| Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
| 1
|
Neanderthal
|
133,400
|
4,446
|
GA
|
Mid
|
| 2
|
Eugenics
|
113,022
|
3,767
|
B
|
Mid
|
| 3
|
Charles Darwin
|
107,800
|
3,593
|
FA
|
Top
|
| 4
|
Sexual dimorphism
|
69,337
|
2,311
|
B
|
High
|
| 5
|
Human evolution
|
68,788
|
2,292
|
C
|
High
|
| 6
|
Cretaceous–Paleogene extinction event
|
65,706
|
2,190
|
FA
|
High
|
| 7
|
Richard Dawkins
|
64,123
|
2,137
|
GA
|
Mid
|
| 8
|
List of common misconceptions
|
63,501
|
2,116
|
List
|
Low
|
| 9
|
Species
|
59,779
|
1,992
|
GA
|
Top
|
| 10
|
Extinction
|
55,344
|
1,844
|
C
|
High
|
| 11
|
Racism
|
45,916
|
1,530
|
B
|
Mid
|
| 12
|
Abiogenesis
|
43,677
|
1,455
|
GA
|
Top
|
| 13
|
Evolution
|
43,027
|
1,434
|
FA
|
Top
|
| 14
|
Scientific racism
|
42,529
|
1,417
|
C
|
Low
|
| 15
|
Cro-Magnon
|
41,055
|
1,368
|
GA
|
Mid
|
| 16
|
Carcinisation
|
39,958
|
1,331
|
Start
|
Mid
|
| 17
|
Scopes trial
|
37,480
|
1,249
|
B
|
High
|
| 18
|
Early modern human
|
37,044
|
1,234
|
B
|
Mid
|
| 19
|
Parthenogenesis
|
36,240
|
1,208
|
C
|
High
|
| 20
|
List of X-Men members
|
36,113
|
1,203
|
List
|
Low
|
| 21
|
Epicanthic fold
|
34,976
|
1,165
|
C
|
Low
|
| 22
|
William Jennings Bryan
|
33,850
|
1,128
|
B
|
High
|
| 23
|
Inbreeding
|
33,132
|
1,104
|
C
|
High
|
| 24
|
Last universal common ancestor
|
31,773
|
1,059
|
GA
|
Top
|
| 25
|
Binomial nomenclature
|
31,146
|
1,038
|
C
|
Low
|
| 26
|
Fossil
|
30,837
|
1,027
|
B
|
Mid
|
| 27
|
Timeline of human evolution
|
30,831
|
1,027
|
C
|
Low
|
| 28
|
Cousin
|
27,528
|
917
|
Start
|
Low
|
| 29
|
Hybrid (biology)
|
26,924
|
897
|
GA
|
High
|
| 30
|
Domestication of the dog
|
25,654
|
855
|
B
|
Low
|
| 31
|
Patrilineality
|
24,225
|
807
|
Start
|
Low
|
| 32
|
Homo floresiensis
|
24,136
|
804
|
B
|
Mid
|
| 33
|
Biodiversity
|
23,626
|
787
|
C
|
Mid
|
| 34
|
Clade
|
22,976
|
765
|
C
|
High
|
| 35
|
Racism in the United States
|
22,891
|
763
|
B
|
High
|
| 36
|
On the Origin of Species
|
22,803
|
760
|
FA
|
Top
|
| 37
|
HeLa
|
22,519
|
750
|
C
|
Low
|
| 38
|
Neontology
|
22,335
|
744
|
Start
|
Mid
|
| 39
|
Natural selection
|
22,253
|
741
|
GA
|
Top
|
| 40
|
Genetics
|
22,054
|
735
|
FA
|
Top
|
| 41
|
Wallace Line
|
22,031
|
734
|
Start
|
Mid
|
| 42
|
Origin of SARS-CoV-2
|
21,251
|
708
|
B
|
Mid
|
| 43
|
Paleontology
|
21,186
|
706
|
GA
|
Top
|
| 44
|
Great Oxidation Event
|
21,096
|
703
|
B
|
Mid
|
| 45
|
Social Darwinism
|
20,777
|
692
|
B
|
Low
|
| 46
|
Cambrian explosion
|
20,727
|
690
|
B
|
High
|
| 47
|
Convergent evolution
|
20,568
|
685
|
GA
|
High
|
| 48
|
Anus
|
20,490
|
683
|
Start
|
Mid
|
| 49
|
Ecology
|
20,141
|
671
|
GA
|
Top
|
| 50
|
Mutation
|
19,323
|
644
|
B
|
Top
|
| 51
|
Altruism
|
18,828
|
627
|
B
|
High
|
| 52
|
Eusociality
|
18,826
|
627
|
GA
|
Mid
|
| 53
|
Pan (genus)
|
18,774
|
625
|
B
|
High
|
| 54
|
Upper Paleolithic
|
18,549
|
618
|
C
|
Low
|
| 55
|
Origin of language
|
18,451
|
615
|
B
|
Low
|
| 56
|
Eugenics in the United States
|
17,670
|
589
|
Start
|
Low
|
| 57
|
Domestication of the cat
|
17,311
|
577
|
C
|
Mid
|
| 58
|
Francis Galton
|
16,975
|
565
|
B
|
Low
|
| 59
|
Australopithecine
|
16,282
|
542
|
C
|
High
|
| 60
|
Living fossil
|
16,194
|
539
|
C
|
Mid
|
| 61
|
Nazi eugenics
|
16,189
|
539
|
C
|
Low
|
| 62
|
Sociality
|
15,878
|
529
|
C
|
Mid
|
| 63
|
Tiktaalik
|
15,872
|
529
|
GA
|
High
|
| 64
|
Evolution of the wolf
|
15,692
|
523
|
B
|
Low
|
| 65
|
Lamarckism
|
15,268
|
508
|
GA
|
High
|
| 66
|
Human taxonomy
|
15,175
|
505
|
C
|
Low
|
| 67
|
Extant taxon
|
15,132
|
504
|
NA
|
NA
|
| 68
|
Fear
|
15,018
|
500
|
B
|
Low
|
| 69
|
History of life
|
14,744
|
491
|
GA
|
Top
|
| 70
|
Population bottleneck
|
14,664
|
488
|
C
|
High
|
| 71
|
Insular dwarfism
|
14,478
|
482
|
C
|
Low
|
| 72
|
Polymorphism (biology)
|
14,209
|
473
|
B
|
High
|
| 73
|
Hardy–Weinberg principle
|
14,093
|
469
|
C
|
High
|
| 74
|
Matrilineality
|
13,976
|
465
|
C
|
Low
|
| 75
|
Herbert Spencer
|
13,928
|
464
|
B
|
Low
|
| 76
|
Alfred Russel Wallace
|
13,673
|
455
|
FA
|
Top
|
| 77
|
Aposematism
|
13,593
|
453
|
GA
|
Mid
|
| 78
|
Camouflage
|
13,530
|
451
|
GA
|
Mid
|
| 79
|
Stromatolite
|
13,470
|
449
|
B
|
Mid
|
| 80
|
Stephen Jay Gould
|
13,411
|
447
|
GA
|
Mid
|
| 81
|
Antimicrobial resistance
|
13,042
|
434
|
B
|
Unknown
|
| 82
|
Earliest known life forms
|
12,857
|
428
|
C
|
Top
|
| 83
|
Darwinism
|
12,829
|
427
|
C
|
High
|
| 84
|
Homology (biology)
|
12,685
|
422
|
GA
|
Top
|
| 85
|
Nordicism
|
12,620
|
420
|
B
|
Low
|
| 86
|
Haplogroup
|
12,617
|
420
|
C
|
Mid
|
| 87
|
Humanoid
|
12,610
|
420
|
Start
|
Mid
|
| 88
|
Bipedalism
|
12,477
|
415
|
B
|
Mid
|
| 89
|
Ronald Fisher
|
12,036
|
401
|
B
|
High
|
| 90
|
Karyotype
|
12,004
|
400
|
C
|
Low
|
| 91
|
The Selfish Gene
|
11,752
|
391
|
B
|
High
|
| 92
|
Sexual selection
|
11,722
|
390
|
GA
|
High
|
| 93
|
Timeline of the evolutionary history of life
|
11,630
|
387
|
B
|
Top
|
| 94
|
Peking Man
|
11,573
|
385
|
GA
|
Mid
|
| 95
|
Evolution of mammals
|
11,516
|
383
|
B
|
High
|
| 96
|
The Naked Woman
|
11,505
|
383
|
Stub
|
Low
|
| 97
|
Thomas Henry Huxley
|
11,351
|
378
|
B
|
Mid
|
| 98
|
Sex differences in intelligence
|
11,279
|
375
|
B
|
Low
|
| 99
|
Selective breeding
|
11,258
|
375
|
C
|
Low
|
| 100
|
R/K selection theory
|
11,134
|
371
|
C
|
High
|
| 101
|
Chicken or the egg
|
11,055
|
368
|
Start
|
Low
|
| 102
|
Ediacaran biota
|
11,037
|
367
|
FA
|
Low
|
| 103
|
Human Y-chromosome DNA haplogroup
|
10,916
|
363
|
C
|
Mid
|
| 104
|
Panthera hybrid
|
10,889
|
362
|
C
|
Low
|
| 105
|
Behavioral modernity
|
10,701
|
356
|
C
|
Low
|
| 106
|
Darwin's finches
|
10,693
|
356
|
C
|
High
|
| 107
|
Archaic humans
|
10,487
|
349
|
NA
|
Low
|
| 108
|
Heritability of IQ
|
10,407
|
346
|
C
|
Mid
|
| 109
|
Origin of birds
|
10,303
|
343
|
B
|
Mid
|
| 110
|
Phylogenetics
|
10,127
|
337
|
B
|
High
|
| 111
|
List of human evolution fossils
|
10,098
|
336
|
List
|
High
|
| 112
|
Jean-Baptiste Lamarck
|
10,090
|
336
|
B
|
Top
|
| 113
|
Human mating strategies
|
9,829
|
327
|
B
|
Low
|
| 114
|
E. O. Wilson
|
9,760
|
325
|
B
|
Mid
|
| 115
|
Ernst Haeckel
|
9,710
|
323
|
B
|
High
|
| 116
|
Major histocompatibility complex
|
9,699
|
323
|
B
|
Low
|
| 117
|
Heritability of autism
|
9,679
|
322
|
C
|
Mid
|
| 118
|
Institutional racism
|
9,660
|
322
|
B
|
Mid
|
| 119
|
Human vestigiality
|
9,357
|
311
|
C
|
Mid
|
| 120
|
Most recent common ancestor
|
9,261
|
308
|
B
|
High
|
| 121
|
Mimicry
|
9,234
|
307
|
GA
|
High
|
| 122
|
Feathered dinosaur
|
9,130
|
304
|
C
|
High
|
| 123
|
Three-domain system
|
9,116
|
303
|
C
|
Mid
|
| 124
|
Evolutionary psychology
|
9,085
|
302
|
C
|
High
|
| 125
|
Evolution of the horse
|
9,070
|
302
|
B
|
Mid
|
| 126
|
Julian Huxley
|
8,673
|
289
|
B
|
Mid
|
| 127
|
Founder effect
|
8,621
|
287
|
C
|
Mid
|
| 128
|
RNA world
|
8,596
|
286
|
C
|
High
|
| 129
|
Lower Paleolithic
|
8,578
|
285
|
C
|
High
|
| 130
|
Red Queen hypothesis
|
8,529
|
284
|
Start
|
Mid
|
| 131
|
Inbreeding depression
|
8,389
|
279
|
C
|
Mid
|
| 132
|
Genetic drift
|
8,340
|
278
|
GA
|
Top
|
| 133
|
Rare Earth hypothesis
|
8,323
|
277
|
B
|
Low
|
| 134
|
Vestigiality
|
8,249
|
274
|
C
|
High
|
| 135
|
Sex differences in human physiology
|
8,188
|
272
|
C
|
High
|
| 136
|
Adaptation
|
8,161
|
272
|
GA
|
Top
|
| 137
|
Stoned ape theory
|
8,157
|
271
|
C
|
Low
|
| 138
|
Survival of the fittest
|
8,121
|
270
|
B
|
Low
|
| 139
|
Common descent
|
8,070
|
269
|
B
|
Top
|
| 140
|
Monophyly
|
8,051
|
268
|
C
|
Mid
|
| 141
|
Island gigantism
|
7,978
|
265
|
C
|
Low
|
| 142
|
Triune brain
|
7,913
|
263
|
Start
|
Low
|
| 143
|
Great American Interchange
|
7,911
|
263
|
C
|
Mid
|
| 144
|
Instinct
|
7,896
|
263
|
C
|
Low
|
| 145
|
Cladistics
|
7,860
|
262
|
C
|
Mid
|
| 146
|
Dysgenics
|
7,816
|
260
|
Start
|
Mid
|
| 147
|
Aquatic ape hypothesis
|
7,766
|
258
|
C
|
Low
|
| 148
|
Sperm competition
|
7,742
|
258
|
Start
|
Mid
|
| 149
|
Evolutionary biology
|
7,689
|
256
|
C
|
Top
|
| 150
|
Species complex
|
7,676
|
255
|
B
|
Mid
|
| 151
|
Sexual cannibalism
|
7,652
|
255
|
B
|
Low
|
| 152
|
Offspring
|
7,644
|
254
|
Start
|
Mid
|
| 153
|
Batesian mimicry
|
7,568
|
252
|
GA
|
Mid
|
| 154
|
Horizontal gene transfer
|
7,532
|
251
|
C
|
High
|
| 155
|
Basal (phylogenetics)
|
7,477
|
249
|
C
|
Mid
|
| 156
|
Linnaean taxonomy
|
7,404
|
246
|
C
|
Mid
|
| 157
|
Fertility
|
7,395
|
246
|
C
|
High
|
| 158
|
Recent human evolution
|
7,280
|
242
|
B
|
Mid
|
| 159
|
Felid hybrids
|
7,272
|
242
|
Start
|
Low
|
| 160
|
Symbiogenesis
|
7,268
|
242
|
GA
|
High
|
| 161
|
Primordial soup
|
7,265
|
242
|
Start
|
Mid
|
| 162
|
Evolution of sexual reproduction
|
7,221
|
240
|
B
|
High
|
| 163
|
Jebel Irhoud
|
7,211
|
240
|
C
|
Low
|
| 164
|
Punctuated equilibrium
|
7,178
|
239
|
GA
|
High
|
| 165
|
Speciation
|
7,098
|
236
|
B
|
High
|
| 166
|
Female promiscuity
|
6,960
|
232
|
C
|
Low
|
| 167
|
Ashkenazi Jewish intelligence
|
6,952
|
231
|
Start
|
Low
|
| 168
|
Lek mating
|
6,917
|
230
|
GA
|
Mid
|
| 169
|
J. B. S. Haldane
|
6,893
|
229
|
C
|
Mid
|
| 170
|
Anthropometry
|
6,764
|
225
|
C
|
Low
|
| 171
|
Signalling theory
|
6,623
|
220
|
GA
|
Mid
|
| 172
|
Evolution of cetaceans
|
6,606
|
220
|
GA
|
Mid
|
| 173
|
Neanderthal genetics
|
6,581
|
219
|
C
|
High
|
| 174
|
Homo longi
|
6,556
|
218
|
GA
|
Low
|
| 175
|
List of related male and female reproductive organs
|
6,516
|
217
|
List
|
Mid
|
| 176
|
Middle Paleolithic
|
6,495
|
216
|
C
|
High
|
| 177
|
Symmetry in biology
|
6,271
|
209
|
C
|
High
|
| 178
|
Evolutionary history of plants
|
6,182
|
206
|
B
|
High
|
| 179
|
Evolution of primates
|
6,080
|
202
|
Start
|
Low
|
| 180
|
Human mitochondrial DNA haplogroup
|
6,069
|
202
|
Start
|
Mid
|
| 181
|
Bergmann's rule
|
6,025
|
200
|
C
|
Low
|
| 182
|
First universal common ancestor
|
5,993
|
199
|
Start
|
Unknown
|
| 183
|
Evolution of human intelligence
|
5,942
|
198
|
Start
|
High
|
| 184
|
Evolutionary origin of religion
|
5,800
|
193
|
C
|
Low
|
| 185
|
Fitness (biology)
|
5,719
|
190
|
B
|
High
|
| 186
|
Objections to evolution
|
5,698
|
189
|
GA
|
Mid
|
| 187
|
Evolution of fish
|
5,654
|
188
|
C
|
High
|
| 188
|
Anisogamy
|
5,648
|
188
|
C
|
High
|
| 189
|
Autosome
|
5,611
|
187
|
Start
|
High
|
| 190
|
Evolutionary algorithm
|
5,555
|
185
|
C
|
Low
|
| 191
|
Missing link (human evolution)
|
5,513
|
183
|
Start
|
Mid
|
| 192
|
Aggressive mimicry
|
5,496
|
183
|
GA
|
Mid
|
| 193
|
Relict (biology)
|
5,490
|
183
|
C
|
Mid
|
| 194
|
History of eugenics
|
5,448
|
181
|
B
|
Low
|
| 195
|
Crown group
|
5,437
|
181
|
C
|
Mid
|
| 196
|
Sexual selection in humans
|
5,417
|
180
|
C
|
Low
|
| 197
|
Variability hypothesis
|
5,385
|
179
|
C
|
Low
|
| 198
|
Cowardice
|
5,354
|
178
|
C
|
Low
|
| 199
|
The Descent of Man, and Selection in Relation to Sex
|
5,337
|
177
|
B
|
High
|
| 200
|
Allopatric speciation
|
5,315
|
177
|
B
|
High
|
| 201
|
Biogeography
|
5,300
|
176
|
Start
|
Mid
|
| 202
|
Müllerian mimicry
|
5,216
|
173
|
GA
|
Mid
|
| 203
|
Anatomically modern human
|
5,204
|
173
|
NA
|
NA
|
| 204
|
Incertae sedis
|
5,152
|
171
|
C
|
Low
|
| 205
|
History of evolutionary thought
|
5,115
|
170
|
FA
|
Top
|
| 206
|
Modern synthesis (20th century)
|
5,077
|
169
|
GA
|
High
|
| 207
|
Apomorphy and synapomorphy
|
5,035
|
167
|
C
|
Low
|
| 208
|
Evolution of birds
|
4,978
|
165
|
C
|
High
|
| 209
|
Killer ape theory
|
4,976
|
165
|
Start
|
Low
|
| 210
|
CpG site
|
4,958
|
165
|
C
|
Mid
|
| 211
|
Sex differences in psychology
|
4,929
|
164
|
C
|
High
|
| 212
|
Lagerstätte
|
4,906
|
163
|
List
|
Mid
|
| 213
|
Sexy son hypothesis
|
4,804
|
160
|
C
|
Mid
|
| 214
|
Religious views of Charles Darwin
|
4,768
|
158
|
B
|
Low
|
| 215
|
Adaptive radiation
|
4,766
|
158
|
B
|
High
|
| 216
|
Human genetic variation
|
4,695
|
156
|
C
|
Mid
|
| 217
|
Spiral Dynamics
|
4,656
|
155
|
C
|
Low
|
| 218
|
Hominina
|
4,643
|
154
|
NA
|
NA
|
| 219
|
Cladogram
|
4,480
|
149
|
C
|
Mid
|
| 220
|
Recapitulation theory
|
4,433
|
147
|
C
|
Mid
|
| 221
|
Speculative evolution
|
4,367
|
145
|
B
|
Low
|
| 222
|
Population genetics
|
4,359
|
145
|
C
|
High
|
| 223
|
Ontogeny
|
4,352
|
145
|
B
|
High
|
| 224
|
Maladaptation
|
4,284
|
142
|
Start
|
Mid
|
| 225
|
Medical genetics of Jews
|
4,247
|
141
|
Start
|
Mid
|
| 226
|
Australopithecus sediba
|
4,244
|
141
|
GA
|
Low
|
| 227
|
Kenyanthropus
|
4,236
|
141
|
GA
|
Low
|
| 228
|
The Passing of the Great Race
|
4,230
|
141
|
C
|
Low
|
| 229
|
Transitional fossil
|
4,224
|
140
|
GA
|
Top
|
| 230
|
Homo juluensis
|
4,206
|
140
|
Start
|
Low
|
| 231
|
Purple Earth hypothesis
|
4,154
|
138
|
Start
|
Mid
|
| 232
|
Climate change adaptation
|
4,117
|
137
|
B
|
Mid
|
| 233
|
Neo-Darwinism
|
4,091
|
136
|
Start
|
Mid
|
| 234
|
Expelled: No Intelligence Allowed
|
4,048
|
134
|
B
|
Low
|
| 235
|
Thomas Hunt Morgan
|
4,004
|
133
|
B
|
High
|
| 236
|
Japanese Paleolithic
|
3,951
|
131
|
Start
|
High
|
| 237
|
Evolutionary anachronism
|
3,932
|
131
|
List
|
Mid
|
| 238
|
Heritability
|
3,927
|
130
|
C
|
Mid
|
| 239
|
Herto Man
|
3,885
|
129
|
GA
|
Low
|
| 240
|
Complex adaptive system
|
3,882
|
129
|
C
|
Mid
|
| 241
|
Genetic diversity
|
3,876
|
129
|
C
|
Mid
|
| 242
|
Rejection of evolution by religious groups
|
3,840
|
128
|
B
|
High
|
| 243
|
Kin selection
|
3,808
|
126
|
GA
|
High
|
| 244
|
David Reich (geneticist)
|
3,808
|
126
|
C
|
Mid
|
| 245
|
Sister group
|
3,764
|
125
|
Start
|
Mid
|
| 246
|
Sexual conflict
|
3,643
|
121
|
Start
|
High
|
| 247
|
Peppered moth
|
3,636
|
121
|
B
|
Low
|
| 248
|
Multiregional origin of modern humans
|
3,629
|
120
|
C
|
Mid
|
| 249
|
Evolution of the eye
|
3,625
|
120
|
C
|
High
|
| 250
|
List of fossil sites
|
3,623
|
120
|
List
|
Top
|
| 251
|
Evolution of the brain
|
3,553
|
118
|
Start
|
High
|
| 252
|
Ernst Mayr
|
3,537
|
117
|
C
|
High
|
| 253
|
Peppered moth evolution
|
3,535
|
117
|
GA
|
High
|
| 254
|
Race suicide
|
3,528
|
117
|
Start
|
Mid
|
| 255
|
Mach bands
|
3,500
|
116
|
Start
|
Mid
|
| 256
|
Islamic views on evolution
|
3,489
|
116
|
C
|
Low
|
| 257
|
Fisherian runaway
|
3,451
|
115
|
Start
|
Low
|
| 258
|
Geological history of oxygen
|
3,436
|
114
|
C
|
Low
|
| 259
|
Evolution as fact and theory
|
3,426
|
114
|
C
|
Low
|
| 260
|
Assortative mating
|
3,375
|
112
|
C
|
Mid
|
| 261
|
Heather Heying
|
3,365
|
112
|
Start
|
Low
|
| 262
|
Cro-Magnon rock shelter
|
3,343
|
111
|
Start
|
Mid
|
| 263
|
Evolutionary developmental biology
|
3,339
|
111
|
GA
|
High
|
| 264
|
Spandrel (biology)
|
3,308
|
110
|
B
|
Mid
|
| 265
|
Systematics
|
3,203
|
106
|
C
|
High
|
| 266
|
Gene flow
|
3,179
|
105
|
Start
|
High
|
| 267
|
Stotting
|
3,176
|
105
|
GA
|
Low
|
| 268
|
Evolutionary game theory
|
3,167
|
105
|
C
|
High
|
| 269
|
Devolution (biology)
|
3,106
|
103
|
C
|
Low
|
| 270
|
March of Progress
|
3,086
|
102
|
C
|
Low
|
| 271
|
The Blind Watchmaker
|
3,080
|
102
|
C
|
Mid
|
| 272
|
Orthogenesis
|
3,079
|
102
|
GA
|
Mid
|
| 273
|
History of biology
|
3,077
|
102
|
FA
|
High
|
| 274
|
Four Fs (evolution)
|
3,069
|
102
|
C
|
Low
|
| 275
|
Genetic variation
|
3,040
|
101
|
Start
|
High
|
| 276
|
Sequence homology
|
3,035
|
101
|
C
|
High
|
| 277
|
Self-preservation
|
3,009
|
100
|
C
|
High
|
| 278
|
Endurance running hypothesis
|
2,978
|
99
|
Start
|
Low
|
| 279
|
Why Is Sex Fun?
|
2,956
|
98
|
C
|
Low
|
| 280
|
Haplodiploidy
|
2,912
|
97
|
C
|
Mid
|
| 281
|
E. coli long-term evolution experiment
|
2,900
|
96
|
B
|
Mid
|
| 282
|
Clonally transmissible cancer
|
2,892
|
96
|
C
|
Low
|
| 283
|
Body plan
|
2,873
|
95
|
C
|
Mid
|
| 284
|
Evolutionarily stable strategy
|
2,828
|
94
|
B
|
Mid
|
| 285
|
Parental investment
|
2,826
|
94
|
Start
|
High
|
| 286
|
Solo Man
|
2,799
|
93
|
FA
|
Low
|
| 287
|
Life history theory
|
2,779
|
92
|
C
|
High
|
| 288
|
Protocell
|
2,768
|
92
|
C
|
Mid
|
| 289
|
Ring species
|
2,763
|
92
|
C
|
High
|
| 290
|
Two-domain system
|
2,726
|
90
|
C
|
Low
|
| 291
|
Handicap principle
|
2,725
|
90
|
GA
|
High
|
| 292
|
Hunter versus farmer hypothesis
|
2,713
|
90
|
C
|
Low
|
| 293
|
Gene-centered view of evolution
|
2,692
|
89
|
B
|
High
|
| 294
|
Frameshift mutation
|
2,678
|
89
|
B
|
High
|
| 295
|
Altruism (biology)
|
2,678
|
89
|
C
|
Mid
|
| 296
|
Evidence of common descent
|
2,676
|
89
|
B
|
Mid
|
| 297
|
Lagar Velho 1
|
2,675
|
89
|
Start
|
Low
|
| 298
|
Theodosius Dobzhansky
|
2,661
|
88
|
C
|
Mid
|
| 299
|
Exaptation
|
2,647
|
88
|
C
|
High
|
| 300
|
Level of support for evolution
|
2,626
|
87
|
C
|
Mid
|
| 301
|
Introduction to evolution
|
2,622
|
87
|
B
|
Mid
|
| 302
|
Jerry Coyne
|
2,619
|
87
|
C
|
Low
|
| 303
|
Reproductive isolation
|
2,617
|
87
|
C
|
High
|
| 304
|
Shadow biosphere
|
2,616
|
87
|
Start
|
Mid
|
| 305
|
Eukaryogenesis
|
2,599
|
86
|
C
|
High
|
| 306
|
Allele frequency
|
2,596
|
86
|
Start
|
Mid
|
| 307
|
Domestication syndrome
|
2,581
|
86
|
C
|
Low
|
| 308
|
Human Diversity Foundation
|
2,576
|
85
|
B
|
Low
|
| 309
|
Coevolution
|
2,519
|
83
|
GA
|
High
|
| 310
|
Parallel evolution
|
2,515
|
83
|
Start
|
High
|
| 311
|
Allometry
|
2,502
|
83
|
C
|
Mid
|
| 312
|
Cline (biology)
|
2,487
|
82
|
C
|
Low
|
| 313
|
Asa Gray
|
2,478
|
82
|
GA
|
Low
|
| 314
|
Evolutionary radiation
|
2,447
|
81
|
Start
|
Mid
|
| 315
|
Sympatric speciation
|
2,442
|
81
|
Start
|
Mid
|
| 316
|
Origin of speech
|
2,431
|
81
|
C
|
Mid
|
| 317
|
John Maynard Smith
|
2,425
|
80
|
C
|
High
|
| 318
|
Group selection
|
2,402
|
80
|
GA
|
High
|
| 319
|
Divergent evolution
|
2,402
|
80
|
Start
|
Mid
|
| 320
|
Gene duplication
|
2,401
|
80
|
C
|
Mid
|
| 321
|
List of examples of convergent evolution
|
2,375
|
79
|
List
|
High
|
| 322
|
Phenotypic plasticity
|
2,365
|
78
|
C
|
Mid
|
| 323
|
The Expression of the Emotions in Man and Animals
|
2,305
|
76
|
C
|
Mid
|
| 324
|
Red Deer Cave people
|
2,293
|
76
|
Start
|
Low
|
| 325
|
Gene polymorphism
|
2,291
|
76
|
Start
|
Mid
|
| 326
|
W. D. Hamilton
|
2,274
|
75
|
C
|
Low
|
| 327
|
Macroevolution
|
2,256
|
75
|
B
|
Top
|
| 328
|
Haldane's rule
|
2,241
|
74
|
C
|
Low
|
| 329
|
Island syndrome
|
2,234
|
74
|
Start
|
Unknown
|
| 330
|
Alloparenting
|
2,231
|
74
|
C
|
Low
|
| 331
|
Ursid hybrid
|
2,227
|
74
|
C
|
Low
|
| 332
|
Acceptance of evolution by religious groups
|
2,220
|
74
|
C
|
Low
|
| 333
|
Evolution of reptiles
|
2,211
|
73
|
C
|
High
|
| 334
|
Neutral theory of molecular evolution
|
2,203
|
73
|
Start
|
High
|
| 335
|
Evolutionary arms race
|
2,203
|
73
|
Start
|
High
|
| 336
|
John Gould
|
2,189
|
72
|
C
|
Mid
|
| 337
|
Gene pool
|
2,151
|
71
|
Start
|
High
|
| 338
|
Panmixia
|
2,143
|
71
|
Start
|
Mid
|
| 339
|
Human sperm competition
|
2,143
|
71
|
C
|
Low
|
| 340
|
Evolutionary computation
|
2,123
|
70
|
C
|
High
|
| 341
|
Drunken monkey hypothesis
|
2,104
|
70
|
Start
|
Low
|
| 342
|
Reciprocal altruism
|
2,079
|
69
|
B
|
Mid
|
| 343
|
Human genetics
|
2,069
|
68
|
Start
|
Mid
|
| 344
|
Duane Gish
|
2,061
|
68
|
B
|
Low
|
| 345
|
Sociobiological theories of rape
|
2,058
|
68
|
C
|
Mid
|
| 346
|
Homo sapiens sapiens
|
2,047
|
68
|
NA
|
NA
|
| 347
|
Evolutionary pressure
|
2,046
|
68
|
C
|
Mid
|
| 348
|
Darwin's Dangerous Idea
|
2,005
|
66
|
C
|
Mid
|
| 349
|
Baldwin effect
|
2,001
|
66
|
GA
|
Low
|
| 350
|
Grandmother hypothesis
|
2,000
|
66
|
C
|
Mid
|
| 351
|
Down House
|
1,988
|
66
|
C
|
Low
|
| 352
|
Primitive (phylogenetics)
|
1,969
|
65
|
Start
|
Mid
|
| 353
|
Genetic divergence
|
1,952
|
65
|
Start
|
High
|
| 354
|
Fish intelligence
|
1,945
|
64
|
B
|
Low
|
| 355
|
Rotating locomotion in living systems
|
1,942
|
64
|
FA
|
High
|
| 356
|
Directional selection
|
1,936
|
64
|
Start
|
Mid
|
| 357
|
Coalescent theory
|
1,936
|
64
|
C
|
Low
|
| 358
|
Oceanic dispersal
|
1,934
|
64
|
Start
|
Low
|
| 359
|
Trivers–Willard hypothesis
|
1,931
|
64
|
Start
|
Low
|
| 360
|
Racist
|
1,927
|
64
|
NA
|
NA
|
| 361
|
Human skeletal changes due to bipedalism
|
1,913
|
63
|
B
|
Mid
|
| 362
|
Evolutionary psychology of religion
|
1,890
|
63
|
C
|
Low
|
| 363
|
Alternatives to Darwinian evolution
|
1,875
|
62
|
B
|
Mid
|
| 364
|
Inclusive fitness
|
1,868
|
62
|
C
|
High
|
| 365
|
George R. Price
|
1,864
|
62
|
C
|
Low
|
| 366
|
Meganthropus
|
1,857
|
61
|
Start
|
Low
|
| 367
|
Fisher's principle
|
1,846
|
61
|
Start
|
Mid
|
| 368
|
Microevolution
|
1,818
|
60
|
C
|
High
|
| 369
|
Struggle for existence
|
1,811
|
60
|
C
|
Mid
|
| 370
|
Parental care
|
1,804
|
60
|
B
|
Mid
|
| 371
|
Taforalt
|
1,773
|
59
|
B
|
Low
|
| 372
|
Nicholas Miklouho-Maclay
|
1,765
|
58
|
C
|
Low
|
| 373
|
Evolution of photosynthesis
|
1,757
|
58
|
Start
|
High
|
| 374
|
Evolutionary mismatch
|
1,753
|
58
|
C
|
Low
|
| 375
|
Last Glacial Maximum refugia
|
1,744
|
58
|
Start
|
Low
|
| 376
|
Evolution of mammalian auditory ossicles
|
1,705
|
56
|
B
|
Mid
|
| 377
|
Evolutionism
|
1,697
|
56
|
C
|
Mid
|
| 378
|
Muller's ratchet
|
1,694
|
56
|
Start
|
Mid
|
| 379
|
Evolution of morality
|
1,688
|
56
|
C
|
High
|
| 380
|
The Third Chimpanzee
|
1,670
|
55
|
C
|
Low
|
| 381
|
Acritarch
|
1,666
|
55
|
C
|
Low
|
| 382
|
Evolution of tetrapods
|
1,658
|
55
|
C
|
High
|
| 383
|
Mutation rate
|
1,657
|
55
|
Start
|
Mid
|
| 384
|
History of ecology
|
1,650
|
55
|
C
|
Mid
|
| 385
|
Racism in the LGBTQ community
|
1,630
|
54
|
C
|
Low
|
| 386
|
Bateman's principle
|
1,626
|
54
|
B
|
Mid
|
| 387
|
Stabilizing selection
|
1,599
|
53
|
Start
|
Mid
|
| 388
|
Dollo's law of irreversibility
|
1,596
|
53
|
Start
|
High
|
| 389
|
Fitness landscape
|
1,583
|
52
|
B
|
High
|
| 390
|
Biology and political orientation
|
1,582
|
52
|
C
|
Low
|
| 391
|
Embryonic diapause
|
1,581
|
52
|
Start
|
Low
|
| 392
|
Entrainment (biomusicology)
|
1,558
|
51
|
Start
|
Low
|
| 393
|
Future generations
|
1,558
|
51
|
Start
|
Low
|
| 394
|
Mate choice in humans
|
1,556
|
51
|
B
|
Unknown
|
| 395
|
Siblicide
|
1,555
|
51
|
Start
|
Low
|
| 396
|
Extended evolutionary synthesis
|
1,554
|
51
|
B
|
High
|
| 397
|
Evolution of cephalopods
|
1,551
|
51
|
C
|
Low
|
| 398
|
Radiation hormesis
|
1,536
|
51
|
B
|
Mid
|
| 399
|
Somatic mutation
|
1,534
|
51
|
C
|
Low
|
| 400
|
Computational phylogenetics
|
1,532
|
51
|
C
|
Mid
|
| 401
|
Background extinction rate
|
1,517
|
50
|
Start
|
Mid
|
| 402
|
Reproductive success
|
1,509
|
50
|
Start
|
High
|
| 403
|
Price equation
|
1,505
|
50
|
C
|
Low
|
| 404
|
Bird hybrid
|
1,504
|
50
|
Start
|
Low
|
| 405
|
Beta diversity
|
1,503
|
50
|
C
|
Mid
|
| 406
|
Pangenesis
|
1,500
|
50
|
C
|
Low
|
| 407
|
Robert Trivers
|
1,493
|
49
|
Start
|
Low
|
| 408
|
Initial Upper Paleolithic
|
1,493
|
49
|
B
|
Unknown
|
| 409
|
Satoshi Kanazawa
|
1,486
|
49
|
C
|
Unknown
|
| 410
|
Mutagenesis
|
1,477
|
49
|
C
|
Mid
|
| 411
|
Heterochrony
|
1,471
|
49
|
GA
|
Mid
|
| 412
|
Project Steve
|
1,458
|
48
|
C
|
Low
|
| 413
|
Anagenesis
|
1,439
|
47
|
C
|
Mid
|
| 414
|
Evolution of cells
|
1,438
|
47
|
Start
|
High
|
| 415
|
Germline mutation
|
1,424
|
47
|
B
|
High
|
| 416
|
Josiah C. Nott
|
1,416
|
47
|
C
|
Low
|
| 417
|
Telescoping generations
|
1,416
|
47
|
Stub
|
Unknown
|
| 418
|
Disappearing blonde gene
|
1,408
|
46
|
Start
|
Low
|
| 419
|
Disruptive selection
|
1,404
|
46
|
C
|
Mid
|
| 420
|
August Weismann
|
1,403
|
46
|
Start
|
High
|
| 421
|
Molecular evolution
|
1,400
|
46
|
C
|
Top
|
| 422
|
Red dress effect
|
1,382
|
46
|
Start
|
Low
|
| 423
|
Genetic pollution
|
1,377
|
45
|
C
|
Low
|
| 424
|
Creation and evolution in public education
|
1,359
|
45
|
B
|
Mid
|
| 425
|
Indel
|
1,348
|
44
|
Start
|
Mid
|
| 426
|
Isua Greenstone Belt
|
1,348
|
44
|
C
|
Mid
|
| 427
|
Embryological origins of the mouth and anus
|
1,343
|
44
|
Start
|
Low
|
| 428
|
Universal Darwinism
|
1,339
|
44
|
C
|
Low
|
| 429
|
Genotype–phenotype distinction
|
1,328
|
44
|
Start
|
High
|
| 430
|
Nothing in Biology Makes Sense Except in the Light of Evolution
|
1,320
|
44
|
C
|
Mid
|
| 431
|
Green-beard effect
|
1,316
|
43
|
Start
|
Low
|
| 432
|
Snaiad
|
1,307
|
43
|
B
|
Low
|
| 433
|
Heterozygote advantage
|
1,301
|
43
|
Start
|
Mid
|
| 434
|
Late Stone Age
|
1,297
|
43
|
Start
|
Low
|
| 435
|
Evolution of nervous systems
|
1,295
|
43
|
B
|
Mid
|
| 436
|
Gene–environment interaction
|
1,287
|
42
|
Start
|
Mid
|
| 437
|
Genetic assimilation
|
1,286
|
42
|
GA
|
Low
|
| 438
|
Metapopulation
|
1,271
|
42
|
B
|
Mid
|
| 439
|
Major histocompatibility complex and sexual selection
|
1,269
|
42
|
C
|
Mid
|
| 440
|
Models of DNA evolution
|
1,267
|
42
|
B
|
Low
|
| 441
|
Tend and befriend
|
1,265
|
42
|
C
|
Low
|
| 442
|
Modern humans
|
1,255
|
41
|
NA
|
NA
|
| 443
|
Motion camouflage
|
1,255
|
41
|
GA
|
Low
|
| 444
|
The 10,000 Year Explosion
|
1,254
|
41
|
B
|
Mid
|
| 445
|
Mutational meltdown
|
1,252
|
41
|
Stub
|
Mid
|
| 446
|
Missing heritability problem
|
1,243
|
41
|
Start
|
Mid
|
| 447
|
Iron–sulfur world hypothesis
|
1,241
|
41
|
C
|
Low
|
| 448
|
Grimaldi man
|
1,241
|
41
|
C
|
Low
|
| 449
|
Origin of avian flight
|
1,240
|
41
|
Start
|
Mid
|
| 450
|
List of prehistoric cartilaginous fish genera
|
1,240
|
41
|
List
|
Mid
|
| 451
|
Costly signaling theory in evolutionary psychology
|
1,232
|
41
|
C
|
Mid
|
| 452
|
Bruniquel Cave
|
1,231
|
41
|
Start
|
Mid
|
| 453
|
Dmanisi
|
1,230
|
41
|
Start
|
Mid
|
| 454
|
Sexual selection in birds
|
1,230
|
41
|
C
|
Low
|
| 455
|
Parapatric speciation
|
1,222
|
40
|
C
|
Mid
|
| 456
|
Jonathan Wells (intelligent design advocate)
|
1,219
|
40
|
B
|
Low
|
| 457
|
Reticulate evolution
|
1,216
|
40
|
C
|
Mid
|
| 458
|
Peptide nucleic acid
|
1,210
|
40
|
Start
|
Low
|
| 459
|
Evolution of biological complexity
|
1,205
|
40
|
C
|
Mid
|
| 460
|
Population biology
|
1,204
|
40
|
Stub
|
Low
|
| 461
|
Balancing selection
|
1,198
|
39
|
Start
|
Mid
|
| 462
|
Snow camouflage
|
1,196
|
39
|
GA
|
Low
|
| 463
|
Ovulatory shift hypothesis
|
1,185
|
39
|
GA
|
Low
|
| 464
|
1860 Oxford evolution debate
|
1,159
|
38
|
B
|
Mid
|
| 465
|
Evolution of lemurs
|
1,154
|
38
|
FA
|
Low
|
| 466
|
Codon usage bias
|
1,143
|
38
|
B
|
Low
|
| 467
|
Outgroup (cladistics)
|
1,139
|
37
|
Start
|
Mid
|
| 468
|
Of Pandas and People
|
1,136
|
37
|
C
|
Low
|
| 469
|
Aerobic fermentation
|
1,136
|
37
|
B
|
Low
|
| 470
|
The Red Queen: Sex and the Evolution of Human Nature
|
1,134
|
37
|
Start
|
Low
|
| 471
|
Henry Walter Bates
|
1,115
|
37
|
C
|
High
|
| 472
|
Evolution of snake venom
|
1,115
|
37
|
GA
|
Mid
|
| 473
|
Evolution of bacteria
|
1,113
|
37
|
C
|
Mid
|
| 474
|
Junkyard tornado
|
1,112
|
37
|
C
|
Low
|
| 475
|
Mating call
|
1,106
|
36
|
C
|
Low
|
| 476
|
Evolutionary taxonomy
|
1,105
|
36
|
C
|
Mid
|
| 477
|
Timeline of fish evolution
|
1,099
|
36
|
List
|
Low
|
| 478
|
Evolutionary anthropology
|
1,096
|
36
|
Start
|
Low
|
| 479
|
Extended female sexuality
|
1,090
|
36
|
B
|
Mid
|
| 480
|
Mutationism
|
1,082
|
36
|
GA
|
Low
|
| 481
|
Evolution of color vision in primates
|
1,082
|
36
|
C
|
Low
|
| 482
|
Homoplasy
|
1,057
|
35
|
Start
|
Low
|
| 483
|
Peripatric speciation
|
1,053
|
35
|
B
|
Mid
|
| 484
|
History of anthropometry
|
1,047
|
34
|
C
|
Low
|
| 485
|
Nuptial gift
|
1,039
|
34
|
Start
|
Mid
|
| 486
|
Cryptic female choice
|
1,035
|
34
|
B
|
Low
|
| 487
|
Saltation (biology)
|
1,033
|
34
|
C
|
Mid
|
| 488
|
Selective sweep
|
1,031
|
34
|
Start
|
Mid
|
| 489
|
List of non-avian dinosaur species preserved with evidence of feathers
|
1,014
|
33
|
List
|
Low
|
| 490
|
Evolution of ageing
|
1,007
|
33
|
B
|
High
|
| 491
|
Endemism in the Hawaiian Islands
|
1,004
|
33
|
Start
|
Low
|
| 492
|
Sociobiology: The New Synthesis
|
1,002
|
33
|
GA
|
Mid
|
| 493
|
Jewish views on evolution
|
1,002
|
33
|
B
|
Low
|
| 494
|
Niche construction
|
999
|
33
|
B
|
Low
|
| 495
|
Evolution of emotion
|
999
|
33
|
Start
|
Unknown
|
| 496
|
Negative selection (natural selection)
|
998
|
33
|
Stub
|
Mid
|
| 497
|
Thrifty gene hypothesis
|
994
|
33
|
B
|
Mid
|
| 498
|
Budgerigar colour genetics
|
993
|
33
|
Start
|
Low
|
| 499
|
Wonderful Life (book)
|
990
|
33
|
Stub
|
Low
|
| 500
|
Gene family
|
979
|
32
|
C
|
High
|
| 501
|
The Greatest Show on Earth: The Evidence for Evolution
|
977
|
32
|
Start
|
Low
|
| 502
|
Joan Roughgarden
|
972
|
32
|
C
|
Unknown
|
| 503
|
Ka/Ks ratio
|
969
|
32
|
C
|
Mid
|
| 504
|
Evolutionary approaches to depression
|
968
|
32
|
Start
|
Low
|
| 505
|
Vertebrate land invasion
|
967
|
32
|
C
|
Mid
|
| 506
|
Yuanmou Man
|
960
|
32
|
GA
|
Low
|
| 507
|
Extinction vortex
|
956
|
31
|
Start
|
Low
|
| 508
|
Female sperm storage
|
956
|
31
|
C
|
Low
|
| 509
|
Zlatý kůň woman
|
954
|
31
|
Start
|
Low
|
| 510
|
Neural Darwinism
|
952
|
31
|
C
|
Unknown
|
| 511
|
Teleology in biology
|
941
|
31
|
GA
|
High
|
| 512
|
Androgenesis
|
939
|
31
|
C
|
Low
|
| 513
|
Strategic pluralism
|
937
|
31
|
Stub
|
Low
|
| 514
|
Adaptationism
|
933
|
31
|
Start
|
Mid
|
| 515
|
Systemic racism
|
927
|
30
|
NA
|
NA
|
| 516
|
Paternal care
|
925
|
30
|
C
|
Low
|
| 517
|
Cognitive tradeoff hypothesis
|
923
|
30
|
C
|
Low
|
| 518
|
Fisher's fundamental theorem of natural selection
|
922
|
30
|
Start
|
Mid
|
| 519
|
Bat wing development
|
920
|
30
|
C
|
Low
|
| 520
|
Snake detection theory
|
917
|
30
|
Start
|
Mid
|
| 521
|
Sexual selection in mammals
|
916
|
30
|
C
|
Low
|
| 522
|
Mate value
|
916
|
30
|
C
|
Low
|
| 523
|
Synonymous substitution
|
911
|
30
|
Start
|
Mid
|
| 524
|
Sperm Wars
|
904
|
30
|
Start
|
Mid
|
| 525
|
David Sloan Wilson
|
902
|
30
|
Start
|
Unknown
|
| 526
|
Autapomorphy
|
897
|
29
|
C
|
Low
|
| 527
|
Angraecum sesquipedale
|
894
|
29
|
B
|
Mid
|
| 528
|
Crocoduck
|
894
|
29
|
C
|
Low
|
| 529
|
Frequency-dependent selection
|
893
|
29
|
Start
|
High
|
| 530
|
Elaine Morgan
|
892
|
29
|
C
|
Low
|
| 531
|
Motoo Kimura
|
887
|
29
|
B
|
High
|
| 532
|
Davis's law
|
866
|
28
|
Start
|
Low
|
| 533
|
Protein superfamily
|
862
|
28
|
B
|
Mid
|
| 534
|
Bayesian inference in phylogeny
|
861
|
28
|
C
|
Low
|
| 535
|
David Krakauer (scientist)
|
856
|
28
|
Start
|
Low
|
| 536
|
Blending inheritance
|
855
|
28
|
GA
|
Low
|
| 537
|
Diana Fleischman
|
855
|
28
|
Start
|
Low
|
| 538
|
Savannah hypothesis
|
850
|
28
|
Start
|
Low
|
| 539
|
Domestication of the goat
|
847
|
28
|
B
|
Mid
|
| 540
|
Experimental evolution
|
846
|
28
|
Start
|
High
|
| 541
|
Population structure (genetics)
|
846
|
28
|
Start
|
Low
|
| 542
|
Polyphenism
|
844
|
28
|
Start
|
Mid
|
| 543
|
Demonic Males
|
842
|
28
|
C
|
Unknown
|
| 544
|
The Genetical Theory of Natural Selection
|
840
|
28
|
Start
|
Mid
|
| 545
|
Cladogenesis
|
834
|
27
|
Start
|
Mid
|
| 546
|
Island hopping
|
829
|
27
|
NA
|
Low
|
| 547
|
Evolution of color vision
|
827
|
27
|
Start
|
Low
|
| 548
|
Cope's rule
|
826
|
27
|
Start
|
Mid
|
| 549
|
Incomplete lineage sorting
|
826
|
27
|
Start
|
Mid
|
| 550
|
James Cowles Prichard
|
824
|
27
|
C
|
High
|
| 551
|
Artificial selection
|
823
|
27
|
NA
|
NA
|
| 552
|
Elizabeth, Lady Hope
|
812
|
27
|
C
|
Low
|
| 553
|
Lantian Man
|
812
|
27
|
GA
|
Low
|
| 554
|
History of creationism
|
809
|
26
|
B
|
Mid
|
| 555
|
Character displacement
|
807
|
26
|
B
|
Mid
|
| 556
|
Alternative abiogenesis scenarios
|
805
|
26
|
C
|
Low
|
| 557
|
Human jaw shrinkage
|
802
|
26
|
Unknown
|
Unknown
|
| 558
|
Glossary of genetics and evolutionary biology
|
800
|
26
|
List
|
Top
|
| 559
|
Endosymbiotic theory
|
788
|
26
|
NA
|
NA
|
| 560
|
Parasite-stress theory
|
788
|
26
|
C
|
Mid
|
| 561
|
The Spandrels of San Marco and the Panglossian Paradigm
|
788
|
26
|
Start
|
Mid
|
| 562
|
Pathological Altruism
|
778
|
25
|
Start
|
Unknown
|
| 563
|
List of Neanderthal fossils
|
776
|
25
|
List
|
Low
|
| 564
|
Mormon views on evolution
|
772
|
25
|
C
|
Low
|
| 565
|
Cooperation (evolution)
|
770
|
25
|
B
|
Mid
|
| 566
|
Plant evolution
|
762
|
25
|
Start
|
High
|
| 567
|
Self-decoration camouflage
|
760
|
25
|
GA
|
Low
|
| 568
|
Canalisation (genetics)
|
753
|
25
|
Start
|
Mid
|
| 569
|
Australopithecus deyiremeda
|
744
|
24
|
GA
|
Low
|
| 570
|
Evolutionary grade
|
734
|
24
|
Start
|
High
|
| 571
|
McLean v. Arkansas
|
726
|
24
|
Start
|
Low
|
| 572
|
Empathy-altruism
|
725
|
24
|
Start
|
Low
|
| 573
|
Chemical defense
|
723
|
24
|
C
|
Low
|
| 574
|
Phenetics
|
720
|
24
|
Start
|
Mid
|
| 575
|
Automimicry
|
719
|
23
|
GA
|
Mid
|
| 576
|
Evolutionary psychiatry
|
718
|
23
|
Stub
|
Low
|
| 577
|
Haplogroup C-V20
|
716
|
23
|
Unknown
|
Unknown
|
| 578
|
George Christopher Williams
|
712
|
23
|
Start
|
Mid
|
| 579
|
Weasel program
|
705
|
23
|
B
|
Low
|
| 580
|
Operational sex ratio
|
702
|
23
|
Start
|
Low
|
| 581
|
Braarudosphaera bigelowii
|
701
|
23
|
Start
|
Low
|
| 582
|
The Major Transitions in Evolution
|
700
|
23
|
Stub
|
Low
|
| 583
|
Machiavellian intelligence hypothesis
|
697
|
23
|
Start
|
Low
|
| 584
|
Parent–offspring conflict
|
695
|
23
|
Start
|
Mid
|
| 585
|
Selection coefficient
|
694
|
23
|
Stub
|
Mid
|
| 586
|
Outline of evolution
|
686
|
22
|
List
|
Top
|
| 587
|
Seminal fluid protein
|
685
|
22
|
Start
|
Low
|
| 588
|
Koobi Fora
|
681
|
22
|
C
|
Mid
|
| 589
|
Long branch attraction
|
675
|
22
|
Start
|
Low
|
| 590
|
Disposable soma theory of aging
|
674
|
22
|
C
|
Mid
|
| 591
|
Single-access key
|
673
|
22
|
C
|
Low
|
| 592
|
Polytomy
|
669
|
22
|
Start
|
Mid
|
| 593
|
Precambrian rabbit
|
666
|
22
|
C
|
Low
|
| 594
|
Unit of selection
|
664
|
22
|
C
|
High
|
| 595
|
Nanjing Man
|
661
|
22
|
C
|
Low
|
| 596
|
Franz Weidenreich
|
658
|
21
|
Start
|
Mid
|
| 597
|
Sex Power Money
|
656
|
21
|
C
|
Low
|
| 598
|
Host–parasite coevolution
|
655
|
21
|
GA
|
Mid
|
| 599
|
Phyletic gradualism
|
646
|
21
|
Start
|
Mid
|
| 600
|
Evolvability
|
640
|
21
|
C
|
High
|
| 601
|
Willi Hennig
|
636
|
21
|
Start
|
Mid
|
| 602
|
Caudal luring
|
625
|
20
|
B
|
Low
|
| 603
|
Reinforcement (speciation)
|
622
|
20
|
GA
|
Mid
|
| 604
|
Gut (anatomy)
|
614
|
20
|
NA
|
Low
|
| 605
|
Evolutionary aesthetics
|
608
|
20
|
C
|
High
|
| 606
|
Natural Theology or Evidences of the Existence and Attributes of the Deity
|
605
|
20
|
GA
|
Low
|
| 607
|
Phylogenetic comparative methods
|
604
|
20
|
C
|
Low
|
| 608
|
Numerical taxonomy
|
602
|
20
|
Start
|
Mid
|
| 609
|
The Vital Question
|
602
|
20
|
GA
|
Low
|
| 610
|
Genetic purging
|
600
|
20
|
Unknown
|
Unknown
|
| 611
|
Expensive tissue hypothesis
|
600
|
20
|
C
|
Low
|
| 612
|
Nina Jablonski
|
599
|
19
|
B
|
Low
|
| 613
|
Ray Lankester
|
598
|
19
|
B
|
Low
|
| 614
|
Evolution of eusociality
|
598
|
19
|
C
|
Low
|
| 615
|
Evolutionary models of human drug use
|
597
|
19
|
C
|
Low
|
| 616
|
Genetic erosion
|
596
|
19
|
C
|
Low
|
| 617
|
Racism on the Internet
|
586
|
19
|
Start
|
Low
|
| 618
|
Patrick Matthew
|
585
|
19
|
B
|
Mid
|
| 619
|
Evolution: The Game of Intelligent Life
|
585
|
19
|
Start
|
Low
|
| 620
|
Ecomorphology
|
582
|
19
|
B
|
Low
|
| 621
|
The Evolution of Desire
|
581
|
19
|
Start
|
Unknown
|
| 622
|
Ornithophily
|
580
|
19
|
B
|
Low
|
| 623
|
Cooperative eye hypothesis
|
578
|
19
|
Start
|
Low
|
| 624
|
Hybrid fruit
|
574
|
19
|
NA
|
NA
|
| 625
|
Biogenesis
|
573
|
19
|
NA
|
High
|
| 626
|
Schizocoely
|
573
|
19
|
Start
|
Mid
|
| 627
|
Allogamy
|
571
|
19
|
Start
|
Mid
|
| 628
|
Disassortative mating
|
570
|
19
|
C
|
Mid
|
| 629
|
Bet hedging (biology)
|
568
|
18
|
B
|
Mid
|
| 630
|
Hologenome theory of evolution
|
565
|
18
|
Start
|
Mid
|
| 631
|
Cryptic species complex
|
564
|
18
|
NA
|
NA
|
| 632
|
Habitable zone for complex life
|
564
|
18
|
C
|
Unknown
|
| 633
|
Darwinian demon
|
563
|
18
|
Stub
|
Low
|
| 634
|
Bateson–Dobzhansky–Muller model
|
561
|
18
|
Unknown
|
Unknown
|
| 635
|
Edward Blyth
|
560
|
18
|
B
|
High
|
| 636
|
Animal weapon
|
557
|
18
|
Start
|
Low
|
| 637
|
E. B. Ford
|
557
|
18
|
C
|
Low
|
| 638
|
Fritz Müller
|
554
|
18
|
B
|
Mid
|
| 639
|
Zoonotic origins of COVID-19
|
553
|
18
|
B
|
Mid
|
| 640
|
Insectivorous Plants
|
548
|
18
|
Start
|
Low
|
| 641
|
Miguelón
|
542
|
18
|
C
|
Unknown
|
| 642
|
PAH world hypothesis
|
541
|
18
|
Start
|
Low
|
| 643
|
Social selection
|
538
|
17
|
C
|
Low
|
| 644
|
Lek paradox
|
536
|
17
|
C
|
Low
|
| 645
|
Psychiatric genetics
|
535
|
17
|
C
|
Mid
|
| 646
|
Buya, Eritrea
|
533
|
17
|
B
|
Low
|
| 647
|
Proavis
|
532
|
17
|
Start
|
Low
|
| 648
|
Directed evolution (transhumanism)
|
528
|
17
|
Stub
|
Low
|
| 649
|
Philosophie zoologique
|
527
|
17
|
GA
|
Low
|
| 650
|
Endless Forms Most Beautiful (book)
|
524
|
17
|
GA
|
Low
|
| 651
|
Icons of Evolution
|
519
|
17
|
C
|
Low
|
| 652
|
Konstantin Mereschkowski
|
515
|
17
|
GA
|
Low
|
| 653
|
Evolutionary ecology
|
513
|
17
|
C
|
Mid
|
| 654
|
Conservative replacement
|
512
|
17
|
Start
|
Low
|
| 655
|
St. George Jackson Mivart
|
511
|
17
|
Start
|
Low
|
| 656
|
Genotype frequency
|
510
|
17
|
Start
|
Mid
|
| 657
|
List of Neanderthal sites
|
510
|
17
|
List
|
Low
|
| 658
|
Klepton
|
510
|
17
|
Start
|
Low
|
| 659
|
Black Queen hypothesis
|
510
|
17
|
Start
|
Low
|
| 660
|
Allan Wilson (biologist)
|
509
|
16
|
C
|
Low
|
| 661
|
Chemoton
|
507
|
16
|
Start
|
Low
|
| 662
|
Man's Place in Nature
|
505
|
16
|
Start
|
Mid
|
| 663
|
Intragenomic conflict
|
502
|
16
|
C
|
Mid
|
| 664
|
Spiegelman's Monster
|
493
|
16
|
Start
|
Low
|
| 665
|
Genetic isolate
|
489
|
16
|
Start
|
Low
|
| 666
|
Ecological speciation
|
488
|
16
|
B
|
High
|
| 667
|
Great Hippocampus Question
|
487
|
16
|
B
|
Low
|
| 668
|
The Evolution of Beauty
|
487
|
16
|
Start
|
Low
|
| 669
|
Evolution of flagella
|
486
|
16
|
Start
|
Mid
|
| 670
|
Vestigial response
|
486
|
16
|
Stub
|
Low
|
| 671
|
Caminalcules
|
486
|
16
|
Start
|
Mid
|
| 672
|
Court jester hypothesis
|
486
|
16
|
C
|
Low
|
| 673
|
Natural Selection (manuscript)
|
485
|
16
|
Stub
|
Low
|
| 674
|
Sex differences in memory
|
485
|
16
|
Start
|
Low
|
| 675
|
Glacial refugium
|
485
|
16
|
Start
|
Low
|
| 676
|
Power, Sex, Suicide
|
484
|
16
|
Stub
|
Low
|
| 677
|
Queen mandibular pheromone
|
484
|
16
|
Start
|
Low
|
| 678
|
WLH-50
|
482
|
16
|
Start
|
Low
|
| 679
|
David Lack
|
480
|
16
|
C
|
Low
|
| 680
|
Vocal learning
|
478
|
15
|
B
|
Low
|
| 681
|
Digital organism
|
477
|
15
|
Stub
|
Low
|
| 682
|
Darwin and women
|
477
|
15
|
Stub
|
Low
|
| 683
|
Mosaic evolution
|
476
|
15
|
Start
|
Low
|
| 684
|
Development of Darwin's theory
|
475
|
15
|
B
|
Mid
|
| 685
|
Mate guarding
|
475
|
15
|
Unknown
|
Mid
|
| 686
|
Muscular evolution in humans
|
471
|
15
|
Start
|
Low
|
| 687
|
The Structure of Evolutionary Theory
|
469
|
15
|
Start
|
Low
|
| 688
|
Genome evolution
|
464
|
15
|
C
|
Top
|
| 689
|
Evolutionary suicide
|
463
|
15
|
Start
|
Low
|
| 690
|
Kettlewell's experiment
|
461
|
15
|
Start
|
Mid
|
| 691
|
Robert Edmond Grant
|
456
|
15
|
Start
|
Low
|
| 692
|
Inheritance of acquired characteristics
|
456
|
15
|
NA
|
NA
|
| 693
|
List of taxa that use parthenogenesis
|
455
|
15
|
B
|
High
|
| 694
|
Evolutionary neuroscience
|
451
|
15
|
Start
|
High
|
| 695
|
Darwinian literary studies
|
445
|
14
|
C
|
Low
|
| 696
|
Sexual selection in scaled reptiles
|
441
|
14
|
Start
|
Low
|
| 697
|
Hybrid zone
|
439
|
14
|
C
|
Mid
|
| 698
|
Museum of Human Evolution
|
439
|
14
|
Start
|
Unknown
|
| 699
|
The Variation of Animals and Plants Under Domestication
|
431
|
14
|
C
|
Low
|
| 700
|
Winner and loser effects
|
430
|
14
|
C
|
Low
|
| 701
|
Secondarily aquatic tetrapods
|
429
|
14
|
Stub
|
Mid
|
| 702
|
Troglomorphism
|
425
|
14
|
Stub
|
Low
|
| 703
|
Quasispecies model
|
423
|
14
|
C
|
Mid
|
| 704
|
Inclusive fitness in humans
|
422
|
14
|
C
|
Low
|
| 705
|
Annual vs. perennial plant evolution
|
418
|
13
|
C
|
Low
|
| 706
|
Emsleyan mimicry
|
415
|
13
|
C
|
Low
|
| 707
|
Origin and function of meiosis
|
413
|
13
|
Start
|
Low
|
| 708
|
Polydactyly in stem-tetrapods
|
408
|
13
|
Start
|
Low
|
| 709
|
Nearly neutral theory of molecular evolution
|
405
|
13
|
Start
|
Low
|
| 710
|
Loren Cordain
|
405
|
13
|
Stub
|
Low
|
| 711
|
Randy Thornhill
|
405
|
13
|
Start
|
Mid
|
| 712
|
List of transitional fossils
|
404
|
13
|
NA
|
NA
|
| 713
|
Female line
|
404
|
13
|
NA
|
NA
|
| 714
|
Rate of evolution
|
403
|
13
|
Start
|
Low
|
| 715
|
Laboratory experiments of speciation
|
402
|
13
|
List
|
Low
|
| 716
|
Richard Prum
|
397
|
13
|
Start
|
Low
|
| 717
|
Megaevolution
|
397
|
13
|
Start
|
Mid
|
| 718
|
Error threshold (evolution)
|
395
|
13
|
C
|
Mid
|
| 719
|
Conservation-induced extinction
|
394
|
13
|
Start
|
Mid
|
| 720
|
Push of the past
|
394
|
13
|
C
|
Low
|
| 721
|
Douglas J. Futuyma
|
393
|
13
|
C
|
Low
|
| 722
|
Herman Bernhard Lundborg
|
392
|
13
|
Start
|
Low
|
| 723
|
Cellularization
|
386
|
12
|
Stub
|
Low
|
| 724
|
Contingency (evolutionary biology)
|
383
|
12
|
Start
|
Low
|
| 725
|
W. Tecumseh Fitch
|
382
|
12
|
Stub
|
Low
|
| 726
|
Proto-mitochondrion
|
379
|
12
|
Start
|
Mid
|
| 727
|
Eugenics in Mexico
|
379
|
12
|
Start
|
Low
|
| 728
|
Viral eukaryogenesis
|
378
|
12
|
Start
|
Mid
|
| 729
|
Evolutionary dynamics
|
377
|
12
|
Stub
|
Mid
|
| 730
|
Evolutionary fauna
|
377
|
12
|
Start
|
Low
|
| 731
|
Religion Explained
|
375
|
12
|
Start
|
Low
|
| 732
|
Precambrian body plans
|
375
|
12
|
B
|
Low
|
| 733
|
History of zoology through 1859
|
373
|
12
|
C
|
High
|
| 734
|
Evolutionary trap
|
372
|
12
|
Start
|
Low
|
| 735
|
Multispecies coalescent process
|
372
|
12
|
Start
|
Low
|
| 736
|
Caveasphaera
|
371
|
12
|
Start
|
Low
|
| 737
|
Fisher's geometric model
|
369
|
12
|
Start
|
Low
|
| 738
|
Evo-devo gene toolkit
|
369
|
12
|
Start
|
Mid
|
| 739
|
Shane Campbell-Staton
|
368
|
12
|
Start
|
Low
|
| 740
|
Idealised population
|
366
|
12
|
C
|
Mid
|
| 741
|
Archaic Homo sapiens
|
366
|
12
|
NA
|
NA
|
| 742
|
Sexual antagonistic coevolution
|
365
|
12
|
Unknown
|
Unknown
|
| 743
|
The Goodness Paradox
|
365
|
12
|
Start
|
Low
|
| 744
|
Tradeoffs for locomotion in air and water
|
361
|
12
|
C
|
Mid
|
| 745
|
Evolution of descended testes in mammals
|
359
|
11
|
Unknown
|
Unknown
|
| 746
|
Emergent evolution
|
357
|
11
|
C
|
Low
|
| 747
|
Evolutionary tradeoff
|
357
|
11
|
Unknown
|
Unknown
|
| 748
|
Qikiqtania
|
355
|
11
|
C
|
Unknown
|
| 749
|
Evolution (TV series)
|
351
|
11
|
Start
|
Low
|
| 750
|
Storage effect
|
350
|
11
|
B
|
Mid
|
| 751
|
Lilliput effect
|
348
|
11
|
Start
|
Low
|
| 752
|
Deep homology
|
347
|
11
|
Start
|
Mid
|
| 753
|
The Origin of Birds
|
344
|
11
|
GA
|
High
|
| 754
|
Evolution of cognition
|
344
|
11
|
C
|
Low
|
| 755
|
On Being the Right Size
|
343
|
11
|
C
|
Mid
|
| 756
|
Nylon-eating bacteria and creationism
|
342
|
11
|
B
|
Low
|
| 757
|
Marcus Feldman
|
342
|
11
|
Start
|
Low
|
| 758
|
Adaptation and Natural Selection
|
340
|
11
|
Start
|
Low
|
| 759
|
Intergradation
|
338
|
11
|
Start
|
Low
|
| 760
|
Rensch's rule
|
337
|
11
|
Start
|
Low
|
| 761
|
Candidatus Atelocyanobacterium thalassa
|
337
|
11
|
C
|
Low
|
| 762
|
Helitron (biology)
|
336
|
11
|
B
|
Low
|
| 763
|
Evolutionary invasion analysis
|
335
|
11
|
Start
|
Low
|
| 764
|
Epic of evolution
|
333
|
11
|
C
|
Low
|
| 765
|
Pseudoextinction
|
331
|
11
|
Start
|
Low
|
| 766
|
Co-adaptation
|
331
|
11
|
C
|
Low
|
| 767
|
History of zoology (1859–present)
|
331
|
11
|
C
|
High
|
| 768
|
Bitter taste evolution
|
330
|
11
|
Start
|
Low
|
| 769
|
Evolutionary physiology
|
327
|
10
|
B
|
High
|
| 770
|
Timeline of zoology
|
327
|
10
|
List
|
Mid
|
| 771
|
What Darwin Got Wrong
|
326
|
10
|
Start
|
Low
|
| 772
|
Biogeographic regions of Europe
|
326
|
10
|
Start
|
Mid
|
| 773
|
Fuyan Cave
|
324
|
10
|
C
|
Low
|
| 774
|
Gavin de Beer
|
323
|
10
|
C
|
Low
|
| 775
|
Viral phylodynamics
|
322
|
10
|
B
|
Low
|
| 776
|
Index of evolutionary biology articles
|
321
|
10
|
List
|
High
|
| 777
|
Scott F. Gilbert
|
321
|
10
|
C
|
Low
|
| 778
|
Alfred Newton
|
320
|
10
|
C
|
Low
|
| 779
|
Dawkins vs. Gould
|
318
|
10
|
Start
|
Low
|
| 780
|
Quantum evolution
|
316
|
10
|
C
|
Mid
|
| 781
|
Evolution of olfaction
|
315
|
10
|
C
|
Low
|
| 782
|
Cultural selection theory
|
314
|
10
|
C
|
Low
|
| 783
|
History of molecular evolution
|
313
|
10
|
C
|
Mid
|
| 784
|
The Theory of Evolution
|
313
|
10
|
Stub
|
Low
|
| 785
|
Turnover-pulse hypothesis
|
312
|
10
|
Start
|
Low
|
| 786
|
Evolution of brachiopods
|
312
|
10
|
Start
|
Low
|
| 787
|
Postcanine megadontia
|
310
|
10
|
C
|
Low
|
| 788
|
Sir William Lawrence, 1st Baronet
|
308
|
10
|
B
|
High
|
| 789
|
William Henry Flower
|
307
|
10
|
B
|
Low
|
| 790
|
Orgel's rules
|
306
|
10
|
Stub
|
Low
|
| 791
|
The Correlation between Relatives on the Supposition of Mendelian Inheritance
|
305
|
10
|
Start
|
Mid
|
| 792
|
Evolutionary developmental psychology
|
305
|
10
|
C
|
Low
|
| 793
|
Biodiversity of Kosovo
|
303
|
10
|
C
|
Low
|
| 794
|
Reciprocity (evolution)
|
302
|
10
|
Unknown
|
Unknown
|
| 795
|
Evolution of hair
|
300
|
10
|
NA
|
NA
|
| 796
|
Evolutionary psychology of language
|
299
|
9
|
Start
|
Low
|
| 797
|
Martha M. Muñoz
|
299
|
9
|
Stub
|
Unknown
|
| 798
|
Paragroup
|
298
|
9
|
Stub
|
Low
|
| 799
|
Molecular Phylogenetics and Evolution
|
298
|
9
|
Stub
|
Low
|
| 800
|
Francis Maitland Balfour
|
296
|
9
|
Start
|
Low
|
| 801
|
Phylotypic stage
|
296
|
9
|
C
|
Low
|
| 802
|
Darwinian threshold
|
295
|
9
|
Start
|
Mid
|
| 803
|
Ancestral sequence reconstruction
|
291
|
9
|
C
|
Low
|
| 804
|
Stenogale
|
291
|
9
|
Stub
|
Low
|
| 805
|
Davidson Black
|
290
|
9
|
C
|
Mid
|
| 806
|
Reproductive suppression
|
290
|
9
|
C
|
Mid
|
| 807
|
Ileret
|
290
|
9
|
Stub
|
Low
|
| 808
|
Zinnia Kumar
|
289
|
9
|
C
|
Low
|
| 809
|
Germ-Soma Differentiation
|
288
|
9
|
C
|
Low
|
| 810
|
Joan E. Strassmann
|
286
|
9
|
Start
|
Low
|
| 811
|
Applications of evolution
|
286
|
9
|
B
|
Low
|
| 812
|
Eukaryote hybrid genome
|
286
|
9
|
B
|
Low
|
| 813
|
Interlocus sexual conflict
|
283
|
9
|
B
|
Mid
|
| 814
|
Behavioral plasticity
|
280
|
9
|
Start
|
Low
|
| 815
|
Red King hypothesis
|
279
|
9
|
Start
|
Low
|
| 816
|
Phylogenetic signal
|
279
|
9
|
C
|
Mid
|
| 817
|
Constructive neutral evolution
|
278
|
9
|
C
|
Low
|
| 818
|
Felsenstein's tree-pruning algorithm
|
277
|
9
|
Stub
|
Low
|
| 819
|
Isolation by distance
|
277
|
9
|
Start
|
Low
|
| 820
|
Edward Bagnall Poulton
|
276
|
9
|
Start
|
Mid
|
| 821
|
Peter J. Bowler
|
274
|
9
|
Start
|
Low
|
| 822
|
Biological constraints
|
272
|
9
|
Start
|
Mid
|
| 823
|
Saldanha man
|
272
|
9
|
Stub
|
Low
|
| 824
|
Cytotaxonomy
|
272
|
9
|
Stub
|
Mid
|
| 825
|
Hybrid incompatibility
|
270
|
9
|
C
|
Low
|
| 826
|
Urban evolution
|
270
|
9
|
C
|
Unknown
|
| 827
|
Evolutionary models of food sharing
|
269
|
8
|
C
|
Low
|
| 828
|
Alpheus Hyatt
|
268
|
8
|
Start
|
Low
|
| 829
|
Psammosere
|
267
|
8
|
Start
|
Mid
|
| 830
|
Henric Sanielevici
|
267
|
8
|
B
|
Low
|
| 831
|
Paul W. Ewald
|
265
|
8
|
Start
|
Low
|
| 832
|
Automixis
|
265
|
8
|
Start
|
Unknown
|
| 833
|
Inversion (evolutionary biology)
|
263
|
8
|
Start
|
Mid
|
| 834
|
Hydrogen hypothesis
|
261
|
8
|
Start
|
Low
|
| 835
|
Evolutionary landscape
|
261
|
8
|
C
|
High
|
| 836
|
Arthur Cain
|
260
|
8
|
C
|
Low
|
| 837
|
Cospeciation
|
256
|
8
|
Start
|
Mid
|
| 838
|
Modern human
|
255
|
8
|
NA
|
NA
|
| 839
|
The Apportionment of Human Diversity
|
255
|
8
|
C
|
Low
|
| 840
|
Ecological fitting
|
253
|
8
|
B
|
Low
|
| 841
|
Sexual selection in insects
|
251
|
8
|
B
|
Low
|
| 842
|
Phylogenetic reconciliation
|
248
|
8
|
Unknown
|
Unknown
|
| 843
|
Shifting balance theory
|
245
|
8
|
Stub
|
Low
|
| 844
|
Mesozoic–Cenozoic radiation
|
245
|
8
|
C
|
Low
|
| 845
|
John Tyler Bonner
|
244
|
8
|
C
|
Mid
|
| 846
|
Homo consumericus
|
244
|
8
|
Start
|
Low
|
| 847
|
Wushan Man
|
243
|
8
|
Start
|
Low
|
| 848
|
Jeremiah Kianga
|
243
|
8
|
Start
|
Low
|
| 849
|
Reciprocal altruism in humans
|
242
|
8
|
Start
|
Low
|
| 850
|
Karl Kessler
|
239
|
7
|
Stub
|
Low
|
| 851
|
Selection shadow
|
239
|
7
|
Start
|
Low
|
| 852
|
Parasite load
|
238
|
7
|
C
|
Low
|
| 853
|
Neofunctionalization
|
238
|
7
|
Start
|
Low
|
| 854
|
Allochronic speciation
|
238
|
7
|
B
|
Mid
|
| 855
|
The Seven Pillars of Life
|
237
|
7
|
Start
|
Low
|
| 856
|
Concerted evolution
|
237
|
7
|
Stub
|
Low
|
| 857
|
William Charles Wells
|
235
|
7
|
B
|
High
|
| 858
|
Tree rearrangement
|
234
|
7
|
Start
|
Low
|
| 859
|
Prejudice from an evolutionary perspective
|
234
|
7
|
Start
|
Low
|
| 860
|
Obligate mutualism
|
233
|
7
|
C
|
Low
|
| 861
|
Gilbertian mimicry
|
232
|
7
|
GA
|
Mid
|
| 862
|
Alloplastic adaptation
|
231
|
7
|
Stub
|
Low
|
| 863
|
Species-typical behavior
|
231
|
7
|
Start
|
Low
|
| 864
|
Key innovation
|
230
|
7
|
Start
|
Mid
|
| 865
|
Rapid modes of evolution
|
228
|
7
|
Unknown
|
Unknown
|
| 866
|
Resource holding potential
|
227
|
7
|
Stub
|
Low
|
| 867
|
Dynamic mutation
|
227
|
7
|
Stub
|
Low
|
| 868
|
Despeciation
|
225
|
7
|
Start
|
Low
|
| 869
|
Wing-assisted incline running
|
225
|
7
|
Start
|
Low
|
| 870
|
Mutation accumulation theory
|
225
|
7
|
C
|
Low
|
| 871
|
History of speciation
|
224
|
7
|
C
|
Low
|
| 872
|
Background selection
|
223
|
7
|
Start
|
Low
|
| 873
|
Philosophy of evolution
|
222
|
7
|
C
|
Mid
|
| 874
|
Clonal interference
|
220
|
7
|
Stub
|
Mid
|
| 875
|
TalkOrigins Archive
|
219
|
7
|
Start
|
Low
|
| 876
|
Evolutionary Psychology (journal)
|
219
|
7
|
Stub
|
Unknown
|
| 877
|
The Genealogical Adam and Eve
|
219
|
7
|
Start
|
Low
|
| 878
|
John Endler
|
218
|
7
|
Start
|
Low
|
| 879
|
Evolution of metal ions in biological systems
|
218
|
7
|
C
|
Low
|
| 880
|
Evolutionary psychology and culture
|
218
|
7
|
Start
|
Low
|
| 881
|
Mimicry in vertebrates
|
216
|
7
|
Start
|
Low
|
| 882
|
Cytonuclear discordance
|
216
|
7
|
Start
|
Unknown
|
| 883
|
Zoology of the Voyage of H.M.S. Beagle
|
215
|
7
|
Stub
|
Low
|
| 884
|
Stephen Blair Hedges
|
215
|
7
|
Start
|
Low
|
| 885
|
Carboniferous-Earliest Permian Biodiversification Event
|
215
|
7
|
NA
|
Low
|
| 886
|
Enterocoely
|
214
|
7
|
Stub
|
Mid
|
| 887
|
Hybrid swarm
|
214
|
7
|
Start
|
Mid
|
| 888
|
Francisc Rainer
|
213
|
7
|
B
|
Low
|
| 889
|
Group living
|
213
|
7
|
Start
|
Low
|
| 890
|
V. C. Wynne-Edwards
|
212
|
7
|
Start
|
Low
|
| 891
|
Ecology and evolutionary biology
|
212
|
7
|
Start
|
Low
|
| 892
|
List of Nepenthes natural hybrids
|
212
|
7
|
List
|
Low
|
| 893
|
Local adaptation
|
212
|
7
|
Unknown
|
Unknown
|
| 894
|
Evolutionary capacitance
|
210
|
7
|
C
|
Mid
|
| 895
|
Society for the Study of Evolution
|
210
|
7
|
Stub
|
Low
|
| 896
|
Natural morality
|
210
|
7
|
Start
|
Low
|
| 897
|
Gard model
|
210
|
7
|
Start
|
Low
|
| 898
|
The Neutral Theory of Molecular Evolution
|
209
|
6
|
Stub
|
Low
|
| 899
|
Undeniable: Evolution and the Science of Creation
|
209
|
6
|
Start
|
Low
|
| 900
|
Coloration evidence for natural selection
|
208
|
6
|
GA
|
Mid
|
| 901
|
Evolutionary theodicy
|
207
|
6
|
C
|
Low
|
| 902
|
Modularity (biology)
|
206
|
6
|
Start
|
Low
|
| 903
|
George Rolleston
|
205
|
6
|
Start
|
Low
|
| 904
|
Calcichordate hypothesis
|
205
|
6
|
Start
|
Mid
|
| 905
|
Polyandry in fish
|
205
|
6
|
C
|
Low
|
| 906
|
Horizontal gene transfer in evolution
|
204
|
6
|
Start
|
High
|
| 907
|
Phagomimicry
|
204
|
6
|
Stub
|
Low
|
| 908
|
How the Snake Lost Its Legs
|
204
|
6
|
GA
|
Low
|
| 909
|
Law of Life
|
202
|
6
|
Stub
|
Low
|
| 910
|
Ruth Mace
|
202
|
6
|
Start
|
Low
|
| 911
|
Unique-event polymorphism
|
200
|
6
|
Start
|
Low
|
| 912
|
Transient masculinization
|
200
|
6
|
C
|
Unknown
|
| 913
|
Melissa A. Wilson
|
198
|
6
|
C
|
Low
|
| 914
|
Herbivore adaptations to plant defense
|
197
|
6
|
B
|
Low
|
| 915
|
Subfunctionalization
|
193
|
6
|
Start
|
Low
|
| 916
|
Largest-scale trends in evolution
|
191
|
6
|
Start
|
High
|
| 917
|
David Hillis
|
190
|
6
|
Start
|
Low
|
| 918
|
GADV-protein world hypothesis
|
190
|
6
|
Start
|
Low
|
| 919
|
Proteinoid
|
189
|
6
|
Start
|
Low
|
| 920
|
Heterotopy
|
188
|
6
|
Stub
|
Low
|
| 921
|
Hox genes in amphibians and reptiles
|
187
|
6
|
C
|
Low
|
| 922
|
Maternal behavior in vertebrates
|
187
|
6
|
C
|
Low
|
| 923
|
Runcaria
|
184
|
6
|
Start
|
Low
|
| 924
|
Hyrax Hill
|
183
|
6
|
B
|
Low
|
| 925
|
Recurrent evolution
|
183
|
6
|
Unknown
|
Unknown
|
| 926
|
Man's Genesis
|
183
|
6
|
Start
|
Low
|
| 927
|
Michael Majerus
|
182
|
6
|
Start
|
Mid
|
| 928
|
Distractive markings
|
182
|
6
|
C
|
Low
|
| 929
|
Human Behavior and Evolution Society
|
181
|
6
|
Start
|
Low
|
| 930
|
Cousin couple
|
181
|
6
|
NA
|
Low
|
| 931
|
Kindred: Neanderthal Life, Love, Death and Art
|
181
|
6
|
Stub
|
Low
|
| 932
|
Mark Ridley (zoologist)
|
180
|
6
|
Stub
|
Low
|
| 933
|
Maternal effect dominant embryonic arrest
|
180
|
6
|
Start
|
Low
|
| 934
|
Talk.origins
|
179
|
5
|
Start
|
Low
|
| 935
|
Biodiversity of Wales
|
179
|
5
|
C
|
Low
|
| 936
|
Developmental bias
|
179
|
5
|
Unknown
|
Unknown
|
| 937
|
Darwin (unit)
|
177
|
5
|
Stub
|
Low
|
| 938
|
Phylogenetic inertia
|
177
|
5
|
Start
|
Mid
|
| 939
|
Nama assemblage
|
176
|
5
|
Start
|
Low
|
| 940
|
Joseph Parker (biologist)
|
176
|
5
|
Start
|
Unknown
|
| 941
|
Andrew Berry (biologist)
|
173
|
5
|
Stub
|
Low
|
| 942
|
Swamping argument
|
173
|
5
|
Stub
|
Low
|
| 943
|
Laura Landweber
|
173
|
5
|
Start
|
Low
|
| 944
|
The Gene Bomb
|
172
|
5
|
Start
|
Mid
|
| 945
|
Victoria Arbour
|
172
|
5
|
Start
|
Low
|
| 946
|
Tip dating
|
172
|
5
|
Stub
|
Low
|
| 947
|
G-value paradox
|
171
|
5
|
C
|
Low
|
| 948
|
Commemoration of Charles Darwin
|
170
|
5
|
C
|
Mid
|
| 949
|
Thorson's rule
|
169
|
5
|
Start
|
Low
|
| 950
|
Tim Lewens
|
169
|
5
|
Start
|
Unknown
|
| 951
|
Mutation bias
|
168
|
5
|
C
|
Mid
|
| 952
|
Intralocus sexual conflict
|
167
|
5
|
Start
|
Mid
|
| 953
|
Adriana Briscoe
|
167
|
5
|
B
|
Low
|
| 954
|
White Sea assemblage
|
167
|
5
|
Stub
|
Low
|
| 955
|
Paul Bujor
|
166
|
5
|
B
|
Low
|
| 956
|
Benjamin Chan
|
166
|
5
|
Start
|
Low
|
| 957
|
Axel Meyer
|
164
|
5
|
Start
|
Unknown
|
| 958
|
Skeletal changes of vertebrates transitioning from water to land
|
163
|
5
|
C
|
Low
|
| 959
|
Formamide-based prebiotic chemistry
|
162
|
5
|
Start
|
Low
|
| 960
|
Inferring horizontal gene transfer
|
161
|
5
|
B
|
Low
|
| 961
|
Sexual strategies theory
|
161
|
5
|
Start
|
Unknown
|
| 962
|
Interactor
|
160
|
5
|
Stub
|
Low
|
| 963
|
Graham Bell (biologist)
|
160
|
5
|
Stub
|
Low
|
| 964
|
Nancy A. Moran
|
160
|
5
|
C
|
Low
|
| 965
|
Patriarch hypothesis
|
159
|
5
|
Unknown
|
Unknown
|
| 966
|
Evolution of Macropodidae
|
159
|
5
|
Start
|
Low
|
| 967
|
Paul Sniegowski
|
159
|
5
|
Start
|
Low
|
| 968
|
Fluctuating selection
|
158
|
5
|
Start
|
Low
|
| 969
|
Corrie Moreau
|
156
|
5
|
C
|
Low
|
| 970
|
The Great Monkey Trial
|
154
|
5
|
Start
|
Low
|
| 971
|
Laura Betzig
|
154
|
5
|
Stub
|
Unknown
|
| 972
|
Strong reciprocity
|
153
|
5
|
B
|
Low
|
| 973
|
James A. Lake
|
153
|
5
|
Start
|
Low
|
| 974
|
ASUDAS
|
153
|
5
|
Start
|
Unknown
|
| 975
|
Adaptive behavior (ecology)
|
152
|
5
|
C
|
Mid
|
| 976
|
Kapthurin Formation
|
151
|
5
|
C
|
Low
|
| 977
|
Genome diversity and karyotype evolution of mammals
|
151
|
5
|
B
|
Low
|
| 978
|
Institute of Human Origins
|
151
|
5
|
Start
|
Low
|
| 979
|
Evolutionary rescue
|
151
|
5
|
Start
|
Low
|
| 980
|
Reductive evolution
|
151
|
5
|
Start
|
Low
|
| 981
|
List of ecoregions with high endemism
|
150
|
5
|
List
|
Low
|
| 982
|
European Society for Evolutionary Biology
|
149
|
4
|
Stub
|
Low
|
| 983
|
Facilitated variation
|
149
|
4
|
Stub
|
Low
|
| 984
|
Scott V. Edwards
|
149
|
4
|
C
|
Low
|
| 985
|
Evolution Without Selection
|
149
|
4
|
Start
|
Low
|
| 986
|
Jeremy Yoder
|
149
|
4
|
Start
|
Low
|
| 987
|
Nonadaptive radiation
|
148
|
4
|
Start
|
Low
|
| 988
|
Preadaptation
|
147
|
4
|
NA
|
Mid
|
| 989
|
Reciprocal causation
|
147
|
4
|
C
|
Low
|
| 990
|
William Kitchen Parker
|
145
|
4
|
Start
|
Low
|
| 991
|
The Panda's Thumb (blog)
|
145
|
4
|
Start
|
Low
|
| 992
|
Dan Willard
|
145
|
4
|
C
|
Low
|
| 993
|
Theology of creationism and evolution
|
143
|
4
|
Start
|
Low
|
| 994
|
Sex differences in sensory systems
|
143
|
4
|
Start
|
Mid
|
| 995
|
Host switch
|
143
|
4
|
C
|
Low
|
| 996
|
Human somatic variation
|
142
|
4
|
C
|
Mid
|
| 997
|
International Year of Biodiversity
|
141
|
4
|
Start
|
High
|
| 998
|
Sulphobes
|
139
|
4
|
Stub
|
Low
|
| 999
|
Phylo (video game)
|
139
|
4
|
Start
|
Low
|
| 1000
|
Molecular drive
|
138
|
4
|
Stub
|
Low
|
