| Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
| 1
|
List of common misconceptions
|
126,642
|
4,221
|
List
|
Low
|
| 2
|
Neanderthal
|
123,136
|
4,104
|
GA
|
Mid
|
| 3
|
Charles Darwin
|
103,772
|
3,459
|
FA
|
Top
|
| 4
|
Eugenics
|
83,935
|
2,797
|
B
|
Mid
|
| 5
|
Human evolution
|
71,559
|
2,385
|
C
|
High
|
| 6
|
Sexual dimorphism
|
68,486
|
2,282
|
B
|
High
|
| 7
|
Cretaceous–Paleogene extinction event
|
60,995
|
2,033
|
FA
|
High
|
| 8
|
Species
|
57,913
|
1,930
|
GA
|
Top
|
| 9
|
Richard Dawkins
|
56,390
|
1,879
|
GA
|
Mid
|
| 10
|
Evolution
|
50,210
|
1,673
|
FA
|
Top
|
| 11
|
Racism
|
44,114
|
1,470
|
B
|
Mid
|
| 12
|
Abiogenesis
|
43,558
|
1,451
|
GA
|
Top
|
| 13
|
Scopes trial
|
41,845
|
1,394
|
B
|
High
|
| 14
|
Scientific racism
|
41,466
|
1,382
|
C
|
Low
|
| 15
|
Extinction
|
40,366
|
1,345
|
C
|
High
|
| 16
|
Early modern human
|
38,776
|
1,292
|
B
|
Mid
|
| 17
|
Parthenogenesis
|
37,889
|
1,262
|
C
|
High
|
| 18
|
Cro-Magnon
|
37,748
|
1,258
|
GA
|
Mid
|
| 19
|
Last universal common ancestor
|
34,734
|
1,157
|
GA
|
Top
|
| 20
|
Binomial nomenclature
|
32,909
|
1,096
|
C
|
Low
|
| 21
|
Carcinisation
|
31,815
|
1,060
|
Start
|
Mid
|
| 22
|
Inbreeding
|
31,170
|
1,039
|
C
|
High
|
| 23
|
Timeline of human evolution
|
30,986
|
1,032
|
C
|
Low
|
| 24
|
William Jennings Bryan
|
30,704
|
1,023
|
B
|
High
|
| 25
|
Epicanthic fold
|
30,235
|
1,007
|
C
|
Low
|
| 26
|
Fossil
|
29,950
|
998
|
B
|
Mid
|
| 27
|
Cousin
|
28,592
|
953
|
Start
|
Low
|
| 28
|
Hybrid (biology)
|
27,706
|
923
|
GA
|
High
|
| 29
|
Paleontology
|
26,713
|
890
|
GA
|
Top
|
| 30
|
Homo floresiensis
|
25,282
|
842
|
B
|
Mid
|
| 31
|
Patrilineality
|
24,585
|
819
|
Start
|
Low
|
| 32
|
Clade
|
24,180
|
806
|
C
|
High
|
| 33
|
On the Origin of Species
|
24,164
|
805
|
FA
|
Top
|
| 34
|
Biodiversity
|
23,999
|
799
|
C
|
Mid
|
| 35
|
Domestication of the dog
|
23,975
|
799
|
B
|
Low
|
| 36
|
List of X-Men members
|
23,973
|
799
|
List
|
Low
|
| 37
|
Natural selection
|
23,968
|
798
|
GA
|
Top
|
| 38
|
Great Oxidation Event
|
22,699
|
756
|
B
|
Mid
|
| 39
|
Population bottleneck
|
22,291
|
743
|
C
|
High
|
| 40
|
Eusociality
|
21,489
|
716
|
GA
|
Mid
|
| 41
|
Neontology
|
21,334
|
711
|
Start
|
Mid
|
| 42
|
Convergent evolution
|
21,307
|
710
|
GA
|
High
|
| 43
|
Genetics
|
20,459
|
681
|
FA
|
Top
|
| 44
|
Altruism
|
20,437
|
681
|
B
|
High
|
| 45
|
Homo longi
|
20,431
|
681
|
GA
|
Low
|
| 46
|
Ecology
|
20,421
|
680
|
GA
|
Top
|
| 47
|
The Naked Woman
|
20,314
|
677
|
Stub
|
Low
|
| 48
|
Mutation
|
20,192
|
673
|
B
|
Top
|
| 49
|
Racism in the United States
|
20,029
|
667
|
B
|
High
|
| 50
|
Social Darwinism
|
19,808
|
660
|
B
|
Low
|
| 51
|
Anus
|
19,525
|
650
|
Start
|
Mid
|
| 52
|
HeLa
|
19,375
|
645
|
C
|
Low
|
| 53
|
Cambrian explosion
|
19,220
|
640
|
B
|
High
|
| 54
|
Sociality
|
18,220
|
607
|
C
|
Mid
|
| 55
|
Origin of language
|
18,131
|
604
|
B
|
Low
|
| 56
|
Fear
|
17,777
|
592
|
B
|
Low
|
| 57
|
History of eugenics
|
17,735
|
591
|
B
|
Low
|
| 58
|
Lamarckism
|
17,571
|
585
|
GA
|
High
|
| 59
|
Island gigantism
|
17,534
|
584
|
C
|
Low
|
| 60
|
Darwinism
|
17,483
|
582
|
C
|
High
|
| 61
|
Wallace Line
|
17,293
|
576
|
Start
|
Mid
|
| 62
|
Living fossil
|
17,123
|
570
|
C
|
Mid
|
| 63
|
Aposematism
|
16,779
|
559
|
GA
|
Mid
|
| 64
|
Karyotype
|
16,527
|
550
|
C
|
Low
|
| 65
|
Upper Paleolithic
|
16,163
|
538
|
C
|
Low
|
| 66
|
Domestication of the cat
|
15,759
|
525
|
C
|
Mid
|
| 67
|
History of life
|
15,496
|
516
|
GA
|
Top
|
| 68
|
Australopithecine
|
15,464
|
515
|
C
|
High
|
| 69
|
Alfred Russel Wallace
|
15,387
|
512
|
FA
|
Top
|
| 70
|
Francis Galton
|
15,117
|
503
|
B
|
Low
|
| 71
|
Stephen Jay Gould
|
15,038
|
501
|
GA
|
Mid
|
| 72
|
Herbert Spencer
|
15,022
|
500
|
B
|
Low
|
| 73
|
Bipedalism
|
14,861
|
495
|
B
|
Mid
|
| 74
|
Extant taxon
|
14,756
|
491
|
NA
|
NA
|
| 75
|
Camouflage
|
14,659
|
488
|
GA
|
Mid
|
| 76
|
Matrilineality
|
14,456
|
481
|
C
|
Low
|
| 77
|
Tiktaalik
|
14,417
|
480
|
GA
|
High
|
| 78
|
Pan (genus)
|
14,330
|
477
|
B
|
High
|
| 79
|
Antimicrobial resistance
|
14,190
|
473
|
B
|
Unknown
|
| 80
|
Humanoid
|
13,968
|
465
|
Start
|
Mid
|
| 81
|
Origin of SARS-CoV-2
|
13,834
|
461
|
B
|
Mid
|
| 82
|
Homology (biology)
|
13,385
|
446
|
GA
|
Top
|
| 83
|
Evolutionary psychology
|
13,196
|
439
|
C
|
High
|
| 84
|
E. O. Wilson
|
13,020
|
434
|
B
|
Mid
|
| 85
|
Sex differences in intelligence
|
12,907
|
430
|
B
|
Low
|
| 86
|
Stromatolite
|
12,879
|
429
|
B
|
Mid
|
| 87
|
Chicken or the egg
|
12,861
|
428
|
C
|
Low
|
| 88
|
Lower Paleolithic
|
12,847
|
428
|
C
|
High
|
| 89
|
The Selfish Gene
|
12,720
|
424
|
B
|
High
|
| 90
|
Heritability of IQ
|
12,692
|
423
|
C
|
Mid
|
| 91
|
Evolution of mammals
|
12,575
|
419
|
B
|
High
|
| 92
|
Panthera hybrid
|
12,490
|
416
|
C
|
Low
|
| 93
|
Human taxonomy
|
12,291
|
409
|
C
|
Low
|
| 94
|
Eugenics in the United States
|
12,284
|
409
|
Start
|
Low
|
| 95
|
Sexual selection
|
11,930
|
397
|
GA
|
High
|
| 96
|
Ediacaran biota
|
11,908
|
396
|
FA
|
Low
|
| 97
|
Peking Man
|
11,887
|
396
|
GA
|
Mid
|
| 98
|
Behavioral modernity
|
11,861
|
395
|
C
|
Low
|
| 99
|
Nordicism
|
11,809
|
393
|
B
|
Low
|
| 100
|
Earliest known life forms
|
11,749
|
391
|
C
|
Top
|
| 101
|
Thomas Henry Huxley
|
11,740
|
391
|
B
|
Mid
|
| 102
|
Most recent common ancestor
|
11,675
|
389
|
B
|
High
|
| 103
|
Timeline of the evolutionary history of life
|
11,523
|
384
|
B
|
Top
|
| 104
|
Mimicry
|
11,445
|
381
|
GA
|
High
|
| 105
|
Haplogroup
|
11,431
|
381
|
C
|
Mid
|
| 106
|
Ronald Fisher
|
11,163
|
372
|
B
|
High
|
| 107
|
Stoned ape theory
|
11,045
|
368
|
C
|
Low
|
| 108
|
Feathered dinosaur
|
10,978
|
365
|
C
|
High
|
| 109
|
Selective breeding
|
10,902
|
363
|
C
|
Low
|
| 110
|
Rejection of evolution by religious groups
|
10,897
|
363
|
B
|
High
|
| 111
|
Human mating strategies
|
10,860
|
362
|
B
|
Low
|
| 112
|
Evolution of sexual reproduction
|
10,807
|
360
|
B
|
High
|
| 113
|
Cladistics
|
10,598
|
353
|
C
|
Mid
|
| 114
|
RNA world
|
10,587
|
352
|
C
|
High
|
| 115
|
R/K selection theory
|
10,547
|
351
|
C
|
High
|
| 116
|
Jean-Baptiste Lamarck
|
10,538
|
351
|
B
|
Top
|
| 117
|
Human Y-chromosome DNA haplogroup
|
10,372
|
345
|
C
|
Mid
|
| 118
|
Origin of birds
|
10,183
|
339
|
B
|
Mid
|
| 119
|
Adaptation
|
10,148
|
338
|
GA
|
Top
|
| 120
|
Polymorphism (biology)
|
10,105
|
336
|
B
|
High
|
| 121
|
Aquatic ape hypothesis
|
10,103
|
336
|
C
|
Low
|
| 122
|
Monophyly
|
9,607
|
320
|
C
|
Mid
|
| 123
|
Objections to evolution
|
9,592
|
319
|
B
|
Mid
|
| 124
|
Ashkenazi Jewish intelligence
|
9,569
|
318
|
Start
|
Low
|
| 125
|
Phylogenetics
|
9,531
|
317
|
B
|
High
|
| 126
|
Human vestigiality
|
9,517
|
317
|
C
|
Mid
|
| 127
|
Species complex
|
9,497
|
316
|
B
|
Mid
|
| 128
|
Archaic humans
|
9,490
|
316
|
NA
|
Low
|
| 129
|
Nazi eugenics
|
9,268
|
308
|
C
|
Low
|
| 130
|
Dysgenics
|
9,247
|
308
|
Start
|
Mid
|
| 131
|
Sex differences in human physiology
|
9,233
|
307
|
C
|
High
|
| 132
|
Symbiogenesis
|
9,232
|
307
|
GA
|
High
|
| 133
|
Institutional racism
|
9,178
|
305
|
B
|
Mid
|
| 134
|
Ernst Haeckel
|
9,140
|
304
|
B
|
High
|
| 135
|
Evolution of the horse
|
8,986
|
299
|
B
|
Mid
|
| 136
|
Sexual cannibalism
|
8,965
|
298
|
B
|
Low
|
| 137
|
Linnaean taxonomy
|
8,907
|
296
|
C
|
Mid
|
| 138
|
Instinct
|
8,879
|
295
|
C
|
Low
|
| 139
|
Recent human evolution
|
8,866
|
295
|
B
|
Mid
|
| 140
|
Vestigiality
|
8,853
|
295
|
C
|
High
|
| 141
|
Red Queen hypothesis
|
8,851
|
295
|
Start
|
Mid
|
| 142
|
Inbreeding depression
|
8,816
|
293
|
C
|
Mid
|
| 143
|
J. B. S. Haldane
|
8,785
|
292
|
C
|
Mid
|
| 144
|
Darwin's finches
|
8,778
|
292
|
C
|
High
|
| 145
|
Major histocompatibility complex
|
8,669
|
288
|
B
|
Low
|
| 146
|
List of human evolution fossils
|
8,647
|
288
|
List
|
High
|
| 147
|
Founder effect
|
8,615
|
287
|
C
|
Mid
|
| 148
|
Three-domain system
|
8,590
|
286
|
C
|
Mid
|
| 149
|
Rare Earth hypothesis
|
8,550
|
285
|
B
|
Low
|
| 150
|
Genetic drift
|
8,476
|
282
|
GA
|
Top
|
| 151
|
Fertility
|
8,460
|
282
|
C
|
High
|
| 152
|
Evolutionary biology
|
8,420
|
280
|
C
|
Top
|
| 153
|
Offspring
|
8,313
|
277
|
Start
|
Mid
|
| 154
|
Julian Huxley
|
8,286
|
276
|
B
|
Mid
|
| 155
|
Hardy–Weinberg principle
|
8,278
|
275
|
C
|
High
|
| 156
|
Horizontal gene transfer
|
8,112
|
270
|
C
|
High
|
| 157
|
Symmetry in biology
|
8,017
|
267
|
C
|
High
|
| 158
|
Signalling theory
|
7,967
|
265
|
GA
|
Mid
|
| 159
|
Batesian mimicry
|
7,945
|
264
|
GA
|
Mid
|
| 160
|
Survival of the fittest
|
7,796
|
259
|
B
|
Low
|
| 161
|
Basal (phylogenetics)
|
7,780
|
259
|
C
|
Mid
|
| 162
|
Common descent
|
7,553
|
251
|
B
|
Top
|
| 163
|
Female promiscuity
|
7,492
|
249
|
C
|
Low
|
| 164
|
Triune brain
|
7,418
|
247
|
Start
|
Low
|
| 165
|
Speciation
|
7,309
|
243
|
B
|
High
|
| 166
|
Middle Paleolithic
|
7,260
|
242
|
C
|
High
|
| 167
|
Jebel Irhoud
|
7,209
|
240
|
C
|
Low
|
| 168
|
Evolution of human intelligence
|
7,136
|
237
|
B
|
High
|
| 169
|
Primordial soup
|
7,124
|
237
|
Start
|
Mid
|
| 170
|
Relict (biology)
|
6,978
|
232
|
C
|
Mid
|
| 171
|
Insular dwarfism
|
6,927
|
230
|
C
|
Low
|
| 172
|
Sex differences in psychology
|
6,829
|
227
|
C
|
High
|
| 173
|
Neanderthal genetics
|
6,785
|
226
|
C
|
High
|
| 174
|
Evolution of birds
|
6,750
|
225
|
C
|
High
|
| 175
|
Lek mating
|
6,671
|
222
|
GA
|
Mid
|
| 176
|
First universal common ancestor
|
6,634
|
221
|
Start
|
Unknown
|
| 177
|
Cowardice
|
6,602
|
220
|
C
|
Low
|
| 178
|
Autosome
|
6,565
|
218
|
Start
|
High
|
| 179
|
Evolutionary origin of religion
|
6,550
|
218
|
C
|
Low
|
| 180
|
Bergmann's rule
|
6,529
|
217
|
C
|
Low
|
| 181
|
Evolution of fish
|
6,517
|
217
|
C
|
High
|
| 182
|
History of evolutionary thought
|
6,408
|
213
|
FA
|
Top
|
| 183
|
Heritability of autism
|
6,403
|
213
|
C
|
Mid
|
| 184
|
Anthropometry
|
6,399
|
213
|
C
|
Low
|
| 185
|
Allopatric speciation
|
6,326
|
210
|
B
|
High
|
| 186
|
Great American Interchange
|
6,322
|
210
|
C
|
Mid
|
| 187
|
Felid hybrids
|
6,314
|
210
|
Start
|
Low
|
| 188
|
Müllerian mimicry
|
6,303
|
210
|
GA
|
Mid
|
| 189
|
Evolution as fact and theory
|
6,218
|
207
|
C
|
Low
|
| 190
|
List of related male and female reproductive organs
|
6,184
|
206
|
List
|
Mid
|
| 191
|
Human mitochondrial DNA haplogroup
|
6,130
|
204
|
Start
|
Mid
|
| 192
|
Aggressive mimicry
|
6,090
|
203
|
GA
|
Mid
|
| 193
|
Evolution of primates
|
6,076
|
202
|
Start
|
Low
|
| 194
|
Evolution of cetaceans
|
6,067
|
202
|
GA
|
Mid
|
| 195
|
Evidence of common descent
|
6,064
|
202
|
B
|
Mid
|
| 196
|
Evolutionary history of plants
|
6,058
|
201
|
B
|
High
|
| 197
|
Modern synthesis (20th century)
|
5,916
|
197
|
GA
|
High
|
| 198
|
Crown group
|
5,901
|
196
|
C
|
Mid
|
| 199
|
The Descent of Man, and Selection in Relation to Sex
|
5,898
|
196
|
B
|
High
|
| 200
|
Incertae sedis
|
5,898
|
196
|
C
|
Low
|
| 201
|
Biogeography
|
5,873
|
195
|
Start
|
Mid
|
| 202
|
Sexual selection in humans
|
5,763
|
192
|
C
|
Low
|
| 203
|
Anisogamy
|
5,685
|
189
|
B
|
High
|
| 204
|
Transitional fossil
|
5,639
|
187
|
GA
|
Top
|
| 205
|
Apomorphy and synapomorphy
|
5,545
|
184
|
C
|
Low
|
| 206
|
Macroevolution
|
5,489
|
182
|
B
|
Top
|
| 207
|
Fitness (biology)
|
5,415
|
180
|
B
|
High
|
| 208
|
Evolutionary algorithm
|
5,370
|
179
|
C
|
Low
|
| 209
|
Sexy son hypothesis
|
5,353
|
178
|
C
|
Mid
|
| 210
|
Kin selection
|
5,346
|
178
|
GA
|
High
|
| 211
|
Complex adaptive system
|
5,281
|
176
|
C
|
Mid
|
| 212
|
Genetic diversity
|
5,278
|
175
|
C
|
Mid
|
| 213
|
Evolutionary developmental biology
|
5,241
|
174
|
GA
|
High
|
| 214
|
Adaptive radiation
|
5,224
|
174
|
B
|
High
|
| 215
|
Variability hypothesis
|
5,222
|
174
|
C
|
Low
|
| 216
|
Population genetics
|
5,201
|
173
|
C
|
High
|
| 217
|
Recapitulation theory
|
5,179
|
172
|
C
|
Mid
|
| 218
|
Missing link (human evolution)
|
5,093
|
169
|
Start
|
Mid
|
| 219
|
Medical genetics of Jews
|
5,020
|
167
|
Start
|
Mid
|
| 220
|
Punctuated equilibrium
|
5,016
|
167
|
GA
|
High
|
| 221
|
Climate change adaptation
|
4,968
|
165
|
B
|
Mid
|
| 222
|
Speculative evolution
|
4,956
|
165
|
B
|
Low
|
| 223
|
Kenyanthropus
|
4,925
|
164
|
GA
|
Low
|
| 224
|
Evolution of the eye
|
4,876
|
162
|
C
|
High
|
| 225
|
Human genetic variation
|
4,865
|
162
|
C
|
Mid
|
| 226
|
Evolution of the brain
|
4,848
|
161
|
Start
|
High
|
| 227
|
The Passing of the Great Race
|
4,814
|
160
|
C
|
Low
|
| 228
|
Religious views of Charles Darwin
|
4,762
|
158
|
B
|
Low
|
| 229
|
Devolution (biology)
|
4,745
|
158
|
C
|
Low
|
| 230
|
Multiregional origin of modern humans
|
4,725
|
157
|
C
|
Mid
|
| 231
|
Assortative mating
|
4,604
|
153
|
C
|
Mid
|
| 232
|
Endurance running hypothesis
|
4,589
|
152
|
Start
|
Low
|
| 233
|
Ontogeny
|
4,566
|
152
|
B
|
High
|
| 234
|
Sperm competition
|
4,558
|
151
|
Start
|
Mid
|
| 235
|
Sexual conflict
|
4,555
|
151
|
Start
|
High
|
| 236
|
Anatomically modern human
|
4,542
|
151
|
NA
|
NA
|
| 237
|
Heritability
|
4,541
|
151
|
C
|
Mid
|
| 238
|
Spiral Dynamics
|
4,497
|
149
|
C
|
Low
|
| 239
|
Ernst Mayr
|
4,466
|
148
|
C
|
High
|
| 240
|
Fisherian runaway
|
4,416
|
147
|
Start
|
Low
|
| 241
|
Australopithecus sediba
|
4,396
|
146
|
GA
|
Low
|
| 242
|
Lagerstätte
|
4,394
|
146
|
List
|
Mid
|
| 243
|
Gene flow
|
4,349
|
144
|
Start
|
High
|
| 244
|
Peppered moth evolution
|
4,322
|
144
|
GA
|
High
|
| 245
|
Systematics
|
4,301
|
143
|
C
|
High
|
| 246
|
Evolution of the wolf
|
4,300
|
143
|
B
|
Low
|
| 247
|
Lagar Velho 1
|
4,263
|
142
|
Start
|
Low
|
| 248
|
Spandrel (biology)
|
4,252
|
141
|
B
|
Mid
|
| 249
|
Homo juluensis
|
4,232
|
141
|
Start
|
Low
|
| 250
|
Parental investment
|
4,229
|
140
|
Start
|
High
|
| 251
|
Herto Man
|
4,217
|
140
|
GA
|
Low
|
| 252
|
Coevolution
|
4,207
|
140
|
GA
|
High
|
| 253
|
Sister group
|
4,193
|
139
|
Start
|
Mid
|
| 254
|
Theodosius Dobzhansky
|
4,192
|
139
|
C
|
Mid
|
| 255
|
Exaptation
|
4,179
|
139
|
C
|
High
|
| 256
|
Orthogenesis
|
4,157
|
138
|
GA
|
Mid
|
| 257
|
Handicap principle
|
4,146
|
138
|
GA
|
High
|
| 258
|
Introduction to evolution
|
4,096
|
136
|
B
|
Mid
|
| 259
|
Maladaptation
|
4,091
|
136
|
Start
|
Mid
|
| 260
|
1860 Oxford evolution debate
|
4,091
|
136
|
B
|
Mid
|
| 261
|
Haplodiploidy
|
4,085
|
136
|
C
|
Mid
|
| 262
|
David Reich (geneticist)
|
4,036
|
134
|
C
|
Mid
|
| 263
|
Gene-centered view of evolution
|
4,031
|
134
|
B
|
High
|
| 264
|
The Blind Watchmaker
|
4,022
|
134
|
C
|
Mid
|
| 265
|
Thomas Hunt Morgan
|
3,999
|
133
|
B
|
High
|
| 266
|
History of biology
|
3,979
|
132
|
FA
|
High
|
| 267
|
Cladogram
|
3,966
|
132
|
C
|
Mid
|
| 268
|
CpG site
|
3,901
|
130
|
C
|
Mid
|
| 269
|
Japanese Paleolithic
|
3,899
|
129
|
Start
|
High
|
| 270
|
Level of support for evolution
|
3,828
|
127
|
C
|
Mid
|
| 271
|
Cro-Magnon rock shelter
|
3,791
|
126
|
Start
|
Mid
|
| 272
|
Hominina
|
3,779
|
125
|
NA
|
NA
|
| 273
|
Sequence homology
|
3,764
|
125
|
C
|
High
|
| 274
|
Neo-Darwinism
|
3,761
|
125
|
Start
|
Mid
|
| 275
|
Group selection
|
3,744
|
124
|
GA
|
High
|
| 276
|
Peppered moth
|
3,641
|
121
|
B
|
Low
|
| 277
|
Evolutionary game theory
|
3,610
|
120
|
C
|
High
|
| 278
|
Parallel evolution
|
3,589
|
119
|
Start
|
High
|
| 279
|
Stotting
|
3,571
|
119
|
GA
|
Low
|
| 280
|
Eukaryogenesis
|
3,570
|
119
|
C
|
High
|
| 281
|
Evolutionarily stable strategy
|
3,559
|
118
|
B
|
Mid
|
| 282
|
Altruism (biology)
|
3,546
|
118
|
C
|
Mid
|
| 283
|
Purple Earth hypothesis
|
3,537
|
117
|
Start
|
Mid
|
| 284
|
Nitroplast
|
3,517
|
117
|
Start
|
Unknown
|
| 285
|
Reproductive isolation
|
3,473
|
115
|
C
|
High
|
| 286
|
Solo Man
|
3,404
|
113
|
FA
|
Low
|
| 287
|
Grandmother hypothesis
|
3,404
|
113
|
C
|
Mid
|
| 288
|
Origin of speech
|
3,380
|
112
|
C
|
Mid
|
| 289
|
List of fossil sites
|
3,376
|
112
|
List
|
Top
|
| 290
|
Ring species
|
3,357
|
111
|
C
|
High
|
| 291
|
Life history theory
|
3,284
|
109
|
C
|
High
|
| 292
|
Islamic views on evolution
|
3,269
|
108
|
C
|
Low
|
| 293
|
Geological history of oxygen
|
3,228
|
107
|
C
|
Low
|
| 294
|
Inclusive fitness
|
3,221
|
107
|
C
|
High
|
| 295
|
Four Fs (evolution)
|
3,192
|
106
|
C
|
Low
|
| 296
|
Jerry Coyne
|
3,183
|
106
|
C
|
Low
|
| 297
|
Killer ape theory
|
3,174
|
105
|
Start
|
Low
|
| 298
|
Microevolution
|
3,173
|
105
|
C
|
High
|
| 299
|
Alloparenting
|
3,173
|
105
|
C
|
Low
|
| 300
|
Evolution of ageing
|
3,146
|
104
|
B
|
High
|
| 301
|
Evolutionary pressure
|
3,131
|
104
|
C
|
Mid
|
| 302
|
Why Is Sex Fun?
|
3,122
|
104
|
C
|
Low
|
| 303
|
Panmixia
|
3,083
|
102
|
Start
|
Mid
|
| 304
|
Expelled: No Intelligence Allowed
|
3,077
|
102
|
B
|
Low
|
| 305
|
Evolutionary mismatch
|
3,074
|
102
|
C
|
Low
|
| 306
|
Evolutionism
|
3,061
|
102
|
C
|
Mid
|
| 307
|
Clonally transmissible cancer
|
3,059
|
101
|
C
|
Low
|
| 308
|
Body plan
|
3,051
|
101
|
C
|
Mid
|
| 309
|
Baldwin effect
|
3,050
|
101
|
GA
|
Low
|
| 310
|
Two-domain system
|
3,027
|
100
|
C
|
Low
|
| 311
|
Genetic variation
|
3,023
|
100
|
Start
|
High
|
| 312
|
Heather Heying
|
3,002
|
100
|
Start
|
Low
|
| 313
|
Computational phylogenetics
|
2,982
|
99
|
C
|
Mid
|
| 314
|
Allometry
|
2,979
|
99
|
C
|
Mid
|
| 315
|
Cline (biology)
|
2,948
|
98
|
C
|
Low
|
| 316
|
Asa Gray
|
2,942
|
98
|
GA
|
Low
|
| 317
|
Evolution of morality
|
2,932
|
97
|
C
|
High
|
| 318
|
Fish intelligence
|
2,913
|
97
|
B
|
Low
|
| 319
|
Red Deer Cave people
|
2,910
|
97
|
Start
|
Low
|
| 320
|
Reciprocal altruism
|
2,896
|
96
|
B
|
Mid
|
| 321
|
Rotating locomotion in living systems
|
2,891
|
96
|
FA
|
High
|
| 322
|
Neutral theory of molecular evolution
|
2,882
|
96
|
Start
|
High
|
| 323
|
The Expression of the Emotions in Man and Animals
|
2,878
|
95
|
C
|
Mid
|
| 324
|
E. coli long-term evolution experiment
|
2,867
|
95
|
B
|
Mid
|
| 325
|
Duane Gish
|
2,849
|
94
|
B
|
Low
|
| 326
|
Haldane's rule
|
2,842
|
94
|
C
|
Low
|
| 327
|
Human genetics
|
2,838
|
94
|
Start
|
Mid
|
| 328
|
Bateman's principle
|
2,824
|
94
|
B
|
Mid
|
| 329
|
Hunter versus farmer hypothesis
|
2,810
|
93
|
C
|
Low
|
| 330
|
Self-preservation
|
2,800
|
93
|
C
|
High
|
| 331
|
Evolutionary arms race
|
2,774
|
92
|
Start
|
High
|
| 332
|
March of Progress
|
2,765
|
92
|
C
|
Low
|
| 333
|
Evolutionary anachronism
|
2,759
|
91
|
List
|
Mid
|
| 334
|
Molecular evolution
|
2,758
|
91
|
C
|
Top
|
| 335
|
Sociobiological theories of rape
|
2,750
|
91
|
C
|
Mid
|
| 336
|
George R. Price
|
2,739
|
91
|
C
|
Low
|
| 337
|
Human Diversity Foundation
|
2,738
|
91
|
B
|
Low
|
| 338
|
Sympatric speciation
|
2,718
|
90
|
Start
|
Mid
|
| 339
|
Allele frequency
|
2,699
|
89
|
Start
|
Mid
|
| 340
|
Satoshi Kanazawa
|
2,693
|
89
|
C
|
Unknown
|
| 341
|
Evolutionary radiation
|
2,657
|
88
|
Start
|
Mid
|
| 342
|
Genetic pollution
|
2,606
|
86
|
C
|
Low
|
| 343
|
Gene duplication
|
2,601
|
86
|
C
|
Mid
|
| 344
|
Protocell
|
2,598
|
86
|
C
|
Mid
|
| 345
|
Primitive (phylogenetics)
|
2,567
|
85
|
Start
|
Mid
|
| 346
|
W. D. Hamilton
|
2,563
|
85
|
C
|
Low
|
| 347
|
Domestication syndrome
|
2,537
|
84
|
C
|
Low
|
| 348
|
Phenotypic plasticity
|
2,520
|
84
|
C
|
Mid
|
| 349
|
Human sperm competition
|
2,504
|
83
|
C
|
Low
|
| 350
|
Ursid hybrid
|
2,482
|
82
|
C
|
Low
|
| 351
|
Meganthropus
|
2,477
|
82
|
Start
|
Low
|
| 352
|
Creation and evolution in public education
|
2,474
|
82
|
B
|
Mid
|
| 353
|
Radiation hormesis
|
2,470
|
82
|
B
|
Mid
|
| 354
|
Acceptance of evolution by religious groups
|
2,457
|
81
|
C
|
Low
|
| 355
|
The Third Chimpanzee
|
2,451
|
81
|
C
|
Low
|
| 356
|
Fitness landscape
|
2,438
|
81
|
B
|
High
|
| 357
|
Fisher's principle
|
2,420
|
80
|
Start
|
Mid
|
| 358
|
Evolution of biological complexity
|
2,413
|
80
|
C
|
Mid
|
| 359
|
Gene pool
|
2,409
|
80
|
Start
|
High
|
| 360
|
Evolution of tetrapods
|
2,405
|
80
|
C
|
High
|
| 361
|
Origin of avian flight
|
2,393
|
79
|
Start
|
Mid
|
| 362
|
Evolution of mammalian auditory ossicles
|
2,392
|
79
|
B
|
Mid
|
| 363
|
Parental care
|
2,388
|
79
|
B
|
Mid
|
| 364
|
Evolution of reptiles
|
2,387
|
79
|
C
|
High
|
| 365
|
Mutation rate
|
2,368
|
78
|
Start
|
Mid
|
| 366
|
Evolution of nervous systems
|
2,353
|
78
|
B
|
Mid
|
| 367
|
Divergent evolution
|
2,350
|
78
|
Start
|
Mid
|
| 368
|
Siblicide
|
2,339
|
77
|
Start
|
Low
|
| 369
|
Muller's ratchet
|
2,334
|
77
|
Start
|
Mid
|
| 370
|
Pangenesis
|
2,316
|
77
|
C
|
Low
|
| 371
|
John Maynard Smith
|
2,310
|
77
|
C
|
High
|
| 372
|
The 10,000 Year Explosion
|
2,269
|
75
|
B
|
Mid
|
| 373
|
Gene polymorphism
|
2,263
|
75
|
Start
|
Mid
|
| 374
|
Shadow biosphere
|
2,260
|
75
|
Start
|
Mid
|
| 375
|
Anagenesis
|
2,258
|
75
|
C
|
Mid
|
| 376
|
Alternatives to Darwinian evolution
|
2,246
|
74
|
B
|
Mid
|
| 377
|
John Gould
|
2,220
|
74
|
C
|
Mid
|
| 378
|
Glaucophyte
|
2,198
|
73
|
Start
|
Unknown
|
| 379
|
Coalescent theory
|
2,168
|
72
|
C
|
Low
|
| 380
|
Evolution of color vision in primates
|
2,160
|
72
|
C
|
Low
|
| 381
|
Darwin's Dangerous Idea
|
2,154
|
71
|
C
|
Mid
|
| 382
|
History of ecology
|
2,143
|
71
|
C
|
Mid
|
| 383
|
Human skeletal changes due to bipedalism
|
2,143
|
71
|
B
|
Mid
|
| 384
|
Racism in the LGBTQ community
|
2,138
|
71
|
C
|
Low
|
| 385
|
Oceanic dispersal
|
2,132
|
71
|
Start
|
Low
|
| 386
|
Mutationism
|
2,127
|
70
|
GA
|
Low
|
| 387
|
Heterozygote advantage
|
2,121
|
70
|
Start
|
Mid
|
| 388
|
Paternal care
|
2,117
|
70
|
C
|
Low
|
| 389
|
Junkyard tornado
|
2,114
|
70
|
C
|
Low
|
| 390
|
Evolution of emotion
|
2,112
|
70
|
Start
|
Unknown
|
| 391
|
Adaptationism
|
2,102
|
70
|
Start
|
Mid
|
| 392
|
Heterochrony
|
2,098
|
69
|
GA
|
Mid
|
| 393
|
Last Glacial Maximum refugia
|
2,088
|
69
|
Start
|
Low
|
| 394
|
Down House
|
2,077
|
69
|
C
|
Low
|
| 395
|
Evolution of photosynthesis
|
2,076
|
69
|
Start
|
High
|
| 396
|
Directional selection
|
2,070
|
69
|
Start
|
Mid
|
| 397
|
Frameshift mutation
|
2,070
|
69
|
B
|
High
|
| 398
|
Gene–environment interaction
|
2,063
|
68
|
Start
|
Mid
|
| 399
|
Modern human
|
2,051
|
68
|
NA
|
NA
|
| 400
|
Ovulatory shift hypothesis
|
2,042
|
68
|
GA
|
Low
|
| 401
|
Cooperation (evolution)
|
2,035
|
67
|
B
|
Mid
|
| 402
|
Reproductive success
|
2,027
|
67
|
Start
|
High
|
| 403
|
Codon usage bias
|
2,026
|
67
|
B
|
Low
|
| 404
|
Nicholas Miklouho-Maclay
|
2,014
|
67
|
C
|
Low
|
| 405
|
Biology and political orientation
|
2,013
|
67
|
C
|
Low
|
| 406
|
Price equation
|
2,011
|
67
|
C
|
Low
|
| 407
|
Trivers–Willard hypothesis
|
2,011
|
67
|
Start
|
Low
|
| 408
|
Universal Darwinism
|
2,001
|
66
|
C
|
Low
|
| 409
|
Struggle for existence
|
1,999
|
66
|
C
|
Mid
|
| 410
|
Homo sapiens sapiens
|
1,987
|
66
|
NA
|
NA
|
| 411
|
Evolutionary computation
|
1,977
|
65
|
C
|
High
|
| 412
|
List of examples of convergent evolution
|
1,965
|
65
|
List
|
High
|
| 413
|
Peripatric speciation
|
1,953
|
65
|
B
|
Mid
|
| 414
|
Jonathan Wells (intelligent design advocate)
|
1,952
|
65
|
B
|
Low
|
| 415
|
Major histocompatibility complex and sexual selection
|
1,943
|
64
|
C
|
Mid
|
| 416
|
Embryonic diapause
|
1,938
|
64
|
Start
|
Low
|
| 417
|
Mach bands
|
1,907
|
63
|
Start
|
Mid
|
| 418
|
Mating call
|
1,887
|
62
|
C
|
Low
|
| 419
|
Nuptial gift
|
1,882
|
62
|
Start
|
Mid
|
| 420
|
Motion camouflage
|
1,876
|
62
|
GA
|
Low
|
| 421
|
Island syndrome
|
1,875
|
62
|
Start
|
Unknown
|
| 422
|
Green-beard effect
|
1,849
|
61
|
Start
|
Low
|
| 423
|
Dollo's law of irreversibility
|
1,846
|
61
|
Start
|
High
|
| 424
|
Red dress effect
|
1,834
|
61
|
Start
|
Low
|
| 425
|
Sexual selection in birds
|
1,828
|
60
|
C
|
Low
|
| 426
|
Acritarch
|
1,808
|
60
|
C
|
Low
|
| 427
|
Selective sweep
|
1,804
|
60
|
Start
|
Mid
|
| 428
|
August Weismann
|
1,795
|
59
|
Start
|
High
|
| 429
|
Thrifty gene hypothesis
|
1,789
|
59
|
B
|
Mid
|
| 430
|
Genotype–phenotype distinction
|
1,777
|
59
|
Start
|
High
|
| 431
|
Missing heritability problem
|
1,774
|
59
|
Start
|
Mid
|
| 432
|
Isua Greenstone Belt
|
1,770
|
59
|
C
|
Mid
|
| 433
|
Robert Trivers
|
1,766
|
58
|
Start
|
Low
|
| 434
|
Jewish views on evolution
|
1,760
|
58
|
B
|
Low
|
| 435
|
Genetic divergence
|
1,760
|
58
|
Start
|
High
|
| 436
|
Somatic mutation
|
1,740
|
58
|
C
|
Low
|
| 437
|
Iron–sulfur world hypothesis
|
1,729
|
57
|
C
|
Low
|
| 438
|
History of creationism
|
1,711
|
57
|
B
|
Mid
|
| 439
|
Mate choice in humans
|
1,698
|
56
|
B
|
Unknown
|
| 440
|
Josiah C. Nott
|
1,696
|
56
|
C
|
Low
|
| 441
|
Mate value
|
1,690
|
56
|
C
|
Low
|
| 442
|
History of anthropometry
|
1,684
|
56
|
C
|
Low
|
| 443
|
Evolution of cephalopods
|
1,673
|
55
|
C
|
Low
|
| 444
|
Evolutionary grade
|
1,668
|
55
|
Start
|
High
|
| 445
|
Balancing selection
|
1,666
|
55
|
Start
|
Mid
|
| 446
|
Stabilizing selection
|
1,660
|
55
|
Start
|
Mid
|
| 447
|
Evolutionary psychology of religion
|
1,660
|
55
|
C
|
Low
|
| 448
|
Autapomorphy
|
1,658
|
55
|
C
|
Low
|
| 449
|
Braarudosphaera bigelowii
|
1,646
|
54
|
Start
|
Low
|
| 450
|
Tend and befriend
|
1,638
|
54
|
C
|
Low
|
| 451
|
Bird hybrid
|
1,636
|
54
|
Start
|
Low
|
| 452
|
Evolutionary anthropology
|
1,634
|
54
|
Start
|
Low
|
| 453
|
Germline mutation
|
1,631
|
54
|
B
|
High
|
| 454
|
Australopithecus deyiremeda
|
1,627
|
54
|
GA
|
Low
|
| 455
|
Evolutionary approaches to depression
|
1,625
|
54
|
C
|
Low
|
| 456
|
Evolution of snake venom
|
1,625
|
54
|
GA
|
Mid
|
| 457
|
Evolutionary taxonomy
|
1,617
|
53
|
C
|
Mid
|
| 458
|
Telescoping generations
|
1,614
|
53
|
Stub
|
Unknown
|
| 459
|
Taforalt
|
1,606
|
53
|
B
|
Low
|
| 460
|
Disruptive selection
|
1,603
|
53
|
C
|
Mid
|
| 461
|
Mutagenesis
|
1,579
|
52
|
C
|
Mid
|
| 462
|
Parent–offspring conflict
|
1,576
|
52
|
Start
|
Mid
|
| 463
|
Future generations
|
1,551
|
51
|
Start
|
Low
|
| 464
|
Snake detection theory
|
1,545
|
51
|
Start
|
Mid
|
| 465
|
Embryological origins of the mouth and anus
|
1,533
|
51
|
Start
|
Low
|
| 466
|
Dmanisi
|
1,528
|
50
|
Start
|
Mid
|
| 467
|
Ka/Ks ratio
|
1,520
|
50
|
C
|
Mid
|
| 468
|
Blending inheritance
|
1,518
|
50
|
GA
|
Low
|
| 469
|
Crocoduck
|
1,518
|
50
|
C
|
Low
|
| 470
|
Precambrian rabbit
|
1,517
|
50
|
C
|
Low
|
| 471
|
Grimaldi man
|
1,517
|
50
|
C
|
Low
|
| 472
|
Angraecum sesquipedale
|
1,515
|
50
|
B
|
Mid
|
| 473
|
Patrick Matthew
|
1,512
|
50
|
B
|
Mid
|
| 474
|
Disappearing blonde gene
|
1,512
|
50
|
Start
|
Low
|
| 475
|
Evolution of color vision
|
1,499
|
49
|
Start
|
Low
|
| 476
|
Female sperm storage
|
1,499
|
49
|
C
|
Low
|
| 477
|
Background extinction rate
|
1,498
|
49
|
Start
|
Mid
|
| 478
|
Initial Upper Paleolithic
|
1,482
|
49
|
B
|
Unknown
|
| 479
|
Evolution of cells
|
1,473
|
49
|
Start
|
High
|
| 480
|
Extended female sexuality
|
1,461
|
48
|
B
|
Mid
|
| 481
|
Aerobic fermentation
|
1,446
|
48
|
B
|
Low
|
| 482
|
Mutational meltdown
|
1,440
|
48
|
Stub
|
Mid
|
| 483
|
Cladogenesis
|
1,438
|
47
|
Start
|
Mid
|
| 484
|
Niche construction
|
1,436
|
47
|
B
|
Low
|
| 485
|
Late Stone Age
|
1,427
|
47
|
Start
|
Low
|
| 486
|
Weasel program
|
1,421
|
47
|
B
|
Low
|
| 487
|
Evolution of eusociality
|
1,407
|
46
|
C
|
Low
|
| 488
|
Sociobiology: The New Synthesis
|
1,399
|
46
|
GA
|
Mid
|
| 489
|
Evolvability
|
1,383
|
46
|
C
|
High
|
| 490
|
Shane Campbell-Staton
|
1,374
|
45
|
Start
|
Low
|
| 491
|
Experimental evolution
|
1,370
|
45
|
Start
|
High
|
| 492
|
Metapopulation
|
1,366
|
45
|
B
|
Mid
|
| 493
|
Homoplasy
|
1,365
|
45
|
Start
|
Low
|
| 494
|
Unit of selection
|
1,363
|
45
|
C
|
High
|
| 495
|
Entrainment (biomusicology)
|
1,359
|
45
|
Start
|
Low
|
| 496
|
Bruniquel Cave
|
1,355
|
45
|
Start
|
Mid
|
| 497
|
Gene family
|
1,347
|
44
|
C
|
High
|
| 498
|
Frequency-dependent selection
|
1,344
|
44
|
Start
|
High
|
| 499
|
Indel
|
1,344
|
44
|
Start
|
Mid
|
| 500
|
Androgenesis
|
1,337
|
44
|
C
|
Low
|
| 501
|
Teleology in biology
|
1,335
|
44
|
GA
|
High
|
| 502
|
Lantian Man
|
1,334
|
44
|
GA
|
Low
|
| 503
|
Sex differences in memory
|
1,331
|
44
|
Start
|
Low
|
| 504
|
Snaiad
|
1,326
|
44
|
B
|
Low
|
| 505
|
Extended evolutionary synthesis
|
1,321
|
44
|
B
|
High
|
| 506
|
Automimicry
|
1,316
|
43
|
GA
|
Mid
|
| 507
|
List of prehistoric cartilaginous fish genera
|
1,314
|
43
|
List
|
Mid
|
| 508
|
Polyphenism
|
1,313
|
43
|
Start
|
Mid
|
| 509
|
Hybrid zone
|
1,305
|
43
|
C
|
Mid
|
| 510
|
History of zoology through 1859
|
1,298
|
43
|
C
|
High
|
| 511
|
Parasite-stress theory
|
1,288
|
42
|
C
|
Mid
|
| 512
|
Outgroup (cladistics)
|
1,283
|
42
|
Start
|
Mid
|
| 513
|
Genetic assimilation
|
1,281
|
42
|
GA
|
Low
|
| 514
|
Costly signaling theory in evolutionary psychology
|
1,275
|
42
|
C
|
Mid
|
| 515
|
Negative selection (natural selection)
|
1,274
|
42
|
Stub
|
Mid
|
| 516
|
Snow camouflage
|
1,272
|
42
|
GA
|
Low
|
| 517
|
Cryptic female choice
|
1,270
|
42
|
B
|
Low
|
| 518
|
Fisher's fundamental theorem of natural selection
|
1,260
|
42
|
Start
|
Mid
|
| 519
|
Long branch attraction
|
1,259
|
41
|
Start
|
Low
|
| 520
|
Genetic erosion
|
1,259
|
41
|
C
|
Low
|
| 521
|
Cooperative eye hypothesis
|
1,257
|
41
|
Start
|
Low
|
| 522
|
Diana Fleischman
|
1,251
|
41
|
Start
|
Low
|
| 523
|
Protein superfamily
|
1,245
|
41
|
B
|
Mid
|
| 524
|
Evolution of lemurs
|
1,243
|
41
|
FA
|
Low
|
| 525
|
Character displacement
|
1,238
|
41
|
B
|
Mid
|
| 526
|
Evolution of bacteria
|
1,232
|
41
|
C
|
Mid
|
| 527
|
Parapatric speciation
|
1,227
|
40
|
C
|
Mid
|
| 528
|
Models of DNA evolution
|
1,225
|
40
|
B
|
Low
|
| 529
|
Koobi Fora
|
1,221
|
40
|
C
|
Mid
|
| 530
|
Racism on the Internet
|
1,220
|
40
|
Start
|
Low
|
| 531
|
Strategic pluralism
|
1,208
|
40
|
Stub
|
Low
|
| 532
|
Drunken monkey hypothesis
|
1,202
|
40
|
Start
|
Low
|
| 533
|
Secondarily aquatic tetrapods
|
1,196
|
39
|
Stub
|
Mid
|
| 534
|
Epic of evolution
|
1,196
|
39
|
C
|
Low
|
| 535
|
Canalisation (genetics)
|
1,188
|
39
|
Start
|
Mid
|
| 536
|
Race suicide
|
1,188
|
39
|
Start
|
Mid
|
| 537
|
Yuanmou Man
|
1,172
|
39
|
GA
|
Low
|
| 538
|
Budgerigar colour genetics
|
1,170
|
39
|
Start
|
Low
|
| 539
|
Origin and function of meiosis
|
1,170
|
39
|
Start
|
Low
|
| 540
|
Population biology
|
1,168
|
38
|
Stub
|
Low
|
| 541
|
Philosophie zoologique
|
1,167
|
38
|
GA
|
Low
|
| 542
|
Operational sex ratio
|
1,153
|
38
|
Start
|
Low
|
| 543
|
Modern humans
|
1,140
|
38
|
NA
|
NA
|
| 544
|
Reticulate evolution
|
1,139
|
37
|
C
|
Mid
|
| 545
|
PAH world hypothesis
|
1,138
|
37
|
Start
|
Low
|
| 546
|
Timeline of fish evolution
|
1,132
|
37
|
List
|
Low
|
| 547
|
Evolutionary ecology
|
1,131
|
37
|
C
|
Mid
|
| 548
|
Motoo Kimura
|
1,123
|
37
|
B
|
High
|
| 549
|
Peptide nucleic acid
|
1,112
|
37
|
Start
|
Low
|
| 550
|
Artificial selection
|
1,111
|
37
|
NA
|
NA
|
| 551
|
Of Pandas and People
|
1,104
|
36
|
C
|
Low
|
| 552
|
Beta diversity
|
1,103
|
36
|
C
|
Mid
|
| 553
|
Davis's law
|
1,098
|
36
|
Start
|
Low
|
| 554
|
Evolutionary neuroscience
|
1,096
|
36
|
Start
|
High
|
| 555
|
James Cowles Prichard
|
1,095
|
36
|
C
|
High
|
| 556
|
Quasispecies model
|
1,094
|
36
|
C
|
Mid
|
| 557
|
Animal weapon
|
1,093
|
36
|
Start
|
Low
|
| 558
|
Fritz Müller
|
1,092
|
36
|
B
|
Mid
|
| 559
|
Evolutionary psychiatry
|
1,090
|
36
|
Stub
|
Low
|
| 560
|
The Red Queen: Sex and the Evolution of Human Nature
|
1,077
|
35
|
Start
|
Low
|
| 561
|
Nothing in Biology Makes Sense Except in the Light of Evolution
|
1,073
|
35
|
C
|
Mid
|
| 562
|
Empathy-altruism
|
1,071
|
35
|
Start
|
Low
|
| 563
|
Vocal learning
|
1,071
|
35
|
B
|
Low
|
| 564
|
Endless Forms Most Beautiful (book)
|
1,070
|
35
|
GA
|
Low
|
| 565
|
Plant evolution
|
1,060
|
35
|
Start
|
High
|
| 566
|
Endemism in the Hawaiian Islands
|
1,053
|
35
|
Start
|
Low
|
| 567
|
The Greatest Show on Earth: The Evidence for Evolution
|
1,045
|
34
|
Start
|
Low
|
| 568
|
Extinction vortex
|
1,035
|
34
|
Start
|
Low
|
| 569
|
Evolutionary trap
|
1,032
|
34
|
Start
|
Low
|
| 570
|
Population structure (genetics)
|
1,027
|
34
|
Start
|
Low
|
| 571
|
Synonymous substitution
|
1,026
|
34
|
Start
|
Mid
|
| 572
|
Klepton
|
1,017
|
33
|
Start
|
Low
|
| 573
|
Evolutionary aesthetics
|
1,016
|
33
|
C
|
High
|
| 574
|
Bat wing development
|
1,011
|
33
|
C
|
Low
|
| 575
|
Domestication of the goat
|
1,010
|
33
|
B
|
Mid
|
| 576
|
Glossary of genetics and evolutionary biology
|
1,009
|
33
|
List
|
Top
|
| 577
|
Sperm Wars
|
1,008
|
33
|
Start
|
Mid
|
| 578
|
Cognitive tradeoff hypothesis
|
1,005
|
33
|
C
|
Low
|
| 579
|
The Genetical Theory of Natural Selection
|
1,004
|
33
|
Start
|
Mid
|
| 580
|
Incomplete lineage sorting
|
999
|
33
|
Start
|
Mid
|
| 581
|
Neural Darwinism
|
984
|
32
|
C
|
Unknown
|
| 582
|
Allogamy
|
980
|
32
|
Start
|
Mid
|
| 583
|
Vestigial response
|
980
|
32
|
Stub
|
Low
|
| 584
|
Island hopping
|
975
|
32
|
NA
|
Low
|
| 585
|
The Spandrels of San Marco and the Panglossian Paradigm
|
973
|
32
|
Start
|
Mid
|
| 586
|
Polytomy
|
972
|
32
|
Start
|
Mid
|
| 587
|
Phenetics
|
962
|
32
|
Start
|
Mid
|
| 588
|
Ornithophily
|
961
|
32
|
B
|
Low
|
| 589
|
Saltation (biology)
|
957
|
31
|
C
|
Mid
|
| 590
|
Mormon views on evolution
|
952
|
31
|
C
|
Low
|
| 591
|
Cope's rule
|
947
|
31
|
Start
|
Mid
|
| 592
|
Intragenomic conflict
|
935
|
31
|
C
|
Mid
|
| 593
|
Systemic racism
|
935
|
31
|
NA
|
NA
|
| 594
|
Bateson–Dobzhansky–Muller model
|
935
|
31
|
Unknown
|
Unknown
|
| 595
|
Selection shadow
|
934
|
31
|
Start
|
Low
|
| 596
|
Savannah hypothesis
|
927
|
30
|
Start
|
Low
|
| 597
|
Last eukaryotic common ancestor
|
916
|
30
|
NA
|
High
|
| 598
|
Wonderful Life (book)
|
913
|
30
|
Stub
|
Low
|
| 599
|
Elizabeth, Lady Hope
|
912
|
30
|
C
|
Low
|
| 600
|
Joan Roughgarden
|
911
|
30
|
C
|
Unknown
|
| 601
|
Demonic Males
|
910
|
30
|
C
|
Unknown
|
| 602
|
Disassortative mating
|
909
|
30
|
C
|
Mid
|
| 603
|
George Christopher Williams
|
907
|
30
|
Start
|
Mid
|
| 604
|
David Sloan Wilson
|
901
|
30
|
Start
|
Unknown
|
| 605
|
Vertebrate land invasion
|
899
|
29
|
C
|
Mid
|
| 606
|
History of zoology (1859–present)
|
895
|
29
|
C
|
High
|
| 607
|
Pseudoextinction
|
894
|
29
|
Start
|
Low
|
| 608
|
Henry Walter Bates
|
892
|
29
|
C
|
High
|
| 609
|
Bet hedging (biology)
|
890
|
29
|
B
|
Mid
|
| 610
|
Machiavellian intelligence hypothesis
|
884
|
29
|
Start
|
Low
|
| 611
|
Psychiatric genetics
|
884
|
29
|
C
|
Mid
|
| 612
|
Darwin and women
|
880
|
29
|
Stub
|
Low
|
| 613
|
Zlatý kůň woman
|
880
|
29
|
Start
|
Low
|
| 614
|
Recurrent evolution
|
871
|
29
|
Unknown
|
Unknown
|
| 615
|
Gut (anatomy)
|
867
|
28
|
NA
|
Low
|
| 616
|
Alternative abiogenesis scenarios
|
866
|
28
|
C
|
Low
|
| 617
|
Insectivorous Plants
|
864
|
28
|
Start
|
Low
|
| 618
|
List of non-avian dinosaur species preserved with evidence of feathers
|
860
|
28
|
List
|
Low
|
| 619
|
Pathological Altruism
|
857
|
28
|
Start
|
Unknown
|
| 620
|
Deep homology
|
850
|
28
|
Start
|
Mid
|
| 621
|
The Vital Question
|
843
|
28
|
GA
|
Low
|
| 622
|
Viral eukaryogenesis
|
839
|
27
|
Start
|
Mid
|
| 623
|
Inheritance of acquired characteristics
|
836
|
27
|
NA
|
NA
|
| 624
|
Genome evolution
|
836
|
27
|
C
|
Top
|
| 625
|
Neofunctionalization
|
832
|
27
|
Start
|
Low
|
| 626
|
Nearly neutral theory of molecular evolution
|
828
|
27
|
Start
|
Low
|
| 627
|
David Krakauer (scientist)
|
823
|
27
|
Start
|
Low
|
| 628
|
Expensive tissue hypothesis
|
821
|
27
|
C
|
Low
|
| 629
|
Muscular evolution in humans
|
813
|
27
|
Start
|
Low
|
| 630
|
Evolutionary psychology and culture
|
811
|
27
|
Start
|
Low
|
| 631
|
Error threshold (evolution)
|
803
|
26
|
C
|
Mid
|
| 632
|
Evolutionary invasion analysis
|
800
|
26
|
Start
|
Low
|
| 633
|
Reinforcement (speciation)
|
795
|
26
|
GA
|
Mid
|
| 634
|
Social selection
|
794
|
26
|
C
|
Low
|
| 635
|
Single-access key
|
789
|
26
|
C
|
Low
|
| 636
|
Tradeoffs for locomotion in air and water
|
788
|
26
|
C
|
Mid
|
| 637
|
Ecological fitting
|
788
|
26
|
B
|
Low
|
| 638
|
The Major Transitions in Evolution
|
787
|
26
|
Stub
|
Low
|
| 639
|
Natural Theology or Evidences of the Existence and Attributes of the Deity
|
778
|
25
|
GA
|
Low
|
| 640
|
Willi Hennig
|
773
|
25
|
Start
|
Mid
|
| 641
|
Psammosere
|
773
|
25
|
Start
|
Mid
|
| 642
|
Numerical taxonomy
|
772
|
25
|
Start
|
Mid
|
| 643
|
Evolutionary models of human drug use
|
771
|
25
|
C
|
Low
|
| 644
|
The Structure of Evolutionary Theory
|
766
|
25
|
Start
|
Low
|
| 645
|
Reciprocity (evolution)
|
766
|
25
|
Unknown
|
Unknown
|
| 646
|
Caudal luring
|
763
|
25
|
B
|
Low
|
| 647
|
Genetic isolate
|
762
|
25
|
Start
|
Low
|
| 648
|
Inclusive fitness in humans
|
761
|
25
|
C
|
Low
|
| 649
|
Host–parasite coevolution
|
760
|
25
|
GA
|
Mid
|
| 650
|
Local adaptation
|
756
|
25
|
Unknown
|
Unknown
|
| 651
|
Lek paradox
|
754
|
25
|
C
|
Low
|
| 652
|
Emergent evolution
|
751
|
25
|
C
|
Low
|
| 653
|
Polydactyly in stem-tetrapods
|
749
|
24
|
Start
|
Low
|
| 654
|
William Charles Wells
|
746
|
24
|
B
|
High
|
| 655
|
History of molecular evolution
|
745
|
24
|
C
|
Mid
|
| 656
|
Chemoton
|
745
|
24
|
Start
|
Low
|
| 657
|
Endosymbiotic theory
|
745
|
24
|
NA
|
NA
|
| 658
|
Great Hippocampus Question
|
742
|
24
|
B
|
Low
|
| 659
|
Hologenome theory of evolution
|
742
|
24
|
Start
|
Mid
|
| 660
|
Intralocus sexual conflict
|
732
|
24
|
Start
|
Mid
|
| 661
|
Conservative replacement
|
716
|
23
|
Start
|
Low
|
| 662
|
Project Steve
|
715
|
23
|
C
|
Low
|
| 663
|
Isolation by distance
|
712
|
23
|
Start
|
Low
|
| 664
|
Sexual antagonistic coevolution
|
712
|
23
|
Unknown
|
Unknown
|
| 665
|
Viral phylodynamics
|
712
|
23
|
B
|
Low
|
| 666
|
Emsleyan mimicry
|
708
|
23
|
C
|
Low
|
| 667
|
Sexual selection in mammals
|
706
|
23
|
C
|
Low
|
| 668
|
Dawkins vs. Gould
|
703
|
23
|
Start
|
Low
|
| 669
|
Evolution of flagella
|
699
|
23
|
Start
|
Mid
|
| 670
|
Ray Lankester
|
697
|
23
|
B
|
Low
|
| 671
|
Winner and loser effects
|
696
|
23
|
C
|
Low
|
| 672
|
Evolutionary suicide
|
694
|
23
|
Start
|
Low
|
| 673
|
Evolution: The Game of Intelligent Life
|
692
|
23
|
Start
|
Low
|
| 674
|
Mate guarding
|
692
|
23
|
Unknown
|
Mid
|
| 675
|
Evo-devo gene toolkit
|
692
|
23
|
Start
|
Mid
|
| 676
|
Ecological speciation
|
687
|
22
|
B
|
High
|
| 677
|
Elaine Morgan
|
683
|
22
|
C
|
Low
|
| 678
|
Idealised population
|
683
|
22
|
C
|
Mid
|
| 679
|
Co-adaptation
|
683
|
22
|
C
|
Low
|
| 680
|
The Evolution of Desire
|
680
|
22
|
Start
|
Unknown
|
| 681
|
The Correlation between Relatives on the Supposition of Mendelian Inheritance
|
677
|
22
|
Start
|
Mid
|
| 682
|
Proavis
|
673
|
22
|
Start
|
Low
|
| 683
|
Bayesian inference in phylogeny
|
671
|
22
|
C
|
Low
|
| 684
|
Court jester hypothesis
|
669
|
22
|
C
|
Low
|
| 685
|
Biogenesis
|
667
|
22
|
NA
|
High
|
| 686
|
E. B. Ford
|
667
|
22
|
C
|
Low
|
| 687
|
Konstantin Mereschkowski
|
667
|
22
|
GA
|
Low
|
| 688
|
Ecomorphology
|
664
|
22
|
B
|
Low
|
| 689
|
Species-typical behavior
|
661
|
22
|
Start
|
Low
|
| 690
|
Facilitated variation
|
660
|
22
|
Stub
|
Low
|
| 691
|
Chemical defense
|
659
|
21
|
C
|
Low
|
| 692
|
List of Neanderthal fossils
|
655
|
21
|
List
|
Low
|
| 693
|
Evolutionary psychology of language
|
648
|
21
|
Start
|
Low
|
| 694
|
Mosaic evolution
|
640
|
21
|
Start
|
Low
|
| 695
|
Gard model
|
639
|
21
|
Start
|
Low
|
| 696
|
Paulinella
|
638
|
21
|
Start
|
Unknown
|
| 697
|
Queen mandibular pheromone
|
638
|
21
|
Start
|
Low
|
| 698
|
Schizocoely
|
637
|
21
|
Start
|
Mid
|
| 699
|
Polyandry in fish
|
636
|
21
|
C
|
Low
|
| 700
|
Evolution of cognition
|
631
|
21
|
C
|
Low
|
| 701
|
Paul W. Ewald
|
627
|
20
|
Start
|
Low
|
| 702
|
Digital organism
|
623
|
20
|
Stub
|
Low
|
| 703
|
Selection coefficient
|
621
|
20
|
Stub
|
Mid
|
| 704
|
Disposable soma theory of aging
|
621
|
20
|
C
|
Mid
|
| 705
|
Paragroup
|
620
|
20
|
Stub
|
Low
|
| 706
|
Troglomorphism
|
620
|
20
|
Stub
|
Low
|
| 707
|
Phylotypic stage
|
620
|
20
|
C
|
Low
|
| 708
|
Genetic purging
|
619
|
20
|
C
|
Unknown
|
| 709
|
Phyletic gradualism
|
618
|
20
|
Start
|
Mid
|
| 710
|
Human jaw shrinkage
|
617
|
20
|
Unknown
|
Unknown
|
| 711
|
Nina Jablonski
|
610
|
20
|
B
|
Low
|
| 712
|
Nanjing Man
|
609
|
20
|
C
|
Low
|
| 713
|
Outline of evolution
|
609
|
20
|
List
|
Top
|
| 714
|
Seminal fluid protein
|
601
|
20
|
Start
|
Low
|
| 715
|
Gilbertian mimicry
|
599
|
19
|
GA
|
Mid
|
| 716
|
Evolution of brachiopods
|
599
|
19
|
Start
|
Low
|
| 717
|
Haplogroup C-V20
|
599
|
19
|
Unknown
|
Unknown
|
| 718
|
Habitable zone for complex life
|
599
|
19
|
C
|
Unknown
|
| 719
|
Helitron (biology)
|
598
|
19
|
B
|
Low
|
| 720
|
Behavioral plasticity
|
598
|
19
|
Start
|
Low
|
| 721
|
Franz Weidenreich
|
597
|
19
|
Start
|
Mid
|
| 722
|
Glacial refugium
|
596
|
19
|
Start
|
Low
|
| 723
|
On Being the Right Size
|
593
|
19
|
C
|
Mid
|
| 724
|
Storage effect
|
593
|
19
|
B
|
Mid
|
| 725
|
Power, Sex, Suicide
|
593
|
19
|
Stub
|
Low
|
| 726
|
List of taxa that use parthenogenesis
|
592
|
19
|
B
|
High
|
| 727
|
Spiegelman's Monster
|
590
|
19
|
Start
|
Low
|
| 728
|
Reproductive suppression
|
589
|
19
|
C
|
Mid
|
| 729
|
Religion Explained
|
585
|
19
|
Start
|
Low
|
| 730
|
Evolutionary capacitance
|
584
|
19
|
C
|
Mid
|
| 731
|
Bitter taste evolution
|
582
|
19
|
Start
|
Low
|
| 732
|
Interlocus sexual conflict
|
579
|
19
|
B
|
Mid
|
| 733
|
Kettlewell's experiment
|
576
|
19
|
Start
|
Mid
|
| 734
|
Development of Darwin's theory
|
574
|
19
|
B
|
Mid
|
| 735
|
Rate of evolution
|
571
|
19
|
Start
|
Low
|
| 736
|
Inversion (evolutionary biology)
|
570
|
19
|
Start
|
Mid
|
| 737
|
Cryptic species complex
|
563
|
18
|
NA
|
NA
|
| 738
|
Evolutionary landscape
|
563
|
18
|
C
|
High
|
| 739
|
Shifting balance theory
|
558
|
18
|
Stub
|
Low
|
| 740
|
Directed evolution (transhumanism)
|
555
|
18
|
Stub
|
Low
|
| 741
|
Biodiversity of Kosovo
|
553
|
18
|
C
|
Low
|
| 742
|
The Evolution of Beauty
|
545
|
18
|
Start
|
Low
|
| 743
|
Prejudice from an evolutionary perspective
|
542
|
18
|
Start
|
Low
|
| 744
|
Hox genes in amphibians and reptiles
|
541
|
18
|
C
|
Low
|
| 745
|
Sex Power Money
|
540
|
18
|
C
|
Low
|
| 746
|
Phylogenetic comparative methods
|
537
|
17
|
C
|
Low
|
| 747
|
Sexual selection in insects
|
537
|
17
|
B
|
Low
|
| 748
|
The Variation of Animals and Plants Under Domestication
|
534
|
17
|
C
|
Low
|
| 749
|
Adaptation and Natural Selection
|
532
|
17
|
Start
|
Low
|
| 750
|
Wing-assisted incline running
|
522
|
17
|
Start
|
Low
|
| 751
|
Robert Edmond Grant
|
521
|
17
|
Start
|
Low
|
| 752
|
Buya, Eritrea
|
520
|
17
|
B
|
Low
|
| 753
|
Intergradation
|
519
|
17
|
Start
|
Low
|
| 754
|
Inferring horizontal gene transfer
|
517
|
17
|
B
|
Low
|
| 755
|
Multispecies coalescent process
|
512
|
17
|
Start
|
Low
|
| 756
|
List of Neanderthal sites
|
508
|
16
|
List
|
Low
|
| 757
|
Eukaryote hybrid genome
|
507
|
16
|
B
|
Low
|
| 758
|
Karyoklepty
|
501
|
16
|
Stub
|
Low
|
| 759
|
Biological constraints
|
500
|
16
|
Start
|
Mid
|
| 760
|
Red King hypothesis
|
500
|
16
|
Start
|
Low
|
| 761
|
Evolutionary tradeoff
|
499
|
16
|
Unknown
|
Unknown
|
| 762
|
Marcus Feldman
|
492
|
16
|
Start
|
Low
|
| 763
|
Group living
|
490
|
16
|
Start
|
Low
|
| 764
|
David Lack
|
488
|
16
|
C
|
Low
|
| 765
|
Modularity (biology)
|
487
|
16
|
Start
|
Low
|
| 766
|
Hybrid incompatibility
|
484
|
16
|
C
|
Low
|
| 767
|
Cellularization
|
480
|
16
|
Stub
|
Low
|
| 768
|
Evolution of descended testes in mammals
|
480
|
16
|
Unknown
|
Unknown
|
| 769
|
Fisher's geometric model
|
479
|
15
|
Start
|
Low
|
| 770
|
Self-decoration camouflage
|
478
|
15
|
GA
|
Low
|
| 771
|
Adaptive behavior (ecology)
|
477
|
15
|
C
|
Mid
|
| 772
|
Proteinoid
|
476
|
15
|
Start
|
Low
|
| 773
|
Edward Bagnall Poulton
|
476
|
15
|
Start
|
Mid
|
| 774
|
Largest-scale trends in evolution
|
475
|
15
|
Start
|
High
|
| 775
|
Host switch
|
475
|
15
|
C
|
Low
|
| 776
|
McLean v. Arkansas
|
474
|
15
|
Start
|
Low
|
| 777
|
Black Queen hypothesis
|
474
|
15
|
Start
|
Low
|
| 778
|
Davidson Black
|
472
|
15
|
C
|
Mid
|
| 779
|
Turnover-pulse hypothesis
|
472
|
15
|
Start
|
Low
|
| 780
|
Unique-event polymorphism
|
472
|
15
|
Start
|
Low
|
| 781
|
Coloration evidence for natural selection
|
472
|
15
|
GA
|
Mid
|
| 782
|
Orgel's rules
|
471
|
15
|
Stub
|
Low
|
| 783
|
Darwinian demon
|
470
|
15
|
Stub
|
Low
|
| 784
|
Infinite sites model
|
470
|
15
|
Start
|
Low
|
| 785
|
Patriarch hypothesis
|
469
|
15
|
Unknown
|
Unknown
|
| 786
|
Candidatus Atelocyanobacterium thalassa
|
469
|
15
|
C
|
Low
|
| 787
|
Clonal interference
|
465
|
15
|
Stub
|
Mid
|
| 788
|
Contingency (evolutionary biology)
|
461
|
15
|
Start
|
Low
|
| 789
|
Darwinian puzzle
|
459
|
15
|
Start
|
Low
|
| 790
|
Enterocoely
|
459
|
15
|
Stub
|
Mid
|
| 791
|
Phylogenetic inertia
|
459
|
15
|
Start
|
Mid
|
| 792
|
Allochronic speciation
|
458
|
15
|
B
|
Mid
|
| 793
|
Gavin de Beer
|
456
|
15
|
C
|
Low
|
| 794
|
Evolutionary physiology
|
456
|
15
|
B
|
High
|
| 795
|
Applications of evolution
|
455
|
15
|
B
|
Low
|
| 796
|
How the Snake Lost Its Legs
|
455
|
15
|
GA
|
Low
|
| 797
|
Quantum evolution
|
454
|
15
|
C
|
Mid
|
| 798
|
Ecological inheritance
|
453
|
15
|
Stub
|
Low
|
| 799
|
Miguelón
|
450
|
15
|
C
|
Unknown
|
| 800
|
St. George Jackson Mivart
|
446
|
14
|
Start
|
Low
|
| 801
|
Evolutionary models of food sharing
|
445
|
14
|
C
|
Low
|
| 802
|
History of speciation
|
445
|
14
|
C
|
Low
|
| 803
|
Identity in social insects
|
441
|
14
|
Start
|
Low
|
| 804
|
Man's Place in Nature
|
438
|
14
|
Start
|
Mid
|
| 805
|
V. C. Wynne-Edwards
|
436
|
14
|
Start
|
Low
|
| 806
|
Constructive neutral evolution
|
435
|
14
|
C
|
Low
|
| 807
|
Mesozoic–Cenozoic radiation
|
434
|
14
|
C
|
Low
|
| 808
|
Heterotopy
|
432
|
14
|
Stub
|
Low
|
| 809
|
Douglas J. Futuyma
|
427
|
14
|
C
|
Low
|
| 810
|
Darwinian literary studies
|
426
|
14
|
C
|
Low
|
| 811
|
Sexual selection in scaled reptiles
|
426
|
14
|
Start
|
Low
|
| 812
|
Icons of Evolution
|
424
|
14
|
C
|
Low
|
| 813
|
Herman Bernhard Lundborg
|
423
|
14
|
Start
|
Low
|
| 814
|
Allan Wilson (biologist)
|
422
|
14
|
C
|
Low
|
| 815
|
Evolutionary developmental psychology
|
421
|
14
|
C
|
Low
|
| 816
|
Evolution of olfaction
|
421
|
14
|
C
|
Low
|
| 817
|
Key innovation
|
418
|
13
|
Start
|
Mid
|
| 818
|
Maternal effect dominant embryonic arrest
|
416
|
13
|
Start
|
Low
|
| 819
|
Evolutionary baggage
|
415
|
13
|
Start
|
Low
|
| 820
|
Museum of Human Evolution
|
415
|
13
|
Start
|
Unknown
|
| 821
|
Swamping argument
|
415
|
13
|
Stub
|
Low
|
| 822
|
Conservation-induced extinction
|
415
|
13
|
Start
|
Mid
|
| 823
|
Edward Blyth
|
414
|
13
|
B
|
High
|
| 824
|
Urban evolution
|
412
|
13
|
C
|
Unknown
|
| 825
|
Phagomimicry
|
409
|
13
|
Stub
|
Low
|
| 826
|
Megaevolution
|
407
|
13
|
Start
|
Mid
|
| 827
|
Zoonotic origins of COVID-19
|
406
|
13
|
B
|
Mid
|
| 828
|
Natural Selection (manuscript)
|
405
|
13
|
Stub
|
Low
|
| 829
|
Parasite load
|
404
|
13
|
C
|
Low
|
| 830
|
Ancestral sequence reconstruction
|
404
|
13
|
B
|
Low
|
| 831
|
Lilliput effect
|
403
|
13
|
Start
|
Low
|
| 832
|
Alfred Newton
|
402
|
13
|
C
|
Low
|
| 833
|
Stenogale
|
402
|
13
|
Stub
|
Low
|
| 834
|
Escape and radiate coevolution
|
398
|
13
|
C
|
Unknown
|
| 835
|
Felsenstein's tree-pruning algorithm
|
397
|
13
|
Stub
|
Low
|
| 836
|
Darwin (unit)
|
396
|
13
|
Stub
|
Low
|
| 837
|
Nylon-eating bacteria and creationism
|
395
|
13
|
B
|
Low
|
| 838
|
Evolutionary rescue
|
395
|
13
|
Start
|
Low
|
| 839
|
Evolutionary theodicy
|
395
|
13
|
C
|
Low
|
| 840
|
The Neanderthals Rediscovered
|
395
|
13
|
GA
|
Low
|
| 841
|
Annual vs. perennial plant evolution
|
394
|
13
|
C
|
Low
|
| 842
|
Hydrogen hypothesis
|
392
|
13
|
Start
|
Low
|
| 843
|
Loren Cordain
|
392
|
13
|
Stub
|
Low
|
| 844
|
The Theory of Evolution
|
390
|
13
|
Stub
|
Low
|
| 845
|
Evolution by gene duplication
|
390
|
13
|
Start
|
High
|
| 846
|
John Tyler Bonner
|
389
|
12
|
C
|
Mid
|
| 847
|
Eugenics in Mexico
|
389
|
12
|
Start
|
Low
|
| 848
|
Concerted evolution
|
387
|
12
|
Stub
|
Low
|
| 849
|
The Neutral Theory of Molecular Evolution
|
386
|
12
|
Stub
|
Low
|
| 850
|
Philosophy of evolution
|
384
|
12
|
C
|
Mid
|
| 851
|
Postcanine megadontia
|
381
|
12
|
C
|
Low
|
| 852
|
Law of Life
|
377
|
12
|
Stub
|
Low
|
| 853
|
Laboratory experiments of speciation
|
377
|
12
|
List
|
Low
|
| 854
|
The Genealogical Adam and Eve
|
376
|
12
|
Start
|
Low
|
| 855
|
Rensch's rule
|
375
|
12
|
Start
|
Low
|
| 856
|
Distractive markings
|
374
|
12
|
C
|
Low
|
| 857
|
Proto-mitochondrion
|
373
|
12
|
Start
|
Mid
|
| 858
|
Eliza Gamble
|
368
|
12
|
Start
|
Low
|
| 859
|
Automixis
|
368
|
12
|
Start
|
Unknown
|
| 860
|
Invasion genetics
|
366
|
12
|
C
|
Low
|
| 861
|
Evolution (TV series)
|
364
|
12
|
Start
|
Low
|
| 862
|
List of transitional fossils
|
363
|
12
|
NA
|
NA
|
| 863
|
The Goodness Paradox
|
363
|
12
|
Start
|
Low
|
| 864
|
Background selection
|
362
|
12
|
Start
|
Low
|
| 865
|
Push of the past
|
361
|
12
|
C
|
Low
|
| 866
|
Germ-Soma Differentiation
|
361
|
12
|
C
|
Low
|
| 867
|
Tree rearrangement
|
360
|
12
|
Start
|
Low
|
| 868
|
William Henry Flower
|
359
|
11
|
B
|
Low
|
| 869
|
Strong reciprocity
|
359
|
11
|
B
|
Low
|
| 870
|
Evidence for speciation by reinforcement
|
358
|
11
|
List
|
Low
|
| 871
|
Fisheries-induced evolution
|
358
|
11
|
C
|
Low
|
| 872
|
River barrier hypothesis
|
356
|
11
|
C
|
Low
|
| 873
|
Commemoration of Charles Darwin
|
354
|
11
|
C
|
Mid
|
| 874
|
Cospeciation
|
349
|
11
|
Start
|
Mid
|
| 875
|
Darwinian threshold
|
349
|
11
|
Start
|
Mid
|
| 876
|
Cytotaxonomy
|
348
|
11
|
Stub
|
Mid
|
| 877
|
Randy Thornhill
|
347
|
11
|
Start
|
Mid
|
| 878
|
Continuity model of British ancestry
|
346
|
11
|
Start
|
Low
|
| 879
|
Francis Maitland Balfour
|
345
|
11
|
Start
|
Low
|
| 880
|
Sex differences in sensory systems
|
344
|
11
|
Start
|
Mid
|
| 881
|
W. Tecumseh Fitch
|
341
|
11
|
Stub
|
Low
|
| 882
|
Caminalcules
|
341
|
11
|
Start
|
Mid
|
| 883
|
Wushan Man
|
340
|
11
|
Start
|
Low
|
| 884
|
Reciprocal altruism in humans
|
340
|
11
|
Start
|
Low
|
| 885
|
Genotype frequency
|
338
|
11
|
Start
|
Mid
|
| 886
|
Mimicry in vertebrates
|
338
|
11
|
Start
|
Low
|
| 887
|
Calcichordate hypothesis
|
337
|
11
|
Start
|
Mid
|
| 888
|
Maternal behavior in vertebrates
|
337
|
11
|
C
|
Low
|
| 889
|
Archaic Homo sapiens
|
336
|
11
|
NA
|
NA
|
| 890
|
Biogeographic regions of Europe
|
336
|
11
|
Start
|
Mid
|
| 891
|
Nonecological speciation
|
336
|
11
|
Start
|
Low
|
| 892
|
Stepwise mutation model
|
335
|
11
|
Stub
|
Low
|
| 893
|
Theology of creationism and evolution
|
333
|
11
|
Start
|
Low
|
| 894
|
Scott F. Gilbert
|
333
|
11
|
C
|
Low
|
| 895
|
Darwinian anthropology
|
332
|
11
|
B
|
Unknown
|
| 896
|
Evolution of metal ions in biological systems
|
332
|
11
|
C
|
Low
|
| 897
|
Talk.origins
|
330
|
11
|
Start
|
Low
|
| 898
|
Precambrian body plans
|
328
|
10
|
B
|
Low
|
| 899
|
Ecological evolutionary developmental biology
|
328
|
10
|
Start
|
Low
|
| 900
|
Predictive adaptive response
|
327
|
10
|
Unknown
|
Unknown
|
| 901
|
Landscape genomics
|
327
|
10
|
Stub
|
Low
|
| 902
|
Common species
|
326
|
10
|
Stub
|
Unknown
|
| 903
|
Phenotypic integration
|
326
|
10
|
C
|
Low
|
| 904
|
Cultural selection theory
|
325
|
10
|
C
|
Low
|
| 905
|
Human-based evolutionary computation
|
324
|
10
|
Start
|
Low
|
| 906
|
Peter J. Bowler
|
323
|
10
|
Start
|
Low
|
| 907
|
Runcaria
|
323
|
10
|
Start
|
Low
|
| 908
|
Social immunity
|
323
|
10
|
B
|
High
|
| 909
|
Phylogenetic reconciliation
|
322
|
10
|
Unknown
|
Unknown
|
| 910
|
Horizontal gene transfer in evolution
|
320
|
10
|
Start
|
High
|
| 911
|
Evolutionary dynamics
|
319
|
10
|
Stub
|
Mid
|
| 912
|
Natural morality
|
314
|
10
|
Start
|
Low
|
| 913
|
Sir William Lawrence, 1st Baronet
|
311
|
10
|
B
|
High
|
| 914
|
Female line
|
311
|
10
|
NA
|
NA
|
| 915
|
Phylogenetic signal
|
310
|
10
|
C
|
Mid
|
| 916
|
Evolutionary fauna
|
306
|
10
|
Start
|
Low
|
| 917
|
Saldanha man
|
305
|
10
|
Stub
|
Low
|
| 918
|
What Darwin Got Wrong
|
304
|
10
|
Start
|
Low
|
| 919
|
Qikiqtania
|
304
|
10
|
C
|
Unknown
|
| 920
|
The Seven Pillars of Life
|
301
|
10
|
Start
|
Low
|
| 921
|
Alpheus Hyatt
|
300
|
10
|
Start
|
Low
|
| 922
|
Evolution of Macropodidae
|
300
|
10
|
Start
|
Low
|
| 923
|
Romanticism in evolution theory
|
300
|
10
|
Start
|
Low
|
| 924
|
Mutation accumulation theory
|
300
|
10
|
C
|
Low
|
| 925
|
Rupert Riedl
|
299
|
9
|
Start
|
Low
|
| 926
|
Molecular Phylogenetics and Evolution
|
299
|
9
|
Stub
|
Low
|
| 927
|
Fuyan Cave
|
299
|
9
|
C
|
Low
|
| 928
|
Male reproductive alliances
|
297
|
9
|
Start
|
Low
|
| 929
|
Punctuated gradualism
|
295
|
9
|
Start
|
Low
|
| 930
|
Resource holding potential
|
289
|
9
|
Stub
|
Low
|
| 931
|
Discredited hypotheses for the Cambrian explosion
|
286
|
9
|
Stub
|
Mid
|
| 932
|
Richard Prum
|
285
|
9
|
Start
|
Low
|
| 933
|
Gender psychology
|
284
|
9
|
NA
|
NA
|
| 934
|
Subfunctionalization
|
283
|
9
|
Start
|
Low
|
| 935
|
Mutation bias
|
283
|
9
|
C
|
Mid
|
| 936
|
Polymorphism in Lepidoptera
|
281
|
9
|
C
|
High
|
| 937
|
Ecology and evolutionary biology
|
280
|
9
|
Start
|
Low
|
| 938
|
Zinnia Kumar
|
280
|
9
|
C
|
Low
|
| 939
|
Index of evolutionary biology articles
|
277
|
9
|
List
|
High
|
| 940
|
Obcell
|
277
|
9
|
Stub
|
Mid
|
| 941
|
Stan Wood (fossil hunter)
|
277
|
9
|
B
|
Unknown
|
| 942
|
Martha M. Muñoz
|
277
|
9
|
Stub
|
Unknown
|
| 943
|
The Origin of Birds
|
274
|
9
|
GA
|
High
|
| 944
|
V0-morph
|
273
|
9
|
Start
|
Low
|
| 945
|
Sexual strategies theory
|
272
|
9
|
Start
|
Unknown
|
| 946
|
Alloplastic adaptation
|
270
|
9
|
Stub
|
Low
|
| 947
|
Ecological selection
|
269
|
8
|
NA
|
Mid
|
| 948
|
V1-morph
|
269
|
8
|
Stub
|
Low
|
| 949
|
Dynamic mutation
|
269
|
8
|
Stub
|
Low
|
| 950
|
Haplotype convergence
|
269
|
8
|
Stub
|
Low
|
| 951
|
Genome diversity and karyotype evolution of mammals
|
266
|
8
|
B
|
Low
|
| 952
|
TalkOrigins Archive
|
265
|
8
|
Start
|
Low
|
| 953
|
The Faith Instinct
|
265
|
8
|
Stub
|
Low
|
| 954
|
Genomic evolution of birds
|
265
|
8
|
C
|
Low
|
| 955
|
Skeletal changes of vertebrates transitioning from water to land
|
263
|
8
|
C
|
Low
|
| 956
|
Transient masculinization
|
262
|
8
|
C
|
Unknown
|
| 957
|
The Apportionment of Human Diversity
|
261
|
8
|
C
|
Low
|
| 958
|
Timeline of zoology
|
260
|
8
|
List
|
Mid
|
| 959
|
The Great Monkey Trial
|
259
|
8
|
Start
|
Low
|
| 960
|
The g Factor: General Intelligence and Its Implications
|
252
|
8
|
Stub
|
Mid
|
| 961
|
Reductive evolution
|
252
|
8
|
Start
|
Low
|
| 962
|
Hybrid swarm
|
251
|
8
|
Start
|
Mid
|
| 963
|
Rapid modes of evolution
|
249
|
8
|
Unknown
|
Unknown
|
| 964
|
David Hillis
|
247
|
8
|
Start
|
Low
|
| 965
|
Evolution of influenza
|
246
|
8
|
NA
|
NA
|
| 966
|
Joan E. Strassmann
|
244
|
8
|
Start
|
Low
|
| 967
|
Contest competition
|
242
|
8
|
Stub
|
Low
|
| 968
|
The Gene Bomb
|
241
|
8
|
Start
|
Mid
|
| 969
|
Escalation hypothesis
|
240
|
8
|
Unknown
|
Unknown
|
| 970
|
Ileret
|
238
|
7
|
Stub
|
Low
|
| 971
|
Interpolation theory
|
237
|
7
|
Start
|
Low
|
| 972
|
Caveasphaera
|
236
|
7
|
Start
|
Low
|
| 973
|
Stephen Blair Hedges
|
232
|
7
|
Start
|
Low
|
| 974
|
Human reproductive ecology
|
231
|
7
|
Start
|
Low
|
| 975
|
Interactor
|
226
|
7
|
Stub
|
Low
|
| 976
|
Preadaptation
|
225
|
7
|
NA
|
Mid
|
| 977
|
Host adaptation
|
225
|
7
|
Start
|
Mid
|
| 978
|
Homo consumericus
|
224
|
7
|
Start
|
Low
|
| 979
|
Of Moths and Men
|
222
|
7
|
Stub
|
Mid
|
| 980
|
International Year of Biodiversity
|
222
|
7
|
Start
|
High
|
| 981
|
Karl Kessler
|
222
|
7
|
Stub
|
Low
|
| 982
|
Effective evolutionary time
|
219
|
7
|
Start
|
Low
|
| 983
|
John Endler
|
218
|
7
|
Start
|
Low
|
| 984
|
Man's Genesis
|
218
|
7
|
Start
|
Low
|
| 985
|
Allometric engineering
|
216
|
7
|
Start
|
Mid
|
| 986
|
List of ecoregions with high endemism
|
216
|
7
|
List
|
Low
|
| 987
|
GADV-protein world hypothesis
|
216
|
7
|
Start
|
Low
|
| 988
|
Developmental bias
|
216
|
7
|
Unknown
|
Unknown
|
| 989
|
Jeremiah Kianga
|
212
|
7
|
Start
|
Low
|
| 990
|
Undeniable: Evolution and the Science of Creation
|
211
|
7
|
Start
|
Low
|
| 991
|
Human somatic variation
|
211
|
7
|
C
|
Mid
|
| 992
|
James A. Lake
|
210
|
7
|
Start
|
Low
|
| 993
|
Transformed cladistics
|
210
|
7
|
C
|
Low
|
| 994
|
Parallel speciation
|
208
|
6
|
Unknown
|
Low
|
| 995
|
Cytonuclear discordance
|
208
|
6
|
Start
|
Unknown
|
| 996
|
Molecular drive
|
206
|
6
|
Stub
|
Low
|
| 997
|
Hologenomics
|
206
|
6
|
Start
|
Low
|
| 998
|
Thomas Roscoe Rede Stebbing
|
205
|
6
|
B
|
Low
|
| 999
|
Henric Sanielevici
|
205
|
6
|
B
|
Low
|
| 1000
|
Formamide-based prebiotic chemistry
|
204
|
6
|
Start
|
Low
|
