Hey, I have another question about evolution by natural selection. Please bear with me, as I'm really trying to understand this topic.
Natural selection:
Mutations occur randomly. Beneficial mutations occur at very low frequency. Beneficial mutations are only 'propagated' through the population when other animals (who don't have the mutation) die from selection pressures. i.e. we don't share genes like bacteria do, we actually have to come from those parents.
Let's take the example of monkeys-to-humans. I was reading this morning about long latency reflexes. When a muscle is stretched, monkeys respond by co-contracting agonist and antagonist muscles. Humans only contract their agonist muscles. These are reflexes, driven by very simple circuits of neurons (probably just 5) which are genetically coded, not learnt.
Other differences between monkeys and humans: size, upright walking, no hair, larger forebrain, speech, etc... These are in ALL humans and NO monkeys.
So, in the simple transition from monkey to human, do these mutations occur sequentially? e.g. a monkey mutates to have no hair, finds this advantageous, all other monkeys die, this monkey reproduces. Then one of his offspring mutates his long-latency reflexes, all other monkeys die, this monkey reproduces to fill the population... etc. This would suggest a series of evolutionary bottlenecks, which (in my vague impression) is not advantageous, and not the case.
Or, do the mutations occur in parallel? If so, how? Two (or more) beneficial mutations occuring in the same monkey is even unlikelier.
Please explain things using solid examples. No analogies please. I don't cope well with abstract thoughts. Details would be most useful.
Thanks
Natural selection:
Mutations occur randomly. Beneficial mutations occur at very low frequency. Beneficial mutations are only 'propagated' through the population when other animals (who don't have the mutation) die from selection pressures. i.e. we don't share genes like bacteria do, we actually have to come from those parents.
Let's take the example of monkeys-to-humans. I was reading this morning about long latency reflexes. When a muscle is stretched, monkeys respond by co-contracting agonist and antagonist muscles. Humans only contract their agonist muscles. These are reflexes, driven by very simple circuits of neurons (probably just 5) which are genetically coded, not learnt.
Other differences between monkeys and humans: size, upright walking, no hair, larger forebrain, speech, etc... These are in ALL humans and NO monkeys.
So, in the simple transition from monkey to human, do these mutations occur sequentially? e.g. a monkey mutates to have no hair, finds this advantageous, all other monkeys die, this monkey reproduces. Then one of his offspring mutates his long-latency reflexes, all other monkeys die, this monkey reproduces to fill the population... etc. This would suggest a series of evolutionary bottlenecks, which (in my vague impression) is not advantageous, and not the case.
Or, do the mutations occur in parallel? If so, how? Two (or more) beneficial mutations occuring in the same monkey is even unlikelier.
Please explain things using solid examples. No analogies please. I don't cope well with abstract thoughts. Details would be most useful.
Thanks
