Uptake and Excretion of Chemicals by Aquatic Fauna

1983 ◽  
Vol 15 (S1) ◽  
pp. 67-78
Author(s):  
V Zitko

Factors influencing the movement of chemicals across biological membranes are: solubility in lipids and in water, chemical stability, ionization, and molecular weight of the chemical. On the part of aquatic fauna, the transport of chemicals is affected by metabolic activity and by the physiological state of the animals. Additional factors include water temperature, hardness or salinity, and presence of other chemicals. The effects of these factors will be discussed and illustrated by examples. The uptake of highly lipid-soluble compounds by fish appears to be determined by their solubility in water, and compounds with extremely low solubility in water are not taken up in spite of their high solubility in lipids. Examples are hexabromo-benzene, highly brominated biphenyls, C24 chlorinated paraffins, and some flame retardants of the Dechlorane series. In addition to solubility in water, there may be a high molecular weight threshold, beyond which compounds are not taken up, and factors based on the chemical structure of the compounds may play a role as well. For example, Dechlorane 604, a tetrabromophenyl norbornene, is accumulated by fish to a much lesser degree than a tribromophenyl norbornene, present as a minor impurity in Dechlorane 604. Chemical and biochemical stability of compounds are additional factors determining the extent of environmental contamination. Examples are the widespread contamination of aquatic biota by two nonachlors, present originally as relatively minor components in technical chlordane, and the contamination by some components of toxaphene. The use of a one compartment model in studies of accumulation and excretion of chemicals by aquatic fauna, and its extension to the determination of lethality curves, will be mentioned.

1966 ◽  
Vol 44 (12) ◽  
pp. 1361-1367 ◽  
Author(s):  
D. C. Moule ◽  
W. M. Thurston

A new method is described for the analysis of water in nonpolar organic liquids. It is based on an isotope dilution procedure and involves the exchange of the water present in the sample with D2O. The change in isotopic composition of the D2O is determined by infrared difference spectroscopy. The method appears to be accurate to ± 0.8%.The principal advantage of this method is that the difficult problem of calibration with organic–water standards is avoided. It is restricted, however, to solvents which have a low solubility in water and do not have exchangeable hydrogens.A series of solubility measurements were carried out for H2O in C6H6 from 10 to 60 °C. The data were fitted to the usual interpolation equation In (f/x) = −A/T + B ln T + C, and the thermodynamic functions of solution, ΔG, ΔH, ΔCP, and ΔS, were computed for the transfer of 1 mole of water from the benzene phase to the vapor phase.


Biosensors ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 12
Author(s):  
Pablo Fanjul-Bolado ◽  
Ronen Fogel ◽  
Janice Limson ◽  
Cristina Purcarea ◽  
Alina Vasilescu

Dithiocarbamate fungicides (DTFs) are widely used to control various fungal diseases in crops and ornamental plants. Maximum residual limits in the order of ppb-ppm are currently imposed by legislation to prevent toxicity problems associated with excessive use of DTFs. The specific analytical determination of DTFs is complicated by their low solubility in water and organic solvents. This review summarizes the current analytical procedures used for the analysis of DTF, including chromatography, spectroscopy, and sensor-based methods and discusses the challenges related to selectivity, sensitivity, and sample preparation. Biosensors based on enzymatic inhibition demonstrated potential as analytical tools for DTFs and warrant further research, considering novel enzymes from extremophilic sources. Meanwhile, Raman spectroscopy and various sensors appear very promising, provided the selectivity issues are solved.


2014 ◽  
Vol 40 (2) ◽  
pp. 91-102 ◽  
Author(s):  
Reza Tajik ◽  
Hasan Asilian Mohabadi ◽  
Ali Khavanin ◽  
Ahmad Jonidi Jafari ◽  
Babak Eshrati

Abstract Polychlorinated biphenyls (PCBs) are one group of persistent organic pollutants (POPs) that are of international concern because of global distribution, persistence, and toxicity. Removal of these compounds from the environment remains a very difficult challenge because the compounds are highly hydrophobic and have very low solubility in water. A 900 W domestic microwave oven, pyrex vessel reactor, pyrex tube connector and condensing system were used in this experiment. Radiation was discontinuous and ray powers were 540, 720 and 900 W. The PCBS were analyzed by GC-ECD. The application of microwave radiation and H2O2/TiO2 agents for the degradation of polychlorinated biphenyl contaminated oil was explored in this study. PCB – contaminated oil was treated in a pyrex reactor by microwave irradiation at 2450 MHz with the addition of H2O2/TiO2. A novel grain TiO2 (GT01) was used. The determination of PCB residues in oil by gas chromatography (GC) revealed that rates of PCB decomposition were highly dependent on microwave power, exposure time, ratio to solvent with transformer oil in 3:1, the optimal amount of GT01 (0.2 g) and 0.116 mol of H2O2 were used in the study. It was suggested that microwave irradiation with the assistance of H2O2/TiO2 might be a potential technology for the degradation of PCB – contaminated oil. The experiments show that MW irradiation, H2O2 oxidant and TiO2 catalyst lead to a degradation efficiency of PCBs only in the presence of ethanol. The results showed that the addition of ethanol significantly enhanced degradation efficiency of PCBs.


2000 ◽  
Vol 25 (0) ◽  
pp. 63-76 ◽  
Author(s):  
Ivanise GAUBEUR ◽  
Maura Vincenza ROSSI ◽  
Koshun IHA ◽  
Maria Encarnación Vázquez SUÁREZ-IHA

The ligand di-2-pyridyl ketone benzoylhydrazone (DPKBH) is widely used for the determination of transition metal ions in environmental samples. Due to its low solubility in water it is used in aqueous-ethanol (1:1) solvent and for higher sensitivity the pH must be properly adjusted. The properties of DPKBH solutions must be known at different ethanol-water percentages in order to achieve higher sensitivity and/or selectivity for metal analysis. The acid-base behavior of this reagent in aqueous-ethanol solvent and the dissociation/ionization constants (pK1 and pK2) of DPKBH have been determined in different aqueous-ethanol solvent mixtures (10, 20, 30 and 50 % V/V of ethanol) from potentiometric titrations at 25.0 ± 0.1° C. As the amount of ethanol increases from 10 to 30% the pK1 and pK2 values increased, but they decreased in 50% of the organic solvent. The results are correlated with the medium composition and its effects.


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