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In some cases, a service may implement a fat method that actually implements multiple processes against multiple abstractions. For instance, a service method that creates an order, creates an associated line item, and reserves inventory. In this case, the method itself must be repartitioned into separate methods, which then may need to be reassigned to appropriate services, such as Order Service or Inventory Service. Many variations on the same basic method result in a lot of very similar looking methods, sometimes referred to as the Swiss Army Knife approach. When this is repeated for all the processes that the service supports, there could be many service interface methods to support just a few basic processes. Having all these variations can be confusing and prone to incorrect use. It is better to compact these into just a few, clear methods. If someone is unsure about the requirements to be implemented, they may throw a lot of extra functionality, methods, and variations, just to cover themselves. This is defensive programming and will result in services that do a lot more than they need to, relative to the actual requirements. The real solution is to get more detailed requirements, validation from users, and business-level prioritization from stakeholders.





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of this oxidised hydroquinone is reduced. From the magnitude of these current peaks, the concentration of hydroquinone can be deduced, and furthermore the hydroquinone peaks can be distinguished from those associated with other species, provided they occur at other potentials. The electron transfer kinetics are represented by the peak separation between the oxidative and reductive peaks. If the kinetics are fast, the two peaks are almost coincident, a peak separation of down to 57 mV being observed. As the kinetics get slower, so the peak separation rises as a greater electrical driving force ( overpotential ) is needed. The voltammetric data therefore provides the basic scienti c characterisation of the electrochemical system, which underpins the production of an electrochemical sensor relating to that system. Hence cyclic voltammetry is very commonly used for the early assessment of electrochemical properties for electroanalytical applications. In practical applications, greater sensitivity can be achieved if pulsed potential waveforms are employed, which has given rise to the existence of several alternative voltammetric methods, closely related to the cyclic voltammetry approach described above. Further details can be obtained from standard texts dealing with so-called dynamic (i.e. electrochemical measurement during current ow) electrochemistry such as Ref. [1].

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