Near-surface distribution of pollutants in coastal waters as assessed by novel polyethylene passive samplers

We report a novel and inexpensive method to provide high resolution vertical measurements of temporally integrated organic contaminants in surface and sub-surface waters in polluted coastal environments. It employs a strip of polyethylene deployed as a passive sampler. Verifications are confirmed via conventional spot sample analyses and against Performance Reference Compound (PRC) calibration methods. Analytes targeted include 16 Polycyclic Aromatic Hydrocarbons, 15 personal care products, 8 organophosphorus flame retardants, 4 antifouling ‘booster’ biocides and 15 n-alkanes. Whilst all contaminants typically revealed homogeneous concentrations from 10 cm to 3 m depth in the selected harbour (< 30% variations), many increased sharply at the air-sea interface. The passive sampler was shown to afford better resolution than could be achieved using conventional analytical techniques at the surface microlayer (SML). Whilst hydrophobicity appeared to be a key factor for the enrichment of many determinants, less correlation was found for the emerging contaminants. © 2017 Elsevier Lt

Calibration and response of an agarose gel based passive sampler to record short pulses of aquatic organic pollutants

publisher: Elsevier articletitle: Calibration and response of an agarose gel based passive sampler to record short pulses of aquatic organic pollutants journaltitle: Talanta articlelink: http://dx.doi.org/10.1016/j.talanta.2016.12.010 content_type: article copyright: © 2016 Elsevier B.V. All rights reserved

Transformation of C60 fullerene aggregates suspended and weathered under realistic environmental conditions

The occurrence, fate and behaviour of carbon nanomaterials in the aquatic environment are dominated by their functionalization, association with organic material and aggregation behaviour. In particular, the degradation of fullerene aggregates in the aquatic environment is a primary influence on their mobility, sorption potential and toxicity. However, the degradation and kinetics of water suspensions of fullerenes remain poorly understood. In the present work, first, an analytical method based on liquid chromatography and high-resolution mass spectrometry (LC-HRMS) for the determination of C60 fullerene and their environmental transformation products was developed. Secondly, a series of C60 fullerene water suspensions were degraded under relevant environmental conditions, controlling the salinity, the humic substances content, the pH and the sunlight irradiation. Up to ten transformation products were tentatively identified, including epoxides and dimers with two C60 units linked via one or two adjacent furane-like rings. Fullerenols were not observed under these environmentally relevant conditions. The kinetics of generation of each transformation product were studied with and without simulated sunlight conditions. The ionic strength of the media, its pH and the humic substances content were observed to modulate the kinetics of generation

Identifying the main sources of Silicate in coastal waters of the southern Gulf of Valencia (Western Mediterranean Sea)

[EN] Silicon is a major nutrient for siliceous primary producers, which can become a potential limiting nutrient in oligotrophic areas. Most of the silicon inputs to the marine environment come from continental discharges, from both superficial and ground waters. This study analyses the main sources of silicon and their dynamics along the southernmost 43 km of shoreline in the Gulf of Valencia (Western Mediterranean Sea). The salinity and silicate concentration in the different compartments (springs, freshwater wells, beach groundwater, surf zone and coastal waters) in this coastal area were determined. In addition, chlorophyll a and phytoplankton community were analyzed in the surf zone and coastal waters. Silicate concentrations in freshwater wells ranged between 130 and 150 mu M, whereas concentrations of this nutrient declined to 49 mu M in freshwater-seawater mixture transects. At the same time, there was a positive gradient in silicate for both freshwater and coastal waters southward. An amount of 18.7 t of dissolved silicate was estimated in the nearest first kilometre nearest to the coastline, 6 t of this silicate belonged to the background sea level. On the other hand, the sum of the main rivers in the area supplies 1.6 t of dissolved silicate per day. This implies that a large amount of the remaining 11.1 t must derive from submarine groundwater discharges, which would thus represent 59% of the coastal dissolved silicate budget. Overall, it is suggested that a subterranean transport pathway must contribute considerably to silicate concentrations throughout this zone, which is characterized as permeable. (c) 2017 Institute of Oceanology of the Polish Academy of Sciences. Production and hosting by Elsevier Sp. z o.o.The authors acknowledge the financial support for this study from the CNPq (Brazil - Grant 303672/2013-7). We are very grateful for the valuable comments of anonymous reviewers on previous versions of the manuscript.Sospedra, J.; Niencheski, LFH.; Falco, S.; Andrade, C.; Attisano, K.; Rodilla, M. (2018). Identifying the main sources of Silicate in coastal waters of the southern Gulf of Valencia (Western Mediterranean Sea). Oceanologia. 60(1):52-64. https://doi.org/10.1016/j.oceano.2017.07.004S526460

Coral Uptake of Inorganic Phosphorus and Nitrogen Negatively Affected by Simultaneous Changes in Temperature and pH

The effects of ocean acidification and elevated seawater temperature on coral calcification and photosynthesis have been extensively investigated over the last two decades, whereas they are still unknown on nutrient uptake, despite their importance for coral energetics. We therefore studied the separate and combined impacts of increases in temperature and pCO2 on phosphate, ammonium, and nitrate uptake rates by the scleractinian coral S. pistillata. Three experiments were performed, during 10 days i) at three pHT conditions (8.1, 7.8, and 7.5) and normal temperature (26°C), ii) at three temperature conditions (26°, 29°C, and 33°C) and normal pHT (8.1), and iii) at three pHT conditions (8.1, 7.8, and 7.5) and elevated temperature (33°C). After 10 days of incubation, corals had not bleached, as protein, chlorophyll, and zooxanthellae contents were the same in all treatments. However, photosynthetic rates significantly decreased at 33°C, and were further reduced for the pHT 7.5. The photosynthetic efficiency of PSII was only decreased by elevated temperature. Nutrient uptake rates were not affected by a change in pH alone. Conversely, elevated temperature (33°C) alone induced an increase in phosphate uptake but a severe decrease in nitrate and ammonium uptake rates, even leading to a release of nitrogen into seawater. Combination of high temperature (33°C) and low pHT (7.5) resulted in a significant decrease in phosphate and nitrate uptake rates compared to control corals (26°C, pHT = 8.1). These results indicate that both inorganic nitrogen and phosphorus metabolism may be negatively affected by the cumulative effects of ocean warming and acidification