Chris S. wrote:It's easy to understand the benefit to an organism that can reproduce both sexually and asexually. Sexual reproduction rolls the genetic dice, giving an organism a chance to have novel and helpful attributes for natural selection to favor (and also, novel and unhelpful attributes that natural selection will cull). Asexual reproduction gives that organism--if it survives--the best chance for spreading its genes. So an organism that has both sexual and asexual modes of reproduction would seem to have the best of both worlds.
But the species documented here would appear to rely on cloning alone, with greatly curtailed benefit of natural selection. So, upon reading your post, my immediate thought was a question: "How does this species evolve to keep up with its enemies?" After a bit of reading, I surmise that it does not evolve, but is a highly successful (perhaps temporarily so), asexually-reproducing variant of a sexually reproducing species. And in the long term, likely to find itself evolutionarily unsuccessful, when its enemies evolve while it does not.
Can someone more competent than I on the evolutionary biology of parthenogenetic insects confirm or correct my thinking?
I probably don't have that level of competence, but my take on the situation agrees with yours.
You'll probably be interested in the "Bionomics of Bagworms" paper that I linked in my previous post. As noted in the abstract, "The unusual mating behavior of bagworms, characterized by ... a high proportion of females that do not mate as adults, challenges conventional wisdom regarding the evolution of mating systems."
The snippet that I quoted earlier is followed by one more sentence that is particularly relevant to the issue you raise. I've added it here in boldface.
Although rare in Lepidoptera, parthenogenesis has evolved independently in many genera of the Psychidae (46, 61, 65, 72). Studies on the genetics of Dahlica triquetrella Hübner reveal the existence of sexual and parthenogenetic (diploid and tetraploid) races whose distributions closely match recent geological history and biotic changes (97, 98 ). Facultative parthenogenesis has not been demonstrated for any sexual species.
One way of making some sense of this situation is that some unknown feature of the bagworm genome makes it particularly prone to falling into the trap of using parthenogenesis as the
only means of reproduction. That route is very effective for a while, and then it becomes just another dead end. (In fairness, most other routes turn out to be dead ends also.)
For this particular bagworm,
Apterona helix, there's another aspect of its ecology that I find quite curious and have no idea how to explain.
As background, I note that it seems this critter will eat almost anything. The list of host plants given by
https://pubs.wsu.edu/ItemDetail.aspx?ProductID=13611 includes these:
alfalfa, almond, apple, baby’s breath (Gypsophila), bean, broccoli, cabbage, clover, Douglas-fir, knapweed, marigold, mustard, oat, pea, pear, plantain, ponderosa pine, quackgrass, radish, raspberry, rhubarb, rose, squash, tomato, turnip, vetch, violet
That list is obviously incomplete, since it does not include the strawberries that mine are eating.
http://ento.psu.edu/extension/factsheet ... se-bagworm gives a more general summary: "It has an extensive host range, which includes most vegetables, ornamentals, legumes, fruit and other trees, and many species of annual herbs."
Further, the beast lives in an apparently impregnable bag, is parthenogenetic so that only a single individual is needed to start an infestation, and is a European import so that local parasites and disease won't be adapted to it.
You would think, taking all this together, that this thing would be the invader from Hades. But it's not. Despite having occupied my yard for around a decade that I've been noticing, the population has never gotten large enough to be a problem. Barely noticeable, really.
Obviously something is keeping the beast well controlled. I have no idea what that is.
--Rik