| Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
| 1
|
Neanderthal
|
215,411
|
6,948
|
GA
|
Mid
|
| 2
|
Charles Darwin
|
124,938
|
4,030
|
FA
|
Top
|
| 3
|
Human evolution
|
88,778
|
2,863
|
C
|
High
|
| 4
|
Eugenics
|
88,185
|
2,844
|
C
|
Mid
|
| 5
|
Sexual dimorphism
|
87,654
|
2,827
|
B
|
High
|
| 6
|
Richard Dawkins
|
68,890
|
2,222
|
GA
|
Mid
|
| 7
|
List of common misconceptions
|
67,717
|
2,184
|
List
|
Low
|
| 8
|
Racism
|
67,076
|
2,163
|
B
|
Mid
|
| 9
|
Species
|
66,920
|
2,158
|
GA
|
Top
|
| 10
|
Cretaceous–Paleogene extinction event
|
65,123
|
2,100
|
FA
|
High
|
| 11
|
Extinction
|
61,500
|
1,983
|
C
|
High
|
| 12
|
Parthenogenesis
|
60,491
|
1,951
|
B
|
High
|
| 13
|
List of X-Men members
|
58,430
|
1,884
|
List
|
Low
|
| 14
|
Biodiversity
|
55,981
|
1,805
|
C
|
Mid
|
| 15
|
Evolution
|
55,978
|
1,805
|
FA
|
Top
|
| 16
|
Abiogenesis
|
49,215
|
1,587
|
GA
|
Top
|
| 17
|
Fossil
|
42,345
|
1,365
|
B
|
Mid
|
| 18
|
Binomial nomenclature
|
41,409
|
1,335
|
C
|
Low
|
| 19
|
Early modern human
|
41,364
|
1,334
|
B
|
Mid
|
| 20
|
Scientific racism
|
40,199
|
1,296
|
C
|
Low
|
| 21
|
Cro-Magnon
|
39,243
|
1,265
|
GA
|
Mid
|
| 22
|
Archaic humans
|
38,983
|
1,257
|
Start
|
Low
|
| 23
|
Scopes trial
|
38,293
|
1,235
|
B
|
High
|
| 24
|
Carcinisation
|
36,078
|
1,163
|
Start
|
Top
|
| 25
|
Inbreeding
|
36,069
|
1,163
|
C
|
High
|
| 26
|
Ecology
|
35,295
|
1,138
|
GA
|
Top
|
| 27
|
Timeline of human evolution
|
35,000
|
1,129
|
C
|
Low
|
| 28
|
Cousin
|
34,955
|
1,127
|
Start
|
Low
|
| 29
|
Paleontology
|
33,670
|
1,086
|
GA
|
Top
|
| 30
|
Genetics
|
32,651
|
1,053
|
FA
|
Top
|
| 31
|
Epicanthic fold
|
32,142
|
1,036
|
C
|
Low
|
| 32
|
Natural selection
|
31,868
|
1,028
|
GA
|
Top
|
| 33
|
William Jennings Bryan
|
31,203
|
1,006
|
B
|
High
|
| 34
|
Mutation
|
30,540
|
985
|
B
|
Top
|
| 35
|
Hybrid (biology)
|
29,981
|
967
|
GA
|
High
|
| 36
|
Altruism
|
29,565
|
953
|
B
|
High
|
| 37
|
Domestication of the dog
|
28,607
|
922
|
B
|
Low
|
| 38
|
On the Origin of Species
|
27,768
|
895
|
FA
|
Top
|
| 39
|
Origin of language
|
27,484
|
886
|
C
|
Low
|
| 40
|
Neontology
|
26,888
|
867
|
Start
|
Mid
|
| 41
|
Homo floresiensis
|
26,789
|
864
|
B
|
Mid
|
| 42
|
Snake detection theory
|
26,140
|
843
|
Start
|
Mid
|
| 43
|
Cambrian explosion
|
25,868
|
834
|
B
|
High
|
| 44
|
Last universal common ancestor
|
25,803
|
832
|
GA
|
Top
|
| 45
|
Patrilineality
|
25,028
|
807
|
Start
|
Low
|
| 46
|
Clade
|
24,948
|
804
|
C
|
High
|
| 47
|
Darwinism
|
24,403
|
787
|
Start
|
High
|
| 48
|
HeLa
|
23,508
|
758
|
C
|
Low
|
| 49
|
Pan (genus)
|
23,279
|
750
|
B
|
High
|
| 50
|
Convergent evolution
|
22,696
|
732
|
GA
|
High
|
| 51
|
Great Oxidation Event
|
21,895
|
706
|
C
|
Mid
|
| 52
|
Eusociality
|
21,670
|
699
|
GA
|
Mid
|
| 53
|
Upper Paleolithic
|
21,612
|
697
|
C
|
Low
|
| 54
|
Anus
|
21,203
|
683
|
Start
|
Mid
|
| 55
|
Lamarckism
|
20,595
|
664
|
GA
|
High
|
| 56
|
Human taxonomy
|
20,041
|
646
|
C
|
Low
|
| 57
|
Extant taxon
|
19,613
|
632
|
NA
|
NA
|
| 58
|
Fear
|
19,431
|
626
|
B
|
Low
|
| 59
|
Haplogroup
|
19,128
|
617
|
C
|
Mid
|
| 60
|
Aposematism
|
19,029
|
613
|
GA
|
Mid
|
| 61
|
Australopithecine
|
18,978
|
612
|
C
|
High
|
| 62
|
Wallace Line
|
18,104
|
584
|
Start
|
Mid
|
| 63
|
Living fossil
|
18,081
|
583
|
C
|
Mid
|
| 64
|
Institutional racism
|
18,010
|
580
|
B
|
Mid
|
| 65
|
Karyotype
|
17,784
|
573
|
C
|
Low
|
| 66
|
History of life
|
17,690
|
570
|
GA
|
Top
|
| 67
|
Panthera hybrid
|
17,472
|
563
|
C
|
Low
|
| 68
|
Antimicrobial resistance
|
16,981
|
547
|
B
|
Unknown
|
| 69
|
Population bottleneck
|
16,931
|
546
|
C
|
High
|
| 70
|
Sociality
|
16,778
|
541
|
C
|
Mid
|
| 71
|
Origin of COVID-19
|
16,729
|
539
|
Start
|
Mid
|
| 72
|
Nordicism
|
16,688
|
538
|
B
|
Low
|
| 73
|
Homology (biology)
|
16,638
|
536
|
GA
|
Top
|
| 74
|
Hardy–Weinberg principle
|
16,467
|
531
|
C
|
High
|
| 75
|
Evolutionary psychology
|
16,436
|
530
|
C
|
High
|
| 76
|
Timeline of the evolutionary history of life
|
16,313
|
526
|
B
|
Top
|
| 77
|
Major histocompatibility complex
|
16,246
|
524
|
B
|
Low
|
| 78
|
Nazi eugenics
|
15,787
|
509
|
C
|
Low
|
| 79
|
Domestication of the cat
|
15,749
|
508
|
C
|
Mid
|
| 80
|
Stephen Jay Gould
|
15,595
|
503
|
GA
|
Mid
|
| 81
|
Matrilineality
|
15,539
|
501
|
C
|
Low
|
| 82
|
Bipedalism
|
15,537
|
501
|
B
|
Mid
|
| 83
|
Selective breeding
|
15,434
|
497
|
C
|
Low
|
| 84
|
The Selfish Gene
|
15,288
|
493
|
B
|
High
|
| 85
|
Eugenics in the United States
|
15,106
|
487
|
Start
|
Low
|
| 86
|
Camouflage
|
14,990
|
483
|
GA
|
Mid
|
| 87
|
Stromatolite
|
14,958
|
482
|
B
|
Mid
|
| 88
|
Phylogenetics
|
14,566
|
469
|
C
|
High
|
| 89
|
Sex differences in intelligence
|
14,322
|
462
|
B
|
Low
|
| 90
|
Genetic drift
|
14,133
|
455
|
GA
|
Top
|
| 91
|
Sexual selection
|
14,091
|
454
|
GA
|
High
|
| 92
|
Alfred Russel Wallace
|
13,944
|
449
|
FA
|
Top
|
| 93
|
Earliest known life forms
|
13,800
|
445
|
C
|
Top
|
| 94
|
Human Y-chromosome DNA haplogroup
|
13,452
|
433
|
C
|
Mid
|
| 95
|
Tiktaalik
|
13,388
|
431
|
GA
|
High
|
| 96
|
Ronald Fisher
|
13,133
|
423
|
B
|
High
|
| 97
|
Three-domain system
|
12,826
|
413
|
C
|
Mid
|
| 98
|
R/K selection theory
|
12,644
|
407
|
C
|
High
|
| 99
|
Stoned ape theory
|
12,331
|
397
|
C
|
Low
|
| 100
|
Evolution of mammals
|
12,226
|
394
|
B
|
High
|
| 101
|
Vestigiality
|
12,217
|
394
|
C
|
High
|
| 102
|
Peking Man
|
12,200
|
393
|
GA
|
Mid
|
| 103
|
Adaptation
|
12,181
|
392
|
GA
|
Top
|
| 104
|
Thomas Henry Huxley
|
12,163
|
392
|
B
|
Mid
|
| 105
|
Origin of birds
|
12,139
|
391
|
B
|
Mid
|
| 106
|
Ediacaran biota
|
11,699
|
377
|
FA
|
Low
|
| 107
|
Jean-Baptiste Lamarck
|
11,653
|
375
|
B
|
Top
|
| 108
|
Mimicry
|
11,590
|
373
|
GA
|
High
|
| 109
|
List of human evolution fossils
|
11,570
|
373
|
List
|
High
|
| 110
|
Ernst Haeckel
|
11,484
|
370
|
B
|
High
|
| 111
|
E. O. Wilson
|
11,453
|
369
|
B
|
Mid
|
| 112
|
Chicken or the egg
|
11,446
|
369
|
Start
|
Low
|
| 113
|
Darwin's finches
|
11,352
|
366
|
C
|
High
|
| 114
|
Anthropometry
|
11,321
|
365
|
C
|
Low
|
| 115
|
Survival of the fittest
|
11,314
|
364
|
B
|
Low
|
| 116
|
Behavioral modernity
|
11,114
|
358
|
C
|
Low
|
| 117
|
Human vestigiality
|
11,078
|
357
|
C
|
Mid
|
| 118
|
Triune brain
|
11,076
|
357
|
Start
|
Low
|
| 119
|
Human mating strategies
|
11,064
|
356
|
B
|
Low
|
| 120
|
Neanderthal genetics
|
11,052
|
356
|
C
|
High
|
| 121
|
Founder effect
|
10,974
|
354
|
C
|
Mid
|
| 122
|
Bruniquel Cave
|
10,825
|
349
|
Start
|
Mid
|
| 123
|
Most recent common ancestor
|
10,797
|
348
|
B
|
High
|
| 124
|
Fertility
|
10,787
|
347
|
C
|
High
|
| 125
|
Evolution of the horse
|
10,518
|
339
|
B
|
Mid
|
| 126
|
Polymorphism (biology)
|
10,497
|
338
|
B
|
High
|
| 127
|
Evolutionary biology
|
10,273
|
331
|
C
|
Top
|
| 128
|
Symbiogenesis
|
10,228
|
329
|
GA
|
High
|
| 129
|
Horizontal gene transfer
|
10,044
|
324
|
C
|
High
|
| 130
|
Homo longi
|
10,034
|
323
|
GA
|
Low
|
| 131
|
Instinct
|
9,998
|
322
|
C
|
Low
|
| 132
|
RNA world
|
9,792
|
315
|
C
|
High
|
| 133
|
Linnaean taxonomy
|
9,784
|
315
|
C
|
Mid
|
| 134
|
Rare Earth hypothesis
|
9,666
|
311
|
B
|
Low
|
| 135
|
Objections to evolution
|
9,657
|
311
|
GA
|
Mid
|
| 136
|
Signalling theory
|
9,650
|
311
|
GA
|
Mid
|
| 137
|
Speciation
|
9,546
|
307
|
C
|
High
|
| 138
|
Basal (phylogenetics)
|
9,536
|
307
|
C
|
Mid
|
| 139
|
Cladistics
|
9,482
|
305
|
C
|
Mid
|
| 140
|
Recent human evolution
|
9,460
|
305
|
B
|
Mid
|
| 141
|
Evolution of sexual reproduction
|
9,252
|
298
|
B
|
High
|
| 142
|
Monophyly
|
9,180
|
296
|
C
|
Mid
|
| 143
|
Offspring
|
9,036
|
291
|
Start
|
Mid
|
| 144
|
Island gigantism
|
8,940
|
288
|
Start
|
Low
|
| 145
|
Feathered dinosaur
|
8,929
|
288
|
C
|
High
|
| 146
|
Lower Paleolithic
|
8,830
|
284
|
C
|
High
|
| 147
|
Red Queen hypothesis
|
8,765
|
282
|
Start
|
Mid
|
| 148
|
Common descent
|
8,719
|
281
|
C
|
Top
|
| 149
|
Primordial soup
|
8,646
|
278
|
Start
|
Mid
|
| 150
|
Anisogamy
|
8,622
|
278
|
C
|
High
|
| 151
|
Evolutionary history of plants
|
8,569
|
276
|
B
|
High
|
| 152
|
Sexual cannibalism
|
8,561
|
276
|
B
|
Low
|
| 153
|
Adaptive radiation
|
8,435
|
272
|
Start
|
High
|
| 154
|
Julian Huxley
|
8,378
|
270
|
B
|
Mid
|
| 155
|
Felid hybrids
|
8,351
|
269
|
Start
|
Low
|
| 156
|
Jebel Irhoud
|
8,283
|
267
|
C
|
Low
|
| 157
|
Symmetry in biology
|
8,265
|
266
|
C
|
High
|
| 158
|
Evolutionary algorithm
|
8,116
|
261
|
C
|
Low
|
| 159
|
Genetic diversity
|
8,017
|
258
|
C
|
Mid
|
| 160
|
Insular dwarfism
|
7,999
|
258
|
C
|
Low
|
| 161
|
Sex differences in human physiology
|
7,993
|
257
|
C
|
High
|
| 162
|
Evolution of human intelligence
|
7,985
|
257
|
Start
|
High
|
| 163
|
Missing link (human evolution)
|
7,968
|
257
|
Start
|
Mid
|
| 164
|
CpG site
|
7,898
|
254
|
C
|
Mid
|
| 165
|
Species complex
|
7,880
|
254
|
B
|
Mid
|
| 166
|
Biogeography
|
7,795
|
251
|
Start
|
Mid
|
| 167
|
Middle Paleolithic
|
7,700
|
248
|
C
|
High
|
| 168
|
Great American Interchange
|
7,693
|
248
|
C
|
Mid
|
| 169
|
Batesian mimicry
|
7,601
|
245
|
GA
|
Mid
|
| 170
|
Punctuated equilibrium
|
7,588
|
244
|
GA
|
High
|
| 171
|
Evolution of primates
|
7,537
|
243
|
Start
|
Low
|
| 172
|
Allopatric speciation
|
7,508
|
242
|
C
|
High
|
| 173
|
Evolution of fish
|
7,460
|
240
|
C
|
High
|
| 174
|
Bergmann's rule
|
7,398
|
238
|
C
|
Low
|
| 175
|
J. B. S. Haldane
|
7,258
|
234
|
C
|
Mid
|
| 176
|
Anatomically modern human
|
7,224
|
233
|
NA
|
NA
|
| 177
|
Evolutionary origin of religion
|
7,220
|
232
|
C
|
Low
|
| 178
|
Human mitochondrial DNA haplogroup
|
7,168
|
231
|
Start
|
Mid
|
| 179
|
Autosome
|
7,125
|
229
|
Start
|
High
|
| 180
|
Fitness (biology)
|
7,097
|
228
|
B
|
High
|
| 181
|
Female promiscuity
|
7,063
|
227
|
C
|
Low
|
| 182
|
Peppered moth evolution
|
7,051
|
227
|
GA
|
High
|
| 183
|
Population genetics
|
6,981
|
225
|
C
|
High
|
| 184
|
Inbreeding depression
|
6,871
|
221
|
Start
|
Mid
|
| 185
|
Lek mating
|
6,801
|
219
|
GA
|
Mid
|
| 186
|
Müllerian mimicry
|
6,788
|
218
|
GA
|
Mid
|
| 187
|
Four Fs (evolution)
|
6,644
|
214
|
C
|
Low
|
| 188
|
Evolution of cetaceans
|
6,559
|
211
|
GA
|
Mid
|
| 189
|
History of evolutionary thought
|
6,334
|
204
|
FA
|
Top
|
| 190
|
Transitional fossil
|
6,309
|
203
|
GA
|
Top
|
| 191
|
Sex differences in psychology
|
6,280
|
202
|
C
|
High
|
| 192
|
List of related male and female reproductive organs
|
6,249
|
201
|
List
|
Mid
|
| 193
|
Evolution of the wolf
|
6,233
|
201
|
B
|
Low
|
| 194
|
Spiral Dynamics
|
6,149
|
198
|
C
|
Low
|
| 195
|
Aquatic ape hypothesis
|
6,091
|
196
|
C
|
Low
|
| 196
|
Religious views of Charles Darwin
|
6,007
|
193
|
B
|
Low
|
| 197
|
Evolution as fact and theory
|
5,969
|
192
|
C
|
Low
|
| 198
|
Recapitulation theory
|
5,955
|
192
|
C
|
Mid
|
| 199
|
Genetic variation
|
5,899
|
190
|
Start
|
High
|
| 200
|
Sexual selection in humans
|
5,881
|
189
|
C
|
Low
|
| 201
|
Evolution of birds
|
5,862
|
189
|
C
|
High
|
| 202
|
The Descent of Man, and Selection in Relation to Sex
|
5,859
|
189
|
Start
|
High
|
| 203
|
Sexy son hypothesis
|
5,817
|
187
|
C
|
Mid
|
| 204
|
The Naked Woman
|
5,803
|
187
|
Stub
|
Low
|
| 205
|
Sympatric speciation
|
5,800
|
187
|
Start
|
Mid
|
| 206
|
Multiregional origin of modern humans
|
5,770
|
186
|
C
|
Mid
|
| 207
|
Human sperm competition
|
5,729
|
184
|
C
|
Low
|
| 208
|
Kin selection
|
5,710
|
184
|
GA
|
High
|
| 209
|
Braarudosphaera bigelowii
|
5,661
|
182
|
Start
|
Low
|
| 210
|
Hominina
|
5,577
|
179
|
NA
|
NA
|
| 211
|
Ontogeny
|
5,567
|
179
|
B
|
High
|
| 212
|
Speculative evolution
|
5,559
|
179
|
B
|
Low
|
| 213
|
Modern synthesis (20th century)
|
5,517
|
177
|
GA
|
High
|
| 214
|
Neo-Darwinism
|
5,470
|
176
|
Start
|
Mid
|
| 215
|
Cladogram
|
5,432
|
175
|
C
|
Mid
|
| 216
|
Introduction to evolution
|
5,422
|
174
|
B
|
Mid
|
| 217
|
Relict (biology)
|
5,416
|
174
|
C
|
Mid
|
| 218
|
Climate change adaptation
|
5,397
|
174
|
B
|
Mid
|
| 219
|
Reproductive isolation
|
5,357
|
172
|
C
|
High
|
| 220
|
Gene flow
|
5,346
|
172
|
Start
|
High
|
| 221
|
Endurance running hypothesis
|
5,269
|
169
|
Start
|
Low
|
| 222
|
Rejection of evolution by religious groups
|
5,259
|
169
|
B
|
High
|
| 223
|
Incertae sedis
|
5,155
|
166
|
C
|
Low
|
| 224
|
Variability hypothesis
|
5,125
|
165
|
C
|
Low
|
| 225
|
Aggressive mimicry
|
5,093
|
164
|
GA
|
Mid
|
| 226
|
Islamic views on evolution
|
5,089
|
164
|
C
|
Low
|
| 227
|
Sperm competition
|
5,028
|
162
|
Start
|
Mid
|
| 228
|
Sequence homology
|
4,908
|
158
|
C
|
High
|
| 229
|
Complex adaptive system
|
4,884
|
157
|
C
|
Mid
|
| 230
|
Apomorphy and synapomorphy
|
4,878
|
157
|
C
|
Low
|
| 231
|
Thomas Hunt Morgan
|
4,877
|
157
|
B
|
High
|
| 232
|
Allele frequency
|
4,837
|
156
|
Start
|
Mid
|
| 233
|
Purple Earth hypothesis
|
4,830
|
155
|
Start
|
Mid
|
| 234
|
Australopithecus sediba
|
4,806
|
155
|
GA
|
Low
|
| 235
|
Frameshift mutation
|
4,774
|
154
|
B
|
High
|
| 236
|
First universal common ancestor
|
4,680
|
150
|
Start
|
Unknown
|
| 237
|
Parental care
|
4,673
|
150
|
B
|
Mid
|
| 238
|
Maladaptation
|
4,667
|
150
|
Start
|
Mid
|
| 239
|
History of eugenics
|
4,666
|
150
|
B
|
Low
|
| 240
|
Lagerstätte
|
4,647
|
149
|
B
|
Mid
|
| 241
|
Peppered moth
|
4,516
|
145
|
B
|
Low
|
| 242
|
Divergent evolution
|
4,498
|
145
|
Start
|
Mid
|
| 243
|
Sister group
|
4,498
|
145
|
Start
|
Low
|
| 244
|
Evolution of the brain
|
4,479
|
144
|
Start
|
High
|
| 245
|
Evolution of the eye
|
4,432
|
142
|
C
|
High
|
| 246
|
List of fossil sites
|
4,430
|
142
|
List
|
Top
|
| 247
|
Crown group
|
4,364
|
140
|
C
|
Mid
|
| 248
|
Herto Man
|
4,345
|
140
|
GA
|
Low
|
| 249
|
Coevolution
|
4,268
|
137
|
GA
|
High
|
| 250
|
Self-preservation
|
4,206
|
135
|
C
|
High
|
| 251
|
Assortative mating
|
4,189
|
135
|
C
|
Mid
|
| 252
|
Kenyanthropus
|
4,178
|
134
|
GA
|
Low
|
| 253
|
Handicap principle
|
4,172
|
134
|
GA
|
High
|
| 254
|
Altruism (biology)
|
4,136
|
133
|
C
|
Mid
|
| 255
|
History of biology
|
4,108
|
132
|
FA
|
High
|
| 256
|
Spandrel (biology)
|
3,998
|
128
|
B
|
Mid
|
| 257
|
Systematics
|
3,994
|
128
|
C
|
High
|
| 258
|
Evolutionary developmental biology
|
3,990
|
128
|
GA
|
High
|
| 259
|
Gene duplication
|
3,975
|
128
|
C
|
Mid
|
| 260
|
Fisherian runaway
|
3,973
|
128
|
Start
|
Low
|
| 261
|
Directional selection
|
3,916
|
126
|
Start
|
Mid
|
| 262
|
Evolution of photosynthesis
|
3,900
|
125
|
Start
|
High
|
| 263
|
Devolution (biology)
|
3,886
|
125
|
C
|
Low
|
| 264
|
Entrainment (biomusicology)
|
3,873
|
124
|
Start
|
Low
|
| 265
|
Haplodiploidy
|
3,803
|
122
|
C
|
Mid
|
| 266
|
Evidence of common descent
|
3,769
|
121
|
B
|
Mid
|
| 267
|
Evolutionary game theory
|
3,750
|
120
|
C
|
High
|
| 268
|
Orthogenesis
|
3,730
|
120
|
GA
|
Mid
|
| 269
|
Parental investment
|
3,728
|
120
|
Start
|
High
|
| 270
|
Domestication syndrome
|
3,726
|
120
|
C
|
Low
|
| 271
|
Killer ape theory
|
3,713
|
119
|
Start
|
Low
|
| 272
|
Phenotypic plasticity
|
3,698
|
119
|
C
|
Mid
|
| 273
|
Geological history of oxygen
|
3,694
|
119
|
C
|
Low
|
| 274
|
Japanese Paleolithic
|
3,667
|
118
|
Start
|
High
|
| 275
|
Future generations
|
3,659
|
118
|
Start
|
Low
|
| 276
|
Level of support for evolution
|
3,645
|
117
|
C
|
Mid
|
| 277
|
Gene pool
|
3,616
|
116
|
Start
|
High
|
| 278
|
List of examples of convergent evolution
|
3,556
|
114
|
List
|
High
|
| 279
|
The Expression of the Emotions in Man and Animals
|
3,538
|
114
|
Start
|
Mid
|
| 280
|
Gene polymorphism
|
3,525
|
113
|
Start
|
Mid
|
| 281
|
Jerry Coyne
|
3,477
|
112
|
Start
|
Low
|
| 282
|
Hunter versus farmer hypothesis
|
3,450
|
111
|
C
|
Low
|
| 283
|
Evolution of reptiles
|
3,402
|
109
|
C
|
High
|
| 284
|
Expelled: No Intelligence Allowed
|
3,365
|
108
|
B
|
Low
|
| 285
|
Solo Man
|
3,352
|
108
|
FA
|
Low
|
| 286
|
Macroevolution
|
3,351
|
108
|
B
|
Top
|
| 287
|
Ursid hybrid
|
3,343
|
107
|
C
|
Low
|
| 288
|
Sexual conflict
|
3,341
|
107
|
Start
|
High
|
| 289
|
Life history theory
|
3,339
|
107
|
C
|
High
|
| 290
|
Allometry
|
3,318
|
107
|
C
|
Mid
|
| 291
|
E. coli long-term evolution experiment
|
3,306
|
106
|
B
|
Mid
|
| 292
|
Body plan
|
3,236
|
104
|
C
|
Mid
|
| 293
|
Ernst Mayr
|
3,196
|
103
|
C
|
High
|
| 294
|
Protocell
|
3,180
|
102
|
C
|
Mid
|
| 295
|
Parallel evolution
|
3,171
|
102
|
Start
|
High
|
| 296
|
History of ecology
|
3,156
|
101
|
C
|
Mid
|
| 297
|
Sociobiological theories of rape
|
3,151
|
101
|
C
|
Mid
|
| 298
|
Acceptance of evolution by religious groups
|
3,133
|
101
|
C
|
Low
|
| 299
|
Ring species
|
3,127
|
100
|
C
|
High
|
| 300
|
Evolutionary computation
|
3,119
|
100
|
C
|
High
|
| 301
|
Heather Heying
|
3,098
|
99
|
Start
|
Low
|
| 302
|
Eukaryogenesis
|
3,094
|
99
|
C
|
High
|
| 303
|
Radiation hormesis
|
3,063
|
98
|
B
|
Mid
|
| 304
|
Evolutionarily stable strategy
|
3,047
|
98
|
B
|
Mid
|
| 305
|
Group selection
|
3,041
|
98
|
GA
|
High
|
| 306
|
Why Is Sex Fun?
|
3,029
|
97
|
C
|
Low
|
| 307
|
List of Neanderthal fossils
|
2,993
|
96
|
List
|
Low
|
| 308
|
Asa Gray
|
2,960
|
95
|
GA
|
Low
|
| 309
|
Reciprocal altruism
|
2,953
|
95
|
B
|
Mid
|
| 310
|
Fisher's principle
|
2,950
|
95
|
Start
|
Mid
|
| 311
|
Gene-centered view of evolution
|
2,921
|
94
|
B
|
High
|
| 312
|
Exaptation
|
2,915
|
94
|
C
|
High
|
| 313
|
Fish intelligence
|
2,889
|
93
|
B
|
Low
|
| 314
|
The Blind Watchmaker
|
2,863
|
92
|
C
|
Mid
|
| 315
|
Darwin's Dangerous Idea
|
2,857
|
92
|
C
|
Mid
|
| 316
|
Evolutionary pressure
|
2,837
|
91
|
C
|
Mid
|
| 317
|
Cro-Magnon rock shelter
|
2,833
|
91
|
Start
|
Mid
|
| 318
|
Disruptive selection
|
2,819
|
90
|
C
|
Mid
|
| 319
|
Stabilizing selection
|
2,768
|
89
|
Start
|
Mid
|
| 320
|
Cline (biology)
|
2,767
|
89
|
C
|
Low
|
| 321
|
Stotting
|
2,762
|
89
|
GA
|
Low
|
| 322
|
Evolutionary taxonomy
|
2,755
|
88
|
C
|
Mid
|
| 323
|
Origin of speech
|
2,727
|
87
|
C
|
Mid
|
| 324
|
Neutral theory of molecular evolution
|
2,725
|
87
|
Start
|
High
|
| 325
|
Alloparenting
|
2,702
|
87
|
C
|
Low
|
| 326
|
Microevolution
|
2,691
|
86
|
C
|
High
|
| 327
|
Haldane's rule
|
2,685
|
86
|
C
|
Low
|
| 328
|
Human skeletal changes due to bipedalism
|
2,676
|
86
|
B
|
Mid
|
| 329
|
Theodosius Dobzhansky
|
2,651
|
85
|
C
|
Mid
|
| 330
|
Negative selection (natural selection)
|
2,643
|
85
|
Stub
|
Mid
|
| 331
|
Somatic mutation
|
2,611
|
84
|
C
|
Low
|
| 332
|
Shadow biosphere
|
2,573
|
83
|
Start
|
Mid
|
| 333
|
Meganthropus
|
2,554
|
82
|
Start
|
Low
|
| 334
|
Beta diversity
|
2,521
|
81
|
C
|
Mid
|
| 335
|
Alternatives to Darwinian evolution
|
2,521
|
81
|
B
|
Mid
|
| 336
|
Evolution of morality
|
2,511
|
81
|
C
|
High
|
| 337
|
Inclusive fitness
|
2,453
|
79
|
C
|
High
|
| 338
|
Rotating locomotion in living systems
|
2,445
|
78
|
FA
|
High
|
| 339
|
Evolutionary radiation
|
2,443
|
78
|
Start
|
Mid
|
| 340
|
Evolutionism
|
2,409
|
77
|
C
|
Mid
|
| 341
|
Mach bands
|
2,385
|
76
|
Start
|
Mid
|
| 342
|
Clonally transmissible cancer
|
2,369
|
76
|
C
|
Low
|
| 343
|
Germline mutation
|
2,363
|
76
|
B
|
High
|
| 344
|
John Maynard Smith
|
2,337
|
75
|
C
|
High
|
| 345
|
Island syndrome
|
2,336
|
75
|
Start
|
Unknown
|
| 346
|
Computational phylogenetics
|
2,320
|
74
|
C
|
Mid
|
| 347
|
Psammosere
|
2,289
|
73
|
Stub
|
Mid
|
| 348
|
Evolutionary arms race
|
2,260
|
72
|
Start
|
High
|
| 349
|
Evolution of tetrapods
|
2,247
|
72
|
C
|
High
|
| 350
|
Evolutionary anachronism
|
2,227
|
71
|
List
|
Mid
|
| 351
|
Homo sapiens sapiens
|
2,205
|
71
|
NA
|
NA
|
| 352
|
Struggle for existence
|
2,204
|
71
|
C
|
Mid
|
| 353
|
Bird hybrid
|
2,168
|
69
|
Start
|
Low
|
| 354
|
March of Progress
|
2,163
|
69
|
C
|
Low
|
| 355
|
Molecular evolution
|
2,143
|
69
|
C
|
Top
|
| 356
|
Coalescent theory
|
2,140
|
69
|
C
|
Low
|
| 357
|
Two-domain system
|
2,133
|
68
|
C
|
Low
|
| 358
|
Heterochrony
|
2,118
|
68
|
GA
|
Mid
|
| 359
|
Disappearing blonde gene
|
2,118
|
68
|
Start
|
Low
|
| 360
|
Bateman's principle
|
2,072
|
66
|
B
|
Mid
|
| 361
|
Genotype–phenotype distinction
|
2,015
|
65
|
Start
|
High
|
| 362
|
Late Stone Age
|
2,001
|
64
|
Start
|
Low
|
| 363
|
Oceanic dispersal
|
1,993
|
64
|
Start
|
Low
|
| 364
|
W. D. Hamilton
|
1,989
|
64
|
C
|
Low
|
| 365
|
Grandmother hypothesis
|
1,987
|
64
|
C
|
Mid
|
| 366
|
Evolution of emotion
|
1,973
|
63
|
Start
|
Unknown
|
| 367
|
Modern humans
|
1,955
|
63
|
NA
|
NA
|
| 368
|
Red Deer Cave people
|
1,951
|
62
|
Start
|
Low
|
| 369
|
Pangenesis
|
1,949
|
62
|
C
|
Low
|
| 370
|
Siblicide
|
1,946
|
62
|
Start
|
Low
|
| 371
|
Duane Gish
|
1,931
|
62
|
C
|
Low
|
| 372
|
Models of DNA evolution
|
1,921
|
61
|
B
|
Low
|
| 373
|
Primitive (phylogenetics)
|
1,854
|
59
|
Start
|
Mid
|
| 374
|
Cognitive tradeoff hypothesis
|
1,836
|
59
|
C
|
Low
|
| 375
|
Panmixia
|
1,822
|
58
|
Start
|
Mid
|
| 376
|
Creation and evolution in public education
|
1,810
|
58
|
B
|
Mid
|
| 377
|
The Third Chimpanzee
|
1,807
|
58
|
C
|
Low
|
| 378
|
Peripatric speciation
|
1,800
|
58
|
B
|
Mid
|
| 379
|
Evolution of mammalian auditory ossicles
|
1,800
|
58
|
B
|
Mid
|
| 380
|
Origin of avian flight
|
1,788
|
57
|
Start
|
Mid
|
| 381
|
Parapatric speciation
|
1,780
|
57
|
C
|
Mid
|
| 382
|
Price equation
|
1,777
|
57
|
C
|
Low
|
| 383
|
Embryological origins of the mouth and anus
|
1,773
|
57
|
Start
|
Low
|
| 384
|
Evolution of cells
|
1,771
|
57
|
Start
|
High
|
| 385
|
Evolution of cephalopods
|
1,762
|
56
|
C
|
Low
|
| 386
|
Baldwin effect
|
1,741
|
56
|
GA
|
Low
|
| 387
|
Evolutionary mismatch
|
1,740
|
56
|
C
|
Low
|
| 388
|
Extended evolutionary synthesis
|
1,733
|
55
|
B
|
High
|
| 389
|
Background extinction rate
|
1,727
|
55
|
Start
|
Mid
|
| 390
|
Biology and political orientation
|
1,704
|
54
|
C
|
Low
|
| 391
|
Reproductive success
|
1,699
|
54
|
Start
|
High
|
| 392
|
Genetic divergence
|
1,682
|
54
|
Start
|
High
|
| 393
|
Heterozygote advantage
|
1,680
|
54
|
Start
|
Mid
|
| 394
|
Diana Fleischman
|
1,678
|
54
|
Start
|
Low
|
| 395
|
Gene family
|
1,667
|
53
|
C
|
High
|
| 396
|
Robert Trivers
|
1,665
|
53
|
Start
|
Low
|
| 397
|
Evolution of ageing
|
1,665
|
53
|
B
|
High
|
| 398
|
Down House
|
1,661
|
53
|
C
|
Low
|
| 399
|
Codon usage bias
|
1,652
|
53
|
B
|
Low
|
| 400
|
Grimaldi man
|
1,648
|
53
|
C
|
Low
|
| 401
|
Fitness landscape
|
1,639
|
52
|
B
|
High
|
| 402
|
Indel
|
1,639
|
52
|
Start
|
Mid
|
| 403
|
Tend and befriend
|
1,631
|
52
|
C
|
Low
|
| 404
|
Evolution of snake venom
|
1,614
|
52
|
GA
|
Mid
|
| 405
|
Taforalt
|
1,599
|
51
|
C
|
Low
|
| 406
|
Muller's ratchet
|
1,593
|
51
|
Start
|
Mid
|
| 407
|
Metapopulation
|
1,590
|
51
|
B
|
Mid
|
| 408
|
Snaiad
|
1,588
|
51
|
B
|
Low
|
| 409
|
Racism in the LGBT community
|
1,573
|
50
|
C
|
Low
|
| 410
|
History of anthropometry
|
1,573
|
50
|
C
|
Low
|
| 411
|
Aerobic fermentation
|
1,557
|
50
|
B
|
Low
|
| 412
|
Population biology
|
1,557
|
50
|
Stub
|
Low
|
| 413
|
Nicholas Miklouho-Maclay
|
1,555
|
50
|
C
|
Low
|
| 414
|
August Weismann
|
1,527
|
49
|
Start
|
High
|
| 415
|
Initial Upper Paleolithic
|
1,527
|
49
|
B
|
Unknown
|
| 416
|
Numerical taxonomy
|
1,513
|
48
|
Start
|
Mid
|
| 417
|
Racist
|
1,484
|
47
|
NA
|
NA
|
| 418
|
Acritarch
|
1,457
|
47
|
C
|
Low
|
| 419
|
Outgroup (cladistics)
|
1,456
|
46
|
Start
|
Mid
|
| 420
|
Evolution of nervous systems
|
1,456
|
46
|
B
|
Mid
|
| 421
|
Evolutionary approaches to depression
|
1,446
|
46
|
Start
|
Low
|
| 422
|
Population structure (genetics)
|
1,429
|
46
|
Start
|
Low
|
| 423
|
Iron–sulfur world hypothesis
|
1,423
|
45
|
C
|
Low
|
| 424
|
Evolution of biological complexity
|
1,423
|
45
|
C
|
Mid
|
| 425
|
Jonathan Wells (intelligent design advocate)
|
1,422
|
45
|
Start
|
Low
|
| 426
|
Mating call
|
1,418
|
45
|
C
|
Low
|
| 427
|
Isua Greenstone Belt
|
1,415
|
45
|
C
|
Mid
|
| 428
|
Evolution of bacteria
|
1,413
|
45
|
C
|
Mid
|
| 429
|
Evolutionary psychology of religion
|
1,410
|
45
|
Start
|
Low
|
| 430
|
Red dress effect
|
1,410
|
45
|
Start
|
Low
|
| 431
|
Homoplasy
|
1,407
|
45
|
Start
|
Low
|
| 432
|
Sexual selection in birds
|
1,403
|
45
|
C
|
Low
|
| 433
|
Vestigial response
|
1,399
|
45
|
Stub
|
Low
|
| 434
|
Mate choice in humans
|
1,390
|
44
|
B
|
Unknown
|
| 435
|
Paternal care
|
1,388
|
44
|
C
|
Low
|
| 436
|
Genetic pollution
|
1,384
|
44
|
C
|
Low
|
| 437
|
The Genetical Theory of Natural Selection
|
1,373
|
44
|
Start
|
Mid
|
| 438
|
David Krakauer (scientist)
|
1,366
|
44
|
Start
|
Low
|
| 439
|
Extinction vortex
|
1,358
|
43
|
Start
|
Low
|
| 440
|
Nuptial gift
|
1,346
|
43
|
Start
|
Mid
|
| 441
|
Lagar Velho 1
|
1,345
|
43
|
Stub
|
Low
|
| 442
|
Costly signaling theory in evolutionary psychology
|
1,333
|
43
|
C
|
Mid
|
| 443
|
List of prehistoric cartilaginous fish genera
|
1,331
|
42
|
List
|
Mid
|
| 444
|
Reproductive suppression
|
1,327
|
42
|
C
|
Mid
|
| 445
|
Neural Darwinism
|
1,323
|
42
|
C
|
Unknown
|
| 446
|
Evolution of lemurs
|
1,292
|
41
|
FA
|
Low
|
| 447
|
Single-access key
|
1,286
|
41
|
C
|
Low
|
| 448
|
Balancing selection
|
1,282
|
41
|
Start
|
Mid
|
| 449
|
1860 Oxford evolution debate
|
1,276
|
41
|
B
|
Mid
|
| 450
|
Niche construction
|
1,273
|
41
|
B
|
Low
|
| 451
|
Nothing in Biology Makes Sense Except in the Light of Evolution
|
1,271
|
41
|
C
|
Mid
|
| 452
|
Ka/Ks ratio
|
1,269
|
40
|
C
|
Mid
|
| 453
|
Motion camouflage
|
1,268
|
40
|
GA
|
Low
|
| 454
|
Evolutionary anthropology
|
1,264
|
40
|
Start
|
Low
|
| 455
|
George R. Price
|
1,258
|
40
|
C
|
Low
|
| 456
|
Embryonic diapause
|
1,256
|
40
|
Start
|
Low
|
| 457
|
Peptide nucleic acid
|
1,242
|
40
|
Start
|
Low
|
| 458
|
Junkyard tornado
|
1,240
|
40
|
C
|
Low
|
| 459
|
Androgenesis
|
1,238
|
39
|
C
|
Low
|
| 460
|
Elizabeth, Lady Hope
|
1,235
|
39
|
C
|
Low
|
| 461
|
Universal Darwinism
|
1,228
|
39
|
C
|
Low
|
| 462
|
Systemic racism
|
1,225
|
39
|
NA
|
NA
|
| 463
|
Ovulatory shift hypothesis
|
1,221
|
39
|
GA
|
Low
|
| 464
|
Anagenesis
|
1,216
|
39
|
C
|
Mid
|
| 465
|
Satoshi Kanazawa
|
1,215
|
39
|
C
|
Unknown
|
| 466
|
List of Neanderthal sites
|
1,201
|
38
|
List
|
Low
|
| 467
|
Josiah C. Nott
|
1,201
|
38
|
C
|
Low
|
| 468
|
Dmanisi
|
1,190
|
38
|
Start
|
Mid
|
| 469
|
Character displacement
|
1,187
|
38
|
B
|
Mid
|
| 470
|
Annual vs. perennial plant evolution
|
1,166
|
37
|
C
|
Low
|
| 471
|
Green-beard effect
|
1,164
|
37
|
Start
|
Low
|
| 472
|
Major histocompatibility complex and sexual selection
|
1,164
|
37
|
C
|
Mid
|
| 473
|
Strategic pluralism
|
1,163
|
37
|
Stub
|
Low
|
| 474
|
Incomplete lineage sorting
|
1,162
|
37
|
Start
|
Mid
|
| 475
|
Endosymbiotic theory
|
1,154
|
37
|
NA
|
NA
|
| 476
|
Timeline of fish evolution
|
1,154
|
37
|
List
|
Low
|
| 477
|
Mutationism
|
1,150
|
37
|
GA
|
Low
|
| 478
|
Snow camouflage
|
1,150
|
37
|
GA
|
Low
|
| 479
|
Hybrid fruit
|
1,147
|
37
|
Stub
|
Low
|
| 480
|
Evolution of color vision in primates
|
1,139
|
36
|
C
|
Low
|
| 481
|
Synonymous substitution
|
1,131
|
36
|
Start
|
Mid
|
| 482
|
Trivers–Willard hypothesis
|
1,116
|
36
|
Start
|
Low
|
| 483
|
Saltation (biology)
|
1,112
|
35
|
C
|
Mid
|
| 484
|
Jewish views on evolution
|
1,108
|
35
|
B
|
Low
|
| 485
|
Mate value
|
1,107
|
35
|
C
|
Low
|
| 486
|
Operational sex ratio
|
1,101
|
35
|
Start
|
Low
|
| 487
|
Bayesian inference in phylogeny
|
1,100
|
35
|
C
|
Low
|
| 488
|
Dollo's law of irreversibility
|
1,097
|
35
|
Start
|
High
|
| 489
|
Plant evolution
|
1,082
|
34
|
Start
|
High
|
| 490
|
Atelocyanobacterium thalassa
|
1,077
|
34
|
C
|
Low
|
| 491
|
Frequency-dependent selection
|
1,070
|
34
|
Start
|
High
|
| 492
|
Caveasphaera
|
1,060
|
34
|
Start
|
Low
|
| 493
|
Polyphenism
|
1,059
|
34
|
Start
|
Mid
|
| 494
|
Cladogenesis
|
1,053
|
33
|
Start
|
Mid
|
| 495
|
Teleology in biology
|
1,053
|
33
|
GA
|
High
|
| 496
|
Wonderful Life (book)
|
1,047
|
33
|
Stub
|
Low
|
| 497
|
Budgerigar colour genetics
|
1,039
|
33
|
Start
|
Low
|
| 498
|
Of Pandas and People
|
1,032
|
33
|
C
|
Low
|
| 499
|
Adaptationism
|
1,030
|
33
|
Start
|
Mid
|
| 500
|
Cooperation (evolution)
|
1,028
|
33
|
B
|
Mid
|
| 501
|
David Sloan Wilson
|
1,020
|
32
|
Start
|
Unknown
|
| 502
|
Modern human
|
1,010
|
32
|
NA
|
NA
|
| 503
|
Outline of evolution
|
1,010
|
32
|
List
|
Top
|
| 504
|
Henry Walter Bates
|
1,006
|
32
|
C
|
High
|
| 505
|
Phenetics
|
1,001
|
32
|
Start
|
Mid
|
| 506
|
Sociobiology: The New Synthesis
|
996
|
32
|
GA
|
Mid
|
| 507
|
Extended female sexuality
|
991
|
31
|
B
|
Mid
|
| 508
|
Seminal fluid protein
|
991
|
31
|
Start
|
Low
|
| 509
|
Canalisation (genetics)
|
988
|
31
|
Start
|
Mid
|
| 510
|
Protein superfamily
|
988
|
31
|
B
|
Mid
|
| 511
|
Last eukaryotic common ancestor
|
983
|
31
|
NA
|
High
|
| 512
|
Mormon views on evolution
|
979
|
31
|
C
|
Low
|
| 513
|
Crocoduck
|
978
|
31
|
C
|
Low
|
| 514
|
Genotype frequency
|
975
|
31
|
Start
|
Mid
|
| 515
|
Davis's law
|
974
|
31
|
Start
|
Low
|
| 516
|
Experimental evolution
|
971
|
31
|
Start
|
High
|
| 517
|
Race suicide
|
955
|
30
|
Start
|
Mid
|
| 518
|
Telescoping generations
|
952
|
30
|
Stub
|
Unknown
|
| 519
|
Endemism in the Hawaiian Islands
|
951
|
30
|
Start
|
Low
|
| 520
|
Savannah hypothesis
|
947
|
30
|
Start
|
Low
|
| 521
|
The Red Queen: Sex and the Evolution of Human Nature
|
944
|
30
|
Start
|
Low
|
| 522
|
Cryptic female choice
|
944
|
30
|
B
|
Low
|
| 523
|
Genome evolution
|
936
|
30
|
C
|
Top
|
| 524
|
Reinforcement (speciation)
|
933
|
30
|
GA
|
Mid
|
| 525
|
Chemical defense
|
926
|
29
|
C
|
Low
|
| 526
|
Host–parasite coevolution
|
924
|
29
|
GA
|
Mid
|
| 527
|
Blending inheritance
|
911
|
29
|
GA
|
Low
|
| 528
|
The Greatest Show on Earth: The Evidence for Evolution
|
907
|
29
|
Start
|
Low
|
| 529
|
Parasite-stress theory
|
906
|
29
|
C
|
Mid
|
| 530
|
Domestication of the goat
|
901
|
29
|
B
|
Mid
|
| 531
|
Female sperm storage
|
897
|
28
|
C
|
Low
|
| 532
|
Phyletic gradualism
|
887
|
28
|
Start
|
Mid
|
| 533
|
Conservative replacement
|
885
|
28
|
Start
|
Low
|
| 534
|
Social selection
|
884
|
28
|
C
|
Low
|
| 535
|
Autapomorphy
|
875
|
28
|
C
|
Low
|
| 536
|
Disposable soma theory of aging
|
874
|
28
|
C
|
Mid
|
| 537
|
Emsleyan mimicry
|
867
|
27
|
C
|
Low
|
| 538
|
Sexual selection in mammals
|
866
|
27
|
C
|
Low
|
| 539
|
Robert Edmond Grant
|
861
|
27
|
Start
|
Low
|
| 540
|
Artificial selection
|
855
|
27
|
NA
|
NA
|
| 541
|
Angraecum sesquipedale
|
855
|
27
|
B
|
Mid
|
| 542
|
Human jaw shrinkage
|
854
|
27
|
Unknown
|
Unknown
|
| 543
|
Evolution of color vision
|
852
|
27
|
Start
|
Low
|
| 544
|
List of non-avian dinosaur species preserved with evidence of feathers
|
849
|
27
|
List
|
Low
|
| 545
|
Joan Roughgarden
|
840
|
27
|
C
|
Unknown
|
| 546
|
Motoo Kimura
|
839
|
27
|
B
|
High
|
| 547
|
Gut (anatomy)
|
838
|
27
|
NA
|
Low
|
| 548
|
Evolutionary psychiatry
|
821
|
26
|
Stub
|
Low
|
| 549
|
Project Steve
|
816
|
26
|
C
|
Low
|
| 550
|
Lantian Man
|
811
|
26
|
GA
|
Low
|
| 551
|
Mosaic evolution
|
808
|
26
|
Start
|
Low
|
| 552
|
History of creationism
|
802
|
25
|
B
|
Mid
|
| 553
|
The Spandrels of San Marco and the Panglossian Paradigm
|
788
|
25
|
Start
|
Mid
|
| 554
|
Ornithophily
|
787
|
25
|
B
|
Low
|
| 555
|
Glossary of genetics and evolutionary biology
|
783
|
25
|
List
|
Top
|
| 556
|
Bet hedging (biology)
|
782
|
25
|
B
|
Mid
|
| 557
|
Allogamy
|
772
|
24
|
Start
|
Mid
|
| 558
|
Yuanmou Man
|
769
|
24
|
GA
|
Low
|
| 559
|
Sperm Wars
|
767
|
24
|
Start
|
Mid
|
| 560
|
Racism on the Internet
|
766
|
24
|
Start
|
Low
|
| 561
|
Haplogroup C-V20
|
753
|
24
|
Unknown
|
Unknown
|
| 562
|
Parent–offspring conflict
|
742
|
23
|
Start
|
Mid
|
| 563
|
Evolutionary ecology
|
741
|
23
|
C
|
Mid
|
| 564
|
Vertebrate land invasion
|
736
|
23
|
C
|
Mid
|
| 565
|
Genetic erosion
|
734
|
23
|
C
|
Low
|
| 566
|
Hologenome theory of evolution
|
731
|
23
|
Start
|
Mid
|
| 567
|
Darwinian demon
|
730
|
23
|
Stub
|
Low
|
| 568
|
Cope's rule
|
719
|
23
|
Start
|
Mid
|
| 569
|
Endless Forms Most Beautiful (book)
|
716
|
23
|
GA
|
Low
|
| 570
|
Directed evolution (transhumanism)
|
716
|
23
|
Stub
|
Low
|
| 571
|
Cytotaxonomy
|
715
|
23
|
Stub
|
Mid
|
| 572
|
Winner and loser effects
|
699
|
22
|
C
|
Low
|
| 573
|
Rate of evolution
|
695
|
22
|
Start
|
Low
|
| 574
|
Evolution of eusociality
|
688
|
22
|
C
|
Low
|
| 575
|
Evolutionary models of human drug use
|
687
|
22
|
C
|
Low
|
| 576
|
Zinnia Kumar
|
685
|
22
|
Start
|
Low
|
| 577
|
Island hopping
|
683
|
22
|
NA
|
Low
|
| 578
|
Precambrian rabbit
|
682
|
22
|
C
|
Low
|
| 579
|
Australopithecus deyiremeda
|
681
|
21
|
GA
|
Low
|
| 580
|
Timeline of zoology
|
679
|
21
|
List
|
Mid
|
| 581
|
Polyandry in fish
|
679
|
21
|
C
|
Low
|
| 582
|
George Christopher Williams
|
675
|
21
|
Start
|
Mid
|
| 583
|
Genetic isolate
|
674
|
21
|
Stub
|
Low
|
| 584
|
Caminalcules
|
673
|
21
|
Start
|
Mid
|
| 585
|
The Vital Question
|
673
|
21
|
GA
|
Low
|
| 586
|
Long branch attraction
|
672
|
21
|
Start
|
Low
|
| 587
|
Koobi Fora
|
672
|
21
|
C
|
Mid
|
| 588
|
Cooperative eye hypothesis
|
672
|
21
|
Start
|
Low
|
| 589
|
The 10,000 Year Explosion
|
671
|
21
|
B
|
Mid
|
| 590
|
Muscular evolution in humans
|
662
|
21
|
Start
|
Low
|
| 591
|
Automimicry
|
659
|
21
|
GA
|
Mid
|
| 592
|
Natural Theology or Evidences of the Existence and Attributes of the Deity
|
657
|
21
|
GA
|
Low
|
| 593
|
Ecological speciation
|
656
|
21
|
B
|
High
|
| 594
|
Evolvability
|
655
|
21
|
C
|
High
|
| 595
|
Polytomy
|
638
|
20
|
Start
|
Mid
|
| 596
|
Development of Darwin's theory
|
633
|
20
|
B
|
Mid
|
| 597
|
PAH world hypothesis
|
630
|
20
|
Start
|
Low
|
| 598
|
Buya, Eritrea
|
625
|
20
|
C
|
Unknown
|
| 599
|
Court jester hypothesis
|
616
|
19
|
C
|
Low
|
| 600
|
Ecomorphology
|
615
|
19
|
B
|
Low
|
| 601
|
Black Queen hypothesis
|
614
|
19
|
Start
|
Low
|
| 602
|
Cryptic species complex
|
608
|
19
|
NA
|
NA
|
| 603
|
Phylogenetic comparative methods
|
605
|
19
|
C
|
Low
|
| 604
|
Fisher's fundamental theorem of natural selection
|
604
|
19
|
Start
|
Mid
|
| 605
|
Habitable zone for complex life
|
604
|
19
|
C
|
Unknown
|
| 606
|
Disassortative mating
|
602
|
19
|
C
|
Mid
|
| 607
|
Biogenesis
|
597
|
19
|
NA
|
High
|
| 608
|
Selection coefficient
|
594
|
19
|
Stub
|
Mid
|
| 609
|
Evolutionary neuroscience
|
591
|
19
|
Start
|
High
|
| 610
|
Reticulate evolution
|
589
|
19
|
C
|
Mid
|
| 611
|
Loren Cordain
|
577
|
18
|
Stub
|
Low
|
| 612
|
Schizocoely
|
575
|
18
|
Start
|
Mid
|
| 613
|
Evolutionary grade
|
571
|
18
|
Start
|
High
|
| 614
|
Precambrian body plans
|
571
|
18
|
B
|
Low
|
| 615
|
Adaptation and Natural Selection
|
563
|
18
|
Start
|
Low
|
| 616
|
Franz Weidenreich
|
560
|
18
|
Stub
|
Mid
|
| 617
|
James Cowles Prichard
|
555
|
17
|
C
|
High
|
| 618
|
Proavis
|
552
|
17
|
Start
|
Low
|
| 619
|
The Major Transitions in Evolution
|
551
|
17
|
Stub
|
Low
|
| 620
|
Bateson–Dobzhansky–Muller model
|
551
|
17
|
Unknown
|
Unknown
|
| 621
|
Evolutionary suicide
|
550
|
17
|
Start
|
Low
|
| 622
|
Elaine Morgan
|
549
|
17
|
C
|
Low
|
| 623
|
Sex Power Money
|
548
|
17
|
C
|
Low
|
| 624
|
Saldanha man
|
545
|
17
|
Stub
|
Low
|
| 625
|
Alternative abiogenesis scenarios
|
545
|
17
|
C
|
Low
|
| 626
|
Unit of selection
|
544
|
17
|
C
|
High
|
| 627
|
Mate guarding
|
530
|
17
|
Unknown
|
Mid
|
| 628
|
Evolution of cognition
|
530
|
17
|
C
|
Low
|
| 629
|
Demonic Males
|
529
|
17
|
C
|
Unknown
|
| 630
|
Evolution of metal ions in biological systems
|
527
|
17
|
C
|
Low
|
| 631
|
Vocal learning
|
526
|
16
|
B
|
Low
|
| 632
|
Bitter taste evolution
|
526
|
16
|
Start
|
Low
|
| 633
|
Darwin and women
|
526
|
16
|
Stub
|
Low
|
| 634
|
Patrick Matthew
|
523
|
16
|
B
|
Mid
|
| 635
|
Group living
|
519
|
16
|
Start
|
Low
|
| 636
|
Weasel program
|
516
|
16
|
B
|
Low
|
| 637
|
Ray Lankester
|
514
|
16
|
B
|
Low
|
| 638
|
Epic of evolution
|
513
|
16
|
C
|
Low
|
| 639
|
Philosophie zoologique
|
505
|
16
|
GA
|
Low
|
| 640
|
Man's Place in Nature
|
502
|
16
|
Start
|
Mid
|
| 641
|
Richard Prum
|
498
|
16
|
Start
|
Low
|
| 642
|
The Evolution of Desire
|
497
|
16
|
Start
|
Unknown
|
| 643
|
Edward Blyth
|
496
|
16
|
B
|
High
|
| 644
|
Fritz Müller
|
496
|
16
|
B
|
Mid
|
| 645
|
Zlatý kůň woman
|
496
|
16
|
Start
|
Low
|
| 646
|
Troglomorphism
|
490
|
15
|
Stub
|
Low
|
| 647
|
Jeremiah Kianga
|
489
|
15
|
Start
|
Low
|
| 648
|
Bat wing development
|
488
|
15
|
Start
|
Low
|
| 649
|
Natural Selection (manuscript)
|
486
|
15
|
Stub
|
Low
|
| 650
|
Evolutionary developmental psychology
|
485
|
15
|
C
|
Low
|
| 651
|
The Evolution of Beauty
|
481
|
15
|
Start
|
Low
|
| 652
|
Eukaryote hybrid genome
|
481
|
15
|
B
|
Low
|
| 653
|
Evolutionary tradeoff
|
477
|
15
|
Unknown
|
Unknown
|
| 654
|
Museum of Human Evolution
|
476
|
15
|
Start
|
Unknown
|
| 655
|
Nina Jablonski
|
475
|
15
|
B
|
Low
|
| 656
|
Randy Thornhill
|
474
|
15
|
Start
|
Mid
|
| 657
|
Sex differences in memory
|
466
|
15
|
Start
|
Low
|
| 658
|
Hybrid zone
|
465
|
15
|
C
|
Mid
|
| 659
|
Lek paradox
|
465
|
15
|
C
|
Low
|
| 660
|
Wushan Man
|
464
|
14
|
Start
|
Low
|
| 661
|
Evolution of flagella
|
460
|
14
|
Start
|
Mid
|
| 662
|
Genetic assimilation
|
457
|
14
|
GA
|
Low
|
| 663
|
The Variation of Animals and Plants Under Domestication
|
456
|
14
|
C
|
Low
|
| 664
|
Power, Sex, Suicide
|
456
|
14
|
Stub
|
Low
|
| 665
|
Spiegelman's Monster
|
454
|
14
|
Start
|
Low
|
| 666
|
List of transitional fossils
|
452
|
14
|
NA
|
NA
|
| 667
|
Kettlewell's experiment
|
451
|
14
|
Start
|
Mid
|
| 668
|
Klepton
|
450
|
14
|
Start
|
Low
|
| 669
|
Evolution: The Game of Intelligent Life
|
449
|
14
|
Start
|
Low
|
| 670
|
What Darwin Got Wrong
|
446
|
14
|
Start
|
Low
|
| 671
|
Insectivorous Plants (book)
|
440
|
14
|
Start
|
Low
|
| 672
|
Darwinian literary studies
|
438
|
14
|
C
|
Low
|
| 673
|
The Goodness Paradox
|
437
|
14
|
Start
|
Low
|
| 674
|
Horizontal gene transfer in evolution
|
436
|
14
|
Start
|
High
|
| 675
|
Great Hippocampus Question
|
435
|
14
|
B
|
Low
|
| 676
|
Glacial refugium
|
435
|
14
|
Stub
|
Low
|
| 677
|
Willi Hennig
|
434
|
14
|
Start
|
Mid
|
| 678
|
Konstantin Mereschkowski
|
433
|
13
|
GA
|
Unknown
|
| 679
|
Intragenomic conflict
|
432
|
13
|
C
|
Mid
|
| 680
|
Nanjing Man
|
432
|
13
|
C
|
Low
|
| 681
|
McLean v. Arkansas
|
430
|
13
|
Start
|
Low
|
| 682
|
Herman Bernhard Lundborg
|
430
|
13
|
Start
|
Low
|
| 683
|
Isolation by distance
|
429
|
13
|
Start
|
Low
|
| 684
|
Reciprocal altruism in humans
|
422
|
13
|
Start
|
Low
|
| 685
|
Reciprocity (evolution)
|
421
|
13
|
Unknown
|
Unknown
|
| 686
|
Ancestral sequence reconstruction
|
421
|
13
|
C
|
Low
|
| 687
|
Secondarily aquatic tetrapods
|
417
|
13
|
Stub
|
Mid
|
| 688
|
Expensive tissue hypothesis
|
414
|
13
|
C
|
Low
|
| 689
|
Allan Wilson (biologist)
|
412
|
13
|
C
|
Low
|
| 690
|
Quantum evolution
|
409
|
13
|
C
|
Mid
|
| 691
|
Inferring horizontal gene transfer
|
408
|
13
|
B
|
Low
|
| 692
|
Evolutionary aesthetics
|
406
|
13
|
C
|
High
|
| 693
|
Laboratory experiments of speciation
|
405
|
13
|
List
|
Low
|
| 694
|
Weapon (biology)
|
404
|
13
|
Stub
|
Low
|
| 695
|
Co-adaptation
|
403
|
13
|
C
|
Low
|
| 696
|
Enterocoely
|
403
|
13
|
Stub
|
Mid
|
| 697
|
Evolutionary fauna
|
403
|
13
|
Start
|
Low
|
| 698
|
St. George Jackson Mivart
|
402
|
12
|
Start
|
Low
|
| 699
|
Postcanine megadontia
|
400
|
12
|
C
|
Low
|
| 700
|
Megaevolution
|
399
|
12
|
Start
|
Mid
|
| 701
|
Evolution of descended testes in mammals
|
399
|
12
|
Unknown
|
Unknown
|
| 702
|
Rensch's rule
|
396
|
12
|
Start
|
Low
|
| 703
|
Origin and function of meiosis
|
396
|
12
|
Start
|
Low
|
| 704
|
Quasispecies model
|
394
|
12
|
C
|
Mid
|
| 705
|
Chemoton
|
393
|
12
|
Start
|
Low
|
| 706
|
Self-decoration camouflage
|
390
|
12
|
GA
|
Low
|
| 707
|
Allochronic speciation
|
390
|
12
|
B
|
Mid
|
| 708
|
Female line
|
390
|
12
|
NA
|
NA
|
| 709
|
Evolutionary dynamics
|
387
|
12
|
Stub
|
Mid
|
| 710
|
Deep homology
|
386
|
12
|
Start
|
Mid
|
| 711
|
Polydactyly in stem-tetrapods
|
386
|
12
|
Start
|
Low
|
| 712
|
Coloration evidence for natural selection
|
386
|
12
|
GA
|
Mid
|
| 713
|
Evolution (TV series)
|
384
|
12
|
Start
|
Low
|
| 714
|
Lilliput effect
|
383
|
12
|
Start
|
Low
|
| 715
|
Index of evolutionary biology articles
|
382
|
12
|
List
|
High
|
| 716
|
Biogeographic regions of Europe
|
381
|
12
|
Start
|
Mid
|
| 717
|
David Lack
|
380
|
12
|
C
|
Low
|
| 718
|
Douglas J. Futuyma
|
376
|
12
|
C
|
Low
|
| 719
|
Error threshold (evolution)
|
376
|
12
|
C
|
Mid
|
| 720
|
Sexual selection in scaled reptiles
|
374
|
12
|
Start
|
Low
|
| 721
|
Inclusive fitness in humans
|
373
|
12
|
C
|
Low
|
| 722
|
History of zoology through 1859
|
370
|
11
|
C
|
High
|
| 723
|
Viral eukaryogenesis
|
370
|
11
|
Start
|
Mid
|
| 724
|
Intergradation
|
370
|
11
|
Start
|
Low
|
| 725
|
Emergent evolution
|
369
|
11
|
C
|
Low
|
| 726
|
History of speciation
|
364
|
11
|
C
|
Low
|
| 727
|
Evolutionary physiology
|
361
|
11
|
B
|
High
|
| 728
|
Homo consumericus
|
358
|
11
|
Start
|
Low
|
| 729
|
Germ-Soma Differentiation
|
358
|
11
|
C
|
Low
|
| 730
|
The Structure of Evolutionary Theory
|
357
|
11
|
Start
|
Low
|
| 731
|
Evo-devo gene toolkit
|
354
|
11
|
Start
|
Mid
|
| 732
|
Social immunity
|
353
|
11
|
B
|
High
|
| 733
|
Eugenics in Mexico
|
351
|
11
|
Start
|
Low
|
| 734
|
Religion Explained
|
350
|
11
|
Start
|
Low
|
| 735
|
Evolutionary trap
|
348
|
11
|
Start
|
Low
|
| 736
|
Helitron (biology)
|
348
|
11
|
B
|
Low
|
| 737
|
Inheritance of acquired characteristics
|
343
|
11
|
NA
|
NA
|
| 738
|
W. Tecumseh Fitch
|
341
|
11
|
Stub
|
Low
|
| 739
|
Evolutionary theodicy
|
336
|
10
|
C
|
Low
|
| 740
|
Dawkins vs. Gould
|
333
|
10
|
Start
|
Low
|
| 741
|
Marcus Feldman
|
330
|
10
|
Start
|
Low
|
| 742
|
Red King hypothesis
|
330
|
10
|
Start
|
Low
|
| 743
|
Sexual antagonistic coevolution
|
329
|
10
|
Unknown
|
Unknown
|
| 744
|
Herbivore adaptations to plant defense
|
326
|
10
|
B
|
Low
|
| 745
|
The Neutral Theory of Molecular Evolution
|
324
|
10
|
Stub
|
Low
|
| 746
|
Viral phylodynamics
|
324
|
10
|
B
|
Low
|
| 747
|
Alfred Newton
|
322
|
10
|
C
|
Low
|
| 748
|
Fuyan Cave
|
322
|
10
|
C
|
Low
|
| 749
|
Evolutionary landscape
|
320
|
10
|
C
|
High
|
| 750
|
Multispecies coalescent process
|
320
|
10
|
Start
|
Low
|
| 751
|
Phylogenetic signal
|
320
|
10
|
C
|
Mid
|
| 752
|
Behavioral plasticity
|
316
|
10
|
Start
|
Low
|
| 753
|
Scott F. Gilbert
|
315
|
10
|
C
|
Low
|
| 754
|
Evolution of hair
|
312
|
10
|
NA
|
NA
|
| 755
|
Constructive neutral evolution
|
312
|
10
|
C
|
Low
|
| 756
|
On Being the Right Size
|
311
|
10
|
C
|
Mid
|
| 757
|
Molecular Phylogenetics and Evolution
|
311
|
10
|
Stub
|
Low
|
| 758
|
Fisheries-induced evolution
|
310
|
10
|
C
|
Low
|
| 759
|
Digital organism
|
307
|
9
|
Stub
|
Low
|
| 760
|
Ileret
|
307
|
9
|
Stub
|
Low
|
| 761
|
Tradeoffs for locomotion in air and water
|
307
|
9
|
C
|
Mid
|
| 762
|
Conservation-induced extinction
|
307
|
9
|
Start
|
Mid
|
| 763
|
Phylotypic stage
|
307
|
9
|
C
|
Low
|
| 764
|
Alloplastic adaptation
|
306
|
9
|
Stub
|
Low
|
| 765
|
Concerted evolution
|
306
|
9
|
Stub
|
Low
|
| 766
|
Icons of Evolution
|
305
|
9
|
C
|
Low
|
| 767
|
Evolution of olfaction
|
305
|
9
|
C
|
Low
|
| 768
|
Biological constraints
|
304
|
9
|
Start
|
Mid
|
| 769
|
Natural morality
|
304
|
9
|
Start
|
Low
|
| 770
|
Nylon-eating bacteria and creationism
|
303
|
9
|
B
|
Low
|
| 771
|
History of zoology (1859–present)
|
301
|
9
|
C
|
High
|
| 772
|
Evolutionary psychology of language
|
301
|
9
|
Start
|
Low
|
| 773
|
Undeniable: Evolution and the Science of Creation
|
301
|
9
|
Start
|
Low
|
| 774
|
Shane Campbell-Staton
|
300
|
9
|
Start
|
Low
|
| 775
|
Push of the past
|
297
|
9
|
C
|
Low
|
| 776
|
Cospeciation
|
296
|
9
|
Start
|
Mid
|
| 777
|
Molecular drive
|
294
|
9
|
Stub
|
Low
|
| 778
|
Recurrent evolution
|
294
|
9
|
Unknown
|
Unknown
|
| 779
|
Francis Maitland Balfour
|
289
|
9
|
Start
|
Low
|
| 780
|
Cytonuclear discordance
|
284
|
9
|
Start
|
Unknown
|
| 781
|
Paragroup
|
283
|
9
|
Stub
|
Low
|
| 782
|
Nearly neutral theory of molecular evolution
|
280
|
9
|
Start
|
Low
|
| 783
|
Shifting balance theory
|
279
|
9
|
Stub
|
Low
|
| 784
|
Automixis
|
279
|
9
|
Start
|
Unknown
|
| 785
|
Selection shadow
|
279
|
9
|
Start
|
Low
|
| 786
|
Pseudoextinction
|
276
|
8
|
Start
|
Low
|
| 787
|
Evolution of brachiopods
|
276
|
8
|
Start
|
Low
|
| 788
|
E. B. Ford
|
274
|
8
|
C
|
Low
|
| 789
|
History of molecular evolution
|
274
|
8
|
C
|
Mid
|
| 790
|
Davidson Black
|
272
|
8
|
C
|
Mid
|
| 791
|
Cultural selection theory
|
272
|
8
|
C
|
Low
|
| 792
|
Cellularization
|
271
|
8
|
Stub
|
Low
|
| 793
|
Paul W. Ewald
|
271
|
8
|
Start
|
Low
|
| 794
|
Edward Bagnall Poulton
|
271
|
8
|
Start
|
Mid
|
| 795
|
Darwinian threshold
|
270
|
8
|
Start
|
Mid
|
| 796
|
Stenogale
|
269
|
8
|
Stub
|
Low
|
| 797
|
Idealised population
|
268
|
8
|
C
|
Mid
|
| 798
|
Felsenstein's tree-pruning algorithm
|
268
|
8
|
Stub
|
Low
|
| 799
|
Neofunctionalization
|
268
|
8
|
Start
|
Low
|
| 800
|
William Henry Flower
|
267
|
8
|
B
|
Low
|
| 801
|
Subfunctionalization
|
267
|
8
|
Start
|
Low
|
| 802
|
Rapid modes of evolution
|
264
|
8
|
Unknown
|
Unknown
|
| 803
|
International Year of Biodiversity
|
264
|
8
|
Start
|
High
|
| 804
|
Biodiversity of Kosovo
|
264
|
8
|
C
|
Low
|
| 805
|
Maternal behavior in vertebrates
|
262
|
8
|
C
|
Low
|
| 806
|
Background selection
|
261
|
8
|
Start
|
Low
|
| 807
|
Phenotypic disparity
|
261
|
8
|
C
|
Mid
|
| 808
|
Parasite load
|
259
|
8
|
C
|
Low
|
| 809
|
Human somatic variation
|
257
|
8
|
C
|
Mid
|
| 810
|
Qikiqtania
|
256
|
8
|
Stub
|
Unknown
|
| 811
|
Evolutionary invasion analysis
|
255
|
8
|
Start
|
Low
|
| 812
|
Law of Life
|
254
|
8
|
Stub
|
Low
|
| 813
|
Urban evolution
|
254
|
8
|
C
|
Unknown
|
| 814
|
Species-typical behavior
|
253
|
8
|
Start
|
Low
|
| 815
|
Joan E. Strassmann
|
252
|
8
|
Start
|
Low
|
| 816
|
Dynamic mutation
|
250
|
8
|
Stub
|
Low
|
| 817
|
Mutation accumulation theory
|
249
|
8
|
C
|
Low
|
| 818
|
Proto-mitochondrion
|
246
|
7
|
Start
|
Mid
|
| 819
|
G-value paradox
|
246
|
7
|
C
|
Low
|
| 820
|
How the Snake Lost Its Legs
|
244
|
7
|
GA
|
Low
|
| 821
|
Clonal interference
|
243
|
7
|
Stub
|
Mid
|
| 822
|
Storage effect
|
240
|
7
|
B
|
Mid
|
| 823
|
The Theory of Evolution
|
238
|
7
|
Stub
|
Low
|
| 824
|
Adaptive behavior (ecology)
|
235
|
7
|
C
|
Mid
|
| 825
|
Fisher's geometric model
|
233
|
7
|
Start
|
Low
|
| 826
|
Peter J. Bowler
|
232
|
7
|
Start
|
Low
|
| 827
|
Inversion (evolutionary biology)
|
230
|
7
|
Start
|
Mid
|
| 828
|
Hydrogen hypothesis
|
227
|
7
|
Start
|
Low
|
| 829
|
Tree rearrangement
|
225
|
7
|
Start
|
Low
|
| 830
|
Evidence for speciation by reinforcement
|
223
|
7
|
List
|
Low
|
| 831
|
Ecological fitting
|
221
|
7
|
B
|
Low
|
| 832
|
Heterotopy
|
221
|
7
|
Stub
|
Low
|
| 833
|
Sexual selection in insects
|
218
|
7
|
B
|
Low
|
| 834
|
The Correlation between Relatives on the Supposition of Mendelian Inheritance
|
216
|
6
|
Start
|
Mid
|
| 835
|
Maternal effect dominant embryonic arrest
|
216
|
6
|
Start
|
Low
|
| 836
|
The Origin of Birds
|
216
|
6
|
GA
|
High
|
| 837
|
Proteinoid
|
213
|
6
|
Start
|
Low
|
| 838
|
Gavin de Beer
|
212
|
6
|
C
|
Low
|
| 839
|
Sir William Lawrence, 1st Baronet
|
212
|
6
|
B
|
High
|
| 840
|
Hybrid swarm
|
211
|
6
|
Start
|
Mid
|
| 841
|
Wing-assisted incline running
|
211
|
6
|
Start
|
Low
|
| 842
|
Nama assemblage
|
210
|
6
|
Start
|
Low
|
| 843
|
Adriana Briscoe
|
209
|
6
|
B
|
Low
|
| 844
|
Evolutionary models of food sharing
|
208
|
6
|
C
|
Low
|
| 845
|
Mutation bias
|
207
|
6
|
C
|
Mid
|
| 846
|
Alpheus Hyatt
|
206
|
6
|
Start
|
Low
|
| 847
|
Biodiversity of Wales
|
206
|
6
|
C
|
Low
|
| 848
|
Evolutionary Psychology (journal)
|
205
|
6
|
Stub
|
Unknown
|
| 849
|
Evolutionary capacitance
|
200
|
6
|
C
|
Mid
|
| 850
|
The Seven Pillars of Life
|
200
|
6
|
Start
|
Low
|
| 851
|
Key innovation
|
200
|
6
|
Start
|
Mid
|
| 852
|
Prejudice from an evolutionary perspective
|
200
|
6
|
Start
|
Low
|
| 853
|
Nancy A. Moran
|
199
|
6
|
C
|
Low
|
| 854
|
Intralocus sexual conflict
|
198
|
6
|
Start
|
Mid
|
| 855
|
GADV-protein world hypothesis
|
198
|
6
|
Start
|
Low
|
| 856
|
Evolution of Macropodidae
|
197
|
6
|
Start
|
Low
|
| 857
|
Evolutionary psychology and culture
|
197
|
6
|
Start
|
Low
|
| 858
|
Escape and radiate coevolution
|
196
|
6
|
C
|
Unknown
|
| 859
|
Applications of evolution
|
194
|
6
|
B
|
Low
|
| 860
|
Modularity (biology)
|
190
|
6
|
Start
|
Low
|
| 861
|
Wonderful life theory
|
189
|
6
|
Stub
|
Low
|
| 862
|
Orgel's rules
|
187
|
6
|
Stub
|
Low
|
| 863
|
Ecology and evolutionary biology
|
187
|
6
|
Start
|
Low
|
| 864
|
List of Nepenthes natural hybrids
|
186
|
6
|
List
|
Low
|
| 865
|
Segregating site
|
186
|
6
|
Start
|
Low
|
| 866
|
Phagomimicry
|
184
|
5
|
Stub
|
Low
|
| 867
|
Interlocus sexual conflict
|
183
|
5
|
B
|
Mid
|
| 868
|
Resource holding potential
|
182
|
5
|
Stub
|
Low
|
| 869
|
Host switch
|
182
|
5
|
C
|
Low
|
| 870
|
Archaic Homo sapiens
|
181
|
5
|
NA
|
NA
|
| 871
|
Runcaria
|
180
|
5
|
Start
|
Low
|
| 872
|
Distractive markings
|
180
|
5
|
C
|
Low
|
| 873
|
Gard model
|
178
|
5
|
Start
|
Low
|
| 874
|
Character evolution
|
178
|
5
|
Unknown
|
Unknown
|
| 875
|
Carboniferous-Earliest Permian Biodiversification Event
|
178
|
5
|
NA
|
Low
|
| 876
|
Evolution by gene duplication
|
176
|
5
|
Start
|
High
|
| 877
|
Hybrid incompatibility
|
176
|
5
|
C
|
Low
|
| 878
|
List of ecoregions with high endemism
|
175
|
5
|
List
|
Low
|
| 879
|
Paul Bujor
|
174
|
5
|
B
|
Low
|
| 880
|
Evolutionary rescue
|
172
|
5
|
Start
|
Low
|
| 881
|
Henric Sanielevici
|
171
|
5
|
B
|
Low
|
| 882
|
Preadaptation
|
168
|
5
|
NA
|
Mid
|
| 883
|
Infinite sites model
|
167
|
5
|
Start
|
Low
|
| 884
|
John Tyler Bonner
|
166
|
5
|
C
|
Mid
|
| 885
|
V. C. Wynne-Edwards
|
163
|
5
|
Start
|
Low
|
| 886
|
Genome Evolution
|
162
|
5
|
NA
|
Top
|
| 887
|
Russell Lande
|
162
|
5
|
Start
|
Low
|
| 888
|
Paraspecies
|
161
|
5
|
Stub
|
Low
|
| 889
|
Hologenomics
|
160
|
5
|
Stub
|
Low
|
| 890
|
David Hillis
|
159
|
5
|
Start
|
Low
|
| 891
|
Michael Majerus
|
158
|
5
|
Start
|
Mid
|
| 892
|
Turnover-pulse hypothesis
|
158
|
5
|
Start
|
Low
|
| 893
|
Skeletal changes of vertebrates transitioning from water to land
|
158
|
5
|
C
|
Low
|
| 894
|
The Apportionment of Human Diversity
|
156
|
5
|
C
|
Low
|
| 895
|
Zoology of the Voyage of H.M.S. Beagle
|
155
|
5
|
Stub
|
Low
|
| 896
|
Hyrax Hill
|
155
|
5
|
B
|
Low
|
| 897
|
Contest competition
|
155
|
5
|
Stub
|
Low
|
| 898
|
Rupert Riedl
|
153
|
4
|
Start
|
Low
|
| 899
|
Mesozoic–Cenozoic radiation
|
152
|
4
|
Stub
|
Low
|
| 900
|
White Sea assemblage
|
152
|
4
|
Stub
|
Low
|
| 901
|
John Endler
|
151
|
4
|
Start
|
Low
|
| 902
|
Alexander von Humboldt Biological Resources Research Institute
|
151
|
4
|
Stub
|
Low
|
| 903
|
Formamide-based prebiotic chemistry
|
149
|
4
|
Start
|
Low
|
| 904
|
Mark Ridley (zoologist)
|
148
|
4
|
Stub
|
Low
|
| 905
|
Axel Meyer
|
143
|
4
|
Start
|
Unknown
|
| 906
|
Laura Landweber
|
143
|
4
|
Start
|
Low
|
| 907
|
Genomic evolution of birds
|
142
|
4
|
C
|
Low
|
| 908
|
Sibling species
|
140
|
4
|
NA
|
NA
|
| 909
|
Landscape genomics
|
140
|
4
|
Stub
|
Low
|
| 910
|
Darwin (unit)
|
138
|
4
|
Stub
|
Low
|
| 911
|
Strong reciprocity
|
136
|
4
|
B
|
Low
|
| 912
|
Institute of Human Origins
|
136
|
4
|
Start
|
Low
|
| 913
|
Human reproductive ecology
|
136
|
4
|
Start
|
Low
|
| 914
|
TalkOrigins Archive
|
134
|
4
|
Start
|
Low
|
| 915
|
Fluctuating selection
|
134
|
4
|
Start
|
Low
|
| 916
|
Phylogenetic inertia
|
133
|
4
|
Start
|
Mid
|
| 917
|
Moritz Wagner (naturalist)
|
132
|
4
|
Start
|
Low
|
| 918
|
Commemoration of Charles Darwin
|
132
|
4
|
C
|
Mid
|
| 919
|
Ecological evolutionary developmental biology
|
132
|
4
|
Start
|
Low
|
| 920
|
Phylo (video game)
|
131
|
4
|
Start
|
Low
|
| 921
|
Founder takes all
|
131
|
4
|
Stub
|
Low
|
| 922
|
Francisc Rainer
|
130
|
4
|
B
|
Low
|
| 923
|
Reciprocal causation
|
130
|
4
|
C
|
Low
|
| 924
|
Interactor
|
129
|
4
|
Stub
|
Low
|
| 925
|
Phylogenetic reconciliation
|
128
|
4
|
Unknown
|
Unknown
|
| 926
|
Autoplastic adaptation
|
127
|
4
|
Stub
|
Low
|
| 927
|
Ecological inheritance
|
127
|
4
|
Stub
|
Low
|
| 928
|
ASUDAS
|
127
|
4
|
Start
|
Unknown
|
| 929
|
Resource defense polygyny
|
127
|
4
|
Stub
|
Unknown
|
| 930
|
Ecological selection
|
126
|
4
|
Start
|
Mid
|
| 931
|
Mimicry in vertebrates
|
126
|
4
|
Start
|
Low
|
| 932
|
Man's Genesis
|
126
|
4
|
Start
|
Low
|
| 933
|
Ruth Mace
|
124
|
4
|
Start
|
Low
|
| 934
|
William Charles Wells
|
123
|
3
|
B
|
High
|
| 935
|
The Neanderthals Rediscovered
|
123
|
3
|
GA
|
Low
|
| 936
|
OneZoom
|
122
|
3
|
Start
|
Unknown
|
| 937
|
Obligate mutualism
|
122
|
3
|
C
|
Low
|
| 938
|
Talk.origins
|
121
|
3
|
Start
|
Low
|
| 939
|
Arthur Cain
|
120
|
3
|
C
|
Low
|
| 940
|
Unique-event polymorphism
|
120
|
3
|
Start
|
Low
|
| 941
|
Thorson's rule
|
118
|
3
|
Start
|
Low
|
| 942
|
Karl Kessler
|
118
|
3
|
Stub
|
Low
|
| 943
|
Kindred: Neanderthal Life, Love, Death and Art
|
118
|
3
|
Stub
|
Low
|
| 944
|
The Great Monkey Trial
|
117
|
3
|
Start
|
Low
|
| 945
|
Harrison's rule
|
116
|
3
|
Unknown
|
Unknown
|
| 946
|
Epididymis evolution from reptiles to mammals
|
116
|
3
|
B
|
Low
|
| 947
|
Facilitated variation
|
115
|
3
|
Stub
|
Low
|
| 948
|
Evolution of Infectious Disease
|
115
|
3
|
Stub
|
Low
|
| 949
|
Darwinian anthropology
|
115
|
3
|
B
|
Unknown
|
| 950
|
Alejandro Rico-Guevara
|
115
|
3
|
Start
|
Unknown
|
| 951
|
Eric Charnov
|
113
|
3
|
Start
|
Low
|
| 952
|
Nonadaptive radiation
|
113
|
3
|
Start
|
Low
|
| 953
|
Egg taphonomy
|
111
|
3
|
C
|
Low
|
| 954
|
WLH-50
|
111
|
3
|
Start
|
Unknown
|
| 955
|
Hox genes in amphibians and reptiles
|
111
|
3
|
C
|
Low
|
| 956
|
Scott V. Edwards
|
111
|
3
|
C
|
Low
|
| 957
|
Graham Bell (biologist)
|
110
|
3
|
Stub
|
Low
|
| 958
|
Non-Darwinian Evolution (paper)
|
109
|
3
|
Stub
|
Low
|
| 959
|
Dan Willard
|
109
|
3
|
C
|
Low
|
| 960
|
Tim Lewens
|
108
|
3
|
Start
|
Unknown
|
| 961
|
Evolutionary approaches to postpartum depression
|
108
|
3
|
C
|
Low
|
| 962
|
Society for the Study of Evolution
|
107
|
3
|
Stub
|
Low
|
| 963
|
Sulphobes
|
107
|
3
|
Stub
|
Low
|
| 964
|
Marcello Barbieri
|
107
|
3
|
Start
|
Low
|
| 965
|
Polymorphism in Lepidoptera
|
106
|
3
|
C
|
High
|
| 966
|
Tip dating
|
104
|
3
|
Stub
|
Low
|
| 967
|
Largest-scale trends in evolution
|
103
|
3
|
Start
|
High
|
| 968
|
James A. Lake
|
103
|
3
|
Start
|
Low
|
| 969
|
Stephen Blair Hedges
|
102
|
3
|
Start
|
Low
|
| 970
|
Identity in social insects
|
101
|
3
|
Start
|
Low
|
| 971
|
Interpolation theory
|
100
|
3
|
Start
|
Low
|
| 972
|
Hyposphene-hypantrum articulation
|
100
|
3
|
Start
|
Low
|
| 973
|
Despeciation
|
100
|
3
|
Start
|
Low
|
| 974
|
Assisted evolution
|
100
|
3
|
C
|
Low
|
| 975
|
Relative rate test
|
99
|
3
|
Start
|
Low
|
| 976
|
Bias in the introduction of variation
|
98
|
3
|
B
|
Low
|
| 977
|
Species group
|
97
|
3
|
NA
|
NA
|
| 978
|
Wallace effect
|
96
|
3
|
NA
|
NA
|
| 979
|
Cousin couple
|
94
|
3
|
NA
|
Low
|
| 980
|
Calcichordate hypothesis
|
94
|
3
|
Start
|
Mid
|
| 981
|
Reductive evolution
|
94
|
3
|
Start
|
Low
|
| 982
|
Grit, not grass hypothesis
|
93
|
3
|
C
|
Low
|
| 983
|
Locomotor mimicry
|
93
|
3
|
Start
|
Low
|
| 984
|
Zachary Blount
|
92
|
2
|
Start
|
Low
|
| 985
|
Nonecological speciation
|
92
|
2
|
Start
|
Low
|
| 986
|
Darwinian puzzle
|
90
|
2
|
Start
|
Low
|
| 987
|
George Rolleston
|
90
|
2
|
Start
|
Low
|
| 988
|
Phylosymbiosis
|
90
|
2
|
Start
|
Low
|
| 989
|
Patty Brennan
|
90
|
2
|
Start
|
Unknown
|
| 990
|
Sex differences in sensory systems
|
89
|
2
|
Start
|
Mid
|
| 991
|
Differential fitness
|
89
|
2
|
C
|
Low
|
| 992
|
Andrew Berry (biologist)
|
87
|
2
|
Stub
|
Low
|
| 993
|
Mosaic coevolution
|
87
|
2
|
Unknown
|
Unknown
|
| 994
|
Ludwig Hermann Plate
|
86
|
2
|
Start
|
Low
|
| 995
|
Evolution Day
|
86
|
2
|
Unknown
|
Unknown
|
| 996
|
Mutation accumulation experiments
|
86
|
2
|
C
|
Low
|
| 997
|
Female sabotage
|
85
|
2
|
Start
|
Low
|
| 998
|
The Panda's Thumb (blog)
|
85
|
2
|
Start
|
Low
|
| 999
|
Swamping argument
|
85
|
2
|
Stub
|
Low
|
| 1000
|
Corrie Moreau
|
85
|
2
|
C
|
Low
|
