bioe 109 summer 2009 lecture 13- part ii human evolution

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BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

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Page 1: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

BIOE 109Summer 2009

Lecture 13- Part IIHuman evolution

Page 2: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Human evolution  

• humans are classified within the superfamily Hominoidea (with gibbons, orangutans, gorillas and chimpanzees).

Page 3: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Human evolution  

• humans are classified within the superfamily Hominoidea (with gibbons, orangutans, gorillas and chimpanzees).

Page 4: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Human evolution  

• humans are classified within the superfamily Hominoidea (with gibbons, orangutans, gorillas and chimpanzees).

Page 5: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Similarity between human and chimpanzee genomes

Page 6: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Comparison of the human and chimpanzee genomes

  

Page 7: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Comparison of the human and chimpanzee genomes

  

• the genome of “Clint” was published September 1, 2005. 

Page 8: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Comparison of the human and chimpanzee genomes

  

• the genome of “Clint” was published September 1, 2005. 

• mean nucleotide divergence between humans and chimps was 1.06%. 

Page 9: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Comparison of the human and chimpanzee genomes

  

• the genome of “Clint” was published September 1, 2005. 

• mean nucleotide divergence between humans and chimps was 1.06%.  

• differ by 1 chromosomal fusion (human chromo. 2) and at least 9 pericentric inversions.  

Page 10: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

The evolution of human chromosome 2

Page 11: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Comparison of the human and chimpanzee genomes

  

• the genome of “Clint” was published September 1, 2005. 

• mean nucleotide divergence between humans and chimps was 1.06%.  

• differ by 1 chromosomal fusion (human chrom. 2) and at least 9 pericentric inversions.  

• 13,454 human and chimp genes with unambiguous homology were aligned. 

Page 12: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Comparison of the human and chimpanzee genomes

  

• the genome of “Clint” was published September 1, 2005. 

• mean nucleotide divergence between humans and chimps was 1.06%.  

• differ by 1 chromosomal fusion (human chrom. 2) and at least 9 pericentric inversions.  

• 13,454 human and chimp genes with unambiguous homology were aligned. 

• 29% of all proteins compared were identical!

Page 13: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

The primate fossil record 

Page 14: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

The primate fossil record 

• primates first appear in the late Cretaceous (about 70 MYA).

Page 15: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

The primate fossil record 

• primates first appear in the late Cretaceous (about 70 MYA).

• the first anthropoid ape fossil dates to Algeria (50 MYA).

Page 16: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

The primate fossil record 

• primates first appear in the late Cretaceous (about 70 MYA).

• the first anthropoid ape fossil dates to Algeria (50 MYA).

• small anthropoid apes found in Egypt (30 MYA) and Kenya (25 MYA).

Page 17: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

The primate fossil record 

• primates first appear in the late Cretaceous (about 70 MYA).

• the first anthropoid ape fossil dates to Algeria (50 MYA).

• small anthropoid apes found in Egypt (30 MYA) and Kenya (25 MYA).

• another gap to 15 MYA when several small hominids roaming N. Africa.

Page 18: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

The primate fossil record 

• primates first appear in the late Cretaceous (about 70 MYA).

• the first anthropoid ape fossil dates to Algeria (50 MYA).

• small anthropoid apes found in Egypt (30 MYA) and Kenya (25 MYA).

• another gap to 15 MYA when several small hominids roaming N. Africa.

• very few fossils from 6 to 14 MYA!

Page 19: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Evolution of Homo sapiens

These 3.6-million-year-old footprints from Laetoli, Tanzania were made

by a pair of individuals who walked side-by-side through fresh ash

from a volcanic eruption.

Page 20: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Time(MYA)

Evolution of Homo sapiens5

4

3

2

1

0

Ardipithecus ramidus (4.4 – 4.2 MYA) Australopithecus anamensis (4.2 – 3.9 MYA)

A. afarensis (“Lucy”, 3.9 – 3.0 MYA)

A. africanus (2.8 – 2.4 MYA)

Homo habilis (2.5 – 1.6 MYA)

H. ergaster (1.8 – 1.5 MYA)

H. erectus (1.2 – 0.4 MYA)

H. heidelbergensis (0.6 – 0.2 MYA)

H. sapiens (0.15 MYA)

Page 21: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Features of early hominid evolution   

Page 22: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Features of early hominid evolution   

1. Exact path of descent unknown

 

Page 23: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Features of early hominid evolution   

1. Exact path of descent unknown

• more hominid species continue to be discovered.

 

Page 24: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Features of early hominid evolution   

1. Exact path of descent unknown

• more hominid species continue to be discovered.

 

Page 25: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Features of early hominid evolution   

1. Exact path of descent unknown

• more hominid species continue to be discovered.

2. Evolution was continuous and gradual

 

Page 26: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Features of early hominid evolution   

1. Exact path of descent unknown

• more hominid species continue to be discovered.

2. Evolution was continuous and gradual

• no sudden “jumps” in size or cranial capacity observed.

 

Page 27: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Features of early hominid evolution   

1. Exact path of descent unknown

• more hominid species continue to be discovered.

2. Evolution was continuous and gradual

• no sudden “jumps” in size or cranial capacity observed.

• cranial capacity increased from 600-800 cm3 to 1200-1400 cm3 over past 2 MY. 

Page 28: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Gradual evolution of human cranial capacity

Page 29: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Features of early hominid evolution   

3. Many hominid species co-existed in Africa

 

Page 30: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Features of early hominid evolution   

3. Many hominid species co-existed in Africa

• notably the “robust” Australopithecines.  

Page 31: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Diversity of fossil hominid species in Africa

Page 32: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Neanderthals – not in my family tree!  

Page 33: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Neanderthals!  

• Homo sapiens neanderthalensis lived in western Europe 400,000 to 30,000 years ago.

Page 34: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Neanderthals!  

• Homo sapiens neanderthalensis lived in western Europe 400,000 to 30,000 years ago.

• average height was about 5’4’’ but weighed about 20 lbs more than H. sapiens sapiens (due to extra muscle). 

Page 35: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Neanderthals!  

• Homo sapiens neanderthalensis lived in western Europe 400,000 to 30,000 years ago.

• average height was about 5’4’’ but weighed about 20 lbs more than H. sapiens sapiens (due to extra muscle).

• in 1997, Neanderthal mtDNA was amplified and sequenced (360 bp). 

Page 36: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Neanderthals!  

• Homo sapiens neanderthalensis lived in western Europe 400,000 to 30,000 years ago.

• average height was about 5’4’’ but weighed about 20 lbs more than H. sapiens sapiens (due to extra muscle).

• in 1997, Neanderthal mtDNA was amplified and sequenced (360 bp).

• recently, 1 million bp of Neanderthal DNA has been sequenced (and the full genome is on the way…). 

Page 37: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Conclusions: 

Page 38: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Conclusions: 1. Neanderthals diverged from the modern human

lineage ~600,000 – 800,00 years ago.

Page 39: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Conclusions: 1. Neanderthals diverged from the modern human

lineage ~600,000 – 800,00 years ago.

2. Little evidence of any introgression of Neanderthal DNA into modern humans.

 

Page 40: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Conclusions: 1. Neanderthals diverged from the modern human

lineage ~600,000 – 800,00 years ago.

2. Little evidence of any introgression of Neanderthal DNA into modern humans.

 3. Effective population size ~3,000 (compared to

13,000 for early modern humans).

Page 41: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

…….. The last refuge

Page 42: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

The evolution of anatomically modern humans

Page 43: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

The evolution of anatomically modern humans

Page 44: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

The evolution of anatomically modern humans

Page 45: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Predictions of the African Replacement model

 

Page 46: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Predictions of the African Replacement model

 

1. Ancestral alleles should trace to Africa. 

Page 47: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Predictions of the African Replacement model

 

1. Ancestral alleles should trace to Africa. 2. Appearance of modern humans should be recent (< 200,000 years).

Page 48: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Predictions of the African Replacement model

 

1. Ancestral alleles should trace to Africa. 2. Appearance of modern humans should be recent (< 200,000 years).

3. Genetic diversity should be greatest in Africa.

Page 49: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Predictions of the African Replacement model

 

1. Ancestral alleles should trace to Africa. 2. Appearance of modern humans should be recent (< 200,000 years).

3. Genetic diversity should be greatest in Africa.

• all three predictions have been confirmed.

Page 50: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Predictions of the African Replacement model

 

1. Ancestral alleles should trace to Africa. 2. Appearance of modern humans should be recent (< 200,000 years).

3. Genetic diversity should be greatest in Africa.

• all three predictions have been confirmed.

•“mitochondrial Eve” and “Y-chromosome Adam” lived in Africa about 150,000 and 60,000 years ago, respectively!

Page 51: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Complete mtDNA genomes from 53 humans

Page 52: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Recent evidence refuting the African replacement hypothesis

Page 53: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Recent evidence refuting the African replacement hypothesis

• in 2005 Alan Templeton reconstructed the history of human populations by analyzing 25 gene trees.

Page 54: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Recent evidence refuting the African replacement hypothesis

• in 2005 Alan Templeton reconstructed the history of human populations by analyzing 25 gene trees.

• his analysis rejects the complete replacement hypothesis with a probability equal to 10-17!

Page 55: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Recent evidence refuting the African replacement hypothesis

• in 2005 Alan Templeton reconstructed the history of human populations by analyzing 25 gene trees.

• his analysis rejects the complete replacement hypothesis with a probability equal to 10-17!

• he detected three waves of migration out of Africa.

Page 56: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

“Out of Africa again and again”

Based on genetic markers

Page 57: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution
Page 58: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Conclusions

1. Evolution is the foundation of all biology!

Page 59: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Conclusions

1. Evolution is the foundation of all biology!

2. Evolution is relevant!

Page 60: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Conclusions

1. Evolution is the foundation of all biology!

2. Evolution is relevant!

• in health and medicine…

Page 61: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Conclusions

1. Evolution is the foundation of all biology!

2. Evolution is relevant!

• in health and medicine…

• in agriculture and natural resources…

Page 62: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Conclusions

1. Evolution is the foundation of all biology!

2. Evolution is relevant!

• in health and medicine…

• in agriculture and natural resources…

• in environmental and conservation issues…

Page 63: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Conclusions

1. Evolution is the foundation of all biology!

2. Evolution is relevant!

• in health and medicine…

• in agriculture and natural resources…

• in environmental and conservation issues…

• in understanding nature and humanity…

Page 64: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Conclusions

3. Natural selection rules!

Page 65: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Conclusions

3. Natural selection rules!

… but can’t do it all.

Page 66: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Conclusions

3. Natural selection rules!

… but can’t do it all.

• can’t simultaneously maximize all components of fitness…

Page 67: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Conclusions

3. Natural selection rules!

… but can’t do it all.

• can’t simultaneously maximize all components of fitness…

• can’t control neutral evolution…

Page 68: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Conclusions

3. Natural selection rules!

… but can’t do it all.

• can’t simultaneously maximize all components of fitness…

• can’t control neutral evolution…

• can’t direct adaptive evolution in small populations…

Page 69: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Conclusions

3. Natural selection rules!

… but can’t do it all.

• can’t simultaneously maximize all components of fitness…

• can’t control neutral evolution…

• can’t direct adaptive evolution in small populations…

• can’t stop aging and death…()

Page 70: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Objectives for the course  

  

Page 71: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Objectives for the course  

1. To foster an approach that may be called “evolutionary” or “population” thinking.   

Page 72: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Objectives for the course  

1. To foster an approach that may be called “evolutionary” or “population” thinking. 

• distinguishes between “proximate” and “ultimate” questions.  

 

Page 73: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Objectives for the course  

1. To foster an approach that may be called “evolutionary” or “population” thinking. 

• distinguishes between “proximate” and “ultimate” questions. • focuses on the importance of genetic variation in natural populations.  

Page 74: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Objectives for the course

2. To foster an understanding of organisms in the context of their evolutionary histories.

Page 75: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Objectives for the course

2. To foster an understanding of organisms in the context of their evolutionary histories.

• necessitates an expansion of perspective to include deep time scales.

Page 76: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Objectives for the course

2. To foster an understanding of organisms in the context of their evolutionary histories.

• necessitates an expansion of perspective to include deep time scales.

• most characters are “inherited” from ancestral species.

Page 77: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Objectives for the course

3. To realize the potential and limits of evolutionary change within species.

Page 78: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Objectives for the course

3. To realize the potential and limits of evolutionary change within species.

• evolution is a “tinkerer” not an engineer.

Page 79: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

Objectives for the course

3. To realize the potential and limits of evolutionary change within species.

• evolution is a “tinkerer” not an engineer.

4. To dispel any preconceived idea that evolution has any ultimate goal in mind.

Page 80: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

The final exam 

Page 81: BIOE 109 Summer 2009 Lecture 13- Part II Human evolution

The final exam

• Time: 6pm- 8pm (2 hours)• Cover lectures 8 (The adaptationist program) through 13 (Human evolution).

Part 1. Multiple choice. 20 questions, 2 points each, 40 points total.

Part 2. Distinctions. Answer 5 out of 6, 4 points each, 20 points total

Part 3. Short answers. 8-10 questions, 2-5 points each, 40 points total.

EXTRA Credit questions!!