24.3 Limits to growth: the logistic differential equation

Before you read this, I suggest you read post 18.15. In post 22.17 we saw the effect of predators on the population of a species: the example I used was the natural control of a rabbit population by foxes. But, in post 16.5, we saw that a population will control itself, without the need for… Continue reading 24.3 Limits to growth: the logistic differential equation

24.2 Thermal vibration of an atom in a crystal: the temperature factor in x-ray crystallography

In post 23.4, we saw that the interpretation of x-ray diffraction patterns from crystals involves a temperature factor because atoms are displaced from their ideal lattice points by thermal vibrations. We have seen that heat is kinetic energy of atomic molecular motion (post 16.35). In a crystalline solid, the atoms must be oscillating about their… Continue reading 24.2 Thermal vibration of an atom in a crystal: the temperature factor in x-ray crystallography

23.10 Frequency analysis and x-ray crystallography

At the beginning of post 23.4, I described two routes to understanding x-ray crystallography. If you prefer the second, less mathematical, route – ignore this post! Before you read this, I suggest you read post 23.8. In post 22.14, we saw that the x-ray diffraction pattern of an object is given by the Fourier transform… Continue reading 23.10 Frequency analysis and x-ray crystallography

23.6 Mutation

Before you read this, I suggest you read post 21.8. In my previous posts (21.11, 21.14 and 21.23), it may appear that genes are constant sources of information that never change. This idea explains most of what we know about why individuals have a different genotype and, therefore, a different phenotype to their parents. But… Continue reading 23.6 Mutation