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Today's post explores another possible use of synthetic sediment: to strengthen the reliability of data generated from samples of natural sediment.
Environmental Data
Environmental samples are collected and analyzed, and environmental professionals interpret that data to guide their decisions about how to manage and steward the environment. The analyses are done by chemists at environmental laboratories. Part of the chemists' job is to check that the instruments used to analyze samples are giving them reliable readings, and to report their "instrument reliability" findings to the client who submitted the samples. There are many types of instrument-checks, but one is to analyze a material (a
reference standard) that contains a precisely known amount of what they're measuring. Doing this isn't to find out what's in the reference standard; it's to "test" the instrument. By comparing the known amount of material in the reference standard to the reading given by the instrument, the chemists get a sense for how well the instrument is working (... how efficiently and accurately it is detecting the material they're measuring). This information is the only way the chemists know how much confidence they can put in the instrument's readings, and whether those readings truly and accurately reflect the actual composition of a field sample containing an unknown amount of material.
Natural Sediment is Alive
Natural sediment is an enormously complex mixture of components (living organisms and non-living material) and those components are actively changing all the time. Very few of those components are stable (almost all components in natural sediment change to some degree, over time). Because of this, natural sediment makes an extremely lousy laboratory reference standard. One interesting component of natural sediment is a material that contains sulfur. It's called acid-volatile sulfide (AVS, for short) because it becomes a gas (volatilizes) when it reacts with acid. AVS is one of those sediment components that constantly changes: it occurs in different amounts from location to location within a sediment bed, and the amount found at any one location changes at a over time (perhaps seasonally to some degree). It's created by the activity of micro-organisms in the sediment munching on organic material and "inhaling" dissolved sulfate ions (think, Epsom salts). The organisms "exhale" sulfide (think, rotten-egg odor), and this sulfide is very reactive and very different than the original sulfate. Sulfide quickly combines with many types of metals in the water to form a new chemical, one that doesn't dissolve in water very well (a precipitate). Sulfide is different from the original sulfate also in that sulfide does not tolerate being around dissolved oxygen. When it reacts with dissolved oxygen in the water, it reverts back to sulfate.. which is again available for those sulfate-"breathing" bacteria to use in their part of the cycle.
One of the most abundant metals in the earth's crust is iron (Fe). Its presence in natural sediment is not usually considered contamination. The natural metal iron (and also another natural metal, manganese; Mn) combines with sulfide to form a dark-brown or black precipitate which stays associated with the sediment (iron sulfide - FeS; manganese sulfide - MnS). In simplistic terms, chemicals like these constitute AVS in natural sediment.
Because of AVS's instability around dissolved oxygen, what happens in natural sediment is that the very thin surface layer of sediment along the sediment bed is in contact with so much dissolved oxygen that almost no FeS or MnS exists. There is a point within sediment where the migration of oxygen from the water above is just balanced by the biological activity of the sulfate-"breathing" bacteria living and growing in the deeper parts of the sediment. At this depth, and below, the sulfate is converted to sulfide faster than the oxygen from above can migrate down, and the AVS can persist without being oxidized.
This "boundary" depth (where the rate of at which sulfide is created (by bacteria) just balances the rate at which oxygen migrates down from the overlying water above) fluctuates wildly based on all sorts of factors and conditions. An important one is the temperature of the water, which dictates not only how much oxygen can dissolve in the water, but also the activity of the bacteria in the water. In cold temperatures (fall/winter), water can hold more dissolved oxygen and bacteria are lethargic: that combination favors a net loss of sulfide (more is oxidized than is produced = low AVS concentrations). During periods of warm temperature (spring/summer), the combination of lower dissolved oxygen in the water and high bacteria activity favors more production than oxidation (high AVS concentrations). So not only do AVS concentrations vary from season to season, but it also varies from place to place, depending on available organic material and dissolved sulfate and how easily dissolved oxygen can penetrate into the sediment.
So... how do chemists and environmental professionals ensure that their AVS instrumentation equipment is accurate if it's always changing?? They don't use a natural sediment sample containing AVS.. that's for sure. They rely on measurements of pure chemical FeS or MnS or other stable metal-sulfide compounds. That's not very realistic when you consider that the "real" samples being analyzed are soil/mud type materials, whereas the "reference" is a pure chemical scooped from a lab bottle. Wouldn't it be more relevant to measure AVS that's associated with a sediment sample?
Sediment Alternative for Reference Standard
In theory, synthetic sediment may be constructed to simulate the complexity of natural sediment, without all the complex changes. In other words, synthetic sediment could be prepared to represent a "snap-shot" in time of a sample of natural sediment. The materials in the synthetic sediment would be consistent in composition and stable through time. Such a material would make an excellent reference standard for sediment analysis. Also, such a synthetic sediment would simulate natural sediment more closely than just measuring a pure sample of the material being measured (which currently is the only way to "instrument-check" for some sediment components). The stability of synthetic sediment against uncontrolled changes like those experience by natural sediment is only part of the equation for a synthetic sediment reference standard. The other part is finding a chemical that acts like AVS in all aspects EXCEPT in its instability when exposed to oxygen. That's the focus of one part of my work: finding a metal sulfide that reacts with acid like natural sediment, but that does NOT oxidize in air or when in contact with dissolved oxygen unlike natural sediment.
Other Stuff.. if you're interested...
Why is reliable data important?
Making an accurate "diagnosis" of the sediment that was sampled depends on how reliable are the lab data. Here's why...
Reliability in the world of scientific data doesn't exactly mean "dependability" like one might think ("It's critical that you be there on time... I'm relying [depending] on you."). Reliability of data is closer in meaning to "confidence" in data. It's the way scientists address the question: "Can I trust this measurement?" Another way of asking this question is: "Does this measurement REALLY reflect what is actually going on in this sample?" I think these and other variations of this question are at the heart of science. We explore the universe by poking and prodding and measuring tiny parts of it, to see what it tells us about itself. If we want an accurate understanding of that part of the universe, the response we get from our poking and prodding needs to accurately reflect what is there. On a very basic level, imagine the consequences of reading the temperature of an oven with a broken (inaccurate; uncalibrated) thermometer. A reading of 70*F on that thermometer may mean the difference between a second degree burn or just a call to the appliance repair shop.
It's the same for scientific endeavors. A measurement of contamination level in soil from a lot that is slated to be converted into a playground needs to accurately reflect what really is there: the "reliability" of that measurement could be the difference between years of fun and laughter, or years of unexplainable skin rashes. In a less dramatic example, data from sediment in a river bottom could suggest possible hazard to the ecology of that river (based on the level of contamination present in the sediment), or the data could indicate a self-adjusting/self-attenuating river with no hazard to the ecology. The interpretation of the data depends heavily on the answer to the question: "How confident are we that those data are accurately reflecting actual conditions in the part of the environment we sampled?" A lot rides on the level of confidence in scientific data.
How do materials get buried under sediment?
Sediment under water bodies (streams, creeks, lakes, estuaries, bays, oceans) are collections of particles of various sizes and compositions. The same way late-season snow storms cover the remnants of earlier snow storms, sediment particles continually settle on the bottom, covering "older" sediment particles. The oxygen and other dissolved material in the water above the sediment surface can migrate into the pore-water between sediment particles. The sediment bed contains a whole host of components, both living and non-living. The living part includes bacteria and the non-living part includes organic material and dissolved salts that are food and "oxidants" for the bacteria. So the more particle material "rains" down onto the sediment surface, the deeper the sediment bed gets, the further away the deeper layers of sediment get from oxygen-rich water. These deep areas are devoid of oxygen and are called anoxic.