In today’s installment, Dr. Marie-Jose Messias
has kindly written a few words explaining the operation of the space-age
looking equipment used in the tracer container to detect the concentration of
dye in the seawater:
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Marie-Jose analysing tracer results |
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The inert molecule CF3SF5 |
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The tracer team - Neill, Ben, Dhruv, Steve, Marie_jose and Andy |
“Our mission is to better
understand how water from the Antarctic Circumpolar Current (ACC) invades the
rest of the world’s oceans. To do this, 80 kg of tracer (trifluoromethyl
sulphur pentafluoride, CF3SF5) were released into the
Pacific side of the ACC in 2009. Since then, we have been tracking its
dispersion vertically (diapycnal mixing) and horizontally (isopycnal mixing) by
collecting water at different depths along its path towards the Atlantic and
measuring its tracer content. Our measuring instrument (which we have named
Electric Barbarella 3000) is very sensitive, and able to detect a concentration
of 5 atomoles (10-18 moles/liter) or 0.5 micrograms of tracer within
a kilometre cube of seawater. It uses a method called ‘purge and trap analysis’
and is coupled to a gas chromatograph.
Everything is carried through the instrument by a flow of the ‘carrier
gas’, Nitrogen (N2). Water samples
flow through into a calibrated volume and then are transferred to a ‘sparge
tower’ under vacuum. The sparge tower is where the dissolved gasses (including
our tracer CF3SF5) present in the water are removed by
bubbles of nitrogen gas. Gases are carried from the water into a ‘trap’, which
is cooled to -110°C, causing the gases to condense and become trapped. We cool
the trap by immersing it in liquid nitrogen vapor. After 3 minutes of sparging,
the trap is lifted out of the liquid nitrogen
and heated to +110° C. This releases the trapped gases into the gas
chromatograph, where the tracer is separated
from the other gasses by going through a series of chromatographic columns. The
amount of tracer present is quantified by an electron capture detector (the
electrophile CF3SF5 ‘captures’ the electrons). Thus we
can tell how much tracer we have in each water sample! The
running time per sample is 9 minutes, giving us just enough time to
compile and check the results from the previous run, and to fetch the new
samples, and maybe make a quick cup of tea...
Next sample please!”
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