Originally posted by scilosopher
Most epigenetics says nothing about acquired characters being passed on.
Originally posted by spookz
gee
i decided to skim a bit and....Alternatively, there is the hypothesis that denies that these charactersitics have to evolve gradually from which derives the 'hopeful monster' theory and which is addressed by some 'evo-devo' researchers. (dr paul)
Originally posted by copper
I don't disagree. But you can't say that post-reproductive organsims are as important to the population as those that can reproduce. Your example didn't really address this. I can't think of an example where a non- or post-reproductive organism is as important to the evolution of the population as one that can pass on its genes.
Originally posted by scilosopher
While the idea of epigenetic inhereitance might be dusty what is understood about it is quite new and cutting edge.
Beak of the Finch is an excellent book. The Grant's work on the Galapagos finches is less a study than a life-long work. I'm not sure I would use the term 'quickly' for the changing beak sizes, but there were measurable differences between generations in beak size, within a population, before and after a drought. There is no question that these differences are the result of evolution by natural selection.Originally posted by 2inquisitive
paulsamuel, I am not very informed about evolutionary theories, but
what is your take on "Beak of the Finch," the book that won the
1995 Pulitzer Prize by Jonathan Weiner? I have not read the book,
but saw a documentary on TV about Rosemary and Peter Grant's
work a few years ago. I'm sure you are aware of their study of the
quickly changing beak sizes of Darwin's finches to reflect the changing
food supply. Does that represent evolution and natural selection
or something else?
http://www.2think.org/tbotf.shtml
I'm not familiar with the work, but I will follow up. It's interesting to see these heat-shock proteins popping up in all kinds of evolutionary studies. I worked on MHC genes for my dissertation and there could be analogous evolutionary forces at work. Since the breadth of evolutionary responses to environmental changes increase with the amount of variation present, this is probably important work (forgive my understatement).Originally posted by scilosopher
canute, I don't think anyone considers Darwin an expert on mutation. He was pretty much in the dark as to the basis for the generation of diversity ...
paulsamuel, what do you think about the CH Waddington hypothesis about selection for sets of alleles that alter biological function. The current incarnation of the idea is demonstrated in the Rutherford and Lindquist paper on hsp90:
http://www.ncbi.nlm.nih.gov/entrez/...ve&db=PubMed&list_uids=12101404&dopt=Abstract
The mechanism they suggest involves both cryptic variation and the possibility for selecting sets of alleles rather than single alleles. The basic idea is that hsp90 a chaperone (meaning it helps avoid misfolded proteins) masks certain allelic variants that bias a pathway towards a different behaviour. If you have multiple variants that encourage this behavior hsp90 can no longer mask the effect (possibly because the alleles are in a protein complex and mutually stabilize eachother). Therefore a population can harbor many mutations that alone have no effect and through sex rapidly generate the set that gives the improved phenotype.
I guess as a molecular biologist I feel uncomfortable speaking about things so abstractly that one looses site of mechanism and such ...
I do recall a study in bacteria where replication repair mechanisms are detered or blocked under induced stress conditions, if I'm not mistaken. Also, isn't there some evidence of directed mutation in ADh genes in molluscs, IIRC?Originally posted by scilosopher
Fair enough. That more mutations happen under stressfull conditions (ie. when things aren't working out so well), is not that diffidult to imagine as a simple reduction in available energy (as during hunger) could clearly encourage mutation as mutation repair requires energy.
However I do not read any of the nuances you put forward into the passage above. Still you've given rise to the first mechanistic hypothesis as to why mutation may be higher at certain times and it has a natural correlation to when you'd want them. Though in multicellular organisms it isn't clear the timing would work out right (hungry mom has baby with more mutations than normal sounds like it would cause problems as much as evolution).
this is not an example of Lamarkian inheritence. There are 2 mechanisms that can explain the loss of characters under these circumstances, selection and drift. Please don't misunderstand me. I am not dismissing the inheritence of acquired characterisitics (I'm discontinuing my use of the term 'Lamarkism' because that is not what he was about). Steele has presented some supporting evidence that is controversial, but still scientific in the Kuhnian sense (see Lamark's Signature, 1998 Perseus Books).Originally posted by spookz
quite possible!
blind cave fish
the mexican tetra fish lives in both caves/underground pools and streams/ponds. the former are blind and without pigmentation. eye development starts the usual way..rudimentary lens and optic cup. within 24 hrs however the cells die, cornea/iris does not develop. eyeball sinks and is covered by skin.
now it is known that shit atrophies without use. how is tho that the tetra passes on this degradation to its offspring.
dont plants do this kinda stuff all the time? if they do, how and why are we so special?
(pdf link p15)
there is more...butterfly wing morphology(p17) and geomyoid rodents (p19)
thoughts on this? on evo devo as a whole?
thanks
I don't get the referenced paper from this link, if you could give me the real ref. i.e. journal, date, vol., pg., i'd appreciate it. TIAOriginally posted by scilosopher
paulsamuel, what do you think about the CH Waddington hypothesis about selection for sets of alleles that alter biological function. The current incarnation of the idea is demonstrated in the Rutherford and Lindquist paper on hsp90:
http://www.ncbi.nlm.nih.gov/entrez/...ve&db=PubMed&list_uids=12101404&dopt=Abstract