The behaviour of particulate trace metals in marine systems: A review.

Changes in the ocean temperature, seawater acidity, and oxygen level are parts of global change that may indirectly impact the biogeochemical cycles of trace metals in the marine system, particularly for the particulate phase. The different factors influencing the level of particulate trace metals are interesting topics for investigation. Following up on marine research in the estuary and coastal areas, we specifically review the distribution of particulate trace metals. This review aims to provide an overview of the progress of studies on particulate metals in the marine environment and to understand the factors that influence the level of particulate metals. Spatially, the distribution of particulate trace metals decreases towards the sea due to the influence of salinity, while the temporal distribution portrays the unique feature of each location that differences in metal sources and phytoplankton bloom periods might cause.

Element pattern in two dominant species of seaweed from Betsukari coastline - Mashike, Hokkaido, Japan.

The present study investigated the monthly of element accumulation in seaweeds. Patterns of As, Ba, Cd, Cu, Fe, Mn, Pb, and Zn concentrations in dominant species of Phaeophyceae and Rhodophyceae, namely Saccharina japonica and Pterocladiella tenuis respectively, collected from the Betsukari coastline-Mashike, Hokkaido, Japan, were investigated. Our results indicated that element accumulation was more related to specific seaweed species than to their supply in seawater concentration. S. japonica was found to be an accumulator of As, whereas P. tenuis notably accumulated Mn. The accumulation of specific elements also affects the coupled patterns between closely related elements. The monthly pattern of Cd was similar to that of As in S. japonica, and it is an element with unknown biological function in the seaweed. The monthly accumulation pattern of Fe and Mn, a well-known closely related element that forms the extracellular surface in seaweed, was found to be similar in P. tenuis. A similar transport mechanism affected the antagonistic pattern of Cd and Zn accumulation in S. japonica. Our data can be employed in the assessment of biomonitoring of element cycles in the environment.

Direct analysis of biodegradable chelating agents based on liquid chromatography/electrospray ionization mass spectrometry using a metal-free hydrophilic interaction liquid chromatographic column.

Recently, biodegradable aminopolycarboxylic acid chelating agents have attracted attention as an alternative to environmentally persistent chelating agents such as ethylenediamine-N,N,N',N'-tetraacetic acid. However, the detection of chelating agents requires complexation with metals or derivatization by esterification reagents, and their direct detection using the currently available analytical methods still represents a challenge. Herein, we describe a direct analytical method for the biodegradable chelating agents ethylenediamine-N,N'-disuccinic acid, 3-hydroxy-2,2'-iminodisuccinic acid, methylglycine-N,N'-diacetic acid, and N,N-bis(carboxymethyl)-L-glutamic acid, via ultra-performance liquid chromatography/electrospray ionization quadrupole/time-of-flight mass spectrometry. Satisfactory retention and separation with a good peak shape were successfully achieved using a metal-free hydrophilic interaction liquid chromatographic column. The calibration curves showed good linearity in the range of 1.0-50 µM with correlation coefficients greater than 0.9988. The detection limits ranged from 0.04 to 0.12 µM. Furthermore, the developed method could be applied to the quantitative analysis of the four chelating agents in biodegradation and photodegradation experiments at the laboratory level. The proposed method, which offers the advantages of quickness, sensitivity, and requiring no complicated pretreatment steps, is expected to contribute significantly to the practical analysis of chelating agents in environmental water samples.