|
|
Plant defence against arsenic toxicity: a key role of arsenate reductase?
Jurčíková, Martina ; Mašková, Petra (advisor) ; Hála, Michal (referee)
Arsenic in its various forms is one of the most toxic environmental contaminants, which is also taken up by plants and can affect their vitality. The risk category is crops where As contamination reduces the overall yield and through which As enters the food chain. Its inorganic (arsenite and arsenate) and organic (methylated) forms are taken up by roots and rhizomes, where they can either accumulate or be translocated and subsequently stored in shoots. Arsenate reductase is an enzyme that catalyses the reduction of arsenate to arsenite, thereby affecting not only the overall toxicity of As in the plant, but also its transport between underground and aboveground organs. However, the interplay of the different mechanisms of As uptake, translocation and detoxification has not been investigated in detail. The aim of this bachelor thesis was to analyze and compare the importance of arsenate reductase in these processes in the model organism Arabidopsis thaliana, in a rice crop and in the arsenic hyperaccumulator Pteris vittata. The different tolerance of these organisms to As and their differences in the preferential site of As deposition in leaves or seeds could be used for different purposes, such as in the phytoremediation of As-contaminated soils, or in limiting the uptake or translocation of As to...
|
|
|
Speciation analysis of arsenic based on volatile species generation and dielectric barrier discharge plasma atomization
Plecháč, Matěj ; Kratzer, Jan (advisor) ; Kaňa, Antonín (referee)
SPECIATION ANALYSIS OF ARSENIC BASED ON VOLATILE SPECIES GENERATION AND DIELECTRIC BARRIER DISCHARGE PLASMA ATOMIZATION Bc. Matěj Plecháč 2024 Abstract Volatile species generation (VSG) comprises a group of techniques based on analyte derivatization in order to form a volatile compound prior to spectrometric detection. Selective analyte conversion from liquid to gas phase results in enhanced analyte introduction efficiency, but also in matrix separation and reduced risk of interferences. Moreover, VSG step can be utilized during speciation analysis or analyte preconcentration. The most frequent atomizers of volatile species are externally heated quartz tubes (QTA). Dielectric barrier discharge (DBD) atomizers have proved to be alternative hydride atomizers to QTA. The significant difference in toxicity of various species of the same element leads to the urgent need to develop new strategies for speciation analysis. Various approaches to speciation analysis of toxicologically relevant arsenic species including inorganic iAsIII and iAsV , monomethylarsonic acid (MMA), dimethylarsinic acid (DMA) and trimethylarsine oxide (TMAsO) by hydride generation atomic absorption spectrometry (HG-AAS) were investigated in this work. All these species can be converted to volatile compounds. i.e. arsane and its methylated...
|
|
|
Speciation analysis of arsenic compounds in environmental samples
Pakosta, Lukáš ; Novotná, Marie (referee) ; Vašinová Galiová, Michaela (advisor)
Arsenic is a toxic element that exists in various species, each having different environmental and health impacts. The presence of arsenic in the environment, especially in water and soil, poses a serious risk to human health. In this bachelor's thesis, the time and temperature for the extraction of arsenic and arsenic species in soil and biota samples were optimized. For the separation of arsenic species, high-performance liquid chromatography was used, and the determination of arsenic species content and total arsenic content was carried out using a triple quadrupole mass spectrometer with inductively coupled plasma. Based on the conducted experiment, the optimal conditions were applied to soil and biota samples from Lužánky Park.
|
|
|
Study of road dust pollution using ICP mass spectrometry
Chalabala, Jan ; Komendová, Renata (referee) ; Vašinová Galiová, Michaela (advisor)
Nowadays, there are many studies focused on road dust as a matrix of interest because of its ability to accumulate contamination with contribution from road traffic. This master thesis is turned into study of road dust pollution from aglomeration of Ulaanbaatar, capital city of Mongolia. There are 113 samples devided on nine sets corresponding to major roads in Ulaanbaatar. Samples have been sieved on three size fractions and then decomposed by aqua regia. Middle size fraction 45–63 µm has been analyzed using ICP-MS mass spektrometry. For purposes of contamination assesment, analyzed elements have been devided into two groups: contaminants (Cr, Cu, Zn, Pb and As) and rare earth elements (REE). Measured contents for elements have been compared with values of geochemical backgroud. Firstly for each set of samples and secondly for each sampling point. For first group of elements (contaminants), antropogenic contamination have been found, especially in the centre of Ulaanbaatar. As a probable source of this contamination, road traffic for Cu, Zn and Pb and coal combustion for Pb a As, have been identified. For REE group hasn´t been found any antropogenic enrichment.
|
|
| |
|
|
Arsenic and arsenic species cycle in environment
Ševčíková, Kateřina ; Sommer, Lumír (referee) ; Dočekalová, Hana (advisor)
This bachelor thesis, based mostly on literature retrieval, deals with monitoring of individual arsenic compounds in the environment and is also reviewing methods used for their analysis. The experimental part is focused on determination of various arsenic in the Oncorhynchus mykiss tissue by HPLC-UV-HG-AFS. Obtained results showed that the arsenic was present in the tissue of the Oncorhynchus mykiss in form of arsenobetaine, which is common for fishes and other aquatic animals and is not toxic even for consuments.
|
|
|
Multicomponental Preconcentration of As, Sb, Se and Te on Modified Silica, Their Determination by ICP-AES (ICP-MS) and Application for Waters
Urbánková, Kristýna ; Řehůřková, Irena (referee) ; Kanický, Viktor (referee) ; Ventura, Karel (referee) ; Sommer, Lumír (advisor)
The determination of inorganic speciations of arsenic, antimony, selenium and tellurium in natural waters demands often separation and preconcentration. Solid phase extraction is a very effective method for these purposes. In this paper the separation and preconcentration of these microelements is realised on the basis of modified silica Separon SGX C18, SGX C8, SGX CN, SGX NH2, SGX Phenyl and strongly basic anion Exchanger SGX AX. The sorption was provided in the presence of cationic surfactants such as benzyldimethyl dodecylammonium bromide (Ajatin), benzyldimethyltetradecylammonium chloride (Zephyramine), 1-ethoxycarbonylpentadecyltrimetrhylammonium bromide (Septonex) and selected complexing agents 4-(2-pyridylazo)resorcinol (PAR), 8-hydroxyquinoline-5-sulphonic acide (8-HQS), 1,2-dihydroxybenzene (PYR), amonium 1-pyrrolidinecarbodithioate (APDC), sodium diethyldithiocarbamate (DTC) or thiourea(Thur). The interactions of the formed ion associate with the sorbent shows a complicated character which has not been cleared as yet. The previous conditioning of the sorbent plays an outstanding role. Thus, the sorption efficiency was studied in the presence and absence of surfactant and of selected organic complexing agents. Moreover, the influence of pH of the sorbed solution as well as the speed and the volume of the solution running through the sorbent and the type and volume of the eluent on the resulting sorption efficiency was evaluated. The sorption was successfully carried out from 50-1000 ml of solution which allows the 100 fold increase of the preconcentration factor and the determination of the microelements in g.l-1 instead of mg.l-1 by using the common ICP-AES. The influence of macroelements occurring in waters as well as B, Be, Bi, Cd, Co, Cr, Cu, Mn, Mo, Ni, Pb, Sr, Ti, V and Zn in comparable concentrations involve less than 5% error. After the quantitative elution of microelements, the organic solvents were evaporated under IR lamps prior to the determination by ICP-AES and |ICP-MS. The conditions for the direct determination of arsenic, antimony, selenium and tellurium in g.l-1 with ICP-MS were also described in detail in the absence and presence of internal standards Ge and Bi. However, even in this case the preconcentration on silica in the presence of surfactant and selected organic complexants was also tested. When the sorption was followed from 500 ml a 50 fold enrichment factor is reached and the sensitivity for the microelements is improved. The direct determination and the sorption of microelements were applied on synthetic and real waters (dirinking, surface, mineral and sea waters). Instrumental and practical detection limits for various water samples were evaluated according to IUPAC. The results from 1000 ml solution of real waters after sorption on modified silica and the final determination of microelements with ICP-AES were compared with those from ICP-MS without sorption using the method of standards addition in the presence of suitable internal standards. By comparison of results for synthetic and real water samples the error of the determination of microelements was evaluated.
|
|
|
Methods for Elemental Speciation of Arsenic Compounds.
Navrátilová, Jana ; Jarošová, Alžběta (referee) ; Golian,, Jozef (referee) ; Šimko, Peter (advisor)
Speciační analýza arsenu v různých matricích s využitím HPLC/ICPMS byla předmětem této práce. Toxicita arsenu závisí na oxidačním stavu a formě, ve které je přítomen. Znalost zastoupení specií arsenu je nutná k hodnocení toxicity a biodostupnosti. Obecně, anorganické specie jsou více toxické než organické. V práci byla studována degradace arsenocukrů v mořských řasách za simulovaných přirodních podmínek. Původní arsenocukry byly transformovány na arseničnan a kyselinu dimethylarseničnou. Arsen vstupuje do rostlin z půdy a vody a následně může vstoupit do potravního řetězce. S ohledem na tuto skutečnost byla speciační analýza provedena u vybraných vzorcích rýže, zakoupených v české obchodní síti. Stanovený celkový obsah arsenu se pohyboval v rozmezí 36.06 µg/kg - 218.11 µg/kg a hlavními speciemi byla kyselina dimethylarseničná a anorganický arsen (54-78%). Mořské ryby a tuky obsahují významnou část arsenu ve formě zvané arsenolipidy. Část práce byla zaměřena na analýzu arsenolipidů u máslové ryby (Lepidocybium flavobrunnrum) s celkovým obsahem arsenu 1.8 mg/kg a 22% celkového arsenu bylo vyextrahováno pomocí hexanu, což potvrzuje lipofilni charakter těchto sloučenin. Hlavní specií stanovenou ve vodném extraktu byl arsenobetain, představující 89%.
|
|
|
Investigation of Miniature Devices for Collection of Hydride Forming Elements in Atomic Spectrometry Methods
Krejčí, Pavel ; Čelechovská, Olga (referee) ; Janoš, Pavel (referee) ; Otruba, Vítězslav (referee) ; Dočekal, Bohumil (advisor)
Capability of a prototype of miniature collection device based on a strip of the molybdenum foil for collecting hydride forming elements (As, Se, Sb and Bi) was studied. The device was combined with a miniature hydrogen diffusion flame for detection by atomic absorption spectrometry. The conditions for trapping and subsequent vaporization of analytes of interest were optimized. A twin-channel hydride generation system was used for study of mutual interference effects of co-generated hydride forming elements. The influence of modification of the molybdenum surface with noble metals - Rh, Pt and Ir on trapping and vaporization processes was also studied and changes of microstructure of the foil surface after modification were investigated using scanning electron microscope equipped with energy dispersive x-ray analyzer and electron backscattered diffraction system. Complementary radiotracer and radiography experiments were performed in order to determine trapping efficiency and to assess the spatial distribution of collected analytes within the device. Practical application of the method was demonstrated on determination of antimony in water samples at trace level. Possibility of multi-element analysis was demonstrated by combining the collection device with atomization and excitation of the analyte in microwave induced plasma and with detection by atomic emission spectrometry method. The results of the experiments proved that tested miniature collection device is capable of trapping analytes that form volatile hydrides. This device can be coupled to various types of atomizers, typically used in spectrometry methods. Thus, very sensitive and specific detection of hydride forming elements can be performed.
|
|
|
Study of Generation, Trapping and Atomization of Hydride Forming Elements for Atomic Spectrometry
Furdíková, Zuzana ; Sommer, Lumír (referee) ; Čelechovská, Olga (referee) ; Řehůřková, Irena (referee) ; Dočekalová, Hana (advisor)
Interference effects of co-generated hydrides of arsenic, antimony, bismuth and selenium on trapping behavior of selenium or antimony hydrides (analytes) within iridium modified, transversely heated graphite tube atomizer (THGA) was investigated. A twin-channel hydride generation system was used for independent separate generation and introduction of analyte and interferent hydrides, i.e. in simultaneous and/or sequential analyte-interferent and interferent-analyte mode of operation. Influence of the analyte and modifier mass, interferent amount, trapping temperature and composition of the gaseous phase was studied. A simple approach for elimination of mutual interference effects by modification of the gaseous phase with oxygen in substoichiometric ratio to chemically generated hydrogen is proposed and suppression of these interference effects is demonstrated. A hypothesis on mechanism of trapping and mutual interference effects is drawn.
|
guest ::
