Page 148 - Introduction to Paleobiology and The Fossil Record
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MACROEVOLUTION AND THE TREE OF LIFE 135
The vast numbers of DNA and RNA
sequences that are generated daily from the A B C B A C A B C
whole diversity of life are stored as letter
codes in open-access databases. Any investi-
gator may download the sequences of any (a)
particular gene or chromosome for as many
species as are available. There are then two A B C D A C B D A D B C C D A B
key processes in extracting a phylogenetic
tree from such data. First, the nucleic acid
sequences must be aligned, that is matched,
so that the code of a particular gene in one D C A B B D A C D B A C B C A D
species is lined up with the same sequence in
another species. Alignment can be diffi cult
because species do not differ only in the place- A D D A
ment of particular base pairs, but sometimes C B A D B C B C A C B D
gaps in the sequence are introduced, or whole
sections may be repeated. Once the sequences
of a number of species are satisfactorily C A B D A B C D B A C D
aligned, the phylogenetic analysis is carried
out. The base-pair codes are treated like the
presence/absence (1/0) codes in a morphologi- (b)
cal data matrix, and a variety of algorithms Figure 5.12 The number of unique trees for
are applied to extract the most likely tree that three (a) and four (b) taxa. These cladograms
explains the data. may be written more simply as (A(BC), (B(AC))
and ((AB)C) for the three-taxon cases, and
The tree of life ((AB)(CD)), ((AC)(BD)), ((AD)(BC)), etc. for the
four-taxon cases. Note that (A(BC)) and (A(CB))
Paleontologists and biologists are using mor- are identical trees, and both versions count as
phology and molecules to put together ever- one.
larger sectors of the tree of life. Desktop
computers are exploding in labs around the
world as analysts ask them to crank out ever- the information in all existing trees. Research-
larger trees. Bear in mind that the number of ers are currently using all methods and
n−2
possible trees is N = (2n − 3)!/(2 (n − 2)!). approaches to draw major sectors of the tree
So for three species, there are three possible of life, and such huge trees will allow paleon-
unique trees. For four species, there are 15 tologists and biologists to carry out many
possible trees (Fig. 5.12), for eight species novel studies of macroevolution.
168,210 possible trees, and for 50 species
about the same number as there are atoms in
the universe. You can do these calculations in Review questions
table 1.3.1 at http://www.talkorigins.org/faqs/ 1 Consider the four logical steps that sum-
comdesc/section1.html. marize natural selection (see p. 119), list
And yet 50 species is not a demanding examples for each of numbers 1–3, and
number. Systematists want to know the com- consider how the mechanism could be
plete tree for all 240 species of primates, all disproved.
4500 species of mammals (now available: 2 Read books and web sites that present
Bininda-Emonds et al. 2007), and so on. evidence for intelligent design (ID). List
Mathematicians tinker with the tree-fi nding some specific examples/case studies that
software so it finds clever ways to fi nd the are cited by ID supporters, and present
best-fitting tree quickly, even though many these in the form of falsifi able scientifi c
millions or billions of potential trees are con- hypotheses.
sidered and rejected. Another approach is to 3 Find 10 paleontological case studies on
link existing trees for parts of the group of speciation, by searching the internet with
interest to create a supertree that summarizes the key words “phyletic gradualism” and