>>So I looked it up, and the russian study used mitochondrial DNA, not nuclear DNA. Nuclear DNA is found in the nucleus of the snake's cells, whereas mitochondrial DNA is found in the mitochondria of their cells.>>
That is correct. mtDNA is also matrilineal, that means all snakes, regardless of female or male, inherited their mtDNA from their mother. Any mtDNA mutation occurring in a male will not be passed on to future generations.
>>I do know that mitochondrial DNA is often used for these studies because it is believed that you can determine how long ago different philogenetic paths diverged based on the similarity of their mitochondrial DNA.>>
mtDNA is not the only molecule that can be used for molecular clocks. Basically any molecule which undergoes neutral mutations through time can be used for such purposes. Serum albumin, a protein found in blood, was used to determine how long ago organisms last shared ancestors by the late Allan Wilson and his students at UC Berkeley beginning way back in the 1970's. Non-neutral mutations often change much less frequently. Sometimes changes to important molecules (such as chlorophyll) are so detrimental to an organism that these molecules change very little over vast expanses of time.
>>Mitochondria are more or less bacterial in nature, so their DNA changes much more rapidly than that of eukaryotes.>>
The rate a molecule changes and the rate the changes are passed on to the next generation depend a great deal on whether the molecule is adaptive and on whether the changes are neutral or not.
>>Due to that fact, mitochondrial DNA can be used to determine how long ago two populations became isolated.>>
Many other molecules can also be used. The molecular clock is not calibrated only with mtDNA. As I pointed out earlier, serum albumin can also be used. The mtDNA data of Utiger et al. can indeed be used to determine how long ago the ratsnakes diverged from one another. That fact alone does not tell us whether any species or groups of species of ratsnakes have evolved evolutionary novelties. For example, mtDNA does not tell us that Lampropeltis has evolved smooth skin and it does not tell us that Pituophis has evolved a vocal cord.
New taxa, such as a new genus, can only be justified by the appearance of new features, at least that is the way it works traditionally according to the Darwinians. Traditional or Darwinian taxonomists do not, for example, put the corn snake and the fox snake into different genera arbitrarily. Snakes of the genus Lampropeltis, OTOH, has been placed by Darwinian taxonomists in their own genus because of the morphological features that they have evolved which make them different from the genus Elaphe. Utiger et al. divided up the genus Elaphe and resurrected about a dozen names from the synonymy of Elaphe without demonstrating or explaining how these genera differ from each other morphologically. Utiger et al. are not Darwinian taxonomists. They are a new school called the cladists. Cladists differ from Darwinians in some very important ways philosophically. Cladists pay no attention to morphological disparity when classifying organisms. Cladists are also intolerant of paraphyletic taxa, whereas Darwinians accept paraphyletic taxa as the same as monophyletic taxa.
Utiger et al. therefore split up Elaphe without regard to any morphological disparity which may or may not exist. If there is no difference morphologically between, say, "Pantherophis" and Elaphe, then it does not bother the cladists or Utiger et al. The flip side of the coin is that they will also lump morphologically disparate species into the same genus. A good example is the proposal to lump Pituophis and New World Elaphe (or 'Pantherophis') into the same genus. The only thing Utiger et al., Burbrink and Lawson, and cladists in general care about is whether a taxon is paraphyletic or polyphyletic. Like the Darwinians, the cladists do not tolerate polyphyletic taxa. Unlike the Darwinians, cladists also do not tolerate paraphyletic taxa.
Just what exactly is paraphyletic taxa and why do the Darwinians tolerate it but the cladists don't? Paraphyletic taxa are taxa that consist of the descendants of a single recent common ancestor, but not all of the descendants. The term recent is important because all life on earth ultimately share a single common ancestor, and therefore any group of species can be called monophyletic. Paraphyletic taxa are therefore not polyphyletic, since polyphyletic groups are comprised of descendants of more than one recent common ancestor. Darwinians consider paraphyletic taxa monophyletic. Darwinians tolerate paraphyletic taxa because they realize that a useful classification can only be achieved if morphologically disparate species are removed from a taxon and placed in a taxon of its own, leaving the parental group paraphyletic. The cladists, OTOH, are following the leads of Willi Hennig, the German scientist who tells his followers that taxa should only consist of one ancestor and all of its descendant species.
If we follow Hennig's lead, then traditional taxa such as Reptilia would be invalid because it is paraphyletic. Indeed the Hennigians redefined Reptilia to include the birds, but to exclude the mammals, the extinct reptilian ancestors of mammals (called the synapsids and therapsids) and also the first organisms that laid amniotic eggs from the Reptilia. The cladists' "Reptilia" is therefore more heterogeneous than traditional Reptilia, and most biologists and lay people alike have ignored the cladists and continue to use Reptilia the traditional way.
So, we now know where the cladists are coming from philosophically. It is the intolerance of paraphyletic taxa which prompted Utiger et al. to split up Elaphe into a dozen or so morphologically indistinguishable genera. It is also the intolerance of paraphyletic taxa which motivated Burbrink and Lawson to propose lumping Pituophis and "Pantherophis" into the same genus. Both the scientific community and the general public should be informed of the motives of the cladists. Both the scientific community and the general public should reject the irrational intolerance of paraphyletic taxa that is unique to cladistic philosophy. The proposed merging of the genus Pituophis with the New World Elaphe should be rejected. The resurrection of the genus "Pantherophis" should also be rejected. There is precedence for such rejection, and the rejection of the cladistic redefinition of Reptilia is such a precedence. Both the scientific community and the general public do not accept the cladists' "Reptilia" (which regards birds as 'reptiles') and both should reject the more recent taxonomic proposals by the cladists on similar grounds.
Perhaps it may be a good idea to figure out if a future taxonomic proposal is made on the basis of the cladists' irrational intolerance of paraphyletic taxa. Simply ask the authors of a proposed taxonomic change whether they include the birds in Reptilia. If they are cladists, and if they are intolerant of paraphyletic taxa, then they would say that birds are reptiles. If they are not cladists but Darwinians, then their answer is that birds are not part of Reptilia. There is no good reason to include birds in Reptilia, and there is no good reason to lump Elaphe ('Pantherophis') with Pituophis. Following cladistic thinking blindly is not a good reason.