Hi Green, in theory, if you reversed a male, and hit him with another males pollen, then half of them should be YYs. Taking one of them and reversing him (if that's even possible which I have no idea if it would be) and hitting him with another YY would give an all YY population. However selecting a YY male from a 50% XY population would involve some lab equipment to start with.
Although very rare an Androdiecious is possible from a herm is it not ? its just that for whatever reason you get a higher percentage of Gynodioecious lines from the herm, but I don't think its impossible,
I think I'm right to say fitness in Y degenerates quicker than that of X I read something about the use of YY in relation to sterile male plants, I do not know how that works, can only presume they reverse the sterile male and use a yy on it but i do not know about that..
Kopite
Kopite: I'm not sure about an androdiecious line through a hermie. The reason we get gynodiecious lines from hermies is because we're using an XX with intersex traits as a pollen donor. I'm not sure YY's occur in naturally, I have a suspicion you'd have to create it through hard work.
Hi Kopite, surely the ratchet theory is more feasible for the evolution of sexes.
Do you have any evidence for that? Are you saying you thought the plants an XXXY because it showed intersex traits without stress? If it had been stressed do you think it would be an XX with intersex genes? I don't think I'm following you.
And on the subject of an XXXY, how do imagine this stuff is inherited. Most agree you get one chromosome from the mom and the dad, that's why with only one Y chromosome on one of the parents you still get a half male population. So on the XXXY are you imagining the kids receiving three chromosomes from the mom? Do you have any links to the scientific literature, wouldn't hemp breeders know by now?
A model for the evolution of gynodioecy from the hermaphrodite or monoecious condition is described, taking into account the effects of partial selfing and inbreeding depression. It is shown that a mutant causing male-sterility can be selected even if the female plants have the same ovule output as the hermaphrodites, but that the conditions for this are very stringent: The product of the selfing rate and the inbreeding depression must exceed one-half. If the females have an increased ovule output, gynodioecy can evolve with lower values of the selfing and inbreeding depression parameters. Expressions for the equilibrium frequency of females and of the male-sterility gene in both the dominant and the recessive case are given. By a similar technique, conditions for the evolution of androdioecy are derived. In a selfing population, these conditions are much less easily satisfied than those for gynodioecy, though in a randomly mating population the conditions are similar: If ovule production is abolished, pollen production must be more than doubled, or vice versa. Since androdioecy is known to be a very rare condition, it seems likely that avoidance of selfing has played a role in the evolution of gynodioecy. Using the equilibria derived for gynodioecy, the conditions for the evolution of subdioecy or dioecy, by means of a partial or total female-sterility mutation, are studied. In contrast to the situation in a hermaphrodite population, a female-sterility gene can be selected in a gynodioecious population if it confers a moderate increase in pollen output; some increase in pollen output is essential. The fate of such a female-sterility gene also depends on its linkage with the male-sterility gene. If this is recessive, and the female-sterility gene is dominant and has an effect in the females as well as the hermaphrodite individuals, then the second mutation will usually be eliminated unless it occurs at a locus tightly linked to the first gene. In other cases there is no such "linkage constraint," though in all situations there may be selection for tighter linkage between the loci; this will result in an initially subdioecious population becoming more fully dioecious. These results agree with some of the facts known about the evolution of dioecy in plants. First, since gynodioecy is more often controlled by a recessive than a dominant gene, male heterogamety should be commoner than female, as is observed. Second, subdioecy should be common, since full dioecy requires not only the correct phenotypic effects of the two genes but also complementary dominance relations and tight linkage; subdioecy is indeed known in many species. The equilibria reached by our model have only one type of female in appreciable frequency, whereas the polleniferous individuals may fall into several genotypic classes; it is often observed that in subdioecious species the males are more variable than the females, regardless of which is the heterogametic sex. Finally, the equilibria generated by our model agree closely with the results of genetical studies of those dioecious species with male-determining Y chromosomes that have been investigated, in which both male-and female-sterility factors have been found, showing complementary dominance relations and no crossing-over between the loci, so that just two gamete types exist. Such a situation can be explained by the operation of the linkage constraint, which ensures that only linked mutations become established and does not require that unlinked genes have been brought together. This is consistent with the fact that dioecious species often have the same chromosome numbers as their bisexual relatives.
Nice reference Kopite, I cant find the full text yet, everyoneone who has it wants to charge for it so far, I'll keep looking, in the mean time I found this which seems fairly relevant.
http://www.nature.com/hdy/journal/v9.../6800697a.html
Hi GitT,
Say for instance you have a plant that looks female and has not been stressed but suddenly becomes a herm showing a few male flowers that you leave to self pollinate, then it wasn't a XX, but more likely XXXY etc, if you look at the early evolution of a dioecious species... note: the herm in the cases I've seen and heard of has come from a plant that has been a bisexual/herm plant and not mono... its how some people believe you get a dioecious line, I don't believe cannabis is true dioecious...
Kopite