 mg/l, with 82% of the wells above the drinking water threshold of 50 mg NO3/l. Nitrate isotopic composition ranged from +5.3‰ to +35.3‰ for δ15N and from +0.4‰ to +17.6‰ for δ 18ON O3, and the samples showed a positive correlation between δ15N and δ 18ON O3, with a εN/εO ratio of 1.8, consistent with denitrification processes. The link between denitrification and pyrite oxidation is demonstrated by coupling chemical data with nitrate and sulfate isotopes. Furthermore, a spatial distribution of samples with significant denitrification was observed, allowing us to determine two main hydrogeological zones where natural attenuation was most effective. In several of the studied points, denitrification processes related to pyrite oxidation predominated and an estimation of the isotopic enrichment factors was performed using the temporal variations of nitrate concentration and the isotopic composition of dissolved nitrate (δ 15NN O3 and δ 18ON O3). Finally, using estimated isotopic enrichment factors, an approximation of the degree of natural attenuation of nitrate was performed on those samples showing clear denitrification, and a median value of 30% of contaminant diminution was obtainedThis work has been financed by CICYT projects CGL2005-08019-C04-01 and 02, CGL-2008-06373-CO3-01 and 02/BTE from the Spanish Government, the local authorities (Consell Comarcal d’Osona), the Catalan Water Agency (Age` ncia Catalana de l’Aigua), the local private association of livestock raising (ASSAPORC), the project SGR2005-00933 from the Catalan Government, the I3P Programme funded by the EU, and the ‘‘Jose´ de Castillejo’’ program of the Spanish Governmen