Organic chemistry is the study of materials that contain carbon atoms
Carbon atoms for the basis for all life on Earth. By building molecules out of carbon, hydrogen, oxygen, nitrogen, sulphur, phosphorous and an array of other elements, we can create and regulate our bodies. Organic compounds range from simple methane gas (CH4) up to very long and complex molecules used to protect our cells from toxic environments. Organic chemists work to identify these molecules, learn where they come from an how they are made, discover their function within the cell and investigate their effects on organisms and the environment.
Organic geochemists look at organic molecules within sediments and the rock record. They can use them to identify the source of organic material, looking to see whether carbon present in a sample came from soils, vegetation, marine algae or a range of other sources. Organic molecules can also be used to investigate the decomposition of material, looking to see how it changes over time, to identify the biological processes that were happening in ancient fossils, to identify the source and economic potential of hydrocarbon deposits, and many more applications.
Permafrost is soil or sediment that is permanently below zero °C
When most people talk about permafrost, they think of frozen, empty soil with very little living on it, in it or near it. They think of a harsh, icy environment with glaciers, blizzards and possibly a few reindeer roaming around. But permafrost is much more varied than this. It does not necessarily have a covering of ice, but can be a thin layer of grass or peat with frozen soil underneath it, there can even be forests growing on the surface with frozen soil underneath them. There can be animals living on it, and bacteria living within the sediment. In fact, the permafrost might not even be on land! Here are just a little information about permafrost and what it contains.
Permafrost soils, which are frozen so solid so you need a pneumatic drill to sample them, cover a quarter of the northern hemisphere land area, and can be up to 1500 m thick. They store more carbon than there is in the entire atmosphere. The very top layer will thaw each summer and freeze each winter, which allows plants to grow and animals to graze, but the lower parts remain frozen all the time. In the southern parts, there can be trees growing on top of the permafrost, this is known as the ‘taiga’. When it is too cold, and the growing season is too short, only grass, moss, shrubs and lichen can survive, this is the ‘tundra’.
Another example of permafrost is frozen methane-ice trapped on the seabed. Subsea permafrost is often ignored, but these icy crystals of frozen, flammable gas and water contain a large amount of trapped carbon, are prone to melting and gas release, and have been blamed for one of the most extreme climate events in geological history.
The last type of permafrost to be discussed here is ‘yedoma’. This is a feature of the very furthest reaches of the Arctic, and is formed by windblown dust freezing together to form a layer of dirty ice and sediment. These thick ice layers are often found on the Arctic coast, where they have no defences against the incoming waves from the Arctic Ocean and are eroded easily. As the Arctic warms, the sea ice that usually protects the coastline from the force of the waves is reduced to nothing, allowing the full power of the sea to erode into the shoreline
Liquid Chromatography is the separation of molecules from a mixture using a liquid carrier medium.
An organic geochemist will often have the problem of having a test tube containing a large amount of different molecules, but only being interested in one or two of them. Much like a child might place felt tip pen and water onto some filter paper to watch the colours run and separate out (with some very artistic results), with liquid chromatography (LC) we split our mixture of molecules up into its individual components so that they can then be analysed. An LC, sometimes known as HPLC where (HP means High Performance or High Pressure), consists of three main parts: the autosampler, the pump, and the column, labelled in the picture below:
The autosampler collects a syringe full of sample from a vial and injects it at the right time onto the column. You can do this job yourself if you have good timing, are very accurate, and have an exceptionally high boredom threshold; the autosampler allows you to queue up a large amount of samples ready to run while you are away from the machine.
The pumps mix two solvents together and push them through the column. Each chemical in your mixture will behave differently when exposed to each solvent, it will be more soluble in one than the other, and will be differently soluble to the other chemicals in the mixture. Often one of the solvents will be polar (have an electrical charge associated with it, e.g., isopropanol alcohol) and the other will be non-polar (be electrically neutral, e.g., hexane). During the sample run, the amount of each solvent being washed through the column will change, and therefore different chemicals will wash through at different times.
The column is a metal tube filled with small solid particles. These are slightly ‘sticky’ to the molecules passing by (they adsorb onto the particle surfaces) and so the chemicals in the samples are not washed through the column that quickly. The solvents that are being used in the experiment remove the molecules from the column particles and move them through the system, until they reach the end of the column and can be detected. At the end of a sample run, the flow on the column is reversed and anything that did not make it through to the end is cleaned out (the ‘backflush’)
The initial observation for this work was that ‘great’ earthquakes, those which measured more than magnitude 8.0, tend to have end points in the same place. An earthquake end point is the limit to the earthquake fault plane movement, shaking will take place outside of this zone but it is most violent in the regions above the fault plate movement. The figure below shows the rupture zones and end points for great South American earthquakes.
An initial inspection of the plate margin (where the incoming Pacific Plate is subducted underneath the South American Plate) suggested that when there are underwater mountains on the Pacific Plate coming into the subduction zone (black blobs on the figure above), these tend to match up with the end points of earthquakes. The figure below shows how topographic features (underwater mountains and ridges) match up with earthquake locations.
To test whether this was a real relationship, or just coincidence, I designed a model that produced earthquakes along the subduction zone. The model had two versions. In version one, earthquakes were placed in line along the subduction zone (as tends to happen in these situations, one earthquake starts at the end point of a previous one) but their end points were not constrained by anything. In the second version, if the earthquake tried to rupture past an incoming topographic feature, the rupture was stopped there.
By applying statistical tests to the model, I showed that the endpoints of earthquakes were far more likely than random chance to be located where topography > 1000m was being subducted. The model also showed that subducting topography led to a reduction in background earthquakes. At earthquake endpoints not associated with topography, there was an increased amount of smaller earthquakes releasing the built-up stress, but this was not seen at earthquake endpoints near to subducting topography. Therefore, subduction of a high seamount or ridge makes the subduction zone earthquake activity decrease (it becomes ‘aseismic’) which prevents both great earthquakes getting past, and smaller earthquakes from occurring.