Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
1
|
Charles Darwin
|
131,711
|
4,390
|
FA
|
Top
|
2
|
Neanderthal
|
116,180
|
3,872
|
GA
|
Mid
|
3
|
Richard Dawkins
|
100,275
|
3,342
|
GA
|
Mid
|
4
|
Eugenics
|
88,164
|
2,938
|
C
|
Mid
|
5
|
Human evolution
|
79,393
|
2,646
|
C
|
High
|
6
|
Sexual dimorphism
|
75,728
|
2,524
|
B
|
High
|
7
|
Species
|
68,565
|
2,285
|
GA
|
Top
|
8
|
List of X-Men members
|
64,000
|
2,133
|
List
|
Low
|
9
|
Cretaceous–Paleogene extinction event
|
63,948
|
2,131
|
FA
|
High
|
10
|
Racism
|
63,152
|
2,105
|
B
|
Mid
|
11
|
Parthenogenesis
|
62,532
|
2,084
|
B
|
High
|
12
|
Extinction
|
58,926
|
1,964
|
C
|
High
|
13
|
Evolution
|
57,794
|
1,926
|
FA
|
Top
|
14
|
List of common misconceptions
|
52,342
|
1,744
|
List
|
Low
|
15
|
Abiogenesis
|
51,994
|
1,733
|
GA
|
Top
|
16
|
Biodiversity
|
48,987
|
1,632
|
C
|
Mid
|
17
|
Fossil
|
45,142
|
1,504
|
B
|
Mid
|
18
|
Scientific racism
|
41,943
|
1,398
|
C
|
Low
|
19
|
Binomial nomenclature
|
40,798
|
1,359
|
C
|
Low
|
20
|
Carcinisation
|
39,864
|
1,328
|
Start
|
Top
|
21
|
Cousin
|
38,823
|
1,294
|
Start
|
Low
|
22
|
Ecology
|
38,813
|
1,293
|
GA
|
Top
|
23
|
Scopes trial
|
38,408
|
1,280
|
B
|
High
|
24
|
Epicanthic fold
|
35,465
|
1,182
|
C
|
Low
|
25
|
Early modern human
|
35,366
|
1,178
|
B
|
Mid
|
26
|
Inbreeding
|
33,767
|
1,125
|
C
|
High
|
27
|
Genetics
|
33,597
|
1,119
|
FA
|
Top
|
28
|
Cro-Magnon
|
32,376
|
1,079
|
GA
|
Mid
|
29
|
Mutation
|
31,991
|
1,066
|
B
|
Top
|
30
|
Natural selection
|
31,904
|
1,063
|
GA
|
Top
|
31
|
On the Origin of Species
|
30,688
|
1,022
|
FA
|
Top
|
32
|
William Jennings Bryan
|
30,543
|
1,018
|
B
|
High
|
33
|
Altruism
|
29,430
|
981
|
B
|
High
|
34
|
Timeline of human evolution
|
29,213
|
973
|
C
|
Low
|
35
|
Paleontology
|
29,128
|
970
|
GA
|
Top
|
36
|
Archaic humans
|
28,316
|
943
|
Start
|
Low
|
37
|
Domestication of the dog
|
28,145
|
938
|
B
|
Low
|
38
|
Origin of language
|
27,579
|
919
|
C
|
Low
|
39
|
Hybrid (biology)
|
27,068
|
902
|
GA
|
High
|
40
|
Darwinism
|
26,722
|
890
|
Start
|
High
|
41
|
Cambrian explosion
|
25,894
|
863
|
B
|
High
|
42
|
Last universal common ancestor
|
25,529
|
850
|
GA
|
Top
|
43
|
Patrilineality
|
24,892
|
829
|
Start
|
Low
|
44
|
Homo floresiensis
|
24,531
|
817
|
B
|
Mid
|
45
|
Neontology
|
24,150
|
805
|
Start
|
Mid
|
46
|
Clade
|
23,742
|
791
|
C
|
High
|
47
|
Anus
|
23,512
|
783
|
Start
|
Mid
|
48
|
Convergent evolution
|
23,383
|
779
|
GA
|
High
|
49
|
Great Oxidation Event
|
22,722
|
757
|
C
|
Mid
|
50
|
HeLa
|
22,661
|
755
|
C
|
Low
|
51
|
Human taxonomy
|
21,243
|
708
|
C
|
Low
|
52
|
Fear
|
20,769
|
692
|
B
|
Low
|
53
|
Population bottleneck
|
20,241
|
674
|
C
|
High
|
54
|
Lamarckism
|
19,365
|
645
|
GA
|
High
|
55
|
Upper Paleolithic
|
19,080
|
636
|
C
|
Low
|
56
|
Eusociality
|
19,015
|
633
|
GA
|
Mid
|
57
|
Earliest known life forms
|
18,925
|
630
|
C
|
Top
|
58
|
Camouflage
|
18,125
|
604
|
GA
|
Mid
|
59
|
Wallace Line
|
18,018
|
600
|
Start
|
Mid
|
60
|
Institutional racism
|
17,942
|
598
|
B
|
Mid
|
61
|
Karyotype
|
17,894
|
596
|
C
|
Low
|
62
|
Aposematism
|
17,723
|
590
|
GA
|
Mid
|
63
|
Haplogroup
|
17,721
|
590
|
C
|
Mid
|
64
|
Extant taxon
|
17,719
|
590
|
NA
|
NA
|
65
|
Stephen Jay Gould
|
17,647
|
588
|
GA
|
Mid
|
66
|
Living fossil
|
17,335
|
577
|
C
|
Mid
|
67
|
Homology (biology)
|
16,900
|
563
|
GA
|
Top
|
68
|
Symbiogenesis
|
16,878
|
562
|
GA
|
High
|
69
|
Stromatolite
|
16,666
|
555
|
B
|
Mid
|
70
|
Tiktaalik
|
16,535
|
551
|
GA
|
High
|
71
|
Timeline of the evolutionary history of life
|
16,024
|
534
|
B
|
Top
|
72
|
Nazi eugenics
|
15,744
|
524
|
C
|
Low
|
73
|
The Selfish Gene
|
15,728
|
524
|
B
|
High
|
74
|
Australopithecine
|
15,696
|
523
|
C
|
High
|
75
|
Sociality
|
15,623
|
520
|
C
|
Mid
|
76
|
Hardy–Weinberg principle
|
15,439
|
514
|
C
|
High
|
77
|
Major histocompatibility complex
|
15,386
|
512
|
B
|
Low
|
78
|
Pan (genus)
|
15,185
|
506
|
B
|
High
|
79
|
Nordicism
|
15,083
|
502
|
B
|
Low
|
80
|
Bipedalism
|
14,962
|
498
|
B
|
Mid
|
81
|
Origin of COVID-19
|
14,958
|
498
|
Start
|
Mid
|
82
|
Alfred Russel Wallace
|
14,852
|
495
|
FA
|
Top
|
83
|
Phylogenetics
|
14,849
|
494
|
C
|
High
|
84
|
Selective breeding
|
14,807
|
493
|
C
|
Low
|
85
|
Matrilineality
|
14,612
|
487
|
C
|
Low
|
86
|
Domestication of the cat
|
14,441
|
481
|
C
|
Mid
|
87
|
Sex differences in intelligence
|
14,107
|
470
|
B
|
Low
|
88
|
Sexual selection
|
14,033
|
467
|
GA
|
High
|
89
|
Antimicrobial resistance
|
13,913
|
463
|
B
|
Unknown
|
90
|
Ronald Fisher
|
13,911
|
463
|
B
|
High
|
91
|
Genetic drift
|
13,828
|
460
|
GA
|
Top
|
92
|
History of life
|
13,605
|
453
|
GA
|
Top
|
93
|
Mimicry
|
13,599
|
453
|
GA
|
High
|
94
|
Stoned ape theory
|
13,523
|
450
|
C
|
Low
|
95
|
Survival of the fittest
|
13,356
|
445
|
B
|
Low
|
96
|
Eugenics in the United States
|
13,221
|
440
|
Start
|
Low
|
97
|
Three-domain system
|
12,917
|
430
|
C
|
Mid
|
98
|
Thomas Henry Huxley
|
12,825
|
427
|
B
|
Mid
|
99
|
Homo longi
|
12,743
|
424
|
GA
|
Low
|
100
|
Jean-Baptiste Lamarck
|
12,724
|
424
|
B
|
Top
|
101
|
Founder effect
|
12,666
|
422
|
C
|
Mid
|
102
|
Human Y-chromosome DNA haplogroup
|
12,603
|
420
|
C
|
Mid
|
103
|
Darwin's finches
|
12,536
|
417
|
C
|
High
|
104
|
Rare Earth hypothesis
|
12,299
|
409
|
B
|
Low
|
105
|
R/K selection theory
|
12,284
|
409
|
C
|
High
|
106
|
Vestigiality
|
12,187
|
406
|
C
|
High
|
107
|
Evolution of mammals
|
12,127
|
404
|
B
|
High
|
108
|
Panthera hybrid
|
12,101
|
403
|
C
|
Low
|
109
|
Fertility
|
12,031
|
401
|
C
|
High
|
110
|
E. O. Wilson
|
11,668
|
388
|
B
|
Mid
|
111
|
Anthropometry
|
11,639
|
387
|
C
|
Low
|
112
|
Triune brain
|
11,479
|
382
|
Start
|
Low
|
113
|
Peking Man
|
11,348
|
378
|
GA
|
Mid
|
114
|
Human vestigiality
|
11,336
|
377
|
C
|
Mid
|
115
|
Ernst Haeckel
|
11,190
|
373
|
B
|
High
|
116
|
Adaptation
|
11,166
|
372
|
GA
|
Top
|
117
|
Chicken or the egg
|
10,921
|
364
|
Start
|
Low
|
118
|
Ediacaran biota
|
10,812
|
360
|
FA
|
Low
|
119
|
Behavioral modernity
|
10,667
|
355
|
C
|
Low
|
120
|
Evolutionary psychology
|
10,632
|
354
|
C
|
High
|
121
|
Origin of birds
|
10,468
|
348
|
B
|
Mid
|
122
|
Evolution of the horse
|
10,417
|
347
|
B
|
Mid
|
123
|
Instinct
|
10,400
|
346
|
C
|
Low
|
124
|
List of human evolution fossils
|
10,380
|
346
|
List
|
High
|
125
|
Most recent common ancestor
|
10,191
|
339
|
B
|
High
|
126
|
Polymorphism (biology)
|
10,103
|
336
|
B
|
High
|
127
|
RNA world
|
10,081
|
336
|
C
|
High
|
128
|
Human mating strategies
|
10,072
|
335
|
B
|
Low
|
129
|
Horizontal gene transfer
|
10,066
|
335
|
C
|
High
|
130
|
Evolutionary biology
|
9,966
|
332
|
C
|
Top
|
131
|
Basal (phylogenetics)
|
9,936
|
331
|
C
|
Mid
|
132
|
Evolution of sexual reproduction
|
9,870
|
329
|
B
|
High
|
133
|
Red Queen hypothesis
|
9,589
|
319
|
Start
|
Mid
|
134
|
Speciation
|
9,525
|
317
|
C
|
High
|
135
|
Cladistics
|
9,504
|
316
|
C
|
Mid
|
136
|
Adaptive radiation
|
8,993
|
299
|
Start
|
High
|
137
|
Bergmann's rule
|
8,956
|
298
|
C
|
Low
|
138
|
Offspring
|
8,948
|
298
|
Start
|
Mid
|
139
|
Linnaean taxonomy
|
8,874
|
295
|
C
|
Mid
|
140
|
Braarudosphaera bigelowii
|
8,850
|
295
|
Start
|
Low
|
141
|
Monophyly
|
8,764
|
292
|
C
|
Mid
|
142
|
Sexual cannibalism
|
8,746
|
291
|
B
|
Low
|
143
|
Punctuated equilibrium
|
8,741
|
291
|
GA
|
High
|
144
|
Feathered dinosaur
|
8,700
|
290
|
C
|
High
|
145
|
Objections to evolution
|
8,691
|
289
|
GA
|
Mid
|
146
|
Common descent
|
8,640
|
288
|
C
|
Top
|
147
|
Symmetry in biology
|
8,611
|
287
|
C
|
High
|
148
|
Primordial soup
|
8,581
|
286
|
Start
|
Mid
|
149
|
Island gigantism
|
8,372
|
279
|
Start
|
Low
|
150
|
Biogeography
|
8,367
|
278
|
Start
|
Mid
|
151
|
Lower Paleolithic
|
8,357
|
278
|
C
|
High
|
152
|
J. B. S. Haldane
|
8,294
|
276
|
C
|
Mid
|
153
|
Julian Huxley
|
8,277
|
275
|
B
|
Mid
|
154
|
Variability hypothesis
|
8,240
|
274
|
C
|
Low
|
155
|
Genetic diversity
|
8,220
|
274
|
C
|
Mid
|
156
|
Jebel Irhoud
|
8,206
|
273
|
C
|
Low
|
157
|
Allopatric speciation
|
8,155
|
271
|
C
|
High
|
158
|
Evolutionary history of plants
|
8,154
|
271
|
B
|
High
|
159
|
CpG site
|
7,876
|
262
|
C
|
Mid
|
160
|
Species complex
|
7,861
|
262
|
B
|
Mid
|
161
|
Anisogamy
|
7,654
|
255
|
C
|
High
|
162
|
Signalling theory
|
7,591
|
253
|
GA
|
Mid
|
163
|
Missing link (human evolution)
|
7,546
|
251
|
Start
|
Mid
|
164
|
Fitness (biology)
|
7,508
|
250
|
B
|
High
|
165
|
Great American Interchange
|
7,499
|
249
|
C
|
Mid
|
166
|
Recent human evolution
|
7,453
|
248
|
B
|
Mid
|
167
|
Autosome
|
7,413
|
247
|
Start
|
High
|
168
|
Insular dwarfism
|
7,391
|
246
|
C
|
Low
|
169
|
Human mitochondrial DNA haplogroup
|
7,272
|
242
|
Start
|
Mid
|
170
|
Lek mating
|
7,118
|
237
|
GA
|
Mid
|
171
|
Evolutionary algorithm
|
7,110
|
237
|
C
|
Low
|
172
|
Female promiscuity
|
7,090
|
236
|
C
|
Low
|
173
|
Sex differences in human physiology
|
7,035
|
234
|
C
|
High
|
174
|
Evolutionary origin of religion
|
7,014
|
233
|
C
|
Low
|
175
|
Transitional fossil
|
6,939
|
231
|
GA
|
Top
|
176
|
Batesian mimicry
|
6,923
|
230
|
GA
|
Mid
|
177
|
Felid hybrids
|
6,922
|
230
|
Start
|
Low
|
178
|
Evolution of fish
|
6,790
|
226
|
C
|
High
|
179
|
Middle Paleolithic
|
6,724
|
224
|
C
|
High
|
180
|
Sympatric speciation
|
6,518
|
217
|
Start
|
Mid
|
181
|
Evolution of human intelligence
|
6,462
|
215
|
Start
|
High
|
182
|
History of evolutionary thought
|
6,457
|
215
|
FA
|
Top
|
183
|
List of related male and female reproductive organs
|
6,405
|
213
|
List
|
Mid
|
184
|
Evolution of primates
|
6,387
|
212
|
Start
|
Low
|
185
|
Recapitulation theory
|
6,383
|
212
|
C
|
Mid
|
186
|
Inbreeding depression
|
6,279
|
209
|
Start
|
Mid
|
187
|
Evolution of cetaceans
|
6,278
|
209
|
GA
|
Mid
|
188
|
The Naked Woman
|
6,261
|
208
|
Stub
|
Low
|
189
|
Evolution of the wolf
|
6,246
|
208
|
B
|
Low
|
190
|
Gene flow
|
6,215
|
207
|
Start
|
High
|
191
|
Müllerian mimicry
|
6,191
|
206
|
GA
|
Mid
|
192
|
Cladogram
|
6,146
|
204
|
C
|
Mid
|
193
|
Religious views of Charles Darwin
|
6,095
|
203
|
B
|
Low
|
194
|
Anatomically modern human
|
6,057
|
201
|
NA
|
NA
|
195
|
Darwin's Dangerous Idea
|
6,039
|
201
|
C
|
Mid
|
196
|
Aquatic ape hypothesis
|
6,011
|
200
|
C
|
Low
|
197
|
The Descent of Man, and Selection in Relation to Sex
|
5,995
|
199
|
Start
|
High
|
198
|
Population genetics
|
5,947
|
198
|
C
|
High
|
199
|
Genetic variation
|
5,937
|
197
|
Start
|
High
|
200
|
Neanderthal genetics
|
5,892
|
196
|
C
|
High
|
201
|
Sex differences in psychology
|
5,877
|
195
|
C
|
High
|
202
|
Sexy son hypothesis
|
5,851
|
195
|
C
|
Mid
|
203
|
Evolution of birds
|
5,823
|
194
|
C
|
High
|
204
|
Introduction to evolution
|
5,744
|
191
|
B
|
Mid
|
205
|
Spiral Dynamics
|
5,658
|
188
|
C
|
Low
|
206
|
Ontogeny
|
5,624
|
187
|
B
|
High
|
207
|
Evolution as fact and theory
|
5,615
|
187
|
C
|
Low
|
208
|
Peppered moth evolution
|
5,504
|
183
|
GA
|
High
|
209
|
Expelled: No Intelligence Allowed
|
5,456
|
181
|
B
|
Low
|
210
|
Sexual selection in humans
|
5,375
|
179
|
C
|
Low
|
211
|
Modern synthesis (20th century)
|
5,373
|
179
|
GA
|
High
|
212
|
Speculative evolution
|
5,367
|
178
|
B
|
Low
|
213
|
Islamic views on evolution
|
5,247
|
174
|
C
|
Low
|
214
|
Apomorphy and synapomorphy
|
5,187
|
172
|
C
|
Low
|
215
|
Reproductive isolation
|
5,164
|
172
|
C
|
High
|
216
|
Human sperm competition
|
5,162
|
172
|
C
|
Low
|
217
|
Devolution (biology)
|
5,112
|
170
|
C
|
Low
|
218
|
Thomas Hunt Morgan
|
5,069
|
168
|
B
|
High
|
219
|
Incertae sedis
|
4,944
|
164
|
C
|
Low
|
220
|
Relict (biology)
|
4,933
|
164
|
C
|
Mid
|
221
|
Divergent evolution
|
4,921
|
164
|
Start
|
Mid
|
222
|
Maladaptation
|
4,889
|
162
|
Start
|
Mid
|
223
|
Directional selection
|
4,876
|
162
|
Start
|
Mid
|
224
|
Purple Earth hypothesis
|
4,766
|
158
|
Start
|
Mid
|
225
|
Frameshift mutation
|
4,760
|
158
|
B
|
High
|
226
|
Kin selection
|
4,714
|
157
|
GA
|
High
|
227
|
Kenyanthropus
|
4,689
|
156
|
GA
|
Low
|
228
|
Assortative mating
|
4,666
|
155
|
C
|
Mid
|
229
|
First universal common ancestor
|
4,658
|
155
|
Start
|
Unknown
|
230
|
Fisherian runaway
|
4,598
|
153
|
Start
|
Low
|
231
|
Climate change adaptation
|
4,568
|
152
|
B
|
Mid
|
232
|
Spandrel (biology)
|
4,489
|
149
|
B
|
Mid
|
233
|
Aggressive mimicry
|
4,437
|
147
|
GA
|
Mid
|
234
|
Complex adaptive system
|
4,405
|
146
|
C
|
Mid
|
235
|
Neo-Darwinism
|
4,403
|
146
|
Start
|
Mid
|
236
|
Australopithecus sediba
|
4,391
|
146
|
GA
|
Low
|
237
|
Evolution of the eye
|
4,361
|
145
|
C
|
High
|
238
|
Systematics
|
4,340
|
144
|
C
|
High
|
239
|
Crown group
|
4,320
|
144
|
C
|
Mid
|
240
|
Peppered moth
|
4,312
|
143
|
B
|
Low
|
241
|
Sequence homology
|
4,269
|
142
|
C
|
High
|
242
|
History of eugenics
|
4,249
|
141
|
B
|
Low
|
243
|
Hunter versus farmer hypothesis
|
4,248
|
141
|
C
|
Low
|
244
|
Multiregional origin of modern humans
|
4,225
|
140
|
C
|
Mid
|
245
|
Sperm competition
|
4,180
|
139
|
Start
|
Mid
|
246
|
Rotating locomotion in living systems
|
4,147
|
138
|
FA
|
High
|
247
|
Lagerstätte
|
4,090
|
136
|
B
|
Mid
|
248
|
Self-preservation
|
4,078
|
135
|
C
|
High
|
249
|
History of biology
|
4,047
|
134
|
FA
|
High
|
250
|
Coevolution
|
4,034
|
134
|
GA
|
High
|
251
|
Evolution of the brain
|
4,019
|
133
|
Start
|
High
|
252
|
Four Fs (evolution)
|
4,000
|
133
|
C
|
Low
|
253
|
Beta diversity
|
3,997
|
133
|
C
|
Mid
|
254
|
Hominina
|
3,987
|
132
|
NA
|
NA
|
255
|
Allele frequency
|
3,954
|
131
|
Start
|
Mid
|
256
|
Sister group
|
3,923
|
130
|
Start
|
Low
|
257
|
Rejection of evolution by religious groups
|
3,912
|
130
|
B
|
High
|
258
|
Disruptive selection
|
3,883
|
129
|
C
|
Mid
|
259
|
Biology and political orientation
|
3,864
|
128
|
C
|
Low
|
260
|
Evolutionary developmental biology
|
3,835
|
127
|
GA
|
High
|
261
|
Herto Man
|
3,820
|
127
|
GA
|
Low
|
262
|
Ernst Mayr
|
3,807
|
126
|
C
|
High
|
263
|
Heather Heying
|
3,784
|
126
|
Start
|
Low
|
264
|
Haplodiploidy
|
3,772
|
125
|
C
|
Mid
|
265
|
Evolutionary game theory
|
3,764
|
125
|
C
|
High
|
266
|
Protocell
|
3,723
|
124
|
C
|
Mid
|
267
|
List of fossil sites
|
3,716
|
123
|
List
|
Top
|
268
|
Altruism (biology)
|
3,696
|
123
|
C
|
Mid
|
269
|
Handicap principle
|
3,691
|
123
|
GA
|
High
|
270
|
Macroevolution
|
3,673
|
122
|
B
|
Top
|
271
|
Evidence of common descent
|
3,670
|
122
|
B
|
Mid
|
272
|
Parental care
|
3,665
|
122
|
B
|
Mid
|
273
|
Gene duplication
|
3,653
|
121
|
C
|
Mid
|
274
|
Phenotypic plasticity
|
3,594
|
119
|
C
|
Mid
|
275
|
List of examples of convergent evolution
|
3,589
|
119
|
List
|
High
|
276
|
Parental investment
|
3,534
|
117
|
Start
|
High
|
277
|
Stabilizing selection
|
3,529
|
117
|
Start
|
Mid
|
278
|
Geological history of oxygen
|
3,517
|
117
|
C
|
Low
|
279
|
Level of support for evolution
|
3,466
|
115
|
C
|
Mid
|
280
|
Atelocyanobacterium thalassa
|
3,464
|
115
|
C
|
Low
|
281
|
Japanese Paleolithic
|
3,446
|
114
|
Start
|
High
|
282
|
Endurance running hypothesis
|
3,431
|
114
|
Start
|
Low
|
283
|
Jeremiah Kianga
|
3,387
|
112
|
Start
|
Low
|
284
|
The Blind Watchmaker
|
3,349
|
111
|
C
|
Mid
|
285
|
Acceptance of evolution by religious groups
|
3,264
|
108
|
C
|
Low
|
286
|
Gene polymorphism
|
3,241
|
108
|
Start
|
Mid
|
287
|
History of ecology
|
3,208
|
106
|
C
|
Mid
|
288
|
Evolutionarily stable strategy
|
3,152
|
105
|
B
|
Mid
|
289
|
Cline (biology)
|
3,146
|
104
|
C
|
Low
|
290
|
Reciprocal altruism
|
3,114
|
103
|
B
|
Mid
|
291
|
Orthogenesis
|
3,100
|
103
|
GA
|
Mid
|
292
|
The Expression of the Emotions in Man and Animals
|
3,093
|
103
|
Start
|
Mid
|
293
|
Body plan
|
3,092
|
103
|
C
|
Mid
|
294
|
Gene-centered view of evolution
|
3,078
|
102
|
B
|
High
|
295
|
Exaptation
|
3,056
|
101
|
C
|
High
|
296
|
Microevolution
|
3,052
|
101
|
C
|
High
|
297
|
Life history theory
|
3,052
|
101
|
C
|
High
|
298
|
Evolution of reptiles
|
3,052
|
101
|
C
|
High
|
299
|
Theodosius Dobzhansky
|
3,048
|
101
|
C
|
Mid
|
300
|
Allometry
|
3,045
|
101
|
C
|
Mid
|
301
|
Parallel evolution
|
3,010
|
100
|
Start
|
High
|
302
|
Evolutionism
|
3,007
|
100
|
C
|
Mid
|
303
|
Sexual conflict
|
3,001
|
100
|
Start
|
High
|
304
|
Sociobiological theories of rape
|
2,973
|
99
|
C
|
Mid
|
305
|
Evolutionary pressure
|
2,953
|
98
|
C
|
Mid
|
306
|
Group selection
|
2,943
|
98
|
GA
|
High
|
307
|
Ring species
|
2,940
|
98
|
C
|
High
|
308
|
Domestication syndrome
|
2,923
|
97
|
C
|
Low
|
309
|
Solo Man
|
2,920
|
97
|
FA
|
Low
|
310
|
Gene pool
|
2,906
|
96
|
Start
|
High
|
311
|
Why Is Sex Fun?
|
2,875
|
95
|
C
|
Low
|
312
|
Radiation hormesis
|
2,856
|
95
|
B
|
Mid
|
313
|
E. coli long-term evolution experiment
|
2,841
|
94
|
B
|
Mid
|
314
|
Fish intelligence
|
2,801
|
93
|
B
|
Low
|
315
|
Evolutionary computation
|
2,795
|
93
|
C
|
High
|
316
|
Clonally transmissible cancer
|
2,783
|
92
|
C
|
Low
|
317
|
Killer ape theory
|
2,755
|
91
|
Start
|
Low
|
318
|
Eukaryogenesis
|
2,749
|
91
|
C
|
High
|
319
|
Future generations
|
2,743
|
91
|
Start
|
Low
|
320
|
March of Progress
|
2,732
|
91
|
C
|
Low
|
321
|
Stotting
|
2,666
|
88
|
GA
|
Low
|
322
|
Island syndrome
|
2,605
|
86
|
Start
|
Unknown
|
323
|
Shadow biosphere
|
2,521
|
84
|
Start
|
Mid
|
324
|
John Maynard Smith
|
2,514
|
83
|
C
|
High
|
325
|
Neutral theory of molecular evolution
|
2,510
|
83
|
Start
|
High
|
326
|
Ursid hybrid
|
2,505
|
83
|
C
|
Low
|
327
|
Alloparenting
|
2,488
|
82
|
C
|
Low
|
328
|
Evolution of photosynthesis
|
2,473
|
82
|
Start
|
High
|
329
|
Mach bands
|
2,463
|
82
|
Start
|
Mid
|
330
|
Human skeletal changes due to bipedalism
|
2,392
|
79
|
B
|
Mid
|
331
|
Duane Gish
|
2,390
|
79
|
C
|
Low
|
332
|
Struggle for existence
|
2,355
|
78
|
C
|
Mid
|
333
|
Alternatives to Darwinian evolution
|
2,330
|
77
|
B
|
Mid
|
334
|
Somatic mutation
|
2,312
|
77
|
C
|
Low
|
335
|
Inclusive fitness
|
2,279
|
75
|
C
|
High
|
336
|
Evolutionary radiation
|
2,278
|
75
|
Start
|
Mid
|
337
|
Haldane's rule
|
2,273
|
75
|
C
|
Low
|
338
|
Homo sapiens sapiens
|
2,268
|
75
|
NA
|
NA
|
339
|
Molecular evolution
|
2,254
|
75
|
C
|
Top
|
340
|
Germline mutation
|
2,222
|
74
|
B
|
High
|
341
|
Evolutionary arms race
|
2,222
|
74
|
Start
|
High
|
342
|
Cro-Magnon rock shelter
|
2,191
|
73
|
Start
|
Mid
|
343
|
Two-domain system
|
2,185
|
72
|
C
|
Low
|
344
|
Coalescent theory
|
2,155
|
71
|
C
|
Low
|
345
|
Meganthropus
|
2,144
|
71
|
Start
|
Low
|
346
|
W. D. Hamilton
|
2,130
|
71
|
C
|
Low
|
347
|
Costly signaling theory in evolutionary psychology
|
2,109
|
70
|
C
|
Mid
|
348
|
Evolution of morality
|
2,066
|
68
|
C
|
High
|
349
|
Pangenesis
|
2,050
|
68
|
C
|
Low
|
350
|
Origin of speech
|
2,044
|
68
|
C
|
Mid
|
351
|
Muller's ratchet
|
2,033
|
67
|
Start
|
Mid
|
352
|
Evolution of tetrapods
|
2,010
|
67
|
C
|
High
|
353
|
Asa Gray
|
1,992
|
66
|
GA
|
Low
|
354
|
Evolutionary anachronism
|
1,973
|
65
|
List
|
Mid
|
355
|
Bateman's principle
|
1,971
|
65
|
B
|
Mid
|
356
|
Fisher's principle
|
1,966
|
65
|
Start
|
Mid
|
357
|
Parapatric speciation
|
1,932
|
64
|
C
|
Mid
|
358
|
Evolutionary suicide
|
1,932
|
64
|
Start
|
Low
|
359
|
Snake detection theory
|
1,925
|
64
|
Start
|
Mid
|
360
|
Disappearing blonde gene
|
1,904
|
63
|
Start
|
Low
|
361
|
Jerry Coyne
|
1,893
|
63
|
Start
|
Low
|
362
|
Evolutionary taxonomy
|
1,889
|
62
|
C
|
Mid
|
363
|
Grandmother hypothesis
|
1,867
|
62
|
C
|
Mid
|
364
|
Bird hybrid
|
1,857
|
61
|
Start
|
Low
|
365
|
Panmixia
|
1,829
|
60
|
Start
|
Mid
|
366
|
Genotype–phenotype distinction
|
1,785
|
59
|
Start
|
High
|
367
|
Nicholas Miklouho-Maclay
|
1,782
|
59
|
C
|
Low
|
368
|
Baldwin effect
|
1,780
|
59
|
GA
|
Low
|
369
|
Evolution of cells
|
1,780
|
59
|
Start
|
High
|
370
|
Evolution of mammalian auditory ossicles
|
1,779
|
59
|
B
|
Mid
|
371
|
Evolutionary mismatch
|
1,775
|
59
|
C
|
Low
|
372
|
Siblicide
|
1,763
|
58
|
Start
|
Low
|
373
|
Evolution of emotion
|
1,760
|
58
|
Start
|
Unknown
|
374
|
Peripatric speciation
|
1,742
|
58
|
B
|
Mid
|
375
|
Outgroup (cladistics)
|
1,739
|
57
|
Start
|
Mid
|
376
|
Heterochrony
|
1,736
|
57
|
GA
|
Mid
|
377
|
Background extinction rate
|
1,729
|
57
|
Start
|
Mid
|
378
|
Negative selection (natural selection)
|
1,728
|
57
|
Stub
|
Mid
|
379
|
Oceanic dispersal
|
1,723
|
57
|
Start
|
Low
|
380
|
Heterozygote advantage
|
1,718
|
57
|
Start
|
Mid
|
381
|
Reproductive success
|
1,713
|
57
|
Start
|
High
|
382
|
Indel
|
1,700
|
56
|
Start
|
Mid
|
383
|
Computational phylogenetics
|
1,690
|
56
|
C
|
Mid
|
384
|
Models of DNA evolution
|
1,687
|
56
|
B
|
Low
|
385
|
The Third Chimpanzee
|
1,682
|
56
|
C
|
Low
|
386
|
Creation and evolution in public education
|
1,678
|
55
|
B
|
Mid
|
387
|
Fitness landscape
|
1,673
|
55
|
B
|
High
|
388
|
Primitive (phylogenetics)
|
1,665
|
55
|
Start
|
Mid
|
389
|
Cognitive tradeoff hypothesis
|
1,646
|
54
|
C
|
Low
|
390
|
Late Stone Age
|
1,645
|
54
|
Start
|
Low
|
391
|
Down House
|
1,640
|
54
|
C
|
Low
|
392
|
Price equation
|
1,627
|
54
|
C
|
Low
|
393
|
Evolution of cephalopods
|
1,622
|
54
|
C
|
Low
|
394
|
Codon usage bias
|
1,619
|
53
|
B
|
Low
|
395
|
Red Deer Cave people
|
1,616
|
53
|
Start
|
Low
|
396
|
Modern humans
|
1,589
|
52
|
NA
|
NA
|
397
|
Robert Trivers
|
1,587
|
52
|
Start
|
Low
|
398
|
Evolution of snake venom
|
1,583
|
52
|
GA
|
Mid
|
399
|
Entrainment (biomusicology)
|
1,576
|
52
|
Start
|
Low
|
400
|
Gene family
|
1,562
|
52
|
C
|
High
|
401
|
Embryological origins of the mouth and anus
|
1,550
|
51
|
Start
|
Low
|
402
|
Homoplasy
|
1,547
|
51
|
Start
|
Low
|
403
|
Extended evolutionary synthesis
|
1,538
|
51
|
B
|
High
|
404
|
Metapopulation
|
1,519
|
50
|
B
|
Mid
|
405
|
Grimaldi man
|
1,508
|
50
|
C
|
Low
|
406
|
Population structure (genetics)
|
1,493
|
49
|
Start
|
Low
|
407
|
Isua Greenstone Belt
|
1,490
|
49
|
C
|
Mid
|
408
|
Red dress effect
|
1,484
|
49
|
Start
|
Low
|
409
|
Tend and befriend
|
1,483
|
49
|
C
|
Low
|
410
|
Sexual selection in birds
|
1,479
|
49
|
C
|
Low
|
411
|
Nothing in Biology Makes Sense Except in the Light of Evolution
|
1,469
|
48
|
C
|
Mid
|
412
|
Aerobic fermentation
|
1,460
|
48
|
B
|
Low
|
413
|
Diana Fleischman
|
1,458
|
48
|
Start
|
Low
|
414
|
Taforalt
|
1,452
|
48
|
C
|
Low
|
415
|
Peptide nucleic acid
|
1,450
|
48
|
Start
|
Low
|
416
|
August Weismann
|
1,448
|
48
|
Start
|
High
|
417
|
Evolution of biological complexity
|
1,442
|
48
|
C
|
Mid
|
418
|
Racism in the LGBT community
|
1,440
|
48
|
C
|
Low
|
419
|
Population biology
|
1,422
|
47
|
Stub
|
Low
|
420
|
Ka/Ks ratio
|
1,417
|
47
|
C
|
Mid
|
421
|
1860 Oxford evolution debate
|
1,413
|
47
|
B
|
Mid
|
422
|
Evolutionary psychology of religion
|
1,400
|
46
|
Start
|
Low
|
423
|
Satoshi Kanazawa
|
1,396
|
46
|
C
|
Unknown
|
424
|
Green-beard effect
|
1,395
|
46
|
Start
|
Low
|
425
|
Acritarch
|
1,392
|
46
|
C
|
Low
|
426
|
Frequency-dependent selection
|
1,389
|
46
|
Start
|
High
|
427
|
Genetic divergence
|
1,386
|
46
|
Start
|
High
|
428
|
History of anthropometry
|
1,380
|
46
|
C
|
Low
|
429
|
David Sloan Wilson
|
1,377
|
45
|
Start
|
Unknown
|
430
|
Anagenesis
|
1,373
|
45
|
C
|
Mid
|
431
|
Numerical taxonomy
|
1,366
|
45
|
Start
|
Mid
|
432
|
Initial Upper Paleolithic
|
1,358
|
45
|
B
|
Unknown
|
433
|
Character displacement
|
1,340
|
44
|
B
|
Mid
|
434
|
Evolution of lemurs
|
1,331
|
44
|
FA
|
Low
|
435
|
Synonymous substitution
|
1,323
|
44
|
Start
|
Mid
|
436
|
Balancing selection
|
1,314
|
43
|
Start
|
Mid
|
437
|
Systemic racism
|
1,313
|
43
|
NA
|
NA
|
438
|
Iron–sulfur world hypothesis
|
1,308
|
43
|
C
|
Low
|
439
|
Mate choice in humans
|
1,307
|
43
|
B
|
Unknown
|
440
|
Mating call
|
1,295
|
43
|
C
|
Low
|
441
|
Junkyard tornado
|
1,288
|
42
|
C
|
Low
|
442
|
Racist
|
1,286
|
42
|
NA
|
NA
|
443
|
Trivers–Willard hypothesis
|
1,281
|
42
|
Start
|
Low
|
444
|
Saltation (biology)
|
1,273
|
42
|
C
|
Mid
|
445
|
George R. Price
|
1,272
|
42
|
C
|
Low
|
446
|
Evolutionary anthropology
|
1,256
|
41
|
Start
|
Low
|
447
|
Endosymbiotic theory
|
1,250
|
41
|
NA
|
NA
|
448
|
Mate value
|
1,239
|
41
|
C
|
Low
|
449
|
Single-access key
|
1,237
|
41
|
C
|
Low
|
450
|
Bayesian inference in phylogeny
|
1,234
|
41
|
C
|
Low
|
451
|
Snaiad
|
1,232
|
41
|
B
|
Low
|
452
|
Embryonic diapause
|
1,228
|
40
|
Start
|
Low
|
453
|
Evolution of bacteria
|
1,228
|
40
|
C
|
Mid
|
454
|
Extinction vortex
|
1,224
|
40
|
Start
|
Low
|
455
|
Dmanisi
|
1,220
|
40
|
Start
|
Mid
|
456
|
Josiah C. Nott
|
1,212
|
40
|
C
|
Low
|
457
|
Origin of avian flight
|
1,210
|
40
|
Start
|
Mid
|
458
|
Race suicide
|
1,210
|
40
|
Start
|
Mid
|
459
|
Jewish views on evolution
|
1,206
|
40
|
B
|
Low
|
460
|
Adaptationism
|
1,199
|
39
|
Start
|
Mid
|
461
|
Snow camouflage
|
1,195
|
39
|
GA
|
Low
|
462
|
Incomplete lineage sorting
|
1,190
|
39
|
Start
|
Mid
|
463
|
Genetic pollution
|
1,186
|
39
|
C
|
Low
|
464
|
David Krakauer (scientist)
|
1,186
|
39
|
Start
|
Low
|
465
|
Evolution of nervous systems
|
1,179
|
39
|
B
|
Mid
|
466
|
Major histocompatibility complex and sexual selection
|
1,178
|
39
|
C
|
Mid
|
467
|
Dollo's law of irreversibility
|
1,172
|
39
|
Start
|
High
|
468
|
Plant evolution
|
1,167
|
38
|
Start
|
High
|
469
|
Hybrid fruit
|
1,166
|
38
|
Stub
|
Low
|
470
|
Androgenesis
|
1,158
|
38
|
C
|
Low
|
471
|
Blending inheritance
|
1,157
|
38
|
GA
|
Low
|
472
|
List of prehistoric cartilaginous fish genera
|
1,153
|
38
|
List
|
Mid
|
473
|
Evolutionary approaches to depression
|
1,150
|
38
|
Start
|
Low
|
474
|
Budgerigar colour genetics
|
1,148
|
38
|
Start
|
Low
|
475
|
Teleology in biology
|
1,147
|
38
|
GA
|
High
|
476
|
Niche construction
|
1,146
|
38
|
B
|
Low
|
477
|
Ovulatory shift hypothesis
|
1,142
|
38
|
GA
|
Low
|
478
|
Mormon views on evolution
|
1,133
|
37
|
C
|
Low
|
479
|
Strategic pluralism
|
1,129
|
37
|
Stub
|
Low
|
480
|
Motion camouflage
|
1,124
|
37
|
GA
|
Low
|
481
|
Nuptial gift
|
1,119
|
37
|
Start
|
Mid
|
482
|
Davis's law
|
1,117
|
37
|
Start
|
Low
|
483
|
Universal Darwinism
|
1,116
|
37
|
C
|
Low
|
484
|
Evolution of ageing
|
1,115
|
37
|
B
|
High
|
485
|
Paternal care
|
1,100
|
36
|
C
|
Low
|
486
|
Caveasphaera
|
1,089
|
36
|
Start
|
Low
|
487
|
Parasite-stress theory
|
1,072
|
35
|
C
|
Mid
|
488
|
Jonathan Wells (intelligent design advocate)
|
1,066
|
35
|
Start
|
Low
|
489
|
Timeline of fish evolution
|
1,050
|
35
|
List
|
Low
|
490
|
Experimental evolution
|
1,047
|
34
|
Start
|
High
|
491
|
Elizabeth, Lady Hope
|
1,044
|
34
|
C
|
Low
|
492
|
Mutationism
|
1,043
|
34
|
GA
|
Low
|
493
|
Wonderful Life (book)
|
1,042
|
34
|
Stub
|
Low
|
494
|
Phenetics
|
1,041
|
34
|
Start
|
Mid
|
495
|
Operational sex ratio
|
1,024
|
34
|
Start
|
Low
|
496
|
Autapomorphy
|
997
|
33
|
C
|
Low
|
497
|
Savannah hypothesis
|
997
|
33
|
Start
|
Low
|
498
|
Extended female sexuality
|
996
|
33
|
B
|
Mid
|
499
|
Endemism in the Hawaiian Islands
|
992
|
33
|
Start
|
Low
|
500
|
Motoo Kimura
|
991
|
33
|
B
|
High
|
501
|
Evolution of color vision in primates
|
987
|
32
|
C
|
Low
|
502
|
Ornithophily
|
984
|
32
|
B
|
Low
|
503
|
The Spandrels of San Marco and the Panglossian Paradigm
|
978
|
32
|
Start
|
Mid
|
504
|
Canalisation (genetics)
|
977
|
32
|
Start
|
Mid
|
505
|
Genotype frequency
|
976
|
32
|
Start
|
Mid
|
506
|
Glossary of genetics and evolutionary biology
|
968
|
32
|
List
|
Top
|
507
|
Conservative replacement
|
967
|
32
|
Start
|
Low
|
508
|
Of Pandas and People
|
961
|
32
|
C
|
Low
|
509
|
Polyphenism
|
960
|
32
|
Start
|
Mid
|
510
|
Protein superfamily
|
960
|
32
|
B
|
Mid
|
511
|
Neural Darwinism
|
959
|
31
|
C
|
Unknown
|
512
|
Sexual selection in mammals
|
951
|
31
|
C
|
Low
|
513
|
Cousin couple
|
949
|
31
|
NA
|
Low
|
514
|
Sociobiology: The New Synthesis
|
939
|
31
|
GA
|
Mid
|
515
|
Project Steve
|
923
|
30
|
C
|
Low
|
516
|
Allogamy
|
921
|
30
|
Start
|
Mid
|
517
|
Female sperm storage
|
920
|
30
|
C
|
Low
|
518
|
Cladogenesis
|
912
|
30
|
Start
|
Mid
|
519
|
Cooperation (evolution)
|
906
|
30
|
B
|
Mid
|
520
|
Artificial selection
|
901
|
30
|
NA
|
NA
|
521
|
The Greatest Show on Earth: The Evidence for Evolution
|
898
|
29
|
Start
|
Low
|
522
|
Parent–offspring conflict
|
896
|
29
|
Start
|
Mid
|
523
|
Angraecum sesquipedale
|
894
|
29
|
B
|
Mid
|
524
|
Crocoduck
|
893
|
29
|
C
|
Low
|
525
|
Human jaw shrinkage
|
884
|
29
|
Unknown
|
Unknown
|
526
|
Domestication of the goat
|
880
|
29
|
B
|
Mid
|
527
|
Cope's rule
|
876
|
29
|
Start
|
Mid
|
528
|
Joan Roughgarden
|
876
|
29
|
C
|
Unknown
|
529
|
Disposable soma theory of aging
|
873
|
29
|
C
|
Mid
|
530
|
Last eukaryotic common ancestor
|
864
|
28
|
NA
|
High
|
531
|
Vertebrate land invasion
|
861
|
28
|
C
|
Mid
|
532
|
List of non-avian dinosaur species preserved with evidence of feathers
|
855
|
28
|
List
|
Low
|
533
|
Evolution of flagella
|
849
|
28
|
Start
|
Mid
|
534
|
Koobi Fora
|
844
|
28
|
C
|
Mid
|
535
|
Henry Walter Bates
|
842
|
28
|
C
|
High
|
536
|
Outline of evolution
|
840
|
28
|
List
|
Top
|
537
|
Emsleyan mimicry
|
826
|
27
|
C
|
Low
|
538
|
Phyletic gradualism
|
825
|
27
|
Start
|
Mid
|
539
|
Lagar Velho 1
|
823
|
27
|
Stub
|
Low
|
540
|
Evolution of color vision
|
819
|
27
|
Start
|
Low
|
541
|
Sperm Wars
|
806
|
26
|
Start
|
Mid
|
542
|
Cryptic female choice
|
806
|
26
|
B
|
Low
|
543
|
Habitable zone for complex life
|
796
|
26
|
C
|
Unknown
|
544
|
Telescoping generations
|
793
|
26
|
Stub
|
Unknown
|
545
|
Fisher's fundamental theorem of natural selection
|
776
|
25
|
Start
|
Mid
|
546
|
Biogenesis
|
775
|
25
|
NA
|
High
|
547
|
Yuanmou Man
|
772
|
25
|
GA
|
Low
|
548
|
Annual vs. perennial plant evolution
|
766
|
25
|
C
|
Low
|
549
|
Darwinian demon
|
764
|
25
|
Stub
|
Low
|
550
|
The Red Queen: Sex and the Evolution of Human Nature
|
761
|
25
|
Start
|
Low
|
551
|
Evolutionary ecology
|
752
|
25
|
C
|
Mid
|
552
|
Proavis
|
751
|
25
|
Start
|
Low
|
553
|
Epic of evolution
|
742
|
24
|
C
|
Low
|
554
|
Elaine Morgan
|
740
|
24
|
C
|
Low
|
555
|
Evolutionary psychiatry
|
730
|
24
|
Stub
|
Low
|
556
|
Hologenome theory of evolution
|
728
|
24
|
Start
|
Mid
|
557
|
Bruniquel Cave
|
727
|
24
|
Start
|
Mid
|
558
|
Polytomy
|
725
|
24
|
Start
|
Mid
|
559
|
List of Neanderthal fossils
|
718
|
23
|
List
|
Low
|
560
|
Lantian Man
|
717
|
23
|
GA
|
Low
|
561
|
Gut (anatomy)
|
715
|
23
|
NA
|
Low
|
562
|
Haplogroup C-V20
|
714
|
23
|
Unknown
|
Unknown
|
563
|
Natural Theology or Evidences of the Existence and Attributes of the Deity
|
712
|
23
|
GA
|
Low
|
564
|
Seminal fluid protein
|
706
|
23
|
Start
|
Low
|
565
|
Host–parasite coevolution
|
699
|
23
|
GA
|
Mid
|
566
|
Caminalcules
|
695
|
23
|
Start
|
Mid
|
567
|
Chemical defense
|
693
|
23
|
C
|
Low
|
568
|
Mosaic evolution
|
692
|
23
|
Start
|
Low
|
569
|
Selection coefficient
|
688
|
22
|
Stub
|
Mid
|
570
|
Reinforcement (speciation)
|
687
|
22
|
GA
|
Mid
|
571
|
George Christopher Williams
|
681
|
22
|
Start
|
Mid
|
572
|
Disassortative mating
|
670
|
22
|
C
|
Mid
|
573
|
Social selection
|
669
|
22
|
C
|
Low
|
574
|
Cytotaxonomy
|
665
|
22
|
Stub
|
Mid
|
575
|
History of creationism
|
660
|
22
|
B
|
Mid
|
576
|
Precambrian rabbit
|
657
|
21
|
C
|
Low
|
577
|
Long branch attraction
|
649
|
21
|
Start
|
Low
|
578
|
Evolvability
|
648
|
21
|
C
|
High
|
579
|
Development of Darwin's theory
|
641
|
21
|
B
|
Mid
|
580
|
Phylogenetic comparative methods
|
634
|
21
|
C
|
Low
|
581
|
Island hopping
|
633
|
21
|
NA
|
Low
|
582
|
Genetic erosion
|
633
|
21
|
C
|
Low
|
583
|
Australopithecus deyiremeda
|
632
|
21
|
GA
|
Low
|
584
|
Unit of selection
|
622
|
20
|
C
|
High
|
585
|
Genome evolution
|
622
|
20
|
C
|
Top
|
586
|
Social immunity
|
622
|
20
|
B
|
High
|
587
|
Sex Power Money
|
622
|
20
|
C
|
Low
|
588
|
Evolutionary grade
|
621
|
20
|
Start
|
High
|
589
|
Robert Edmond Grant
|
620
|
20
|
Start
|
Low
|
590
|
Glacial refugium
|
619
|
20
|
Stub
|
Low
|
591
|
Genetic isolate
|
617
|
20
|
Stub
|
Low
|
592
|
Cooperative eye hypothesis
|
616
|
20
|
Start
|
Low
|
593
|
Philosophie zoologique
|
615
|
20
|
GA
|
Low
|
594
|
Willi Hennig
|
611
|
20
|
Start
|
Mid
|
595
|
The Genetical Theory of Natural Selection
|
609
|
20
|
Start
|
Mid
|
596
|
Mate guarding
|
608
|
20
|
Unknown
|
Mid
|
597
|
The Vital Question
|
608
|
20
|
GA
|
Low
|
598
|
Muscular evolution in humans
|
602
|
20
|
Start
|
Low
|
599
|
Evolutionary models of human drug use
|
594
|
19
|
C
|
Low
|
600
|
Ecological speciation
|
590
|
19
|
B
|
High
|
601
|
The Major Transitions in Evolution
|
588
|
19
|
Stub
|
Low
|
602
|
Evolution (TV series)
|
585
|
19
|
Start
|
Low
|
603
|
Bateson–Dobzhansky–Muller model
|
584
|
19
|
Unknown
|
Unknown
|
604
|
PAH world hypothesis
|
583
|
19
|
Start
|
Low
|
605
|
Ecomorphology
|
583
|
19
|
B
|
Low
|
606
|
Reticulate evolution
|
583
|
19
|
C
|
Mid
|
607
|
Evolution of eusociality
|
582
|
19
|
C
|
Low
|
608
|
Automimicry
|
577
|
19
|
GA
|
Mid
|
609
|
Precambrian body plans
|
577
|
19
|
B
|
Low
|
610
|
Schizocoely
|
576
|
19
|
Start
|
Mid
|
611
|
Loren Cordain
|
576
|
19
|
Stub
|
Low
|
612
|
Psammosere
|
572
|
19
|
Stub
|
Mid
|
613
|
Bat wing development
|
570
|
19
|
Start
|
Low
|
614
|
Nina Jablonski
|
568
|
18
|
B
|
Low
|
615
|
Racism on the Internet
|
564
|
18
|
Start
|
Low
|
616
|
List of transitional fossils
|
562
|
18
|
NA
|
NA
|
617
|
Vocal learning
|
560
|
18
|
B
|
Low
|
618
|
Bet hedging (biology)
|
557
|
18
|
B
|
Mid
|
619
|
Cryptic species complex
|
555
|
18
|
NA
|
NA
|
620
|
Endless Forms Most Beautiful (book)
|
553
|
18
|
GA
|
Low
|
621
|
The 10,000 Year Explosion
|
552
|
18
|
B
|
Mid
|
622
|
Origin and function of meiosis
|
552
|
18
|
Start
|
Low
|
623
|
Vestigial response
|
544
|
18
|
Stub
|
Low
|
624
|
Evolution of cognition
|
544
|
18
|
C
|
Low
|
625
|
Weasel program
|
543
|
18
|
B
|
Low
|
626
|
St. George Jackson Mivart
|
542
|
18
|
Start
|
Low
|
627
|
Randy Thornhill
|
537
|
17
|
Start
|
Mid
|
628
|
Patrick Matthew
|
533
|
17
|
B
|
Mid
|
629
|
Hybrid zone
|
531
|
17
|
C
|
Mid
|
630
|
Rate of evolution
|
529
|
17
|
Start
|
Low
|
631
|
Timeline of zoology
|
526
|
17
|
List
|
Mid
|
632
|
Court jester hypothesis
|
524
|
17
|
C
|
Low
|
633
|
Buya, Eritrea
|
524
|
17
|
C
|
Unknown
|
634
|
Konstantin Mereschkowski
|
523
|
17
|
GA
|
Unknown
|
635
|
McLean v. Arkansas
|
523
|
17
|
Start
|
Low
|
636
|
Franz Weidenreich
|
521
|
17
|
Stub
|
Mid
|
637
|
Spiegelman's Monster
|
516
|
17
|
Start
|
Low
|
638
|
Black Queen hypothesis
|
516
|
17
|
Start
|
Low
|
639
|
Man's Place in Nature
|
514
|
17
|
Start
|
Mid
|
640
|
Evolutionary tradeoff
|
512
|
17
|
Unknown
|
Unknown
|
641
|
Herman Bernhard Lundborg
|
508
|
16
|
Start
|
Low
|
642
|
Polyandry in fish
|
506
|
16
|
C
|
Low
|
643
|
Darwin and women
|
506
|
16
|
Stub
|
Low
|
644
|
Alternative abiogenesis scenarios
|
504
|
16
|
C
|
Low
|
645
|
James Cowles Prichard
|
503
|
16
|
C
|
High
|
646
|
Kettlewell's experiment
|
501
|
16
|
Start
|
Mid
|
647
|
Evolution: The Game of Intelligent Life
|
485
|
16
|
Start
|
Low
|
648
|
The Evolution of Desire
|
485
|
16
|
Start
|
Unknown
|
649
|
Zlatý kůň woman
|
484
|
16
|
Start
|
Low
|
650
|
Fritz Müller
|
482
|
16
|
B
|
Mid
|
651
|
Winner and loser effects
|
481
|
16
|
C
|
Low
|
652
|
Darwinian literary studies
|
472
|
15
|
C
|
Low
|
653
|
List of Neanderthal sites
|
469
|
15
|
List
|
Low
|
654
|
Ray Lankester
|
465
|
15
|
B
|
Low
|
655
|
Adaptation and Natural Selection
|
464
|
15
|
Start
|
Low
|
656
|
Lek paradox
|
464
|
15
|
C
|
Low
|
657
|
Klepton
|
464
|
15
|
Start
|
Low
|
658
|
Shane Campbell-Staton
|
460
|
15
|
Start
|
Low
|
659
|
Great Hippocampus Question
|
457
|
15
|
B
|
Low
|
660
|
Genetic assimilation
|
456
|
15
|
GA
|
Low
|
661
|
Intragenomic conflict
|
454
|
15
|
C
|
Mid
|
662
|
Lilliput effect
|
453
|
15
|
Start
|
Low
|
663
|
Evo-devo gene toolkit
|
452
|
15
|
Start
|
Mid
|
664
|
Secondarily aquatic tetrapods
|
448
|
14
|
Stub
|
Mid
|
665
|
Edward Blyth
|
445
|
14
|
B
|
High
|
666
|
Evolutionary dynamics
|
441
|
14
|
Stub
|
Mid
|
667
|
Group living
|
439
|
14
|
Start
|
Low
|
668
|
Quantum evolution
|
436
|
14
|
C
|
Mid
|
669
|
Inheritance of acquired characteristics
|
435
|
14
|
NA
|
NA
|
670
|
Troglomorphism
|
433
|
14
|
Stub
|
Low
|
671
|
Bitter taste evolution
|
433
|
14
|
Start
|
Low
|
672
|
History of zoology through 1859
|
429
|
14
|
C
|
High
|
673
|
Error threshold (evolution)
|
428
|
14
|
C
|
Mid
|
674
|
Wushan Man
|
427
|
14
|
Start
|
Low
|
675
|
Enterocoely
|
426
|
14
|
Stub
|
Mid
|
676
|
The Structure of Evolutionary Theory
|
425
|
14
|
Start
|
Low
|
677
|
Co-adaptation
|
424
|
14
|
C
|
Low
|
678
|
Directed evolution (transhumanism)
|
421
|
14
|
Stub
|
Low
|
679
|
Emergent evolution
|
418
|
13
|
C
|
Low
|
680
|
Demonic Males
|
417
|
13
|
C
|
Unknown
|
681
|
David Lack
|
415
|
13
|
C
|
Low
|
682
|
Evolutionary fauna
|
414
|
13
|
Start
|
Low
|
683
|
Expensive tissue hypothesis
|
414
|
13
|
C
|
Low
|
684
|
The Evolution of Beauty
|
411
|
13
|
Start
|
Low
|
685
|
Icons of Evolution
|
410
|
13
|
C
|
Low
|
686
|
Chemoton
|
410
|
13
|
Start
|
Low
|
687
|
Evolutionary developmental psychology
|
409
|
13
|
C
|
Low
|
688
|
Quasispecies model
|
407
|
13
|
C
|
Mid
|
689
|
Evolutionary neuroscience
|
406
|
13
|
Start
|
High
|
690
|
Natural Selection (manuscript)
|
404
|
13
|
Stub
|
Low
|
691
|
Laboratory experiments of speciation
|
404
|
13
|
List
|
Low
|
692
|
Sex differences in memory
|
403
|
13
|
Start
|
Low
|
693
|
The Variation of Animals and Plants Under Domestication
|
402
|
13
|
C
|
Low
|
694
|
Sir William Lawrence, 1st Baronet
|
400
|
13
|
B
|
High
|
695
|
Viral eukaryogenesis
|
395
|
13
|
Start
|
Mid
|
696
|
Sexual selection in scaled reptiles
|
393
|
13
|
Start
|
Low
|
697
|
Isolation by distance
|
391
|
13
|
Start
|
Low
|
698
|
Allan Wilson (biologist)
|
387
|
12
|
C
|
Low
|
699
|
Saldanha man
|
386
|
12
|
Stub
|
Low
|
700
|
Dawkins vs. Gould
|
385
|
12
|
Start
|
Low
|
701
|
Religion Explained
|
382
|
12
|
Start
|
Low
|
702
|
Museum of Human Evolution
|
381
|
12
|
Start
|
Unknown
|
703
|
Evolutionary aesthetics
|
381
|
12
|
C
|
High
|
704
|
Undeniable: Evolution and the Science of Creation
|
379
|
12
|
Unknown
|
Unknown
|
705
|
Richard Prum
|
377
|
12
|
Start
|
Low
|
706
|
Neofunctionalization
|
377
|
12
|
Start
|
Low
|
707
|
Power, Sex, Suicide
|
375
|
12
|
Stub
|
Low
|
708
|
Self-decoration camouflage
|
375
|
12
|
GA
|
Low
|
709
|
Natural morality
|
371
|
12
|
Start
|
Low
|
710
|
Evolutionary physiology
|
362
|
12
|
B
|
High
|
711
|
Polydactyly in stem-tetrapods
|
359
|
11
|
Start
|
Low
|
712
|
Inclusive fitness in humans
|
356
|
11
|
C
|
Low
|
713
|
Evolutionary models of food sharing
|
356
|
11
|
C
|
Low
|
714
|
Evolution of descended testes in mammals
|
356
|
11
|
Unknown
|
Unknown
|
715
|
What Darwin Got Wrong
|
355
|
11
|
Start
|
Low
|
716
|
Deep homology
|
352
|
11
|
Start
|
Mid
|
717
|
E. B. Ford
|
351
|
11
|
C
|
Low
|
718
|
Evolutionary trap
|
349
|
11
|
Start
|
Low
|
719
|
Cytonuclear discordance
|
349
|
11
|
Start
|
Unknown
|
720
|
Postcanine megadontia
|
348
|
11
|
C
|
Low
|
721
|
History of zoology (1859–present)
|
346
|
11
|
C
|
High
|
722
|
Marcus Feldman
|
343
|
11
|
Start
|
Low
|
723
|
Weapon (biology)
|
342
|
11
|
Stub
|
Low
|
724
|
Helitron (biology)
|
340
|
11
|
B
|
Low
|
725
|
Nanjing Man
|
334
|
11
|
C
|
Low
|
726
|
Molecular Phylogenetics and Evolution
|
333
|
11
|
Stub
|
Low
|
727
|
Douglas J. Futuyma
|
332
|
11
|
C
|
Low
|
728
|
Rensch's rule
|
331
|
11
|
Start
|
Low
|
729
|
Reciprocal altruism in humans
|
330
|
11
|
Start
|
Low
|
730
|
Intergradation
|
329
|
10
|
Start
|
Low
|
731
|
Ancestral sequence reconstruction
|
329
|
10
|
C
|
Low
|
732
|
The Goodness Paradox
|
329
|
10
|
Start
|
Low
|
733
|
Edward Bagnall Poulton
|
327
|
10
|
Start
|
Mid
|
734
|
Biogeographic regions of Europe
|
323
|
10
|
Start
|
Mid
|
735
|
W. Tecumseh Fitch
|
320
|
10
|
Stub
|
Low
|
736
|
On Being the Right Size
|
319
|
10
|
C
|
Mid
|
737
|
The Origin of Birds
|
319
|
10
|
GA
|
High
|
738
|
Nylon-eating bacteria and creationism
|
318
|
10
|
B
|
Low
|
739
|
Inferring horizontal gene transfer
|
318
|
10
|
B
|
Low
|
740
|
The Neutral Theory of Molecular Evolution
|
316
|
10
|
Stub
|
Low
|
741
|
Nearly neutral theory of molecular evolution
|
314
|
10
|
Start
|
Low
|
742
|
Allochronic speciation
|
313
|
10
|
B
|
Mid
|
743
|
Multispecies coalescent process
|
310
|
10
|
Start
|
Low
|
744
|
Insectivorous Plants (book)
|
309
|
10
|
Start
|
Low
|
745
|
Evolution of brachiopods
|
308
|
10
|
Start
|
Low
|
746
|
Background selection
|
306
|
10
|
Start
|
Low
|
747
|
Tradeoffs for locomotion in air and water
|
306
|
10
|
C
|
Mid
|
748
|
Megaevolution
|
306
|
10
|
Start
|
Mid
|
749
|
Scott F. Gilbert
|
306
|
10
|
C
|
Low
|
750
|
Proto-mitochondrion
|
303
|
10
|
Start
|
Mid
|
751
|
Index of evolutionary biology articles
|
300
|
10
|
List
|
High
|
752
|
Stenogale
|
300
|
10
|
Stub
|
Low
|
753
|
History of speciation
|
298
|
9
|
C
|
Low
|
754
|
The Seven Pillars of Life
|
297
|
9
|
Start
|
Low
|
755
|
Phylotypic stage
|
295
|
9
|
C
|
Low
|
756
|
Behavioral plasticity
|
294
|
9
|
Start
|
Low
|
757
|
Digital organism
|
293
|
9
|
Stub
|
Low
|
758
|
Fuyan Cave
|
293
|
9
|
C
|
Low
|
759
|
Evolutionary theodicy
|
289
|
9
|
C
|
Low
|
760
|
Homo consumericus
|
288
|
9
|
Start
|
Low
|
761
|
Zinnia Kumar
|
287
|
9
|
Start
|
Low
|
762
|
Proteinoid
|
286
|
9
|
Start
|
Low
|
763
|
Shifting balance theory
|
285
|
9
|
Stub
|
Low
|
764
|
Mutation accumulation theory
|
284
|
9
|
C
|
Low
|
765
|
The Theory of Evolution
|
283
|
9
|
Stub
|
Low
|
766
|
Cospeciation
|
283
|
9
|
Start
|
Mid
|
767
|
Cellularization
|
282
|
9
|
Stub
|
Low
|
768
|
Conservation-induced extinction
|
282
|
9
|
Start
|
Mid
|
769
|
Sexual antagonistic coevolution
|
279
|
9
|
Unknown
|
Unknown
|
770
|
Phylogenetic signal
|
279
|
9
|
C
|
Mid
|
771
|
Sexual selection in insects
|
274
|
9
|
B
|
Low
|
772
|
Evolutionary invasion analysis
|
273
|
9
|
Start
|
Low
|
773
|
Qikiqtania
|
273
|
9
|
Stub
|
Unknown
|
774
|
Alloplastic adaptation
|
272
|
9
|
Stub
|
Low
|
775
|
Coloration evidence for natural selection
|
270
|
9
|
GA
|
Mid
|
776
|
Michael Majerus
|
268
|
8
|
Start
|
Mid
|
777
|
Ileret
|
268
|
8
|
Stub
|
Low
|
778
|
Rupert Riedl
|
266
|
8
|
Start
|
Low
|
779
|
Heterotopy
|
266
|
8
|
Stub
|
Low
|
780
|
Red King hypothesis
|
266
|
8
|
Start
|
Low
|
781
|
Nama assemblage
|
265
|
8
|
Start
|
Low
|
782
|
Davidson Black
|
263
|
8
|
C
|
Mid
|
783
|
Subfunctionalization
|
262
|
8
|
Start
|
Low
|
784
|
Fisher's geometric model
|
262
|
8
|
Start
|
Low
|
785
|
William Henry Flower
|
261
|
8
|
B
|
Low
|
786
|
Constructive neutral evolution
|
261
|
8
|
C
|
Low
|
787
|
Storage effect
|
259
|
8
|
B
|
Mid
|
788
|
Darwinian threshold
|
259
|
8
|
Start
|
Mid
|
789
|
Cultural selection theory
|
258
|
8
|
C
|
Low
|
790
|
Concerted evolution
|
258
|
8
|
Stub
|
Low
|
791
|
Horizontal gene transfer in evolution
|
258
|
8
|
Start
|
High
|
792
|
G-value paradox
|
258
|
8
|
C
|
Low
|
793
|
Pseudoextinction
|
256
|
8
|
Start
|
Low
|
794
|
History of molecular evolution
|
256
|
8
|
C
|
Mid
|
795
|
Modern human
|
254
|
8
|
NA
|
NA
|
796
|
Evolution of metal ions in biological systems
|
254
|
8
|
C
|
Low
|
797
|
Francis Maitland Balfour
|
253
|
8
|
Start
|
Low
|
798
|
Dynamic mutation
|
251
|
8
|
Stub
|
Low
|
799
|
International Year of Biodiversity
|
248
|
8
|
Start
|
High
|
800
|
Adaptive behavior (ecology)
|
246
|
8
|
C
|
Mid
|
801
|
Inversion (evolutionary biology)
|
246
|
8
|
Start
|
Mid
|
802
|
Germ-Soma Differentiation
|
246
|
8
|
C
|
Low
|
803
|
Ecological evolutionary developmental biology
|
244
|
8
|
Start
|
Low
|
804
|
Biological constraints
|
243
|
8
|
Start
|
Mid
|
805
|
Human somatic variation
|
242
|
8
|
C
|
Mid
|
806
|
The Correlation between Relatives on the Supposition of Mendelian Inheritance
|
241
|
8
|
Start
|
Mid
|
807
|
Automixis
|
241
|
8
|
Start
|
Unknown
|
808
|
Evolution of olfaction
|
239
|
7
|
C
|
Low
|
809
|
Biodiversity of Kosovo
|
239
|
7
|
C
|
Low
|
810
|
Wonderful life theory
|
236
|
7
|
Stub
|
Low
|
811
|
Paragroup
|
235
|
7
|
Stub
|
Low
|
812
|
Alfred Newton
|
234
|
7
|
C
|
Low
|
813
|
Recurrent evolution
|
233
|
7
|
Unknown
|
Unknown
|
814
|
Hydrogen hypothesis
|
227
|
7
|
Start
|
Low
|
815
|
Ecology and evolutionary biology
|
227
|
7
|
Start
|
Low
|
816
|
Peter J. Bowler
|
227
|
7
|
Start
|
Low
|
817
|
Push of the past
|
226
|
7
|
C
|
Low
|
818
|
Gavin de Beer
|
223
|
7
|
C
|
Low
|
819
|
Tree rearrangement
|
223
|
7
|
Start
|
Low
|
820
|
Contest competition
|
223
|
7
|
Stub
|
Low
|
821
|
Herbivore adaptations to plant defense
|
221
|
7
|
B
|
Low
|
822
|
Evolutionary landscape
|
221
|
7
|
C
|
High
|
823
|
Idealised population
|
220
|
7
|
C
|
Mid
|
824
|
Molecular drive
|
219
|
7
|
Stub
|
Low
|
825
|
Parasite load
|
217
|
7
|
C
|
Low
|
826
|
Urban evolution
|
216
|
7
|
C
|
Unknown
|
827
|
Orgel's rules
|
209
|
6
|
Stub
|
Low
|
828
|
Evolutionary psychology and culture
|
208
|
6
|
Start
|
Low
|
829
|
Paul W. Ewald
|
207
|
6
|
Start
|
Low
|
830
|
Hybrid swarm
|
207
|
6
|
Start
|
Mid
|
831
|
Evolutionary capacitance
|
206
|
6
|
C
|
Mid
|
832
|
Law of Life
|
206
|
6
|
Stub
|
Low
|
833
|
Wing-assisted incline running
|
206
|
6
|
Start
|
Low
|
834
|
Selection shadow
|
205
|
6
|
Start
|
Low
|
835
|
V. C. Wynne-Edwards
|
204
|
6
|
Start
|
Low
|
836
|
Turnover-pulse hypothesis
|
204
|
6
|
Start
|
Low
|
837
|
GADV-protein world hypothesis
|
204
|
6
|
Start
|
Low
|
838
|
Man's Genesis
|
204
|
6
|
Start
|
Low
|
839
|
Russell Lande
|
203
|
6
|
Start
|
Low
|
840
|
Interlocus sexual conflict
|
202
|
6
|
B
|
Mid
|
841
|
Laura Landweber
|
202
|
6
|
Start
|
Low
|
842
|
Alpheus Hyatt
|
201
|
6
|
Start
|
Low
|
843
|
Viral phylodynamics
|
201
|
6
|
B
|
Low
|
844
|
Segregating site
|
201
|
6
|
Start
|
Low
|
845
|
Modularity (biology)
|
199
|
6
|
Start
|
Low
|
846
|
David Hillis
|
198
|
6
|
Start
|
Low
|
847
|
Joan E. Strassmann
|
197
|
6
|
Start
|
Low
|
848
|
Maternal effect dominant embryonic arrest
|
197
|
6
|
Start
|
Low
|
849
|
TalkOrigins Archive
|
196
|
6
|
Start
|
Low
|
850
|
Eugenics in Mexico
|
195
|
6
|
Start
|
Low
|
851
|
Maternal behavior in vertebrates
|
195
|
6
|
C
|
Low
|
852
|
Eukaryote hybrid genome
|
195
|
6
|
B
|
Low
|
853
|
Reproductive suppression
|
194
|
6
|
C
|
Mid
|
854
|
Evidence for speciation by reinforcement
|
194
|
6
|
List
|
Low
|
855
|
Human reproductive ecology
|
194
|
6
|
Start
|
Low
|
856
|
Evolutionary psychology of language
|
191
|
6
|
Start
|
Low
|
857
|
SK 847
|
191
|
6
|
Start
|
Low
|
858
|
Host switch
|
191
|
6
|
C
|
Low
|
859
|
Paraspecies
|
186
|
6
|
Stub
|
Low
|
860
|
Felsenstein's tree-pruning algorithm
|
185
|
6
|
Stub
|
Low
|
861
|
Biodiversity of Wales
|
184
|
6
|
C
|
Low
|
862
|
Mesozoic–Cenozoic radiation
|
184
|
6
|
Stub
|
Low
|
863
|
Skeletal changes of vertebrates transitioning from water to land
|
184
|
6
|
C
|
Low
|
864
|
Clonal interference
|
183
|
6
|
Stub
|
Mid
|
865
|
Prejudice from an evolutionary perspective
|
182
|
6
|
Start
|
Low
|
866
|
Carboniferous-Earliest Permian Biodiversification Event
|
182
|
6
|
NA
|
Low
|
867
|
Assisted evolution
|
181
|
6
|
C
|
Low
|
868
|
List of ecoregions with high endemism
|
179
|
5
|
List
|
Low
|
869
|
Intralocus sexual conflict
|
177
|
5
|
Start
|
Mid
|
870
|
Infinite sites model
|
177
|
5
|
Start
|
Low
|
871
|
Harrison's rule
|
177
|
5
|
Unknown
|
Unknown
|
872
|
Hyrax Hill
|
176
|
5
|
B
|
Low
|
873
|
Distractive markings
|
176
|
5
|
C
|
Low
|
874
|
Runcaria
|
175
|
5
|
Start
|
Low
|
875
|
Mutation bias
|
175
|
5
|
C
|
Mid
|
876
|
Species-typical behavior
|
174
|
5
|
Start
|
Low
|
877
|
Applications of evolution
|
174
|
5
|
B
|
Low
|
878
|
Gard model
|
174
|
5
|
Start
|
Low
|
879
|
Ecological fitting
|
173
|
5
|
B
|
Low
|
880
|
Formamide-based prebiotic chemistry
|
173
|
5
|
Start
|
Low
|
881
|
Phylo (video game)
|
172
|
5
|
Start
|
Low
|
882
|
Key innovation
|
171
|
5
|
Start
|
Mid
|
883
|
How the Snake Lost Its Legs
|
171
|
5
|
GA
|
Low
|
884
|
John Tyler Bonner
|
170
|
5
|
C
|
Mid
|
885
|
Resource defense polygyny
|
169
|
5
|
Stub
|
Unknown
|
886
|
Genomic evolution of birds
|
168
|
5
|
C
|
Low
|
887
|
Resource holding potential
|
167
|
5
|
Stub
|
Low
|
888
|
Zoology of the Voyage of H.M.S. Beagle
|
165
|
5
|
Stub
|
Low
|
889
|
Evolution by gene duplication
|
165
|
5
|
Start
|
High
|
890
|
Karl Kessler
|
164
|
5
|
Stub
|
Low
|
891
|
The Apportionment of Human Diversity
|
164
|
5
|
C
|
Low
|
892
|
Archaic Homo sapiens
|
163
|
5
|
NA
|
NA
|
893
|
Phylogenetic inertia
|
161
|
5
|
Start
|
Mid
|
894
|
Evolutionary Psychology (journal)
|
155
|
5
|
Stub
|
Unknown
|
895
|
Phagomimicry
|
155
|
5
|
Stub
|
Low
|
896
|
Interactor
|
154
|
5
|
Stub
|
Low
|
897
|
Mark Ridley (zoologist)
|
154
|
5
|
Stub
|
Low
|
898
|
Arthur Cain
|
151
|
5
|
C
|
Low
|
899
|
Autoplastic adaptation
|
151
|
5
|
Stub
|
Low
|
900
|
Dan Willard
|
151
|
5
|
C
|
Low
|
901
|
OneZoom
|
150
|
5
|
Start
|
Unknown
|
902
|
Talk.origins
|
147
|
4
|
Start
|
Low
|
903
|
Evolutionary rescue
|
146
|
4
|
Start
|
Low
|
904
|
John Endler
|
144
|
4
|
Start
|
Low
|
905
|
Egg taphonomy
|
144
|
4
|
C
|
Low
|
906
|
Mimicry in vertebrates
|
144
|
4
|
Start
|
Low
|
907
|
Hybrid incompatibility
|
144
|
4
|
C
|
Low
|
908
|
Escape and radiate coevolution
|
143
|
4
|
C
|
Unknown
|
909
|
Thorson's rule
|
142
|
4
|
Start
|
Low
|
910
|
Unique-event polymorphism
|
141
|
4
|
Start
|
Low
|
911
|
Commemoration of Charles Darwin
|
141
|
4
|
C
|
Mid
|
912
|
Nancy A. Moran
|
141
|
4
|
C
|
Low
|
913
|
Society for the Study of Evolution
|
139
|
4
|
Stub
|
Low
|
914
|
Reciprocal causation
|
139
|
4
|
C
|
Low
|
915
|
Evolutionary approaches to postpartum depression
|
139
|
4
|
C
|
Low
|
916
|
Ecotron
|
139
|
4
|
Stub
|
Low
|
917
|
Hologenomics
|
138
|
4
|
Stub
|
Low
|
918
|
William Charles Wells
|
137
|
4
|
B
|
High
|
919
|
Darwinian puzzle
|
136
|
4
|
Start
|
Low
|
920
|
Moritz Wagner (naturalist)
|
136
|
4
|
Start
|
Low
|
921
|
Preadaptation
|
135
|
4
|
NA
|
Mid
|
922
|
Sibling species
|
135
|
4
|
NA
|
NA
|
923
|
Phylogenetic reconciliation
|
135
|
4
|
Unknown
|
Unknown
|
924
|
Fluctuating selection
|
134
|
4
|
Start
|
Low
|
925
|
Alexander von Humboldt Biological Resources Research Institute
|
133
|
4
|
Stub
|
Low
|
926
|
Evolution of Macropodidae
|
133
|
4
|
Start
|
Low
|
927
|
Suzanne Leclercq
|
132
|
4
|
Start
|
Low
|
928
|
Differential fitness
|
132
|
4
|
C
|
Low
|
929
|
Andrew Berry (biologist)
|
131
|
4
|
Stub
|
Low
|
930
|
Eric Charnov
|
130
|
4
|
Start
|
Low
|
931
|
Founder takes all
|
130
|
4
|
Stub
|
Low
|
932
|
Facilitated variation
|
129
|
4
|
Stub
|
Low
|
933
|
Marcello Barbieri
|
129
|
4
|
Start
|
Low
|
934
|
White Sea assemblage
|
129
|
4
|
Stub
|
Low
|
935
|
Francisc Rainer
|
128
|
4
|
B
|
Low
|
936
|
Nonadaptive radiation
|
128
|
4
|
Start
|
Low
|
937
|
Swamping argument
|
127
|
4
|
Stub
|
Low
|
938
|
Grit, not grass hypothesis
|
127
|
4
|
C
|
Low
|
939
|
ASUDAS
|
126
|
4
|
Start
|
Unknown
|
940
|
Despeciation
|
124
|
4
|
Start
|
Low
|
941
|
Character evolution
|
124
|
4
|
Unknown
|
Unknown
|
942
|
Relative rate test
|
123
|
4
|
Start
|
Low
|
943
|
Landscape genomics
|
123
|
4
|
Stub
|
Low
|
944
|
Interpolation theory
|
121
|
4
|
Start
|
Low
|
945
|
Non-Darwinian Evolution (paper)
|
121
|
4
|
Stub
|
Low
|
946
|
Ecological selection
|
120
|
4
|
Start
|
Mid
|
947
|
Ruth Mace
|
120
|
4
|
Start
|
Low
|
948
|
List of Nepenthes natural hybrids
|
118
|
3
|
List
|
Low
|
949
|
Scott V. Edwards
|
118
|
3
|
C
|
Low
|
950
|
Brandon Gaut
|
115
|
3
|
C
|
Unknown
|
951
|
Institute of Human Origins
|
114
|
3
|
Start
|
Low
|
952
|
Katie Hinde
|
114
|
3
|
C
|
Low
|
953
|
Reductive evolution
|
114
|
3
|
Start
|
Low
|
954
|
Axel Meyer
|
113
|
3
|
Start
|
Unknown
|
955
|
Kindred: Neanderthal Life, Love, Death and Art
|
113
|
3
|
Stub
|
Low
|
956
|
Identity in social insects
|
112
|
3
|
Start
|
Low
|
957
|
WLH-50
|
112
|
3
|
Start
|
Unknown
|
958
|
Graham Bell (biologist)
|
111
|
3
|
Stub
|
Low
|
959
|
Evolution Day
|
111
|
3
|
Unknown
|
Unknown
|
960
|
The Great Monkey Trial
|
110
|
3
|
Start
|
Low
|
961
|
Discredited hypotheses for the Cambrian explosion
|
110
|
3
|
Stub
|
Mid
|
962
|
Eliza Gamble
|
110
|
3
|
Start
|
Low
|
963
|
Patty Brennan
|
110
|
3
|
Start
|
Unknown
|
964
|
Adriana Briscoe
|
108
|
3
|
B
|
Low
|
965
|
Epididymis evolution from reptiles to mammals
|
107
|
3
|
B
|
Low
|
966
|
Bias in the introduction of variation
|
106
|
3
|
B
|
Low
|
967
|
Wallace effect
|
105
|
3
|
NA
|
NA
|
968
|
Reciprocal food sharing
|
105
|
3
|
NA
|
Low
|
969
|
Jeremy Yoder
|
105
|
3
|
Start
|
Low
|
970
|
Cancer selection
|
104
|
3
|
C
|
Low
|
971
|
Transformed cladistics
|
103
|
3
|
C
|
Low
|
972
|
Darwin (unit)
|
102
|
3
|
Stub
|
Low
|
973
|
Tim Lewens
|
100
|
3
|
Start
|
Unknown
|
974
|
James A. Lake
|
100
|
3
|
Start
|
Low
|
975
|
The Different Forms of Flowers on Plants of the Same Species
|
100
|
3
|
Start
|
Low
|
976
|
Endogenosymbiosis
|
100
|
3
|
Start
|
Low
|
977
|
Polymorphism in Lepidoptera
|
98
|
3
|
C
|
High
|
978
|
Gender psychology
|
98
|
3
|
NA
|
NA
|
979
|
Diversitas
|
96
|
3
|
C
|
Low
|
980
|
Strong reciprocity
|
96
|
3
|
B
|
Low
|
981
|
Stephen Blair Hedges
|
95
|
3
|
Start
|
Low
|
982
|
Stan Wood (fossil hunter)
|
94
|
3
|
Stub
|
Unknown
|
983
|
Charles Ofria
|
93
|
3
|
Stub
|
Low
|
984
|
European Society for Evolutionary Biology
|
92
|
3
|
Stub
|
Low
|
985
|
Henric Sanielevici
|
92
|
3
|
B
|
Low
|
986
|
Hyposphene-hypantrum articulation
|
92
|
3
|
Start
|
Low
|
987
|
Romanticism in evolution theory
|
92
|
3
|
Start
|
Low
|
988
|
Evolution of hair
|
91
|
3
|
NA
|
NA
|
989
|
Ludwig Hermann Plate
|
91
|
3
|
Start
|
Low
|
990
|
Sulphobes
|
90
|
3
|
Stub
|
Low
|
991
|
Nonecological speciation
|
90
|
3
|
Start
|
Low
|
992
|
Kinetotroph
|
90
|
3
|
Start
|
Low
|
993
|
The Panda's Thumb (blog)
|
89
|
2
|
Start
|
Low
|
994
|
Sex differences in sensory systems
|
89
|
2
|
Start
|
Mid
|
995
|
Human evolutionary developmental biology
|
89
|
2
|
C
|
Mid
|
996
|
Locomotor mimicry
|
89
|
2
|
Start
|
Low
|
997
|
Largest-scale trends in evolution
|
88
|
2
|
Start
|
High
|
998
|
Female sabotage
|
85
|
2
|
Start
|
Low
|
999
|
Ecological inheritance
|
85
|
2
|
Stub
|
Low
|
1000
|
George Rolleston
|
84
|
2
|
Start
|
Low
|