Download Using MacClade

Lab #2: Interpreting phylogenetic trees
Objectives:
1. To learn how to interpret phylogenetic trees
2. To compare different trees as alternative hypotheses
3. To interpret characters mapped onto trees as evolutionary hypotheses
I BACKGROUND MATERIAL
The evolutionary relationships among organisms are always going to be hypothetical:
scientists can never go back in time and actually observe the evolution of a group.
The formulation of an initial hypothesis about relationships among groups is the
process of making observations and constructing a phylogeny, which is a testable
hypothesis. This hypothesis can then be tested by the collection of additional data.
In this laboratory exercise, you will become familiar with some of the techniques
used by systematic biologists to develop hypotheses about the evolutionary history
of living things. We have developed several alternative hypotheses proposing the
evolutionary relationships among eighteen insect taxa in a program called MacClade.
You can use this program to explore the differences among these trees, and then
map phenotypic characteristics onto the trees. Using these mappings, you can
explore how different trees produce different evolutionary hypotheses for each
character.
A. THE CHALLENGE OF SYSTEMATICS AND REMOTE INFERENCE
(Sys·tem·at·ics n: the study of systems and classification, especially the science
of classifying organisms)
Both theoretical and practical problems make inferring evolutionary history (a
discipline known as systematics) one of the most challenging of the life science
disciplines. Like other disciplines in biology, systematics proceeds through the
experimental cycle, depending on the construction of hypotheses from observations
and the rejection or retention of these hypotheses based on new data. What
makes systematics unique is that while these hypotheses address events in the
past, often million of years ago, they are based on observations made today. This
process is known as remote inference, and you will be employing it in this lab. We
shall in all likelihood never see major new characteristics evolving over long periods
of time, so we must use observations of both extant organisms and fossils to
construct hypotheses concerning the origin of novel phenotypes. Often, within a
group of related organisms like the insects, phenotypes can be observed to fall into
what appear as logically linked steps: one type is apparently similar to another type.
These patterns of similarity can be used to formulate hypotheses that can then be
tested against trees of phylogenetic relatedness that are derived from
independent data sets.
B. TERMINOLOGY
Taxon n (plural: taxa): Any of the groups to which organisms are assigned
according to the principles of taxonomy, including species, genus, family, order,
class, phylum, etc.
Phylogenetic tree: A branching diagram in which the branching portrays the
hypothesized evolutionary relationships and the sequence of hypothetical ancestors
linking observed taxa.
Character: An observable aspect of the phenotype of an organism. A character
may be genetic (which DNA base is at a particular position in a particular gene
sequence), morphological (the shape of a bone or tooth), or behavioral (when
behavior is genetically determined, such as in mating behavior or song type).
Character state: Across taxa, the detailed structure of a character is likely to
vary (if it does not, the character is said to be uninformative). The actual
description of a character for a particular taxa is its character state. In
systematic analyses, character states are coded numerically, with zero (0) assigned
to the character state of the outgroup.
Character state matrix: A table of characters where the state of the character in
each taxon is coded numerically.
Ingroup: The group of organisms in an evolutionary study in which relationships are
determined based on the presence of shared characteristics and comparison to the
outgroup. There are usually numerous taxa within the ingroup.
Outgroup: The taxon least related to any other taxon in an evolutionary study, to
which members of the ingroup are compared. There may be one or multiple
outgroups in a study.
C. PHYLOGENETIC HYPOTHESES
Phylogenetic hypotheses are hypotheses about the evolutionary relationships among
taxa or among character states. They generally are expressed by biologists in the
form of networks (no “ancester” or root given) or trees (a hypothetical common
ancestor or root given). They describe the pattern of speciation that analysis of
the data indicate. Trees are built by counting the number of changes (steps from
one character state to another) that occur for each of the characters included in
the data set. The tree that requires the smallest number of steps over all the
characters is assumed to be the best hypothesis. This is a principal known as
parsimony, or Occams’ Razor. In science, the first choice hypothesis should be the
simplest.
It is common for complex groups like “insects” for there to be many alternative
trees that are equally parsimonious. Biologists then combine all parsimonious trees,
often resulting in a bush. The junctures with multiple branches are referred to as
polytomies.
In this lab, we will explore the use of hypothetical trees in testing hypotheses
concerning character evolution, by posing hypotheses about the evolution of a
character and then mapping the character onto a tree to test our hypothesis
(where a tree is an assumption about evolutionary relationships). Comparisons among
different trees will allow us to examine how our hypothesis fares with different
initial assumptions about relationships.
Using the Tree of Life
First, open FireFox (Mozilla) and choose the Tree of Life bookmark. It should go
directly to the insects. Note that on the Tree of Life, the “tree” for the insect
groups looks like a garden rake. What does this tell you about scientists’ current
understanding of the relationships among insects?
Browse the tree for the following groups that we will be working with, and think
about how they resemble each other. Pay particular attention to the presence and
number of wings, the descriptions of social behavior and feeding habits.
Hemipteroid groups -- cicadas and leaf-hoppers, aphids
Endopterygota groups -- lacewings (Neuroptera); June beetles (Coleoptera);
Trichoptera, Lepidoptera, paper wasp (Hymenoptera), houseflies (Diptera)
Embiidina (web spinners)
Zoraptera
Plecoptera (stone flies)
Orthoptera (crickets & grasshoppers)
Phasmida (walking sticks)
Isoptera (termites)
Mantodea (mantids)
Dermaptera (earwigs)
Collembola (springtails)
Using the MacClade
Open MacClade and choose “Phylogenetics lab”. If MacClade opens to show trees,
then under “windows”, choose “Data Editor”, and it will switch to show the data
matrix. Look at the list of insects, and familiarize yourself with the different
groups. Some of them should be very familiar (Lepidoptera), and likely some of
them are unknown to you. Take some time to look at the collections provided, and
to examine photographs on the Tree of Life webpage for insects.
In some groups, a particular member of the group has been chosen, while in others
there is no particular type. For example, for Lepidoptera, we are including all
members (moths, butterflies, skippers). In contrast, for Diptera (flies), houseflies
are specified. Under “Characters”, open two windows: Character List and State
Names & Symbols. Tab through the “State Names & Symbols” table until you reach
the character “adult mouthparts”. Note that for this trait, the character state will
depend upon which fly we choose as an example: the mouthparts on a housefly are
quite different from the mouthparts on a mosquito. There are two other groups
for which particular species have been chosen. Examine the character states
across all characters for these two groups and be sure you understand why in this
lab exercise we had to choose particular types for these groups.
Tab through the State Names and Symbols list again and become familiar with the
different states. What exactly does each description mean, and how is it related
to the biology of the organism?
Now we are ready to look at some trees. Under “Windows”, select Tree Window.
Your Characters and State Names & Symbols windows should stay open; if they
don’t, reopen them. The tree should be black; if it isn’t go to the “Trace” pull-down
menu and turn Trace off. A mini-window will also open inside the tree window. It
gives you the tree name and its length (the number of steps or changes in the
entire tree: shorter is more parsimonious).
In this window, you can scroll from tree to tree. Scroll until a tree named
“Polytomy” is displayed. This is the same tree (drawn differently) as the rake on
the Tree of Life web page.
Scroll through all the trees on the list. How are they different from one another?
Which tree is most parsimonious (shortest treelength)? Think about the organisms
listed, and consider whether the hypothesized relationships among them are
consistent with the general body shape that they have.
Return to the polytomy tree, and under the “Trace” pull-down menu, turn Trace on
by selecting Trace Character. A second mini-window will appear, which tells you
which character you are displaying the trace of. Scroll until you are displaying
“metamorphosis”.
The tree now displays an hypothesized pattern of evolution of the character
“metamorphosis”, the window lists the title of the character that is being displayed
and the number of evolutionary steps (changes from one state to another) that are
represented by that particular tree. Each character state has a color, and
“equivocal” is hatched. When a character state is “equivocal”, it means that in this
program, two or more character states are possible for that particular branch in
that particular tree. Are any branches “equivocal” for this character?
The tree mappings also present hypothetical ancestral states for a character: the
phenotype that a hypothetical ancestor would have. What is the ancestral state
for metamorphosis?
Scroll through the other characters. How do the ancestral states compare to the
character states for the outgroup? It should be clear that the polytomy is not
very informative for answering questions about the pattern of evolution of
characters. List all characters with the identified ancestral state for the polytomy
tree in Table 1 (write equivocal if there is no ancestral state):
Character
Ancestral State
(polytomy)
number
of steps
Ancestral State
(tree _____)
number
of steps
Return to the tracing of metamorphosis, and select another tree from the tree list.
Note in column 4 which tree number you have chosen.
Again, scroll through the different characters. Note any differences in ancestral
states in the above table. How does the increased resolution improve our
understanding of the evolution of these characters?
Character tracing:
Now that you are familiar with the function of the character tracing, you will test
hypotheses about character evolution. To illustrate how this is done, we will do one
character, social structure, together.
Social structure. It is commonly hypothesized that extended parental care is a
pre-condition for the evolution of complex social structure in animals. Therefore,
we would hypothesize that the pathway for the evolution of social behavior would
take the path:
none ––> extended parental care ––> extended families ––> social.
We can test this hypothesis by mapping social behavior onto a tree. In tree 1, the
ancestral state is “no social structure”. However, do the relationships among
groups with parental care, extended families, and sociality show the evolutionary
pattern we’ve hypothesized? How many steps are in this mapping?
Move through the different trees. Examine how the different tree structures
affect the hypothesis on the evolution of social structure. As tests of the above
hypothesis on the evolution of social structure, these trees range from complete
rejection to luke-warm support. Which tree supplies the best support for the
hypothesis?
It is very important to note that when testing hypotheses about the evolution of
characters, biologists ought not to choose among trees based upon the character
mapping. The tree is built using characters that are not the subject of current
study. Indeed, under the best circumstances, the characters used to build the tree
will have no obvious biological link to the characters being mapped. Commonly these
days, the characters used are gene sequences and protein structure.
Exercises:
I. Choose one character from the following list:
Wing folding
Silk spinning
Wings
Examine the character states for your chosen character, and if needed look at
either the insects on display or on the Tree of Life. Below, write an evolutionary
hypothesis concerning the pathway of change of these characters, noting the
original (ancestral) state and the transitions that seem logical to you.
Go to tree 1, then choose your character from the character list. Does this
mapping support or reject your hypothesis? Note that if key branches on the tree
are labeled “equivocal”, that tree is uninformative for your hypothesis.
Scroll through the fully resolved trees. Describe in Table 2 below how each tree
affects your evaluation of the hypothesized evolutionary pathway for the character
you’ve chosen:
Tree
number of steps
evaluation of hypothesis
II. Choose two characters from the following list, and repeat the exercise:
Adult mouthparts
food (adult)
food (larvae)
mating behavior
Character_______________
Tree
number of steps
evaluation of hypothesis
Character______________
Tree
number of steps
evaluation of hypothesis
Draw one of the trees below, and hand-map onto the tree the points of change for
each character you’ve chosen, as illustrated in lecture. Count the number of
changes, including reversals. Be sure you understand how the mapping is done, and
how this tree is identical to the tree produced by MacClade.