A review of marine water sampling methods for trace metals

2020 ◽  
Vol 21 (3-4) ◽  
pp. 267-290 ◽  
Author(s):  
A. E. Noble ◽  
C. B. Tuit ◽  
J. P. Maney ◽  
A. D. Wait
2009 ◽  
Vol 6 (6) ◽  
pp. 7247-7285 ◽  
Author(s):  
N. P. Peranginangin ◽  
B. K. Richards ◽  
T. S. Steenhuis

Abstract. Accurate soil water sampling is needed for monitoring of pesticide leaching through the vadose zone, especially in soils with significant preferential flowpaths. We assessed the effectiveness of wick and gravity pan lysimeters as well as ceramic cups (installed 45–60 cm deep) in strongly-structured silty clay loam (Hudson series) and weakly-structured fine sandy loam (Arkport series) soils. Simulated rainfall (10–14 cm in 4 d, approximately equal to a 10-yr, 24 h storm) was applied following concurrent application of agronomic rates (0.2 g m−2) of atrazine (6-chloro-N2-ethyl-N4-isopropyl-1,3,5-triazine-2,4-diamine) and 2,4-D (2,4-dichloro-phenoxy-acetic acid) immediately following application of a chloride tracer (22–44 g m−2). Preferential flow mechanisms were observed in both soils, with herbicide and tracer mobility greater than would be predicted by uniform flow. Preferential flow was more dominant in the Hudson soil, with earlier breakthroughs observed. Mean wick and gravity pan sampler percolate concentrations at 60 cm depth ranged from 96 to 223 μg L−1 for atrazine and 54 to 78 μg L−1 for 2,4-D at the Hudson site, and from 7 to 22 μg L−1 for atrazine and 0.5 to 2.8 μg L−1 for 2,4-D at the Arkport site. Gravity and wick pan lysimeters had comparably good collection efficiencies at elevated soil moisture levels, whereas wick pan samplers performed better at lower moisture contents. Cup samplers performed poorly with wide variations in collections and solute concentrations.


1948 ◽  
Vol 40 (6) ◽  
pp. 625-630
Author(s):  
George W. Schucker

2011 ◽  
Vol 15 (1) ◽  
Author(s):  
AP Edorh ◽  
E Montcho ◽  
K Gnandi ◽  
P Guédénon ◽  
L Koumolou ◽  
...  

1995 ◽  
Vol 29 (9) ◽  
pp. 2051-2054 ◽  
Author(s):  
Steven E. Bufflap ◽  
Herbert E. Allen

2012 ◽  
Vol 46 (20) ◽  
pp. 11220-11226 ◽  
Author(s):  
Hyojin Kim ◽  
James K. B. Bishop ◽  
Todd J. Wood ◽  
Inez Y. Fung

PLoS ONE ◽  
2017 ◽  
Vol 12 (5) ◽  
pp. e0176541 ◽  
Author(s):  
Izumi Katano ◽  
Ken Harada ◽  
Hideyuki Doi ◽  
Rio Souma ◽  
Toshifumi Minamoto

The article is devoted to the development of a generalized methodology for calculating the joint characteristics of the effect of modified spectrum water. Water quality control is important to recognize because of water pollution and disease. A framework for a review of water quality should be defined to ensure that if water quality is measured as appropriate, it should be expected. Basically, water quality monitors to ensure water safety are both sleepy and standard waters nearby and global. Various water sampling methods and technology can be used to determine the level and quantity of a chemical in water as test water. The article describes how to prepare water used in hydrogen generators, to prepare solutions, chromatographic samples, capillary electrophoresis, high performance liquid chromatography (HPLC), and other analyzers that require the use of high purity water. The study showed that the use of spring water with a modified spectrum leads to positive statistically significant changes. The article presents results according to the absolute measurements of the luminosity of water. As a result of the calculations, graphical dependencies of the joint characteristics of the efficiency of using spectrograph. A CDS / (Pt-TiO2) pumice was created without creating a Titania composite in the pumice in accordance with the floating coating, so that photocatalysis did not cause problems in the separation of the titanium solution. European Microscopy Emission Range (FESEM), Microscope Transmission (TEM), Used UV Visible Diffusion Spectroscopy (UV-Vis DRS), such as Photocatalyst Characterization.


2006 ◽  
Vol 3 (3) ◽  
pp. 199 ◽  
Author(s):  
Kate A. Howell ◽  
Eric P. Achterberg ◽  
Alan D. Tappin ◽  
Paul J. Worsfold

Environmental Context. Trace metals play an essential role in the growth and function of aquatic organisms; however, enhanced metal concentrations can have detrimental effects on ecosystems. The distribution of metals between filterable and filter-retained phases is key to their bioavailability and biogeochemical cycling. Studies on rivers have shown that separating dissolved metals from particle-associated metals may introduce significant artefacts in the resulting filtrate concentrations. Comparable studies on turbid estuarine waters are necessary to improve the design of water sampling programmes. Abstract. Total filterable and colloidal metals were measured in the Tamar Estuary. The colloidal fraction (Mc) was highly variable for each metal, both spatially and temporally. In April 2001, Alc and Coc were higher in the river than the estuary, Cdc, Crc and Pbc were lower, and Mnc and Uc were similar. In September 2001, Cdc was higher in the river than the estuary. Colloidal Al and Mn were positively correlated with concentrations of suspended particles, whereas the colloid contents of the other metals were primarily determined by additional factors. The effect of the colloidal metal content on resultant metal filtrate concentrations, as a function of sample volume filtered, was examined. The amount of Al, Cd, Cu, Pb, and U in the filtrate decreased significantly in at least one case, whereas Mn initially increased in some cases. There was no change for Co, Cr, and Zn. The implications of these results for the study of trace metals in moderately turbid estuaries are discussed.


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