Bluefin tuna reveal global patterns of mercury pollution and bioavailability in the world's oceans.

Bluefin tuna (BFT), highly prized among consumers, accumulate high levels of mercury (Hg) as neurotoxic methylmercury (MeHg). However, how Hg bioaccumulation varies among globally distributed BFT populations is not understood. Here, we show mercury accumulation rates (MARs) in BFT are highest in the Mediterranean Sea and decrease as North Pacific Ocean > Indian Ocean > North Atlantic Ocean. Moreover, MARs increase in proportion to the concentrations of MeHg in regional seawater and zooplankton, linking MeHg accumulation in BFT to MeHg bioavailability at the base of each subbasin's food web. Observed global patterns correspond to levels of Hg in each ocean subbasin; the Mediterranean, North Pacific, and Indian Oceans are subject to geogenic enrichment and anthropogenic contamination, while the North Atlantic Ocean is less so. MAR in BFT as a global pollution index reflects natural and human sources and global thermohaline circulation.

Spatiotemporal Variations in Dissolved Elemental Mercury in the River-Dominated and Monsoon-Influenced East China Sea: Drivers, Budgets, and Implications.

Distinct spatiotemporal distributions of sea surface dissolved elemental mercury (DEM) and its air-sea exchange flux were observed in the river-dominated and monsoon-influenced East China Sea (ECS). Spatially, DEM concentrations were higher in the nearshore Changjiang diluted water (90 ± 20 to 260 ± 40 fM) than in the offshore Kuroshio water (60 ± 10 to 160 ± 40 fM) and correlated with salinity and total Hg concentrations, suggesting that the total Hg discharged from the Changjiang river is a controlling factor. In summer, monsoon-driven coastal upwelling formed a transient nearshore water mass with very elevated DEM concentrations (290 ± 20 to 320 ± 70 fM). Seasonally, DEM concentrations in all water masses were the highest in summer (120 ± 30 to 320 ± 70 fM). Estimated rate coefficients for DEM production varied seasonally and strongly correlated with sea surface temperature (SST). Hg0 evasion fluxes also peaked in summer (670 ± 380 pmol m-2 day-1), while in winter, DEM was close to equilibrium with gaseous elemental mercury in the atmosphere. Based on the air-sea Hg fluxes for all four seasons from this study and regional atmospheric deposition fluxes from others, we conclude that the ECS is a net sink of Hg annually, but it is a source of Hg to the atmosphere in summer. Moreover, the contribution of the ECS to Hg evasion may increase as a result of flood-associated high Changjiang discharge and rising SST.

Prokaryotic assemblages and metagenomes in pelagic zones of the South China Sea.

BACKGROUND: Prokaryotic microbes, the most abundant organisms in the ocean, are remarkably diverse. Despite numerous studies of marine prokaryotes, the zonation of their communities in pelagic zones has been poorly delineated. By exploiting the persistent stratification of the South China Sea (SCS), we performed a 2-year, large spatial scale (10, 100, 1000, and 3000 m) survey, which included a pilot study in 2006 and comprehensive sampling in 2007, to investigate the biological zonation of bacteria and archaea using 16S rRNA tag and shotgun metagenome sequencing. RESULTS: Alphaproteobacteria dominated the bacterial community in the surface SCS, where the abundance of Betaproteobacteria was seemingly associated with climatic activity. Gammaproteobacteria thrived in the deep SCS, where a noticeable amount of Cyanobacteria were also detected. Marine Groups II and III Euryarchaeota were predominant in the archaeal communities in the surface and deep SCS, respectively. Bacterial diversity was higher than archaeal diversity at all sampling depths in the SCS, and peaked at mid-depths, agreeing with the diversity pattern found in global water columns. Metagenomic analysis not only showed differential %GC values and genome sizes between the surface and deep SCS, but also demonstrated depth-dependent metabolic potentials, such as cobalamin biosynthesis at 10 m, osmoregulation at 100 m, signal transduction at 1000 m, and plasmid and phage replication at 3000 m. When compared with other oceans, urease at 10 m and both exonuclease and permease at 3000 m were more abundant in the SCS. Finally, enriched genes associated with nutrient assimilation in the sea surface and transposase in the deep-sea metagenomes exemplified the functional zonation in global oceans. CONCLUSIONS: Prokaryotic communities in the SCS stratified with depth, with maximal bacterial diversity at mid-depth, in accordance with global water columns. The SCS had functional zonation among depths and endemically enriched metabolic potentials at the study site, in contrast to other oceans.

Mercury bioaccumulation and trophic transfer in Pacific Saury from the North Pacific Ocean.

This study investigates mercury (Hg) dynamics in Pacific Saury (Cololabis saira) across the North Pacific Ocean, specifically off East Japan in 2018. Saury traits vary with total mercury (THg) concentrations in muscle tissues ranging from 0.017 to 0.082 µg g-1 w. w., averaging of 0.042 (n = 46). A positive correlation between THg and saury length (Knob length, 270-319 mm) indicates increased Hg concentration with size. Stable isotopic tracers suggest Pacific Euphausiids (Krill) are significant contributors to the saury diet (>70% of total). Significant correlations between logarithm THg concentration (Log THg) and δ15N (‰) (R2 = 0.70) demonstrate Hg trophic biomagnification, with regional variations. Comparative analysis between the eastern (ENPO) and western North Pacific Ocean (WNPO) indicates differences, with WNPO saury exhibiting lower δ15N values and higher THg levels than ENPO saury. This suggests that the WNPO, located near East Asia, the world's largest Hg emitter, experiences elevated Hg levels in seawater due to anthropogenic release. Overall, this study advances understanding of Pacific Saury's ecological interactions and Hg bioaccumulations, emphasizing the importance of species-specific behaviors and regional influences in ecological studies.

Rapid increase of pCO2 and seawater acidification along Kuroshio at the east edge of the East China Sea.

Rates of seawater acidification and rise of partial pressure of CO2 (pCO2) at ocean margins are highly uncertain. In this study, nine years of time-series data sampled during 2010-2018 along Kuroshio Current near the East China Sea (ECS) were investigated. We found trends of surface seawater pCO2 at 3.70 ± 0.57 µatm year-1 and pH at -0.0033 ± 0.0009 unityear-1, both of which were significantly greater than those reported from other oceanic time series. Mechanistic analysis showed that seawater warming caused rapid rates of pCO2 increase and acidification under sustained DIC increase. The faster pCO2 growth relative to the atmosphere resulted in the CO2 uptake through the air-sea exchange declining by ~50 % (~-0.8 to -0.4 mol C m-2 year-1) over the study period. Our results imply that rapidly warming boundary currents could potentially present an elevated pCO2 trend, leading to a gradual reduction and eventual loss of oceanic CO2 uptake under climate change.

Probing the outfall-related anomalous Hg levels in the Danshuei Estuarine Coastal, Taiwan.

Seasonal and spatial distributions of total mercury (THg) in the Danshuei Estuary and adjacent coastal areas near the ocean outfall of Taipei, Taiwan, have been successfully investigated from May 2003 to January 2005. We found spatio-temporal variation in THg levels in the Danshuei coastal area was the result of sources and supplies of Hg. High THg concentrations in sediments and seawater were particularly found near the effluent outfall. Average THg levels (avg.: 9-22 ng L-1) were much higher than those in surrounding coastal seawaters (avg.:1-2 ng L-1). Organic carbon contents then played vital roles in controlling water and sedimentary Hg concentrations and occurrences. Hg enrichment factor (EF) as an index of contamination status in surface sediments of the Danshuei coastal area averaged 2.0 ± 0.8 (EFs > 1), indicating an extra non-crustal source from anthropogenic loadings. It implies the Dansheui coastal environment nearby the sewer outfall is facing Hg pollution.

Tungsten and other heavy metal contamination in aquatic environments receiving wastewater from semiconductor manufacturing.

Through analyses of water and sediments, we investigate tungsten and 14 other heavy metals in a stream receiving treated effluents from a semiconductor manufacturer-clustered science park in Taiwan. Treated effluents account for ∼ 50% of total annual river discharge and <1% of total sediment discharge. Dissolved tungsten concentrations in the effluents abnormally reach 400 µg/L, as compared to the world river average concentration of <0.1 µg/L. Particulate tungsten concentrations are up to 300 µg/g in suspended and deposited sediments, and the corresponding enrichment factors are three orders of magnitude higher than average crust composition. Surprisingly, the estimated amount of tungsten exported to the adjacent ocean is 23.5 t/yr, which can approximate the amount from the Yangtze River should it be unpolluted. This study highlights the urgency of investigating the biological effect of such contamination.

Alteromonas tagae sp. nov. and Alteromonas simiduii sp. nov., mercury-resistant bacteria isolated from a Taiwanese estuary.

Two mercury-resistant strains of heterotrophic, aerobic, marine bacteria, designated AT1(T) and AS1(T), were isolated from water samples collected from the Er-Jen River estuary, Tainan, Taiwan. Cells were Gram-negative rods that were motile by means of a single polar flagellum. Buds and prosthecae were produced. The two isolates required NaCl for growth and grew optimally at about 30 degrees C, 2-4 % NaCl and pH 7-8. They grew aerobically and were incapable of anaerobic growth by fermenting glucose or other carbohydrates. They grew and expressed Hg(2+)-reducing activity in liquid media containing HgCl(2). Strain AS1(T) reduced nitrate to nitrite. The predominant isoprenoid quinone was Q(8) (91.3-99.9 %). The polar lipids of strain AT1(T) consisted of phosphatidylethanolamine (46.6 %), phosphatidylglycerol (28.9 %) and sulfolipid (24.5 %), whereas those of AS1(T) comprised phosphatidylethanolamine (48.2 %) and phosphatidylglycerol (51.8 %). The two isolates contained C(16 : 1)omega7c and/or iso-C(15 : 0) 2-OH (22.4-33.7 %), C(16 : 0) (19.0-22.7 %) and C(18 : 1)omega7c (11.3-11.7 %) as the major fatty acids. Strains AT1(T) and AS1(T) had DNA G+C contents of 43.1 and 45.3 mol%, respectively. Phylogeny based on 16S rRNA gene sequences, together with data from morphological, physiological and chemotaxonomic characterization, indicated that the two isolates could be classified as representatives of two novel species in the genus Alteromonas, for which the names Alteromonas tagae sp. nov. (type strain AT1(T)=BCRC 17571(T)=JCM 13895(T)) and Alteromonas simiduii sp. nov. (type strain AS1(T)=BCRC 17572(T)=JCM 13896(T)) are proposed.

Modern and historic atmospheric mercury fluxes in northern Alaska: Global sources and Arctic depletion.

We reconstruct from lake-sediment archives atmospheric Hg deposition to Arctic Alaska over the last several centuries and constrain a contemporary lake/watershed mass-balance with real-time measurement of Hg fluxes in rainfall, runoff, and evasion. Results indicate that (a) anthropogenic Hg impact in the Arctic is of similar magnitude to that at temperate latitudes; (b) whole-lake Hg sedimentation determined from 55 210Pb-dated cores from the five small lakes demonstrates a 3-fold increase in atmospheric Hg deposition since the advent of the Industrial Revolution; (c) because of high soil Hg concentrations and relatively low atmospheric deposition fluxes, erosional inputs to these lakes are more significant than in similar temperate systems; (d) volatilization accounts for about 20% of the Hg losses (evasion and sedimentation); and (e) another source term is needed to balance the evasional and sedimentation sinks. This additional flux (1.21+/-0.74 microg m(-2) yr(-1)) is comparable to direct atmospheric Hg deposition and may be due to some combination of springtime Arctic depletion and more generalized deposition of reactive gaseous Hg species.

Determination of methylmercury in environmental matrixes by on-line flow injection and atomic fluorescence spectrometry.

The precision and bias of monomethylmercury (MMHg) determinations in environmental samples can be improved by directly coupling and automating the numerous steps involved with analysis of this toxic Hg species. We developed a simple and robust mercury speciation analyzer (MSA) for measurement of MMHg in environmental matrixes. This on-line hyphenated system couples the main analytical steps, including sample introduction, aqueous-phase ethylation, Tenax preconcentration, and gas chromatographic separation, to cold vapor atomic fluorescence detection and data acquisition. Here we describe the MMHg-MSA, present results of laboratory optimization and performance tests, and compare the reproducibility between dual analytical channels. With alternating sample concentration and analysis, a dual-channel system permits six high-accuracy MMHg determinations per hour. Additional advantages compared to the traditional manual method include ease of operation and high precision (<5% relative standard deviation). The MSA is applicable to the determination of MMHg in various environmental matrixes, and it can be fully automated. This method was validated by analysis of MMHg in certified reference materials of sediment and biological tissue. Estimated detection limits for MMHg with the MSA are approximately 0.01 ng g(-1) for a 0.1-g sample of dry sediment or fish and approximately 0.01 ng L(-1) for 0.15 L of water.

Determination of the mercury complexation characteristics of dissolved organic matter in natural waters with "reducible Hg" titrations.

A new method for the determination of the concentration and conditional stability constant of dissolved organic matter that binds mercury (Hg) has been developed using an in vitro assay of reducible Hg. The technique is a wet chemical analogue to electrochemical approaches now in use for ligand studies of many other trace transition metals in natural waters. Ligand characteristics are obtained from additions of ionic Hg to buffered lake, river water, and seawater and determination of the wet chemically reducible fraction following equilibration of the spike. This approach is robust, as demonstrated by (i) analysis using three reducing agents of varying strengths, (ii) replicate analyses, (iii) comparison to well-characterized complexing species (chloride and EDTA) using a competitive ion-exchange resin, and (iv) kinetic studies. Results indicate that Hg-complexing equivalents are present in the dissolved phase (<0.2 microm) ranging from <1 to >60 nN concentrations and with log conditional stability constants (log K') in the range of 21-24. Only one ligand class was found in the natural waters analyzed. There was indirect evidence for a class of organic ligands that formed reducible complexes with Hg in freshwater. Such ligand characteristics indicate that the vast majority of ionic inorganic Hg dissolved in freshwater and coastal saltwaters is associated with organic complexes. Concentrations, affinities, and kinetics implicate multidentate chelation sites as the principal complexing moieties for Hg and discourage the use of humic carboxylic acids as a proxy for the ligands/functional groups.