Development of a Frugal, In Situ Sensor Implementing a Ratiometric Method for Continuous Monitoring of Turbidity in Natural Waters.

Turbidity is a commonly used indicator of water quality in continental and marine waters and is mostly caused by suspended and colloidal particles such as organic and inorganic particles. Many methods are available for the measurement of turbidity, ranging from the Secchi disk to infrared light-based benchtop or in situ turbidimeters as well as acoustic methods. The operational methodologies of the large majority of turbidity instruments involve the physics of light scattering and absorption by suspended particles when light is passed through a sample. As such, in the case of in situ monitoring in water bodies, the measurement of turbidity is highly influenced by external light and biofouling. Our motivation for this project is to propose an open-source, low-cost in situ turbidity sensor with a suitable sensitivity and operating range to operate in low-to-medium-turbidity natural waters. This prototype device combines two angular photodetectors and two infrared light sources with different positions, resulting in two different types of light detection, namely nephelometric (i.e., scattering) and attenuation light, according to the ISO 7027 method. The mechanical design involves 3D-printed parts by stereolithography, which are compatible with commercially available waterproof enclosures, thus ensuring easy integration for future users. An effort was made to rely on mostly off-the-shelf electronic components to encourage replication of the system, with the use of a highly integrated photometric front-end commonly used in portable photoplethysmography systems. The sensor was tested in laboratory conditions against a commercial benchtop turbidimeter with Formazin standards. The monitoring results were analyzed, obtaining a linear trendline from 0 to 50 Nephelometric Turbidity Unit (NTU) and an accuracy of +/-0.4 NTU in the 0 to 10 NTU range with a response time of less than 100 ms.

On-site determination of polynuclear aromatic hydrocarbons in seawater by stir bar sorptive extraction (SBSE) and thermal desorption GC-MS.

The identification and quantification of semi-volatile contaminants dissolved in water is currently done in laboratory after a sampling step. This procedure is not satisfactory first because risks of samples contamination and analytes losses remain, in particular when these are present in ultra-trace concentrations, and secondly because procedures are time-consuming. The coupling of the stir bar sorptive extraction (SBSE), a new device of extraction technique, and a new generation of gas chromatography mass spectrometry (GC-MS), the field apparatus EM 640S from Bruker, could be an answer to the challenge of on-site analysis. This analytical system was used to analyze 24 PAHs, among them 15 EPA priority pollutants. It was shown that this coupling led to encouraging results with LODs around the sub-ppt level for most of the compounds and R.S.D. included between 1 and 48%. The existence of competition phenomena between the various analytes inside the absorbent phase was demonstrated with the release (up to 80%) of light compounds. This result shows the necessity to work on the kinetic domain rather than on the thermodynamic equilibrium that is influenced by nature and concentration of other compounds. The matrix effects were also studied through the comparative analysis of ultrapure water, artificial and natural seawaters spiked with PAHs and the influence of ionic strength and particulate organic matter was investigated.

An autonomous nutrient analyzer for oceanic long-term in situ biogeochemical monitoring.

An autonomous nutrient analyzer in situ (ANAIS) has been developed to monitor nitrate, silicate, and phosphate concentrations while deployed at sea at pressure (down to 1000 m). Detection is made by spectrophotometry. The instrument uses solenoid-driven diaphragm pumps to propel the sample, the standards, and the reagents through a microconduit, flow injection-style thermostated manifold. The analyzers are placed in an equipressure container filled with oil. The analyzers operate until a pressure of 100 bar and show a linear response up to 40 microM nitrate, 150 microM silicate, and 5 microM phosphate with a detection limit less than 0.1, 0.5, and 0.1 microM and an accuracy of 1, 1, and 3% for nitrate, silicate, and phosphate, respectively. The measurement protocol includes three steps over 13 min: rinsing with the sample stream, reagents introduction, and absorbance detection. Field tests comprise ANAIS nitrate, silicate, and phosphate testing alone in the surface ocean. Phosphate results are not yet fully satisfactory. The instrument implemented on top of a YOYO vertical eulerian profiler was then deployed successfully in the northwestern Mediterranean Sea acquiring 30 nitrate profiles between 200 and 1100 m over a 15-day period. This chemical analyzer can be a valuable observing asset adapted on any type of oceanographic platform.