The thesis deals with the legal regulation of territorial protection of water in terms of quantity, which is contained in the Water Act. I am only focusing on the Protected Areas of Natural Water Accumulation and Surface Water Accumulation Protected Areas as they have significant potential to reduce the effects of drought. Both areas are viewed through common problem, which is the point of view of the amount of water. The legal regulation of the territorial protection of waters in terms of quantity is discussed in connection with other laws. The aim of this work is to answer the question whether the legal regulation of territorial protection of waters in terms of quantity in the Water Act is sufficient to enable the Czech Republic to adapt adequately to the ongoing climate change, that ultimately causes the loss of water. The first part of the thesis deals with sources of legal regulation of territorial protection of water in terms of quantity, further includes the systematics of the Water Act and the Strategy on Adaptation to Climate Change in the Czech Republic (Adaptation Strategy of the Czech Republic). The second part analyses the Protected Areas of Natural Water Accumulation, prohibitions therein contained prohibitions, exemption from prohibitions and damage compensation. The third part deals...

Le nord du Chili est soumis à un contexte climatique aride à semi-aride présentant une variabilité saisonnière et inter-annuelle forte. Dans cette région les zones de haute altitude soutiennent les parties plus basses des bassins versants, mais la ressource en eau reste malgré tout limitée. Afin d'améliorer les méthodes de gestion de l'eau dans ces bassins versants, il est important de préciser le rôle des zones de haute altitude dans le soutien des parties basses, mais aussi de caractériser les modalités de transfert et d'interaction entre les compartiments constitutifs de l'hydrosystème. Ce travail porte sur la caractérisation du fonctionnement hydrologique du bassin versant de l'Elqui depuis la tête de bassin, située au cœur de la cordillère des Andes, jusqu'aux vallées de la zone inférieure situées entre 500 et 2000 mètres d'altitude. En tête de bassin, les processus d'interaction entre les compartiments cryosphériques, hydrologiques et hydrogéologiques, et leurs impacts sur le transfert des masses d'eau vers l'aval de la zone d'étude sont caractérisés. Le comportement hydrologique des sous bassins versant partiellement ou non‑englacés est également étudié. Dans la zone inférieure du bassin, l'étude porte principalement sur les processus d'interactions surface-souterrain en contexte semi‑aride et sur les impacts des forçages climatiques et anthropiques sur ces derniers. Cette étude s'appuie sur plus de 40 ans de données hydro-météorologiques disponibles sur la zone inférieure du bassin, complétés par des mesures hydrologiques sur la zone supérieure (> 2000 mètres d'altitude) et des prélèvements chimiques (majeurs et traces) et isotopiques (²D, 18O) sur la totalité de la zone d'étude, réalisés entre 2011 et 2013.Ces travaux ont montré que le modèle conceptuel de fonctionnement du bassin versant de l'Elqui généralement accepté était incomplet. Dans la zone supérieure, l'étude d'un bassin versant englacé a permis de montrer que le rôle de la cryosphère dépasse la fonction de production d'eau, avec certains compartiments stockant temporairement de l'eau en période humide et la libérant en période sèche. Ce processus permet d'amortir la variabilité temporelle des précipitations et du taux de fonte en altitude. Les analyses physico-chimiques réalisées dans le bassin versant ont également permis d'identifier des compartiments aquifères ignorés jusqu'à maintenant, comme les compartiments volcanique et plutonique. En améliorant les connaissances sur les processus d'interactions entre compartiments cryosphériques, hydrologiques et hydrogéologiques, les résultats de ce travail ont apporté des précisions sur le fonctionnement hydrologique de la zone de haute altitude. Cela a permis l'estimation des impacts potentiels de la variabilité climatique sur ces processus d'interactions et leurs conséquences sur la disponibilité et la qualité de la ressource. Dans la zone inférieure, la caractérisation des interactions surface-souterrain a montré qu'il existe un fort potentiel d'interaction entre le compartiment hydrologique et le compartiment alluvial, mais également entre le compartiment alluvial et le socle plutonique. L'étude des données hydrologiques et physico-chimiques a permis de caractériser le type d'échanges se déroulant entre les compartiments. Dans certains secteurs le processus dominant est la recharge du compartiment alluvial par le compartiment hydrologique, tandis que pour d'autres il existe une alternance entre période de drainage du compartiment alluvial par le compartiment hydrologique et période de recharge du compartiment alluvial. La réponse de ces processus face aux impacts des forçages climatiques et anthropiques contraindra la disponibilité et la qualité de la ressource dans les années à venir. Ainsi, les résultats apportés par ce travail permettront certainement de mieux anticiper les modifications futures du fonctionnement hydrologique des bassins versant montagneux en contexte semi-arides. / The north Chile is affected by an arid to semi-arid climate, associated with a strong seasonal to inter-annual variability. In this region, while mountainous areas are supporting low areas, the availability of water resources remains limited. In order to improve the water management in these basins, it is necessary to precise how the high areas support the low areas, and to characterize water transfers and interaction processes between the constitutive compartments of the hydrosystem. This work concern the characterization of the hydrodynamic behavior of the Elqui watershed from the headwaters, in the Andes, to the valleys, ranging between 500 and 2000 m.a.s.l.In the headwaters, the interactions processes between cryospheric and hydrologic compartments and their impact on water transfers to the low areas are characterized. The behavior of unglacierized or partially glacierized watershed is also studied. In the low area of the watershed, the study mainly considers groundwater-surface water interactions under semi-arid context and the impact of the climatic variability on these processes. This study is based on more than 40 years of hydro-meteorological data available in the lower zone of the basin, completed by hydrological measurements in the upper zone (> 2000 m.a.s.l.) and chemical (majors and traces elements) and isotopic samples (²D, 18O) over the whole study area realized between 2011 and 2013.This work demonstrated that the conceptual model of the Elqui basin hydrological behavior, generally accepted, was incomplete. In the high area (> 2000 m.a.s.l.), the study of a glacierized watershed show that the function of the cryosphere overpass the water production with some compartments storing water during humid periods and draining their water content during dry periods. This process buffers the temporal variability of precipitations and melting rates in the high area. Physico-chemical analysis, allows to identify some ignored aquifer compartments, as the volcanic and plutonic compartments. The results of this study improve the knowledge about interactions processes between cryospheric, hydrologic and hydrogeologic compartments, which precise the hydrological functioning of the high area. The interpretation of the hydrological behavior of the high altitude area allows to better understand the way that it support the low area, and the way that climate variability may affects it.In the low area, results show that the groundwater-surface water interaction potential is good between alluvial and hydrological compartments, but also between the plutonic and the alluvial compartments. The study of hydro-meteorological and physico-chemical data allowed to characterize the type of exchanges that take place between groundwater and surface water. In some sectors the main process is the recharge of the alluvial compartment by the hydrological compartment, while in other sectors the processes show a seasonal variability with periods of alluvial compartment recharge and periods of hydrological compartment support. The answer of these processes face to climatic and anthropic forcing will constrain the evolution of the availability and quality of the water resources in the Elqui basin. Finally, the results of this study will certainly allow to better anticipate the future modifications of the semi-arid mountainous watershed hydrological functioning.

An automated on-line SPE-LC-MS/MS method was developed for the quantitation of multiple classes of antibiotics in environmental waters. High sensitivity in the low ng/L range was accomplished by using large volume injections with 10-mL of sample. Positive confirmation of analytes was achieved using two selected reaction monitoring (SRM) transitions per antibiotic and quantitation was performed using an internal standard approach. Samples were extracted using online solid phase extraction, then using column switching technique; extracted samples were immediately passed through liquid chromatography and analyzed by tandem mass spectrometry. The total run time per each sample was 20 min. The statistically calculated method detection limits for various environmental samples were between 1.2 and 63 ng/L. Furthermore, the method was validated in terms of precision, accuracy and linearity. The developed analytical methodology was used to measure the occurrence of antibiotics in reclaimed waters (n=56), surface waters (n=53), ground waters (n=8) and drinking waters (n=54) collected from different parts of South Florida. In reclaimed waters, the most frequently detected antibiotics were nalidixic acid, erythromycin, clarithromycin, azithromycin trimethoprim, sulfamethoxazole and ofloxacin (19.3-604.9 ng/L). Detection of antibiotics in reclaimed waters indicates that they can’t be completely removed by conventional wastewater treatment process. Furthermore, the average mass loads of antibiotics released into the local environment through reclaimed water were estimated as 0.248 Kg/day. Among the surface waters samples, Miami River (reaching up to 580 ng/L) and Black Creek canal (up to 124 ng/L) showed highest concentrations of antibiotics. No traces of antibiotics were found in ground waters. On the other hand, erythromycin (monitored as anhydro erythromycin) was detected in 82% of the drinking water samples (n.d-66 ng/L). The developed approach is suitable for both research and monitoring applications. Major metabolites of antibiotics in reclaimed wates were identified and quantified using high resolution benchtop Q-Exactive orbitrap mass spectrometer. A phase I metabolite of erythromycin was tentatively identified in full scan based on accurate mass measurement. Using extracted ion chromatogram (XIC), high resolution data-dependent MS/MS spectra and metabolic profiling software the metabolite was identified as desmethyl anhydro erythromycin with molecular formula C36H63NO12 and m/z 702.4423. The molar concentration of the metabolite to erythromycin was in the order of 13 %. To my knowledge, this is the first known report on this metabolite in reclaimed water. Another compound acetyl-sulfamethoxazole, a phase II metabolite of sulfamethoxazole was also identified in reclaimed water and mole fraction of the metabolite represent 36 %, of the cumulative sulfamethoxazole concentration. The results were illustrating the importance to include metabolites also in the routine analysis to obtain a mass balance for better understanding of the occurrence, fate and distribution of antibiotics in the environment. Finally, all the antibiotics detected in reclaimed and surface waters were investigated to assess the potential risk to the aquatic organisms. The surface water antibiotic concentrations that represented the real time exposure conditions revealed that the macrolide antibiotics, erythromycin, clarithromycin and tylosin along with quinolone antibiotic, ciprofloxacin were suspected to induce high toxicity to aquatic biota. Preliminary results showing that, among the antibiotic groups tested, macrolides posed the highest ecological threat, and therefore, they may need to be further evaluated with, long-term exposure studies considering bioaccumulation factors and more number of species selected. Overall, the occurrence of antibiotics in aquatic environment is posing an ecological health concern.

<p>U doktorskoj disertaciji evaluirani su interkorelacioni rezultati odnosa ključnih fizičko-hemijskih parametara i katjona metala u površinskoj vodi Dunava, Tise (na po tri selektovana reprezentativna lokaliteta) i kanala Dunav-Tisa-Dunav (na dva lokaliteta). U<br />Kanalu Dunav-Tisa-Dunav praćene su i rezidualne katjonske koncentracije metala u sedimentu. Na osnovu podataka prisutnosti katjona metala u heterogenom sistemu tečno/čvrsto izračunate su po prvi put konstante podeonih procesa za ispitivane katjone metala. Primenom multivarijantnih statističkih metoda analizirani su korelacioni odnosi između ključnih fizičko-hemijskih parametara i koncentracionih nivoa rezidula katjona teških, lakih i semimetala. Faktorskom analizom (PCA) i klaster analizom sa dendogramima tumačeni, analizirani i diskutovani su dobijeni rezultati. Za optimalnog uočavanja korelacionih odnosa primenjeno je unapređeno rangiranje određenih skupova podataka (interkorelacije ključnih fizičko-hemijskih parametara i rezidua katjona metala) i grafički prikazanih Haseovih dijagrama primenom DART softvera (Decision Analysis by Ranking Techniques) za definisani model procene uticaja raspodele katjona toksičnih metala u heterogenom sistemu tečno/čvrsto na kvalitet površinskih voda.</p> / <p>In the doctoral thesis are evaluated inter correlational results of key physicochemical parameters and metal cations in surface water of Danube, Tisa (on three selected representative sampling points) and canal Danube-Tisa-Danube (on two sampling sites). In the canal Danube-Tisa-Danube are also followed residual metal cations concentrations in sediment. Based on metal cations presence data in heterogeneous system liquid/solid for the first time partitioning processes constants are calculated for<br />selected metal cations. Appling multivariate statistical methods correlations between key physicochemical parameters and concentration levels of residual heavy, light and semimetals cations are analysed. Using factorial analyse (PCA) and cluster analyse with dendograms obtained results were interpreted, analysed and discussed. For optimal comprehension of correlations, advanced method ranking of finite order sets is applied (inter correlations key physicochemical parameters and residual metal cations) and graphically shown Hasse diagrams obtained by DART software (Decision Analysis by Ranking Techniques) for defined impact assessment model of toxic metal cations partitioning in heterogeneous system liquid/solid for surface water quality.</p>

Les contaminants d’intérêt émergent (CIEs) ont fait l’objet d’un nombre croissant d’études ces dernières années, notamment dans les milieux aquatiques. Il existe cependant certains manques de connaissances concernant leur occurrence et leur distribution dans les systèmes hydrologiques complexes, notamment la distribution verticale à travers différentes masses d’eau. Les variations saisonnières entre conditions estivales et hivernales restent difficiles à établir en raison des conditions météorologiques hivernales rigoureuses au Canada, limitant l’accessibilité des échantillons. Ainsi, ce projet de maîtrise a porté sur l’étude de 90 CIEs, comprenant des pesticides, des produits pharmaceutiques et marqueurs anthropiques, des hormones et des substances perfluorées dans un environnement océanographique, soit l’Estuaire et le Golfe du Saint-Laurent (EGSL). Deux expéditions ont été menées en conditions hivernales (hivers 2019 et 2020) et une en conditions estivales (été 2019). Ces missions ont permis d’évaluer, dans un premier temps, la distribution spatiale des CIEs dans l’eau de surface le long de l’EGSL, puis, dans un second temps, la variation des concentrations de surface associées aux différentes températures, salinités, couvertures de glace, processus de dégradation ou débit du fleuve des saisons. Par ailleurs, un échantillonnage à plusieurs profondeurs durant l’hiver 2020 a permis de dresser un profil vertical des concentrations le long de l’Estuaire et du Golfe du Saint-Laurent. Finalement, la filtration de larges volumes d’eau de surface durant l’hiver 2020 a permis d’évaluer la concentration des CIEs adsorbés sur la matière en suspension (phase particulaire) et conséquemment, le partitionnement entre la phase dissoute et particulaire, influencé par la variation de la salinité et de la quantité de matière en suspension. Les analyses ont été effectuées grâce au développement et à la validation d’une nouvelle méthode multi-résidus impliquant la chromatographie liquide à ultra-haute performance (UHPLC) couplée à la spectrométrie de masse à haute résolution (HRMS). À notre connaissance, il s’agit de la première étude à caractériser divers contaminants émergents dans les eaux de l’Estuaire et du Golfe du Saint-Laurent, particulièrement pendant la période hivernale et à travers la colonne d’eau. / Contaminants of Emerging Concern (CECs) have been increasingly studied since recent years, for instance in aquatic ecosystems. However, there exist significant knowledge gaps regarding their occurrence and distribution in complex hydrological systems, including their vertical distribution in different water bodies. Seasonal variations between summer and winter conditions are also difficult to establish because of the rigorous winter weather conditions in Canada, restricting the accessibility of samples. Thus, this project focused on the study of 90 CECs, including pesticides, pharmaceuticals and anthropogenic markers, hormones, and perfluorinated substances in an oceanographic environment, namely the St. Lawrence Estuary and Gulf (SLEG). Two expeditions were conducted under winter conditions (winters 2019 and 2020) and one under summer conditions (summer 2019). These expeditions first assessed the spatial distribution of CECs along the SLEG and, secondly, the seasonal and annual variations of the concentrations associated with the different temperatures, salinities, ice cover, degradation processes or seasonal river flow. In addition, sampling at multiple depths during the winter of 2020 allowed for documenting the vertical profiles of CECs throughout the SLEG. Finally, the filtration of large volumes of surface water during the winter of 2020 allowed for the evaluation of the CECs adsorbed onto suspended particle matter (SPM) and consequently, the partitioning between dissolved and particulate phases, influenced by salinity and SPM variations. Analyses were performed following the development and validation of a new multi-residue method involving ultra-high performance liquid chromatography (UHPLC) coupled with high-resolution mass spectrometry (HRMS). To the best of our knowledge, this is the first study to report the occurrence of emerging contaminants in the SLEG, especially during the winter season and across the water column.

The goal of this thesis was to determine the operational and technical parameters of the separation objects in water treatment. The first part is a theoretical and provides basic information on this issue. The second part contains the evaluation criteria created by the obtained information for individual objects and gained in practice by personal visits of selected treatment plants of water. In the last part we can find application of these criteria in water treatment in practice. There is also included the final evaluation of the researched condition.

Pharmaceuticals are biological active compounds with different functional groups, physico-chemical and biological properties. These chemical compounds are called as “new contaminants” which cumulate in various environmental components. These contaminants input to environment from industrial processes, hospitals and health care institutions or household sources and these pollutants can to negatively interact with environmental components. Pharmaceuticals are separated according to structure and their effects to live organisms. On the basis of drug consumption in Czech Republic the non-steroidal anti-inflammatory drugs are the most using pharmaceuticals, because these drugs can be obtain without prescriptions. The choosing analgesics for study were monitored in waste water from waste waters treatment plant (WWTP Brno – Modřice) and in surface water from two sampling sites of river Kretinka. Pharmaceuticals were monitored in surface waters in Czech Republic, in Scotland (river Thurso) and in Taiwan (river Erren, Agongdian, Yanshuei and canal of Tainan) Solid phase extraction (SPE) is used for extraction of study pharmaceutical from water system. The high performance liquid chromatography (HPLC) with diode array detection or mass spectrometry was used for determination of drugs in surface waters from Czech Republic. The water samples from Scotland and Taiwan were analysed and the high performance liquid chromatography with mass spectrometry (HPLC/MS) was used for determination of pharmaceuticals. The method of HPLC/MS enables the determination of study compounds in the very low range of concentrations (ng ? l-1). All monitored pharmaceuticals were identified and quantified in water samples from river Kretinka in Czech Republic, river Thurso (Scotland) and rivers Erren, Agongdian, Yanshuei and canal of Tainan in Taiwan and the obtained data were compared.

This work is focused on the study of penetration of pesticides and pharmaceuticals in the aquatic environment. The aim was to develop and verify the optimal method for long-term monitoring of the occurrence of selected pesticides and pharmaceuticals in surface waters. Two frequently used analgesics ibuprofen and diclofenac, and carbamazepine that is used to treat epilepsy, were chosen from the group of drugs. A group of 41 pesticides were selected for monitoring too. The attention was focused on a group of urea pesticides and phenoxyacetic acids, as well as on selected pesticides falling to the group of priority substances or identified as environmental quality standards. Some of pesticides were selected because their consumption in the Czech Republic exceeds 30 tons a year. Liquid chromatography with tandem mass spectrometry (LC / MS / MS) was used for the determination of selected analytes in surface waters. Two optimized analytical method were developed. Ten analytes were determined in negative ion mode and 34 analytes in positive ion mode. Solid phase extraction (SPE) was used for purification and concentration of the samples. Developed methodology was validated and used for monitoring of selected compounds in samples of surface waters from the Morava River basin. Samples were collected on the rivers Morava and Svratka monthly for two years. Samples from the river Blata and stream Nivnička were collected for one year. Surface water samples were also collected from the river Litava. Four samples were taken throughout the length of the flow during one day. Smaller streams were chosen for monitoring because of the probability of occurrence of pesticides. They flow abundantly agriculturally cultivated areas. Drugs ibuprofen and diclofenac were detected in all taken samples, carbamazepine mostly. Among the most commonly occurring pesticides were bentazon, diuron, isoproturon, carbendazim, MCPA, MCPP, propiconazole, tebuconazole and 2,4-D.

This work is focused on the determination of polar pesticides in surface and waste waters. In this study Mecoprop-P, MCPA, Dichlorprop-P, 2,4-D and MCPBA in differently loaded surface waters and communal waters from sewage treatment plants were analyzed. These herbicides are included in the group identified as environmental quality standards. Some of herbicides (2,4-D and MCPA) were selected because their consumption in the Czech Republic exceeds 30 tons a year. Samples were collected prom three rivers near town of Jaroměř (Elbe, Úpa and Metuje Rivers), from one river near the town of Brno (Svratka River) and from inflow and outflow of two sewage treatment plants (WWTP Jaroměř, WWTP Brno – Modřice). Particular rivers were chosen for monitoring due to the probability of occurrence of herbicides, because they flow through agriculturally cultivated areas. Solid phase extraction (SPE) was used for the isolation of target compounds and their concentration. Gas chromatography with tandem mass spectrometry (GC/MS/MS) was used for the determination of target analytes in surface and waste waters. Selected herbicides were detected in all collected samples.

Cette thèse porte sur l’étude de quelques questions liées à l’identifiabilité et l’identification d’un problème inverse non-linéaire de source. Il s’agit de l’identification d’une source ponctuelle dépendante du temps constituant le second membre d’une équation de type advection-dispersion-réaction à coefficients variables. Dans le cas monodimensionnel, la souplesse du modèle stationnaire nous a permis de développer des réponses théoriques concernant le nombre des capteurs nécessaires et leurs emplacements permettant d’identifier la source recherchée d’une façon unique. Ces résultats nous ont beaucoup aidés à définir la ligne de conduite à suivre afin d’apporter des réponses similaires pour le modèle transitoire. Quant au modèle bidimensionnel transitoire, en utilisant quelques résultats de nulle contrôlabilité frontière et des mesures de l’état sur la frontière sortie et de son flux sur la frontière entrée du domaine étudié, nous avons établi un théorème d’identifiabilité et une méthode d’identification permettant de localiser les deux coordonnées de la position de la source recherchée comme étant l’unique solution d’un système non-linéaire de deux équations, et de transformer l’identification de sa fonction de débit en la résolution d’un problème de déconvolution. La dernière partie de cette thèse discute la difficulté principale rencontrée dans ce genre de problèmes inverses à savoir la non identifiabilité d’une source dans sa forme abstraite, propose une alternative permettant de surmonter cette difficulté dans le cas particulier où le but est d’identifier le temps limite à partir duquel la source impliquée a cessé d’émettre, et donc ouvre la porte sur de nouveaux horizons. / The thesis deals with the two main issues identifiability and identification related to a nonlinear inverse source problem. This problem consists in the identification of a time-dependent point source occurring in the right hand-side of an advection-dispersion-reaction equation with spatially varying coefficients. Starting from the stationnary case in the one-dimensional model, we derived theoritical results defining the necessary number of sensors and their positions that enable to uniquely determine the sought source. Those results gave us a good visibility on how to proceed in order to obtain similar results for the time-dependent (evolution) case. As far as the two-dimensional evolution model is concerned, using some boundary null controllability results and the records of the generated state on the inflow boundary and its flux on the outflow boundary of the monitored domain, we established a constructive identifiability theorem as well as an identification method that localizes the two coordinates of the sought source position as the unique solution of a nonlinear system of two equations and transforms the identification of its time-dependent intensity function into solving a deconvolution problem. The last part of this thesis highlights the main difficulty encountred in such inverse problems namely the nonidentifiabilityof a source in its abstract form, proposes a method that enables to overcome this difficulty in the particular case where the aim is to identify the time active limit of the involved source. And thus, this last part opens doors on new horizons and prospects.