A new paper in The American Naturalist by Carl Rothfels and his colleagues (reference and free download below) shows that fern species that diverged in the very distant past can still form hybrids. That’s an interesting result, but I’m not sure about the authors’ conclusion that this revises our notion about how fast species can form in some groups, and I’m absolutely sure that the way creationists have distorted the paper’s findings is bogus. But let’s look first at the science.
The authors found a single fern in the French Pyrenees that looked as if it were intermediate in appearance between two distantly related genera of ferns, Cystopteris and Gymnocarpium. These genera were so diverged that they had been placed in different families. Suspecting that this individual (which was sterile) was indeed a hybrid between species in those long-diverged genera, they subjected it to DNA and chromosome analysis. (The hybrid individual was give the name “xCystocarpium roskanianum,” with the “x” denoting the likelihood that it resulted from a cross.)
Sequencing a single nuclear gene (gapCp “short”) in the parents, the hybrid, and many species in both putative hybrid genera, the authors wanted to see whether the hybrid had a mixture of genes from these putative parents, as we’d expect if the hybrid were indeed a hybrid. They also dated the branches of the tree using five genes that had been sequenced previously. The gene sequences were further used to construct a phylogeny, or evolutionary tree, of the two groups, so they could determine how long ago they diverged.
Finally, Rothfels et al. made meiotic chromosome squashes of the putative hybrid and of species in the parental genera, which showed how the chromosomes of the hybrid paired up during meiosis (the process of gamete formation). That could also show if the chromosomes of the putative hybrid appeared to be a mixture of chromosomes from the two parental groups, and if anything went wrong in the hybrids to make them sterile.
The results:
- The hybrid did indeed appear to have a mixture of alleles (gene forms) from the parental genera: it had four versions of the gapCp gene, two closely related to Cystopteris and the other two to Gymnocarpium. This verifies the putative hybrid as a genuine hybrid between genera. (The two Gymnocarpium alleles were themselves long diverged, indicating that one parental species was itself an “allotetraploid” produced by an ancient hybridization between two species within Gymnocarpium.) The similarity of these two gene sequences to that in a living species suggested that one parent was the cosmopolitan species G. dryopteris, which has 160 chromosomes. (Ferns have huge chromosome numbers!) The other parent was tentatively identified as a member of the European C. fragilis complex, which is a mixture of polyploids with chromosome numbers ranging from 168 to about 336 (it’s hard to count a lot of tiny chromosomes in a squashed three-dimensional cell).
- The chromosome analysis showed about 160 chromosomes in the hybrid, which is close to what one expects in a hybrid between these species (½ x 160 + ½ x 168 = 164). The exact number of chromosomes is hard to determine because of course chromosomes pair during meiosis (remember freshman biology?). Here’s a picture of prophase in the hybrid, when the chromosomes begin to pair up and are already themselves duplicated. Some of the chromosomes are paired, but others are not, which is expected if some pairing occurs between “homologous” chromosomes within one parental species’ genome but not between chromosomes from different genera.

Below you can see another picture of meiosis during metaphase, when the chromosomes move to the “metaphase plate” to divide into the daughter cells. You can see that some chromosomes are properly aligned here, but others are floating around in the cytoplasm. That means that there will be a willy-nilly division of chromosomes to each daughter cell that forms the haploid spore (fern reproduction is complicated; see here for more details). And the spore, which forms the ‘gametophyte’—the haploid plantlet that, producing sperm and eggs, produces a diploid plant—will not contain a full complement of genetic material. It’s as if a human male or female produced a sperm or egg that lacked several chromosomes: that individual would be sterile because any “zygote” that formed via fertilization would be inviable in the early stages. No fetus would be formed.

So although the hybrid fern was indeed a hybrid, and it was “viable,” because it grew into an adult plant, that plant was nevertheless sterile, and therefore a one-off anomaly that was not in itself a member of a new species. Further, because the two parental species were reproductively isolated, producing a viable but completely sterile hybrid, they are clearly members of different biological species and cannot exchange genes. .
- The calibrated molecular data show that two parental genera diverged roughly 58 million years ago (confidence interval between 40-76 million years). That is the oldest known divergence between any pair of species that can form hybrids. To show how long that is, whales and hippos diverged only 54 million years ago, and humans and lemurs about 74 million years ago. This observation is the equivalent, then, of getting a viable hybrid between hippos and whales, or between humans and lemurs! But there are a few cases of animals that are almost as long diverged producing hybrids. In our book Speciation, Allen Orr and I give the record for animals: a viable hybrid between the domestic chicken and the African helmeted guinea fowl, species that diverged abut 54 million years ago (the hybrid was anomalous, and there’s no record of its fertility). So it is possible for anciently diverged groups to form viable hybrids in animals, and possibly in flowering plants.
- Finally, by looking at the genetic divergence between forms of the gapCp gene in parental species and hybrids, we can judge how long ago the hybridization even took place. The genetic differences are very small, so the hybrid must have formed fairly recently. Even though it’s a single plant, it can propagate clonally through the growth of rhizomes, so it’s at least possible that the hybrid could have been around for a very long time. It wasn’t, though.
The authors hypothesize that ferns may be uniquely able to form viable hybrids in nature between long diverged species because of a feature of their reproductive system: sperm and eggs join simply through meeting in a film of water on the gametophyte, so there’s no need for the complicated forms of sexual behavior in animals, or the use of pollinators in many flowering plants. Those forms of fertilization raise the possibility of other forms of reproductive isolation that couldn’t evolve in ferns—for example, a difference in mating pheromones in animals or of pollinators in plants. This, say the authors, may slow down the rate of species formation in ferns because “genetic incompatibilities may form more slowly.” In other words, if some of the features that cause reproductive isolation in other species can’t evolve in ferns, then ferns may speciate more slowly.
The problem is that while the hybrid fern is viable, it’s also completely sterile, so there are at least enough incompatibilities (perhaps in chromosome number) to make the parents full biological species. Thus, we don’t yet have enough evidence to show that the process of species formation is slower in ferns than in other species. Perhaps the evolution of “prezygotic isolation” (reproductive barriers arising before fertilization, like ecological or sexual isolation) is slower in ferns than in other species, but we don’t yet know how much of a contributor such isolation is to speciation, and we certainly don’t have enough data to draw general conclusions about the rate of species formation from a single hybrid.
Nevertheless, the paper is a good one, documenting with high confidence the formation of a viable hybrid between anciently diverged species, and producing a Guinness-style record for ability to form viable hybrids. (It’s a pity that Guinness doesn’t confer records like this!)
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Over at the Baptist Press (the news site of the creationist Southern Baptist Convention), Discovery Institute hack Casey Luskin used this paper to argue that the ferns violate the theory of evolution. The article is called “New fern discovery a ‘problem’ for evolutionists,” Needless to say, there’s not a problem. The entire paper of Rothfels et al. fails to mention any problem with evolutionary theory. What they found, after all, was simply a surprising ability to form viable hybrids between long diverged species. But that doesn’t at all “fail to affirm the evolutionary paradigm,” as Luskin claims, for evolutionary theory says nothing about how long species can be separated and still form viable hybrids. And remember, these are still distinct parental species—the hybrids are viable but (to use a phrase from drosophilist Duane Jeffrey) are “as sterile as crowbars.”
Here’s another criticism by Luskin:
The researchers concluded the fern’s discovery implies the diversity of species that exists today may not be wholly accounted for by adaptation, but may also be the product of varied rates of the speciation clock, the rate at which a type of organism develops reproductive incompatibility with other related species.
This is completely false. The authors simply suggest that the “speciation” clock may run more slowly in ferns than in other species, though I suggest we need more data before concluding that. But even if it did, that wouldn’t constitute a violation of the “evolutionary paradigm”, since we expect some groups to speciate at different rates. Orr and I talk about this in our book. If speciation is, by and large, a byproduct of adaptation, and different groups adapt at different rates (again, completely expected), then of course different groups will form species at different rates. In the last chapter of Speciation, we deal with this exact issue, analyzing what selective forces may lead to different rates of speciation.
Nowhere do Rothfels et al. suggest that speciation may not be accounted for by adaptation. What they do suggest is that the adaptations of different groups (i.e., the reproductive system of ferns versus other taxa), may make them speciate at different rates. This may be a form of “species selection,” in which the diversity of groups, a higher-level property, depends on their lower-level properties. Orr and I discuss this issue in our last chapter, but it’s certainly no flaw in Darwinism, for it’s possible for natural selection to operate on different levels of the biological hierarchy.
Finally, Fazale Rana, a “biochemist” at Reasons to Believe (Hugh Ross’s old-earth creationist organization) says that the new paper “attests to creationism in two ways”:
- “First, ‘it represents a problem for evolutionists because it shows there are things being discovered that fail to affirm the evolutionary paradigm,’ Rana said. ‘You wouldn’t expect that hybridization to take place. It’s the work of a creator used to create a novel organism.'”
As I said, there is no a priori expectation on how fast hybridization can disappear over time, so it’s not a problem for evolutionists.
- “Second, a species that can adapt to the environment and give rise to a sister species demonstrates God’s design in giving living things the ability to respond to changes in the environment.”
We already have a way for species to respond to changes in the environment without the need for a god. It’s called “natural selection.” Rana appears mired in the pre-1859 era—the last time that rational people saw design as prima facie evidence for God.
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h/t: Bob F.