Uncommon Descent Serving The Intelligent Design Community

Homology and Homoplasy

Share
Facebook
Twitter
LinkedIn
Flipboard
Print
Email

In the response to a recent post a commenter asks what “homologous” means and whether similarity is the same as homology.  In this post I will give a brief (and hopefully plain language) overview of “homology” and the related concept of “homoplasy.”

More...

Here is the standard Neo-Darwinian explanation of homology and homoplasy: 

Suppose two organisms have a similar feature.  The features are “homologous” if they were inherited by the organisms from a similar feature in a common ancestor.  In other words, the features are homologous if they result from a shared genetic ancestry.  Bat wings and human arms are homologous because they are similar structures inherited from a shared mammalian ancestor.   

On the other hand, the features are not homologous, but “homoplasious” if they were not inherited by the organisms from a similar feature in a common ancestor.  In other words, the features are homoplasious if they did not result from a shared genetic ancestry.  Homoplasious structures evolved independently more than once in a process known as convergent evolution.  Bird wings and insect wings are homoplasious; they are similar and perform the same function, but they do not result from common genetic ancestry.  Homoplasious features are also called “analogous features.” 

The difficulty is determining whether similar structures are homologous or homoplasious, because similarity, does not necessarily imply common ancestry.  As Gavin De Beer points out: 

“Homologous structures need not be controlled by identical genes, and homology of phenotypes does not imply similarity of genotypes.”  Gavin De Beer, Homology, an Unsolved Problem (London: Oxford University Press, 1971), 16. 

Roger Lewin adds:  “The key issue is the ability correctly to infer a genetic relationship between two species on the basis of a similarity in appearance, at gross and detailed levels of anatomy.  Sometimes this approach . . . can be deceptive, partly because similarity does not necessarily imply an identical genetic heritage:  a shark (which is a fish) and a porpoise (which is a mammal) look similar.”  Roger Lewin, Bones of Contention: Controversies in the Search for Human Origins (New York: Simon and Schuster, 1987), 123. 

Scientists attempt to determine homology through “outgroup comparisons.”  An “outgroup” is a group of organisms (a taxon) that diverged from two other groups (taxa) before they diverged from one another.  In other words, two of the taxa are more closely related to each other than they are to the third group, because they share a common ancestor with each other that they do not share with the outgroup.  The more closely related groups are called the “ingroup.”  Outgroup organisms are thus near relatives of ingroup organisms but not part of the ingroup. 

Researchers use outgroup comparisons to determine the “polarity” (that is the direction) of evolution.  Because the ingroup branched off from the common ancestor after the outgroup, scientists can assume that any character the ingroup shares with the outgroup must have been inherited from the ingroup’s common ancestor.  In other words, a character state that is present in both the outgroup and the ingroup is ancestral, and a character state that is in the ingroup only is not ancestral but derived. 

Now the problem with using homology to show common ancestry is that it is quite circular.  Jonathan Wells points this out: 

“Many biology textbooks define homology as similarity due to common ancestry, yet claim that it is evidence for common ancestry.  For example, Starr and Taggart’s Biology: The Unity and Diversity of Life (8th Edition, 1998) states that the “pattern of macroevolution–that is, change from the form of a common ancestor–is called morphological divergence…. Homology [is] a similarity in one or more body parts in different organisms that share a common ancestor…. Homologous structures provide very strong evidence of morphological divergence.” (pp. 318-319)  In a section on “The Evidence for Evolution” in the teacher’s edition of Johnson’s Biology: Visualizing Life (1998), students are told that “homologous structures are structures that share a common ancestor,” and an accompanying note tells the teacher that “such structures point to a common ancestry.” (p. 178)  According to Campbell, Reece and Mitchell’s Biology (5th Edition, 1999), “similarity in characteristics resulting from common ancestry is known as homology, and such anatomical signs of evolution are called homologous structures. Comparative anatomy is consistent with all other evidence in testifying [to] evolution.” (p. 424) Raven and Johnson’s Biology (5th Edition, 1999), in a section titled “The evidence for macroevolution is extensive,” includes the following: “Homology: Many organisms exhibit organs that are similar in structure to those in a recent common ancestor. This is evidence of evolutionary relatedness.” A few pages later, the same textbook explicitly defines homologous structures as “structures with different appearances and functions that all derived from the same body part in a common ancestor.” (pp. 412, 416) Audesirk, Audesirk and Byers’s Life On Earth (2nd Edition, 2000) calls homology “evidence of relatedness” in a section titled “Comparative Anatomy Provides Structural Evidence of Evolution.” The textbook tells students: “Internally similar structures are called homologous structures, meaning that they have the same evolutionary origin despite possible differences in function. Studies of comparative anatomy have long been used to determine the relationships among organisms, on the grounds that the more similar the internal structures of two species, the more closely related the species must be, that is, the more recently they must have diverged from a common ancestor.” (p. 236)”

Comments
Barry A: In the response to a recent post a commenter asks what “homologous” means and whether similarity is the same as homology. It was the hobbit leaf that made me do it! But thank you for the post it demonstrates the subjective-ness/ specious argument of Nick Matzke's post on PT. As for the "poof" model- if that is what the data leads us to then so-be-it. IOW if it is demonstrated that the level of change required for any CD model is not capable via any method then what options are left?Joseph
September 7, 2006
September
09
Sep
7
07
2006
07:45 PM
7
07
45
PM
PDT
Reciprocating Bill, Tell me how any naturalistic explanation of evolution that tries to fit the data isn't also based on a "poof" model. Somehow each major taxon or novel body part or function magically appeared at some time in the distant past without an obvious predecessor. That what the whole argument is about, our "poof" models versus their "poof" models. Let the students decide which "poof" makes the most sense.jerry
September 7, 2006
September
09
Sep
7
07
2006
07:44 PM
7
07
44
PM
PDT
Reciprocating Bill, I’m curious. I have never expressed an opinion regarding common descent on this blog. Upon what evidence is your pronouncement in 3 based?BarryA
September 7, 2006
September
09
Sep
7
07
2006
07:30 PM
7
07
30
PM
PDT
"Show me where I am wrong." Okay again. The third option, and the one I have settled on as the best explanation, is front loading. The first life on earth was designed to diversify according to a plan and needed no assistance along the way. Consider a fertilized human egg cell. It is front loaded with all the information it needs to diversify into myriad cell types, tissue types, and organ types that compose a human being. Nothing is left to chance in this process formally called ontogenesis. I posit that phylogenesis is the same process on a different scale with nothing left to chance. This of course prompts the question of where the phylogenetic stem cell (my term for the common ancestor of all life on this planet) came from. Granted that's a hard question and it may not be answerable but it isn't the only such hard question. The question of where matter and energy came from (the origin of the observable universe) is even harder. Still we struggle to explain what we can even when the trail of evidence leads to a brick wall we cannot see through, over, or around.DaveScot
September 7, 2006
September
09
Sep
7
07
2006
07:24 PM
7
07
24
PM
PDT
See ISCID Encyclopedia http://www.iscid.org/encyclopedia/Sequelog Sequelog The term 'sequelog' denotes a nucleotide or amino acid sequence that is similar, to a specified extent, to another sequence. This term is strictly about sequential similarity and implies nothing about evolutionary relatedness and functional properties of sequences. Defined by Alexander Varshavsky See also: homolog, ortholog, paralog, pseudoortholog, pseudoparalog, spalog, xenolog ----------------- Spalog http://www.iscid.org/encyclopedia/Spalog The term 'spalog' (pronounced [spailog]) denotes a 3-D structure that is spatially similar, to a specified extent, to another 3-D structure. This term is strictly about spatial similarity and implies nothing about evolutionary relatedness and functional properties of structures. Defined by Alexander Varshavsky See also: homolog, ortholog, paralog, pseudoortholog, pseudoparalog, sequelog, xenolog Web Resources On Spalog The trouble with homology Orthologs, Paralogs and Evolutionary Genomics CV of Alexander VarshavskyDLH
September 7, 2006
September
09
Sep
7
07
2006
07:01 PM
7
07
01
PM
PDT
Mine was a serious comment. Your ID choices are descent with meddling, or repeated "poofs." Since BarryA would like to doubt descent, he is left with "poof." Show me where I am wrong.Reciprocating Bill
September 7, 2006
September
09
Sep
7
07
2006
06:49 PM
6
06
49
PM
PDT
Okay. POOF! You're now in the moderation sandbox.DaveScot
September 7, 2006
September
09
Sep
7
07
2006
06:33 PM
6
06
33
PM
PDT
Bring on the "Poof" model!Reciprocating Bill
September 7, 2006
September
09
Sep
7
07
2006
05:32 PM
5
05
32
PM
PDT
1 2

Leave a Reply