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Evolutionary History of Biological Diversity AP Chapter 26

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Page 1: Evolutionary History of Biological Diversity AP Chapter 26

Evolutionary History of Biological Diversity

AP Chapter 26

Page 2: Evolutionary History of Biological Diversity AP Chapter 26

The Tree of Life

Page 3: Evolutionary History of Biological Diversity AP Chapter 26

Investigating the Tree of Life

• Phylogeny is the evolutionary history of a species or group of related species

• The discipline of systematics classifies organisms and determines their evolutionary relationships

• Systematists use fossil, molecular, and genetic data to infer evolutionary relationships

Page 4: Evolutionary History of Biological Diversity AP Chapter 26

• Taxonomy is the ordered division and naming of organisms

• In the 18th century, Carolus Linnaeus published a system of taxonomy based on resemblances

• Two key features of his system remain useful today: two-part names for species and hierarchical classification

Page 5: Evolutionary History of Biological Diversity AP Chapter 26

Binomial Nomenclature

• The two-part scientific name of a species is called a binomial: first genus, second species

• The first letter of the genus is capitalized, and the entire species name is italicized

• Both parts together name the species (not the specific epithet alone)

Page 6: Evolutionary History of Biological Diversity AP Chapter 26

Fig. 26-3Species:Pantherapardus

Genus: Panthera

Family: Felidae

Order: Carnivora

Class: Mammalia

Phylum: Chordata

Kingdom: Animalia

ArchaeaDomain: EukaryaBacteria

Page 7: Evolutionary History of Biological Diversity AP Chapter 26

Linking Classification and Phylogeny

• Systematists depict evolutionary relationships in branching phylogenetic trees

• Linnaean classification and phylogeny can differ from each other

Page 8: Evolutionary History of Biological Diversity AP Chapter 26

Fig. 26-4Species

Canislupus

Pantherapardus

Taxideataxus

Lutra lutra

Canislatrans

Order Family Genus

Carn

ivora

Felid

aeM

ustelid

aeC

anid

ae

Can

isL

utra

Taxid

eaP

anth

era

Page 9: Evolutionary History of Biological Diversity AP Chapter 26

• A phylogenetic tree represents a hypothesis about evolutionary relationships

• Each branch point represents the divergence of two species

• Sister taxa are groups that share an immediate common ancestor

• A polytomy is a branch from which more than two groups emerge

Page 10: Evolutionary History of Biological Diversity AP Chapter 26

Fig. 26-5

Sistertaxa

ANCESTRALLINEAGE

Taxon A

PolytomyCommon ancestor oftaxa A–F

Branch point(node)

Taxon B

Taxon C

Taxon D

Taxon E

Taxon F

Page 11: Evolutionary History of Biological Diversity AP Chapter 26

What We Can and Cannot Learn from Phylogenetic Trees

• Phylogenetic trees do show patterns of descent

• Phylogenetic trees do not indicate when species evolved or how much genetic change occurred in a lineage

Page 12: Evolutionary History of Biological Diversity AP Chapter 26

Applying Phylogenetics• Phylogeny provides important information

about similar characteristics in closely related species

• A phylogeny was used to identify the species of whale from which “whale meat” originated

• Phylogenies of anthrax bacteria helped researchers identify the source of a particular strain of anthrax

Page 13: Evolutionary History of Biological Diversity AP Chapter 26

Does hamburger meat have horse meat in it?

Page 14: Evolutionary History of Biological Diversity AP Chapter 26

• When constructing a phylogeny, systematists need to distinguish whether a similarity is the result of homology or analogy

• Homology is similarity due to shared ancestry

• Analogy is similarity in function due to convergent evolution

Page 15: Evolutionary History of Biological Diversity AP Chapter 26

Fig. 26-7

Homologies/Analogies?

Page 16: Evolutionary History of Biological Diversity AP Chapter 26

• Convergent evolution occurs when similar environmental pressures and natural selection produce similar (analogous) adaptations in organisms from different evolutionary lineages

Page 17: Evolutionary History of Biological Diversity AP Chapter 26

Being careful about homoplasies

Bird heats and mammal hearts are analogous because they evolved independently of each other (homoplasies). According to data, bird and mammals are in separate clades.

Page 18: Evolutionary History of Biological Diversity AP Chapter 26

• The same with bat and bird wings.They are homologous as forelimbs, but analogous as functional wings.

• Homology can be distinguished from analogy by comparing fossil evidence and the degree of complexity

Ancestors of bats could not fly!

Page 19: Evolutionary History of Biological Diversity AP Chapter 26

Evaluating Molecular Homologies

• Systematists use computer programs and mathematical tools when analyzing comparable DNA segments from different organisms

Page 20: Evolutionary History of Biological Diversity AP Chapter 26

• Organisms with similar morphologies or DNA sequences are likely to be more closely related than organisms with different structures or sequences

Page 21: Evolutionary History of Biological Diversity AP Chapter 26

Fig. 26-8

Deletion

Insertion

1

2

3

4

Page 22: Evolutionary History of Biological Diversity AP Chapter 26

ACGTGCACG

AGTGAGG

Determining Best Fit

ACGTGCACG

A GTG AGG

Page 23: Evolutionary History of Biological Diversity AP Chapter 26

Cladistics

• Cladistics groups organisms by common descent

• A clade is a group of species that includes an ancestral species and all its descendants

• Clades can be nested in larger clades, but not all groupings of organisms qualify as clades (need common ancestor)

Page 24: Evolutionary History of Biological Diversity AP Chapter 26

• A valid clade is monophyletic, signifying that it consists of the ancestor species and all its descendants

• A paraphyletic grouping consists of an ancestral species and some, but not all, of the descendants

• A polyphyletic grouping consists of various species that lack a common ancestor

Page 25: Evolutionary History of Biological Diversity AP Chapter 26

Fig. 26-10

A A A

BBB

C C C

DDD

E E E

FFF

G G G

Group IIIGroup II

Group I

(a) Monophyletic group (clade) (b) Paraphyletic group (c) Polyphyletic group

A valid clade is monophyletic, signifying that it consists of the ancestor species and all its descendants

A paraphyletic grouping consists of an ancestral species and some, but not all, of descendants

A polyphyletic grouping consists of various species that lack a common ancestor

Page 26: Evolutionary History of Biological Diversity AP Chapter 26

The yellow group (sauropsids) is monophyletic, the blue group (traditional reptiles) is

paraphyletic, and the red group (warm-blooded animals) is polyphyletic

Page 27: Evolutionary History of Biological Diversity AP Chapter 26

• Cladograms are constructed by grouping organisms together based on their shared derived characteristics.

http://highered.mcgraw-hill.com/sites/9834092339/student_view0/chapter23/animation_-_phylogenetic_trees.html

Page 28: Evolutionary History of Biological Diversity AP Chapter 26

• A shared ancestral (or primitive) character is a character that originated in an ancestor of the taxon

• A shared derived character is an evolutionary novelty unique to a particular clade

• A character can be both ancestral and derived, depending on the context

Page 29: Evolutionary History of Biological Diversity AP Chapter 26

A cladogram showing derived characters

Page 30: Evolutionary History of Biological Diversity AP Chapter 26
Page 31: Evolutionary History of Biological Diversity AP Chapter 26

Plesiomorphies and apomorphiesanother fancy way of talking about primitve and

derived characters

• A plesiomorphy is an "ancestral", "less specialized", or "primitive" character.

• An apomorphy is a "derived", "specialized", or "advanced" character. Every taxon possesses a

• mixture of plesiomorphies and apomorphies.

Page 32: Evolutionary History of Biological Diversity AP Chapter 26

• An outgroup is a species or group of species that is closely related to the ingroup, the various species being studied but does not claim immediate common ancestry.

• Used to differentiate between shared derived and shared ancestral characteristics

Page 33: Evolutionary History of Biological Diversity AP Chapter 26

Fig. 26-11

TAXA

Lan

cele

t(o

utg

rou

p)

Lam

pre

y

Sal

aman

der

Leo

par

d

Tu

rtle

Tu

na

Vertebral column(backbone)

Hinged jaws

Four walking legs

Amniotic (shelled) egg

CH

AR

AC

TE

RS

Hair

(a) Character table

Hair

Hinged jaws

Vertebralcolumn

Four walking legs

Amniotic egg

(b) Phylogenetic tree

Salamander

Leopard

Turtle

Lamprey

Tuna

Lancelet(outgroup)

0

0 0

0

0

0

0 0

0

0

0 0

0 0 0 1

11

111

1

11

1

1

11

11

Page 34: Evolutionary History of Biological Diversity AP Chapter 26

Venn diagramscan be constructed tomake a cladogram.

Page 35: Evolutionary History of Biological Diversity AP Chapter 26

http://www.bu.edu/gk12/eric/cladogram.pdf

Our example

Page 36: Evolutionary History of Biological Diversity AP Chapter 26
Page 37: Evolutionary History of Biological Diversity AP Chapter 26

Phylogenetic Trees with Proportional Branch Lengths

• In some trees, the length of a branch can reflect the number of genetic changes that have taken place in a particular DNA sequence in that lineage

• But no actual numbers are given

Page 38: Evolutionary History of Biological Diversity AP Chapter 26

Fig. 26-12

Drosophila

Lancelet

Zebrafish

Frog

Human

Chicken

Mouse

The branch lengths are proportional to the amount of genetic change.

Page 39: Evolutionary History of Biological Diversity AP Chapter 26

• In some trees, branch length can represent chronological time, and branching points can be determined from the fossil record

• The shorter branches are between taxa, the more related they are, particularly in molecular data.

Page 40: Evolutionary History of Biological Diversity AP Chapter 26

Fig. 26-13

Drosophila

Lancelet

Zebrafish

Frog

Human

Chicken

Mouse

CENOZOIC

Present65.5

MESOZOIC

251

Millions of years ago

PALEOZOIC

542

Page 41: Evolutionary History of Biological Diversity AP Chapter 26

How do systemists deal with a lot of data to make a tree?

They narrow possibilities by applying the principles of maximum parsimony and maximum likelihood

- Fewest evolutionary events

- fewer derived characters overall

- Most likely sequence of events based on DNA analysis – more

similar DNA sequences more likely related

Page 42: Evolutionary History of Biological Diversity AP Chapter 26

Fig. 26-15-1

Species I

Three phylogenetic hypotheses:

Species II Species III

I

II

III

I

III

IIIII

III

Page 43: Evolutionary History of Biological Diversity AP Chapter 26

Fig. 26-15-4

Species I

Site

Species II

Species III

I

II

III

I

III

IIIII

III

Ancestralsequence

1/C1/C

1/C

1/C

1/C

4321

C

C C

C

T

T

T

T

T

T A

AA

A G

G

I I

I

II

II

II

III

III

III3/A

3/A

3/A3/A

3/A

2/T2/T

2/T 2/T

2/T4/C

4/C

4/C

4/C

4/C

I I

I

II

II

II

III

III

III

7 events7 events6 events

The best one isthe first onedue to less changes.

Page 44: Evolutionary History of Biological Diversity AP Chapter 26

Computer programs are used to search for trees that are parsimonious and likely.

Page 45: Evolutionary History of Biological Diversity AP Chapter 26

Occam's razor (also written as Ockham's razor from William of Ockham (c. 1287 – 1347), is a principle of parsimony, economy, or succinctness used in problem-solving. It states that among competing hypotheses, the hypothesis with the fewest assumptions should be selected.

Page 46: Evolutionary History of Biological Diversity AP Chapter 26

Fig. 26-UN5

Page 47: Evolutionary History of Biological Diversity AP Chapter 26

Fig. 26-UN10

Answer to questionIn book.

Page 48: Evolutionary History of Biological Diversity AP Chapter 26

Phylogenetic Trees are Hypotheses

• The best hypotheses for phylogenetic trees fit the most data: morphological, molecular, and fossil

• Time is implied, not explicitly stated unless coordinated with a time line.

Page 49: Evolutionary History of Biological Diversity AP Chapter 26

A cladogram with time attached

Page 50: Evolutionary History of Biological Diversity AP Chapter 26

An organism’s evolutionary history is documented in its genome

• Comparing nucleic acids or other molecules to infer relatedness is a valuable tool for tracing organisms’ evolutionary history

Page 51: Evolutionary History of Biological Diversity AP Chapter 26

Gene Duplications and Gene Families

• Gene duplication provides more opportunities for evolutionary changes

• Orthologous genes are found in a single copy in the genome and can diverge only after speciation occurs

• Paralogous genes result from gene duplication, so are found in more than one copy in the genome and can diverge within the clade that carries them and often evolve new functions

Page 52: Evolutionary History of Biological Diversity AP Chapter 26

Fig. 26-18

(b) Paralogous genes

(a) Orthologous genes

Ancestral gene

Paralogous genes

Ancestral species

Speciation withdivergence of gene

Gene duplication and divergence

Species A after many generations

Species A Species B

Species A

Orthologous genes

Page 53: Evolutionary History of Biological Diversity AP Chapter 26

Molecular clocks help track evolutionary time

• A molecular clock uses constant rates of mutation in some genes to estimate the absolute time of evolutionary change.• They are calibrated against branches whose dates are known from the fossil record.

Page 54: Evolutionary History of Biological Diversity AP Chapter 26

What genes are used?

• DNA that codes for rRNA changes relatively slowly and is useful for investigating branching points hundreds of millions of years ago

• mtDNA evolves rapidly and can be used to explore recent evolutionary events

Page 55: Evolutionary History of Biological Diversity AP Chapter 26

Neutral Theory

• Neutral theory states that much evolutionary change in genes and proteins has no effect on fitness and therefore is not influenced by Darwinian selection

• It states that the rate of molecular change in these genes and proteins should be regular like a clock

Page 56: Evolutionary History of Biological Diversity AP Chapter 26

Fig. 26-19

Divergence time (millions of years)

Nu

mb

er o

f m

uta

tio

ns

120

90

90

60

60

30

300

0

The green dots are primates species whose proteins appear to have evolved more slowly than those of other mammals.

A molecular clock for mammals based on protein mutations.

Estimate the divergence time for aMammal with a total of 30 mutations?

Page 57: Evolutionary History of Biological Diversity AP Chapter 26

Difficulties with Molecular Clocks

• The molecular clock does not run as smoothly as neutral theory predicts

• Irregularities result from natural selection in which some DNA changes are favored over others

• Estimates of evolutionary divergences older than the fossil record have a high degree of uncertainty

• The use of multiple genes may improve estimates

Page 58: Evolutionary History of Biological Diversity AP Chapter 26

New information continues to revise our understanding of

the tree of life

• Recently, we have gained insight into the very deepest branches of the tree of life through molecular systematics

Page 59: Evolutionary History of Biological Diversity AP Chapter 26

From Two Kingdoms to Three Domains

• Early taxonomists (Linnaeus) classified all species as either plants or animals

• Later, five kingdoms were recognized: Monera (prokaryotes), Protista, Plantae, Fungi, and Animalia

• In the late 70’s, the kingdom Monera was split into the eubacteria and the archaebacteria.

Page 60: Evolutionary History of Biological Diversity AP Chapter 26
Page 61: Evolutionary History of Biological Diversity AP Chapter 26

• More recently, the the three-domain system has been adopted: Bacteria, Archaea, and Eukarya

Page 62: Evolutionary History of Biological Diversity AP Chapter 26

Fig. 26-21

Fungi

EUKARYA

Trypanosomes

Green algaeLand plants

Red algae

ForamsCiliates

Dinoflagellates

Diatoms

Animals

AmoebasCellular slime molds

Leishmania

Euglena

Green nonsulfur bacteria

Thermophiles

Halophiles

Methanobacterium

Sulfolobus

ARCHAEA

COMMONANCESTOR

OF ALLLIFE

BACTERIA

(Plastids, includingchloroplasts)

Greensulfur bacteria

(Mitochondrion)

Cyanobacteria

ChlamydiaSpirochetes

Red lines aremulticellular.

First toemerge.

Page 63: Evolutionary History of Biological Diversity AP Chapter 26

The origins of life and the three domains are difficult to classify due to horizontal gene transfer.

Page 64: Evolutionary History of Biological Diversity AP Chapter 26

Classification is a work in progress?

Page 65: Evolutionary History of Biological Diversity AP Chapter 26

A Simple Tree of All Life

• The tree of life suggests that eukaryotes and archaea are more closely related to each other than to bacteria

• The tree of life is based largely on rRNA genes, as these have evolved slowly

Page 66: Evolutionary History of Biological Diversity AP Chapter 26

• There have been substantial interchanges of genes between organisms in different domains

• Horizontal gene transfer is the movement of genes from one genome to another

• Horizontal gene transfer complicates efforts to build a tree of life

Page 67: Evolutionary History of Biological Diversity AP Chapter 26

Fig. 26-23

ArchaeaBacteria

Eukarya

A ring oflife. Thedomains emerged fromthe ring.

Page 68: Evolutionary History of Biological Diversity AP Chapter 26

• If endosymbiosis occurred, eukaryotes are simultaneously most closely related to bacteria AND archae.

Page 69: Evolutionary History of Biological Diversity AP Chapter 26
Page 70: Evolutionary History of Biological Diversity AP Chapter 26