Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
1
|
Neanderthal
|
109,586
|
3,535
|
GA
|
Mid
|
2
|
Charles Darwin
|
104,644
|
3,375
|
FA
|
Top
|
3
|
Richard Dawkins
|
104,532
|
3,372
|
GA
|
Mid
|
4
|
List of X-Men members
|
90,734
|
2,926
|
List
|
Low
|
5
|
Eugenics
|
87,861
|
2,834
|
B
|
Mid
|
6
|
List of common misconceptions
|
85,050
|
2,743
|
List
|
Low
|
7
|
Sexual dimorphism
|
74,599
|
2,406
|
B
|
High
|
8
|
Human evolution
|
71,304
|
2,300
|
C
|
High
|
9
|
Cretaceous–Paleogene extinction event
|
61,331
|
1,978
|
FA
|
High
|
10
|
Species
|
57,237
|
1,846
|
GA
|
Top
|
11
|
Racism
|
54,292
|
1,751
|
B
|
Mid
|
12
|
William Jennings Bryan
|
53,864
|
1,737
|
B
|
High
|
13
|
Parthenogenesis
|
50,923
|
1,642
|
B
|
High
|
14
|
Extinction
|
46,491
|
1,499
|
C
|
High
|
15
|
Evolution
|
44,125
|
1,423
|
FA
|
Top
|
16
|
Abiogenesis
|
42,248
|
1,362
|
GA
|
Top
|
17
|
Biodiversity
|
41,287
|
1,331
|
C
|
Mid
|
18
|
Epicanthic fold
|
41,234
|
1,330
|
C
|
Low
|
19
|
Cousin
|
39,946
|
1,288
|
Start
|
Low
|
20
|
Carcinisation
|
39,606
|
1,277
|
Start
|
Top
|
21
|
Homo floresiensis
|
38,517
|
1,242
|
B
|
Mid
|
22
|
Inbreeding
|
36,440
|
1,175
|
C
|
High
|
23
|
Early modern human
|
35,915
|
1,158
|
B
|
Mid
|
24
|
Scientific racism
|
35,190
|
1,135
|
C
|
Low
|
25
|
Clade
|
33,471
|
1,079
|
C
|
High
|
26
|
Binomial nomenclature
|
33,066
|
1,066
|
C
|
Low
|
27
|
Cro-Magnon
|
32,045
|
1,033
|
GA
|
Mid
|
28
|
Genetics
|
30,925
|
997
|
FA
|
Top
|
29
|
Archaic humans
|
30,827
|
994
|
Start
|
Low
|
30
|
Scopes trial
|
30,400
|
980
|
B
|
High
|
31
|
Last universal common ancestor
|
30,121
|
971
|
GA
|
Top
|
32
|
Fossil
|
29,658
|
956
|
B
|
Mid
|
33
|
Ecology
|
29,270
|
944
|
GA
|
Top
|
34
|
Timeline of human evolution
|
29,050
|
937
|
C
|
Low
|
35
|
Karyotype
|
27,311
|
881
|
C
|
Low
|
36
|
Wallace Line
|
27,163
|
876
|
Start
|
Mid
|
37
|
Eusociality
|
27,140
|
875
|
GA
|
Mid
|
38
|
Hybrid (biology)
|
26,889
|
867
|
GA
|
High
|
39
|
Domestication of the dog
|
26,575
|
857
|
B
|
Low
|
40
|
Paleontology
|
25,421
|
820
|
GA
|
Top
|
41
|
Altruism
|
24,645
|
795
|
B
|
High
|
42
|
Origin of language
|
24,627
|
794
|
C
|
Low
|
43
|
Patrilineality
|
24,281
|
783
|
Start
|
Low
|
44
|
Rare Earth hypothesis
|
23,047
|
743
|
B
|
Low
|
45
|
Neontology
|
22,547
|
727
|
Start
|
Mid
|
46
|
Feathered dinosaur
|
22,029
|
710
|
C
|
High
|
47
|
Natural selection
|
22,007
|
709
|
GA
|
Top
|
48
|
On the Origin of Species
|
21,826
|
704
|
FA
|
Top
|
49
|
Mutation
|
21,809
|
703
|
B
|
Top
|
50
|
Cambrian explosion
|
20,594
|
664
|
B
|
High
|
51
|
HeLa
|
20,365
|
656
|
C
|
Low
|
52
|
Upper Paleolithic
|
20,199
|
651
|
C
|
Low
|
53
|
Darwinism
|
20,198
|
651
|
C
|
High
|
54
|
Great Oxidation Event
|
19,630
|
633
|
C
|
Mid
|
55
|
Convergent evolution
|
19,201
|
619
|
GA
|
High
|
56
|
Anus
|
17,678
|
570
|
Start
|
Mid
|
57
|
Lamarckism
|
17,055
|
550
|
GA
|
High
|
58
|
History of life
|
16,911
|
545
|
GA
|
Top
|
59
|
Fear
|
16,741
|
540
|
B
|
Low
|
60
|
Human taxonomy
|
16,708
|
538
|
C
|
Low
|
61
|
Haplogroup
|
16,632
|
536
|
C
|
Mid
|
62
|
Stoned ape theory
|
16,488
|
531
|
C
|
Low
|
63
|
Extant taxon
|
16,413
|
529
|
NA
|
NA
|
64
|
Nordicism
|
16,345
|
527
|
B
|
Low
|
65
|
Australopithecine
|
15,732
|
507
|
C
|
High
|
66
|
Pan (genus)
|
15,707
|
506
|
B
|
High
|
67
|
Human vestigiality
|
15,416
|
497
|
C
|
Mid
|
68
|
Domestication of the cat
|
15,338
|
494
|
C
|
Mid
|
69
|
Sociality
|
15,245
|
491
|
C
|
Mid
|
70
|
The Selfish Gene
|
14,971
|
482
|
B
|
High
|
71
|
Population bottleneck
|
14,940
|
481
|
C
|
High
|
72
|
Living fossil
|
14,876
|
479
|
C
|
Mid
|
73
|
Aposematism
|
14,720
|
474
|
GA
|
Mid
|
74
|
Institutional racism
|
14,344
|
462
|
B
|
Mid
|
75
|
Matrilineality
|
14,062
|
453
|
C
|
Low
|
76
|
Chicken or the egg
|
13,792
|
444
|
Start
|
Low
|
77
|
Timeline of the evolutionary history of life
|
13,528
|
436
|
B
|
Top
|
78
|
Stephen Jay Gould
|
13,468
|
434
|
GA
|
Mid
|
79
|
Antimicrobial resistance
|
13,435
|
433
|
B
|
Unknown
|
80
|
Human Y-chromosome DNA haplogroup
|
13,353
|
430
|
C
|
Mid
|
81
|
Bipedalism
|
13,225
|
426
|
B
|
Mid
|
82
|
Stromatolite
|
13,121
|
423
|
B
|
Mid
|
83
|
Alfred Russel Wallace
|
12,888
|
415
|
FA
|
Top
|
84
|
Ernst Haeckel
|
12,842
|
414
|
B
|
High
|
85
|
Homology (biology)
|
12,825
|
413
|
GA
|
Top
|
86
|
Earliest known life forms
|
12,319
|
397
|
C
|
Top
|
87
|
Sex differences in intelligence
|
12,250
|
395
|
B
|
Low
|
88
|
Camouflage
|
12,164
|
392
|
GA
|
Mid
|
89
|
Phylogenetics
|
12,090
|
390
|
B
|
High
|
90
|
Peking Man
|
11,860
|
382
|
GA
|
Mid
|
91
|
Ronald Fisher
|
11,416
|
368
|
B
|
High
|
92
|
Triune brain
|
11,363
|
366
|
Start
|
Low
|
93
|
Thomas Henry Huxley
|
11,341
|
365
|
B
|
Mid
|
94
|
Evolutionary psychology
|
11,125
|
358
|
C
|
High
|
95
|
Tiktaalik
|
11,053
|
356
|
GA
|
High
|
96
|
Origin of SARS-CoV-2
|
11,049
|
356
|
C
|
Mid
|
97
|
Selective breeding
|
10,911
|
351
|
C
|
Low
|
98
|
Sex differences in human physiology
|
10,731
|
346
|
C
|
High
|
99
|
Sexual selection
|
10,710
|
345
|
GA
|
High
|
100
|
Haplodiploidy
|
10,438
|
336
|
C
|
Mid
|
101
|
Mimicry
|
10,414
|
335
|
GA
|
High
|
102
|
Nazi eugenics
|
10,380
|
334
|
C
|
Low
|
103
|
Origin of birds
|
10,241
|
330
|
B
|
Mid
|
104
|
R/K selection theory
|
10,212
|
329
|
C
|
High
|
105
|
Behavioral modernity
|
10,172
|
328
|
C
|
Low
|
106
|
Lower Paleolithic
|
10,139
|
327
|
C
|
High
|
107
|
Horizontal gene transfer
|
10,113
|
326
|
C
|
High
|
108
|
Panthera hybrid
|
9,949
|
320
|
C
|
Low
|
109
|
Vestigiality
|
9,854
|
317
|
C
|
High
|
110
|
Evolution of mammals
|
9,782
|
315
|
B
|
High
|
111
|
E. O. Wilson
|
9,729
|
313
|
B
|
Mid
|
112
|
Survival of the fittest
|
9,675
|
312
|
B
|
Low
|
113
|
Most recent common ancestor
|
9,601
|
309
|
B
|
High
|
114
|
Eugenics in the United States
|
9,600
|
309
|
Start
|
Low
|
115
|
Major histocompatibility complex
|
9,599
|
309
|
B
|
Low
|
116
|
Jean-Baptiste Lamarck
|
9,506
|
306
|
B
|
Top
|
117
|
Anthropometry
|
9,493
|
306
|
C
|
Low
|
118
|
Evolutionary biology
|
9,320
|
300
|
C
|
Top
|
119
|
Adaptation
|
9,281
|
299
|
GA
|
Top
|
120
|
Genetic drift
|
9,249
|
298
|
GA
|
Top
|
121
|
Three-domain system
|
9,150
|
295
|
C
|
Mid
|
122
|
Jebel Irhoud
|
9,109
|
293
|
C
|
Low
|
123
|
Sexual cannibalism
|
8,941
|
288
|
B
|
Low
|
124
|
Human mating strategies
|
8,901
|
287
|
B
|
Low
|
125
|
Instinct
|
8,814
|
284
|
C
|
Low
|
126
|
Founder effect
|
8,759
|
282
|
C
|
Mid
|
127
|
Ediacaran biota
|
8,674
|
279
|
FA
|
Low
|
128
|
Insular dwarfism
|
8,601
|
277
|
C
|
Low
|
129
|
RNA world
|
8,453
|
272
|
C
|
High
|
130
|
Hardy–Weinberg principle
|
8,247
|
266
|
C
|
High
|
131
|
Recent human evolution
|
8,200
|
264
|
B
|
Mid
|
132
|
List of human evolution fossils
|
8,166
|
263
|
List
|
High
|
133
|
Offspring
|
7,983
|
257
|
Start
|
Mid
|
134
|
Fertility
|
7,900
|
254
|
C
|
High
|
135
|
Polymorphism (biology)
|
7,810
|
251
|
B
|
High
|
136
|
Evolution of the horse
|
7,749
|
249
|
B
|
Mid
|
137
|
Monophyly
|
7,718
|
248
|
C
|
Mid
|
138
|
Julian Huxley
|
7,713
|
248
|
B
|
Mid
|
139
|
Symbiogenesis
|
7,711
|
248
|
GA
|
High
|
140
|
Cladistics
|
7,650
|
246
|
C
|
Mid
|
141
|
Basal (phylogenetics)
|
7,646
|
246
|
C
|
Mid
|
142
|
Primordial soup
|
7,603
|
245
|
Start
|
Mid
|
143
|
Island gigantism
|
7,564
|
244
|
C
|
Low
|
144
|
Heather Heying
|
7,554
|
243
|
Start
|
Low
|
145
|
Female promiscuity
|
7,396
|
238
|
C
|
Low
|
146
|
Evolutionary origin of religion
|
7,385
|
238
|
C
|
Low
|
147
|
Middle Paleolithic
|
7,384
|
238
|
C
|
High
|
148
|
Aquatic ape hypothesis
|
7,357
|
237
|
C
|
Low
|
149
|
Common descent
|
7,299
|
235
|
B
|
Top
|
150
|
Autosome
|
7,258
|
234
|
Start
|
High
|
151
|
Red Queen hypothesis
|
7,081
|
228
|
Start
|
Mid
|
152
|
Linnaean taxonomy
|
7,020
|
226
|
C
|
Mid
|
153
|
Missing link (human evolution)
|
6,858
|
221
|
Start
|
Mid
|
154
|
J. B. S. Haldane
|
6,851
|
221
|
C
|
Mid
|
155
|
The Naked Woman
|
6,850
|
220
|
Stub
|
Low
|
156
|
Human mitochondrial DNA haplogroup
|
6,806
|
219
|
Start
|
Mid
|
157
|
Darwin's finches
|
6,771
|
218
|
C
|
High
|
158
|
Evolution of sexual reproduction
|
6,740
|
217
|
B
|
High
|
159
|
Felid hybrids
|
6,700
|
216
|
Start
|
Low
|
160
|
Anisogamy
|
6,675
|
215
|
C
|
High
|
161
|
Symmetry in biology
|
6,630
|
213
|
C
|
High
|
162
|
Speciation
|
6,490
|
209
|
B
|
High
|
163
|
Batesian mimicry
|
6,441
|
207
|
GA
|
Mid
|
164
|
Signalling theory
|
6,430
|
207
|
GA
|
Mid
|
165
|
Bergmann's rule
|
6,415
|
206
|
C
|
Low
|
166
|
Homo longi
|
6,325
|
204
|
GA
|
Low
|
167
|
Objections to evolution
|
6,324
|
204
|
GA
|
Mid
|
168
|
Great American Interchange
|
6,298
|
203
|
C
|
Mid
|
169
|
Evolutionary history of plants
|
6,256
|
201
|
B
|
High
|
170
|
Aggressive mimicry
|
6,181
|
199
|
GA
|
Mid
|
171
|
Species complex
|
6,132
|
197
|
B
|
Mid
|
172
|
Evolution of human intelligence
|
6,043
|
194
|
Start
|
High
|
173
|
Climate change adaptation
|
5,917
|
190
|
B
|
Mid
|
174
|
Biogeography
|
5,796
|
186
|
Start
|
Mid
|
175
|
Lek mating
|
5,681
|
183
|
GA
|
Mid
|
176
|
Cowardice
|
5,672
|
182
|
Start
|
Low
|
177
|
Allopatric speciation
|
5,630
|
181
|
B
|
High
|
178
|
Evolutionary algorithm
|
5,605
|
180
|
C
|
Low
|
179
|
Variability hypothesis
|
5,590
|
180
|
C
|
Low
|
180
|
Anatomically modern human
|
5,562
|
179
|
NA
|
NA
|
181
|
Maladaptation
|
5,550
|
179
|
Start
|
Mid
|
182
|
Punctuated equilibrium
|
5,531
|
178
|
GA
|
High
|
183
|
Ontogeny
|
5,513
|
177
|
B
|
High
|
184
|
Recapitulation theory
|
5,492
|
177
|
C
|
Mid
|
185
|
Grandmother hypothesis
|
5,440
|
175
|
C
|
Mid
|
186
|
Müllerian mimicry
|
5,367
|
173
|
GA
|
Mid
|
187
|
First universal common ancestor
|
5,363
|
173
|
Start
|
Unknown
|
188
|
Inbreeding depression
|
5,320
|
171
|
Start
|
Mid
|
189
|
Evolution of fish
|
5,258
|
169
|
C
|
High
|
190
|
Sex differences in psychology
|
5,254
|
169
|
C
|
High
|
191
|
Human sperm competition
|
5,200
|
167
|
C
|
Low
|
192
|
Evolution of primates
|
5,116
|
165
|
Start
|
Low
|
193
|
Sexual selection in humans
|
5,096
|
164
|
C
|
Low
|
194
|
Fitness (biology)
|
5,079
|
163
|
B
|
High
|
195
|
Evolution of cetaceans
|
4,967
|
160
|
GA
|
Mid
|
196
|
Genetic diversity
|
4,950
|
159
|
C
|
Mid
|
197
|
The Descent of Man, and Selection in Relation to Sex
|
4,925
|
158
|
Start
|
High
|
198
|
List of related male and female reproductive organs
|
4,916
|
158
|
List
|
Mid
|
199
|
Adaptive radiation
|
4,889
|
157
|
Start
|
High
|
200
|
Relict (biology)
|
4,878
|
157
|
C
|
Mid
|
201
|
Evolution of the wolf
|
4,867
|
157
|
B
|
Low
|
202
|
CpG site
|
4,852
|
156
|
C
|
Mid
|
203
|
Neanderthal genetics
|
4,664
|
150
|
C
|
High
|
204
|
Australopithecus sediba
|
4,656
|
150
|
GA
|
Low
|
205
|
History of biology
|
4,644
|
149
|
FA
|
High
|
206
|
Incertae sedis
|
4,643
|
149
|
C
|
Low
|
207
|
Sexy son hypothesis
|
4,643
|
149
|
C
|
Mid
|
208
|
Spiral Dynamics
|
4,637
|
149
|
C
|
Low
|
209
|
Modern synthesis (20th century)
|
4,626
|
149
|
GA
|
High
|
210
|
Religious views of Charles Darwin
|
4,622
|
149
|
B
|
Low
|
211
|
History of evolutionary thought
|
4,585
|
147
|
FA
|
Top
|
212
|
Population genetics
|
4,464
|
144
|
C
|
High
|
213
|
Evolution of birds
|
4,455
|
143
|
C
|
High
|
214
|
Hominina
|
4,404
|
142
|
NA
|
NA
|
215
|
Evolution as fact and theory
|
4,373
|
141
|
C
|
Low
|
216
|
Systematics
|
4,316
|
139
|
C
|
High
|
217
|
Expelled: No Intelligence Allowed
|
4,252
|
137
|
B
|
Low
|
218
|
Genetic variation
|
4,189
|
135
|
Start
|
High
|
219
|
Introduction to evolution
|
4,119
|
132
|
B
|
Mid
|
220
|
Devolution (biology)
|
4,059
|
130
|
C
|
Low
|
221
|
Speculative evolution
|
4,047
|
130
|
B
|
Low
|
222
|
Lagerstätte
|
4,027
|
129
|
B
|
Mid
|
223
|
Transitional fossil
|
3,997
|
128
|
GA
|
Top
|
224
|
Hybrid fruit
|
3,994
|
128
|
Stub
|
Low
|
225
|
Herto Man
|
3,987
|
128
|
GA
|
Low
|
226
|
Crown group
|
3,975
|
128
|
C
|
Mid
|
227
|
Sociobiological theories of rape
|
3,964
|
127
|
C
|
Mid
|
228
|
Complex adaptive system
|
3,885
|
125
|
C
|
Mid
|
229
|
Purple Earth hypothesis
|
3,873
|
124
|
Start
|
Mid
|
230
|
Apomorphy and synapomorphy
|
3,853
|
124
|
C
|
Low
|
231
|
Spandrel (biology)
|
3,851
|
124
|
B
|
Mid
|
232
|
The Blind Watchmaker
|
3,832
|
123
|
C
|
Mid
|
233
|
Kin selection
|
3,792
|
122
|
GA
|
High
|
234
|
Sperm competition
|
3,790
|
122
|
Start
|
Mid
|
235
|
Neo-Darwinism
|
3,741
|
120
|
Start
|
Mid
|
236
|
Sexual conflict
|
3,671
|
118
|
Start
|
High
|
237
|
Sister group
|
3,648
|
117
|
Start
|
Mid
|
238
|
Thomas Hunt Morgan
|
3,615
|
116
|
B
|
High
|
239
|
Evolution of the brain
|
3,542
|
114
|
Start
|
High
|
240
|
Kenyanthropus
|
3,484
|
112
|
GA
|
Low
|
241
|
Four Fs (evolution)
|
3,473
|
112
|
C
|
Low
|
242
|
Multiregional origin of modern humans
|
3,456
|
111
|
C
|
Mid
|
243
|
Self-preservation
|
3,406
|
109
|
C
|
High
|
244
|
History of eugenics
|
3,373
|
108
|
B
|
Low
|
245
|
List of fossil sites
|
3,350
|
108
|
List
|
Top
|
246
|
Evolution of the eye
|
3,328
|
107
|
C
|
High
|
247
|
Geological history of oxygen
|
3,252
|
104
|
C
|
Low
|
248
|
Assortative mating
|
3,230
|
104
|
C
|
Mid
|
249
|
Evolutionary developmental biology
|
3,221
|
103
|
GA
|
High
|
250
|
Japanese Paleolithic
|
3,182
|
102
|
Start
|
High
|
251
|
Peppered moth
|
3,181
|
102
|
B
|
Low
|
252
|
Islamic views on evolution
|
3,180
|
102
|
C
|
Low
|
253
|
Endurance running hypothesis
|
3,174
|
102
|
Start
|
Low
|
254
|
Duane Gish
|
3,147
|
101
|
C
|
Low
|
255
|
Rejection of evolution by religious groups
|
3,113
|
100
|
B
|
High
|
256
|
Fisherian runaway
|
3,054
|
98
|
Start
|
Low
|
257
|
Cladogram
|
3,052
|
98
|
C
|
Mid
|
258
|
Cline (biology)
|
3,036
|
97
|
C
|
Low
|
259
|
Parental investment
|
3,012
|
97
|
Start
|
High
|
260
|
Allele frequency
|
3,007
|
97
|
Start
|
Mid
|
261
|
Altruism (biology)
|
2,913
|
93
|
C
|
Mid
|
262
|
Body plan
|
2,913
|
93
|
C
|
Mid
|
263
|
Level of support for evolution
|
2,901
|
93
|
C
|
Mid
|
264
|
Sequence homology
|
2,900
|
93
|
C
|
High
|
265
|
Ring species
|
2,898
|
93
|
C
|
High
|
266
|
Gene-centered view of evolution
|
2,882
|
92
|
B
|
High
|
267
|
Solo Man
|
2,866
|
92
|
FA
|
Low
|
268
|
Peppered moth evolution
|
2,842
|
91
|
GA
|
High
|
269
|
Why Is Sex Fun?
|
2,839
|
91
|
C
|
Low
|
270
|
Ernst Mayr
|
2,828
|
91
|
C
|
High
|
271
|
Orthogenesis
|
2,827
|
91
|
GA
|
Mid
|
272
|
Evolution of reptiles
|
2,787
|
89
|
C
|
High
|
273
|
Hunter versus farmer hypothesis
|
2,784
|
89
|
C
|
Low
|
274
|
Domestication syndrome
|
2,747
|
88
|
C
|
Low
|
275
|
Allometry
|
2,742
|
88
|
C
|
Mid
|
276
|
Evolutionarily stable strategy
|
2,741
|
88
|
B
|
Mid
|
277
|
Protocell
|
2,733
|
88
|
C
|
Mid
|
278
|
History of ecology
|
2,710
|
87
|
C
|
Mid
|
279
|
Evolutionary game theory
|
2,696
|
86
|
C
|
High
|
280
|
Gene flow
|
2,680
|
86
|
Start
|
High
|
281
|
E. coli long-term evolution experiment
|
2,674
|
86
|
B
|
Mid
|
282
|
Ursid hybrid
|
2,639
|
85
|
C
|
Low
|
283
|
Evidence of common descent
|
2,632
|
84
|
B
|
Mid
|
284
|
Eukaryogenesis
|
2,623
|
84
|
C
|
High
|
285
|
Handicap principle
|
2,609
|
84
|
GA
|
High
|
286
|
Reproductive isolation
|
2,608
|
84
|
C
|
High
|
287
|
Theodosius Dobzhansky
|
2,591
|
83
|
C
|
Mid
|
288
|
March of Progress
|
2,557
|
82
|
C
|
Low
|
289
|
The Expression of the Emotions in Man and Animals
|
2,536
|
81
|
Start
|
Mid
|
290
|
Future generations
|
2,531
|
81
|
Start
|
Low
|
291
|
Shadow biosphere
|
2,504
|
80
|
Start
|
Mid
|
292
|
Exaptation
|
2,468
|
79
|
C
|
High
|
293
|
Life history theory
|
2,454
|
79
|
C
|
High
|
294
|
Acceptance of evolution by religious groups
|
2,440
|
78
|
C
|
Low
|
295
|
Nicholas Miklouho-Maclay
|
2,419
|
78
|
C
|
Low
|
296
|
Parental care
|
2,409
|
77
|
B
|
Mid
|
297
|
List of examples of convergent evolution
|
2,408
|
77
|
List
|
High
|
298
|
Cro-Magnon rock shelter
|
2,407
|
77
|
Start
|
Mid
|
299
|
Satoshi Kanazawa
|
2,406
|
77
|
C
|
Unknown
|
300
|
Stotting
|
2,402
|
77
|
GA
|
Low
|
301
|
Evolutionary computation
|
2,393
|
77
|
C
|
High
|
302
|
Gene polymorphism
|
2,363
|
76
|
Start
|
Mid
|
303
|
Fish intelligence
|
2,353
|
75
|
B
|
Low
|
304
|
Sympatric speciation
|
2,352
|
75
|
Start
|
Mid
|
305
|
John Maynard Smith
|
2,335
|
75
|
C
|
High
|
306
|
Group selection
|
2,323
|
74
|
GA
|
High
|
307
|
Macroevolution
|
2,299
|
74
|
B
|
Top
|
308
|
Clonally transmissible cancer
|
2,292
|
73
|
C
|
Low
|
309
|
Origin of speech
|
2,261
|
72
|
C
|
Mid
|
310
|
Haldane's rule
|
2,257
|
72
|
C
|
Low
|
311
|
Alloparenting
|
2,235
|
72
|
C
|
Low
|
312
|
Gene duplication
|
2,217
|
71
|
C
|
Mid
|
313
|
Evolutionary radiation
|
2,205
|
71
|
Start
|
Mid
|
314
|
Coevolution
|
2,176
|
70
|
GA
|
High
|
315
|
W. D. Hamilton
|
2,167
|
69
|
C
|
Low
|
316
|
Killer ape theory
|
2,151
|
69
|
Start
|
Low
|
317
|
Lagar Velho 1
|
2,149
|
69
|
Stub
|
Low
|
318
|
Homo sapiens sapiens
|
2,140
|
69
|
NA
|
NA
|
319
|
Inclusive fitness
|
2,139
|
69
|
C
|
High
|
320
|
Parallel evolution
|
2,129
|
68
|
Start
|
High
|
321
|
Motion camouflage
|
2,127
|
68
|
GA
|
Low
|
322
|
Phenotypic plasticity
|
2,108
|
68
|
C
|
Mid
|
323
|
Frameshift mutation
|
2,103
|
67
|
B
|
High
|
324
|
Biology and political orientation
|
2,088
|
67
|
C
|
Low
|
325
|
Divergent evolution
|
2,075
|
66
|
Start
|
Mid
|
326
|
Asa Gray
|
2,069
|
66
|
GA
|
Low
|
327
|
Human skeletal changes due to bipedalism
|
2,046
|
66
|
B
|
Mid
|
328
|
Evolutionary pressure
|
2,037
|
65
|
C
|
Mid
|
329
|
Rotating locomotion in living systems
|
2,018
|
65
|
FA
|
High
|
330
|
Mach bands
|
2,009
|
64
|
Start
|
Mid
|
331
|
Evolutionary anachronism
|
1,997
|
64
|
List
|
Mid
|
332
|
Radiation hormesis
|
1,993
|
64
|
B
|
Mid
|
333
|
Meganthropus
|
1,974
|
63
|
Start
|
Low
|
334
|
Two-domain system
|
1,965
|
63
|
C
|
Low
|
335
|
Darwin's Dangerous Idea
|
1,951
|
62
|
C
|
Mid
|
336
|
Island syndrome
|
1,945
|
62
|
Start
|
Unknown
|
337
|
Somatic mutation
|
1,916
|
61
|
C
|
Low
|
338
|
Evolution of morality
|
1,898
|
61
|
C
|
High
|
339
|
Gene pool
|
1,893
|
61
|
Start
|
High
|
340
|
Alternatives to Darwinian evolution
|
1,886
|
60
|
B
|
Mid
|
341
|
Primitive (phylogenetics)
|
1,857
|
59
|
Start
|
Mid
|
342
|
Bruniquel Cave
|
1,833
|
59
|
Start
|
Mid
|
343
|
Reciprocal altruism
|
1,821
|
58
|
B
|
Mid
|
344
|
Evolution of emotion
|
1,818
|
58
|
Start
|
Unknown
|
345
|
Fisher's principle
|
1,799
|
58
|
Start
|
Mid
|
346
|
Extended evolutionary synthesis
|
1,796
|
57
|
B
|
High
|
347
|
Evolution of mammalian auditory ossicles
|
1,793
|
57
|
B
|
Mid
|
348
|
Baldwin effect
|
1,758
|
56
|
GA
|
Low
|
349
|
Down House
|
1,756
|
56
|
C
|
Low
|
350
|
Pangenesis
|
1,713
|
55
|
C
|
Low
|
351
|
Evolutionism
|
1,705
|
55
|
C
|
Mid
|
352
|
Disappearing blonde gene
|
1,701
|
54
|
Start
|
Low
|
353
|
Modern humans
|
1,688
|
54
|
NA
|
NA
|
354
|
Struggle for existence
|
1,655
|
53
|
C
|
Mid
|
355
|
Microevolution
|
1,642
|
52
|
C
|
High
|
356
|
Late Stone Age
|
1,639
|
52
|
Start
|
Low
|
357
|
The Third Chimpanzee
|
1,614
|
52
|
C
|
Low
|
358
|
Evolution of cells
|
1,613
|
52
|
Start
|
High
|
359
|
Evolution of photosynthesis
|
1,603
|
51
|
Start
|
High
|
360
|
Mate choice in humans
|
1,598
|
51
|
B
|
Unknown
|
361
|
Jerry Coyne
|
1,585
|
51
|
Start
|
Low
|
362
|
Bateman's principle
|
1,566
|
50
|
B
|
Mid
|
363
|
August Weismann
|
1,560
|
50
|
Start
|
High
|
364
|
Neutral theory of molecular evolution
|
1,554
|
50
|
Start
|
High
|
365
|
Panmixia
|
1,542
|
49
|
Start
|
Mid
|
366
|
Strategic pluralism
|
1,533
|
49
|
Stub
|
Low
|
367
|
Evolutionary arms race
|
1,522
|
49
|
Start
|
High
|
368
|
Germline mutation
|
1,521
|
49
|
B
|
High
|
369
|
Genotype–phenotype distinction
|
1,499
|
48
|
Start
|
High
|
370
|
Creation and evolution in public education
|
1,494
|
48
|
B
|
Mid
|
371
|
Oceanic dispersal
|
1,494
|
48
|
Start
|
Low
|
372
|
Embryological origins of the mouth and anus
|
1,487
|
47
|
Start
|
Low
|
373
|
Price equation
|
1,478
|
47
|
C
|
Low
|
374
|
Snake detection theory
|
1,456
|
46
|
Start
|
Mid
|
375
|
Heterochrony
|
1,449
|
46
|
GA
|
Mid
|
376
|
Evolutionary psychology of religion
|
1,439
|
46
|
Start
|
Low
|
377
|
Molecular evolution
|
1,435
|
46
|
C
|
Top
|
378
|
Fitness landscape
|
1,431
|
46
|
B
|
High
|
379
|
Robert Trivers
|
1,426
|
46
|
Start
|
Low
|
380
|
Grimaldi man
|
1,426
|
46
|
C
|
Low
|
381
|
Coalescent theory
|
1,425
|
45
|
C
|
Low
|
382
|
Tend and befriend
|
1,419
|
45
|
C
|
Low
|
383
|
Reproductive success
|
1,414
|
45
|
Start
|
High
|
384
|
Red dress effect
|
1,403
|
45
|
Start
|
Low
|
385
|
Taforalt
|
1,401
|
45
|
C
|
Low
|
386
|
George R. Price
|
1,394
|
44
|
C
|
Low
|
387
|
Racism in the LGBT community
|
1,380
|
44
|
C
|
Low
|
388
|
Beta diversity
|
1,374
|
44
|
C
|
Mid
|
389
|
Cognitive tradeoff hypothesis
|
1,370
|
44
|
C
|
Low
|
390
|
Evolutionary mismatch
|
1,362
|
43
|
C
|
Low
|
391
|
Nuptial gift
|
1,361
|
43
|
Start
|
Mid
|
392
|
Evolution of biological complexity
|
1,357
|
43
|
C
|
Mid
|
393
|
Evolutionary taxonomy
|
1,356
|
43
|
C
|
Mid
|
394
|
Evolution of snake venom
|
1,354
|
43
|
GA
|
Mid
|
395
|
Aerobic fermentation
|
1,346
|
43
|
B
|
Low
|
396
|
Red Deer Cave people
|
1,338
|
43
|
Start
|
Low
|
397
|
Background extinction rate
|
1,336
|
43
|
Start
|
Mid
|
398
|
Siblicide
|
1,327
|
42
|
Start
|
Low
|
399
|
Evolution of tetrapods
|
1,321
|
42
|
C
|
High
|
400
|
Muller's ratchet
|
1,312
|
42
|
Start
|
Mid
|
401
|
Initial Upper Paleolithic
|
1,308
|
42
|
B
|
Unknown
|
402
|
Acritarch
|
1,292
|
41
|
C
|
Low
|
403
|
Junkyard tornado
|
1,291
|
41
|
C
|
Low
|
404
|
Timeline of zoology
|
1,286
|
41
|
List
|
Mid
|
405
|
Nothing in Biology Makes Sense Except in the Light of Evolution
|
1,271
|
41
|
C
|
Mid
|
406
|
Bird hybrid
|
1,269
|
40
|
Start
|
Low
|
407
|
Population biology
|
1,267
|
40
|
Stub
|
Low
|
408
|
Evolution of cephalopods
|
1,256
|
40
|
C
|
Low
|
409
|
Computational phylogenetics
|
1,254
|
40
|
C
|
Mid
|
410
|
Evolutionary approaches to depression
|
1,235
|
39
|
Start
|
Low
|
411
|
Dmanisi
|
1,225
|
39
|
Start
|
Mid
|
412
|
Franz Weidenreich
|
1,221
|
39
|
Stub
|
Mid
|
413
|
Racist
|
1,203
|
38
|
NA
|
NA
|
414
|
Ovulatory shift hypothesis
|
1,203
|
38
|
GA
|
Low
|
415
|
Systemic racism
|
1,197
|
38
|
NA
|
NA
|
416
|
E. B. Ford
|
1,188
|
38
|
C
|
Low
|
417
|
Directional selection
|
1,181
|
38
|
Start
|
Mid
|
418
|
1860 Oxford evolution debate
|
1,178
|
38
|
B
|
Mid
|
419
|
Embryonic diapause
|
1,161
|
37
|
Start
|
Low
|
420
|
Stabilizing selection
|
1,154
|
37
|
Start
|
Mid
|
421
|
Evolutionary anthropology
|
1,139
|
36
|
Start
|
Low
|
422
|
Anagenesis
|
1,124
|
36
|
C
|
Mid
|
423
|
Indel
|
1,122
|
36
|
Start
|
Mid
|
424
|
List of prehistoric cartilaginous fish genera
|
1,120
|
36
|
List
|
Mid
|
425
|
Major histocompatibility complex and sexual selection
|
1,115
|
35
|
C
|
Mid
|
426
|
Mating call
|
1,108
|
35
|
C
|
Low
|
427
|
Mate value
|
1,106
|
35
|
C
|
Low
|
428
|
Iron–sulfur world hypothesis
|
1,102
|
35
|
C
|
Low
|
429
|
Heterozygote advantage
|
1,100
|
35
|
Start
|
Mid
|
430
|
Josiah C. Nott
|
1,100
|
35
|
C
|
Low
|
431
|
Isua Greenstone Belt
|
1,095
|
35
|
C
|
Mid
|
432
|
Genetic divergence
|
1,090
|
35
|
Start
|
High
|
433
|
Balancing selection
|
1,084
|
34
|
Start
|
Mid
|
434
|
Budgerigar colour genetics
|
1,081
|
34
|
Start
|
Low
|
435
|
History of anthropometry
|
1,080
|
34
|
C
|
Low
|
436
|
Snow camouflage
|
1,080
|
34
|
GA
|
Low
|
437
|
Peptide nucleic acid
|
1,061
|
34
|
Start
|
Low
|
438
|
Race suicide
|
1,058
|
34
|
Start
|
Mid
|
439
|
Codon usage bias
|
1,057
|
34
|
B
|
Low
|
440
|
Extended female sexuality
|
1,056
|
34
|
B
|
Mid
|
441
|
Teleology in biology
|
1,054
|
34
|
GA
|
High
|
442
|
Parapatric speciation
|
1,051
|
33
|
C
|
Mid
|
443
|
Crocoduck
|
1,051
|
33
|
C
|
Low
|
444
|
Negative selection (natural selection)
|
1,045
|
33
|
Stub
|
Mid
|
445
|
Homoplasy
|
1,035
|
33
|
Start
|
Low
|
446
|
Green-beard effect
|
1,033
|
33
|
Start
|
Low
|
447
|
Models of DNA evolution
|
1,028
|
33
|
B
|
Low
|
448
|
Braarudosphaera bigelowii
|
1,023
|
33
|
Start
|
Low
|
449
|
Evolution of bacteria
|
1,012
|
32
|
C
|
Mid
|
450
|
Caveasphaera
|
994
|
32
|
Start
|
Low
|
451
|
Origin of avian flight
|
984
|
31
|
Start
|
Mid
|
452
|
Universal Darwinism
|
984
|
31
|
C
|
Low
|
453
|
David Krakauer (scientist)
|
973
|
31
|
Start
|
Low
|
454
|
Evolution of nervous systems
|
969
|
31
|
B
|
Mid
|
455
|
Niche construction
|
967
|
31
|
B
|
Low
|
456
|
Jewish views on evolution
|
966
|
31
|
B
|
Low
|
457
|
Snaiad
|
964
|
31
|
B
|
Low
|
458
|
History of zoology through 1859
|
962
|
31
|
C
|
High
|
459
|
Evolution of ageing
|
958
|
30
|
B
|
High
|
460
|
Genetic pollution
|
958
|
30
|
C
|
Low
|
461
|
Polyandry in fish
|
953
|
30
|
C
|
Low
|
462
|
Female sperm storage
|
949
|
30
|
C
|
Low
|
463
|
Peripatric speciation
|
947
|
30
|
B
|
Mid
|
464
|
Saltation (biology)
|
944
|
30
|
C
|
Mid
|
465
|
Parasite-stress theory
|
941
|
30
|
C
|
Mid
|
466
|
David Sloan Wilson
|
940
|
30
|
Start
|
Unknown
|
467
|
Jonathan Wells (intelligent design advocate)
|
928
|
29
|
Start
|
Low
|
468
|
Spiegelman's Monster
|
919
|
29
|
Start
|
Low
|
469
|
Trivers–Willard hypothesis
|
911
|
29
|
Start
|
Low
|
470
|
Paternal care
|
910
|
29
|
C
|
Low
|
471
|
The Greatest Show on Earth: The Evidence for Evolution
|
908
|
29
|
Start
|
Low
|
472
|
Mutationism
|
904
|
29
|
GA
|
Low
|
473
|
Last eukaryotic common ancestor
|
903
|
29
|
NA
|
High
|
474
|
Numerical taxonomy
|
898
|
28
|
Start
|
Mid
|
475
|
Henry Walter Bates
|
887
|
28
|
C
|
High
|
476
|
Costly signaling theory in evolutionary psychology
|
883
|
28
|
C
|
Mid
|
477
|
Elizabeth, Lady Hope
|
882
|
28
|
C
|
Low
|
478
|
List of non-avian dinosaur species preserved with evidence of feathers
|
882
|
28
|
List
|
Low
|
479
|
Evolution of lemurs
|
881
|
28
|
FA
|
Low
|
480
|
Wonderful Life (book)
|
873
|
28
|
Stub
|
Low
|
481
|
Metapopulation
|
871
|
28
|
B
|
Mid
|
482
|
Extinction vortex
|
865
|
27
|
Start
|
Low
|
483
|
Disruptive selection
|
860
|
27
|
C
|
Mid
|
484
|
Endemism in the Hawaiian Islands
|
858
|
27
|
Start
|
Low
|
485
|
Experimental evolution
|
850
|
27
|
Start
|
High
|
486
|
Timeline of fish evolution
|
843
|
27
|
List
|
Low
|
487
|
List of Neanderthal fossils
|
842
|
27
|
List
|
Low
|
488
|
Sociobiology: The New Synthesis
|
838
|
27
|
GA
|
Mid
|
489
|
Domestication of the goat
|
838
|
27
|
B
|
Mid
|
490
|
Gene family
|
837
|
27
|
C
|
High
|
491
|
Telescoping generations
|
833
|
26
|
Stub
|
Unknown
|
492
|
Diana Fleischman
|
833
|
26
|
Start
|
Low
|
493
|
Entrainment (biomusicology)
|
826
|
26
|
Start
|
Low
|
494
|
Adaptationism
|
825
|
26
|
Start
|
Mid
|
495
|
Sexual selection in birds
|
822
|
26
|
C
|
Low
|
496
|
Population structure (genetics)
|
821
|
26
|
Start
|
Low
|
497
|
Outline of evolution
|
821
|
26
|
List
|
Top
|
498
|
Androgenesis
|
816
|
26
|
C
|
Low
|
499
|
Phenetics
|
810
|
26
|
Start
|
Mid
|
500
|
Bayesian inference in phylogeny
|
808
|
26
|
C
|
Low
|
501
|
Human jaw shrinkage
|
805
|
25
|
Unknown
|
Unknown
|
502
|
Outgroup (cladistics)
|
804
|
25
|
Start
|
Mid
|
503
|
History of creationism
|
798
|
25
|
B
|
Mid
|
504
|
Evolutionary ecology
|
797
|
25
|
C
|
Mid
|
505
|
Davis's law
|
794
|
25
|
Start
|
Low
|
506
|
Ka/Ks ratio
|
793
|
25
|
C
|
Mid
|
507
|
Evolutionary models of human drug use
|
792
|
25
|
C
|
Low
|
508
|
The Red Queen: Sex and the Evolution of Human Nature
|
787
|
25
|
Start
|
Low
|
509
|
Savannah hypothesis
|
784
|
25
|
Start
|
Low
|
510
|
Klepton
|
764
|
24
|
Start
|
Low
|
511
|
Blending inheritance
|
763
|
24
|
GA
|
Low
|
512
|
Of Pandas and People
|
762
|
24
|
C
|
Low
|
513
|
Conservation-induced extinction
|
760
|
24
|
Start
|
Mid
|
514
|
Artificial selection
|
757
|
24
|
NA
|
NA
|
515
|
Canalisation (genetics)
|
752
|
24
|
Start
|
Mid
|
516
|
Evolution of color vision
|
752
|
24
|
Start
|
Low
|
517
|
Dollo's law of irreversibility
|
750
|
24
|
Start
|
High
|
518
|
Gut (anatomy)
|
749
|
24
|
NA
|
Low
|
519
|
Hologenome theory of evolution
|
749
|
24
|
Start
|
Mid
|
520
|
Lantian Man
|
741
|
23
|
GA
|
Low
|
521
|
Seminal fluid protein
|
741
|
23
|
Start
|
Low
|
522
|
Frequency-dependent selection
|
730
|
23
|
Start
|
High
|
523
|
Motoo Kimura
|
728
|
23
|
B
|
High
|
524
|
Evolution of color vision in primates
|
725
|
23
|
C
|
Low
|
525
|
Synonymous substitution
|
720
|
23
|
Start
|
Mid
|
526
|
Plant evolution
|
717
|
23
|
Start
|
High
|
527
|
Endless Forms Most Beautiful (book)
|
716
|
23
|
GA
|
Low
|
528
|
Polyphenism
|
711
|
22
|
Start
|
Mid
|
529
|
Yuanmou Man
|
710
|
22
|
GA
|
Low
|
530
|
Character displacement
|
696
|
22
|
B
|
Mid
|
531
|
The 10,000 Year Explosion
|
694
|
22
|
B
|
Mid
|
532
|
Candidatus Atelocyanobacterium thalassa
|
690
|
22
|
C
|
Low
|
533
|
Evolutionary psychiatry
|
688
|
22
|
Stub
|
Low
|
534
|
Sperm Wars
|
679
|
21
|
Start
|
Mid
|
535
|
Joan Roughgarden
|
678
|
21
|
C
|
Unknown
|
536
|
Operational sex ratio
|
677
|
21
|
Start
|
Low
|
537
|
Cooperation (evolution)
|
674
|
21
|
B
|
Mid
|
538
|
Endosymbiotic theory
|
674
|
21
|
NA
|
NA
|
539
|
Evolution of flagella
|
673
|
21
|
Start
|
Mid
|
540
|
Neural Darwinism
|
671
|
21
|
C
|
Unknown
|
541
|
Parent–offspring conflict
|
668
|
21
|
Start
|
Mid
|
542
|
Protein superfamily
|
662
|
21
|
B
|
Mid
|
543
|
George Christopher Williams
|
658
|
21
|
Start
|
Mid
|
544
|
Cladogenesis
|
657
|
21
|
Start
|
Mid
|
545
|
Elaine Morgan
|
657
|
21
|
C
|
Low
|
546
|
Angraecum sesquipedale
|
649
|
20
|
B
|
Mid
|
547
|
Single-access key
|
644
|
20
|
C
|
Low
|
548
|
Autapomorphy
|
634
|
20
|
C
|
Low
|
549
|
Mormon views on evolution
|
634
|
20
|
C
|
Low
|
550
|
Automimicry
|
630
|
20
|
GA
|
Mid
|
551
|
Koobi Fora
|
629
|
20
|
C
|
Mid
|
552
|
Cope's rule
|
626
|
20
|
Start
|
Mid
|
553
|
Project Steve
|
619
|
19
|
C
|
Low
|
554
|
Haplogroup C-V20
|
619
|
19
|
Unknown
|
Unknown
|
555
|
Cryptic female choice
|
617
|
19
|
B
|
Low
|
556
|
Precambrian rabbit
|
615
|
19
|
C
|
Low
|
557
|
The Major Transitions in Evolution
|
613
|
19
|
Stub
|
Low
|
558
|
Shane Campbell-Staton
|
604
|
19
|
Start
|
Low
|
559
|
The Spandrels of San Marco and the Panglossian Paradigm
|
601
|
19
|
Start
|
Mid
|
560
|
Evolutionary grade
|
584
|
18
|
Start
|
High
|
561
|
Allogamy
|
583
|
18
|
Start
|
Mid
|
562
|
Incomplete lineage sorting
|
583
|
18
|
Start
|
Mid
|
563
|
Social selection
|
578
|
18
|
C
|
Low
|
564
|
Robert Edmond Grant
|
577
|
18
|
Start
|
Low
|
565
|
Conservative replacement
|
576
|
18
|
Start
|
Low
|
566
|
Annual vs. perennial plant evolution
|
576
|
18
|
C
|
Low
|
567
|
Biogenesis
|
565
|
18
|
NA
|
High
|
568
|
Machiavellian intelligence hypothesis
|
563
|
18
|
Start
|
Low
|
569
|
The Evolution of Desire
|
563
|
18
|
Start
|
Unknown
|
570
|
Sexual selection in mammals
|
560
|
18
|
C
|
Low
|
571
|
Mosaic evolution
|
552
|
17
|
Start
|
Low
|
572
|
McLean v. Arkansas
|
549
|
17
|
Start
|
Low
|
573
|
Natural Theology or Evidences of the Existence and Attributes of the Deity
|
549
|
17
|
GA
|
Low
|
574
|
Disassortative mating
|
547
|
17
|
C
|
Mid
|
575
|
Host–parasite coevolution
|
544
|
17
|
GA
|
Mid
|
576
|
Racism on the Internet
|
543
|
17
|
Start
|
Low
|
577
|
Cryptic species complex
|
541
|
17
|
NA
|
NA
|
578
|
Unit of selection
|
538
|
17
|
C
|
High
|
579
|
Development of Darwin's theory
|
534
|
17
|
B
|
Mid
|
580
|
James Cowles Prichard
|
533
|
17
|
C
|
High
|
581
|
Vestigial response
|
532
|
17
|
Stub
|
Low
|
582
|
Disposable soma theory of aging
|
529
|
17
|
C
|
Mid
|
583
|
PAH world hypothesis
|
528
|
17
|
Start
|
Low
|
584
|
Buya, Eritrea
|
521
|
16
|
C
|
Unknown
|
585
|
Darwinian demon
|
520
|
16
|
Stub
|
Low
|
586
|
Darwin and women
|
519
|
16
|
Stub
|
Low
|
587
|
Sex Power Money
|
519
|
16
|
C
|
Low
|
588
|
Australopithecus deyiremeda
|
517
|
16
|
GA
|
Low
|
589
|
Genetic isolate
|
516
|
16
|
Stub
|
Low
|
590
|
The Genetical Theory of Natural Selection
|
513
|
16
|
Start
|
Mid
|
591
|
Evolvability
|
510
|
16
|
C
|
High
|
592
|
Cooperative eye hypothesis
|
507
|
16
|
Start
|
Low
|
593
|
Nina Jablonski
|
504
|
16
|
B
|
Low
|
594
|
Genetic purging
|
503
|
16
|
Unknown
|
Unknown
|
595
|
The Vital Question
|
502
|
16
|
GA
|
Low
|
596
|
Evolution: The Game of Intelligent Life
|
499
|
16
|
Start
|
Low
|
597
|
Loren Cordain
|
499
|
16
|
Stub
|
Low
|
598
|
Schizocoely
|
497
|
16
|
Start
|
Mid
|
599
|
Evolution of eusociality
|
497
|
16
|
C
|
Low
|
600
|
Ornithophily
|
493
|
15
|
B
|
Low
|
601
|
Weasel program
|
489
|
15
|
B
|
Low
|
602
|
Winner and loser effects
|
488
|
15
|
C
|
Low
|
603
|
Polytomy
|
486
|
15
|
Start
|
Mid
|
604
|
Female line
|
484
|
15
|
NA
|
NA
|
605
|
Emsleyan mimicry
|
482
|
15
|
C
|
Low
|
606
|
Proavis
|
480
|
15
|
Start
|
Low
|
607
|
Long branch attraction
|
479
|
15
|
Start
|
Low
|
608
|
Reticulate evolution
|
478
|
15
|
C
|
Mid
|
609
|
Island hopping
|
477
|
15
|
NA
|
Low
|
610
|
Cytotaxonomy
|
477
|
15
|
Stub
|
Mid
|
611
|
Ray Lankester
|
476
|
15
|
B
|
Low
|
612
|
Phyletic gradualism
|
476
|
15
|
Start
|
Mid
|
613
|
Phylogenetic comparative methods
|
476
|
15
|
C
|
Low
|
614
|
Laboratory experiments of speciation
|
476
|
15
|
List
|
Low
|
615
|
Muscular evolution in humans
|
473
|
15
|
Start
|
Low
|
616
|
Fisher's fundamental theorem of natural selection
|
469
|
15
|
Start
|
Mid
|
617
|
Chemical defense
|
469
|
15
|
C
|
Low
|
618
|
Vertebrate land invasion
|
468
|
15
|
C
|
Mid
|
619
|
Demonic Males
|
466
|
15
|
C
|
Unknown
|
620
|
The Evolution of Beauty
|
466
|
15
|
Start
|
Low
|
621
|
Evolutionary suicide
|
464
|
14
|
Start
|
Low
|
622
|
Zinnia Kumar
|
464
|
14
|
C
|
Low
|
623
|
Zlatý kůň woman
|
460
|
14
|
Start
|
Low
|
624
|
Philosophie zoologique
|
459
|
14
|
GA
|
Low
|
625
|
Man's Place in Nature
|
459
|
14
|
Start
|
Mid
|
626
|
Directed evolution (transhumanism)
|
459
|
14
|
Stub
|
Low
|
627
|
Genotype frequency
|
454
|
14
|
Start
|
Mid
|
628
|
Great Hippocampus Question
|
449
|
14
|
B
|
Low
|
629
|
Mate guarding
|
444
|
14
|
Unknown
|
Mid
|
630
|
Genome evolution
|
444
|
14
|
C
|
Top
|
631
|
Willi Hennig
|
443
|
14
|
Start
|
Mid
|
632
|
St. George Jackson Mivart
|
442
|
14
|
Start
|
Low
|
633
|
Caminalcules
|
440
|
14
|
Start
|
Mid
|
634
|
Glacial refugium
|
439
|
14
|
Stub
|
Low
|
635
|
Herman Bernhard Lundborg
|
438
|
14
|
Start
|
Low
|
636
|
Precambrian body plans
|
435
|
14
|
B
|
Low
|
637
|
Fritz Müller
|
434
|
14
|
B
|
Mid
|
638
|
Intragenomic conflict
|
434
|
14
|
C
|
Mid
|
639
|
Dawkins vs. Gould
|
433
|
13
|
Start
|
Low
|
640
|
Phagomimicry
|
430
|
13
|
Stub
|
Low
|
641
|
Alternative abiogenesis scenarios
|
430
|
13
|
C
|
Low
|
642
|
Edward Blyth
|
427
|
13
|
B
|
High
|
643
|
Cytonuclear discordance
|
427
|
13
|
Start
|
Unknown
|
644
|
Evolution of cognition
|
426
|
13
|
C
|
Low
|
645
|
Sex differences in memory
|
420
|
13
|
Start
|
Low
|
646
|
Reinforcement (speciation)
|
417
|
13
|
GA
|
Mid
|
647
|
Genetic erosion
|
416
|
13
|
C
|
Low
|
648
|
Bat wing development
|
415
|
13
|
Start
|
Low
|
649
|
Inheritance of acquired characteristics
|
414
|
13
|
NA
|
NA
|
650
|
Evolutionary physiology
|
414
|
13
|
B
|
High
|
651
|
Weapon (biology)
|
413
|
13
|
Stub
|
Low
|
652
|
The Variation of Animals and Plants Under Domestication
|
407
|
13
|
C
|
Low
|
653
|
Natural Selection (manuscript)
|
404
|
13
|
Stub
|
Low
|
654
|
Evolutionary aesthetics
|
403
|
13
|
C
|
High
|
655
|
Evolution of metal ions in biological systems
|
401
|
12
|
C
|
Low
|
656
|
Glossary of genetics and evolutionary biology
|
400
|
12
|
List
|
Top
|
657
|
The Goodness Paradox
|
399
|
12
|
Start
|
Low
|
658
|
Habitable zone for complex life
|
397
|
12
|
C
|
Unknown
|
659
|
Wushan Man
|
395
|
12
|
Start
|
Low
|
660
|
Chemoton
|
395
|
12
|
Start
|
Low
|
661
|
Richard Prum
|
395
|
12
|
Start
|
Low
|
662
|
Bet hedging (biology)
|
395
|
12
|
B
|
Mid
|
663
|
Ecomorphology
|
393
|
12
|
B
|
Low
|
664
|
Rate of evolution
|
390
|
12
|
Start
|
Low
|
665
|
Darwinian literary studies
|
388
|
12
|
C
|
Low
|
666
|
Troglomorphism
|
386
|
12
|
Stub
|
Low
|
667
|
Ecological speciation
|
385
|
12
|
B
|
High
|
668
|
List of transitional fossils
|
379
|
12
|
NA
|
NA
|
669
|
Polydactyly in stem-tetrapods
|
375
|
12
|
Start
|
Low
|
670
|
Viral eukaryogenesis
|
374
|
12
|
Start
|
Mid
|
671
|
Evolutionary neuroscience
|
373
|
12
|
Start
|
High
|
672
|
Origin and function of meiosis
|
373
|
12
|
Start
|
Low
|
673
|
Konstantin Mereschkowski
|
372
|
12
|
GA
|
Unknown
|
674
|
Co-adaptation
|
372
|
12
|
C
|
Low
|
675
|
Saldanha man
|
370
|
11
|
Stub
|
Low
|
676
|
Court jester hypothesis
|
369
|
11
|
C
|
Low
|
677
|
Selection coefficient
|
367
|
11
|
Stub
|
Mid
|
678
|
Self-decoration camouflage
|
367
|
11
|
GA
|
Low
|
679
|
Error threshold (evolution)
|
365
|
11
|
C
|
Mid
|
680
|
Genetic assimilation
|
365
|
11
|
GA
|
Low
|
681
|
Black Queen hypothesis
|
365
|
11
|
Start
|
Low
|
682
|
Patrick Matthew
|
362
|
11
|
B
|
Mid
|
683
|
Bateson–Dobzhansky–Muller model
|
362
|
11
|
Unknown
|
Unknown
|
684
|
Religion Explained
|
361
|
11
|
Start
|
Low
|
685
|
List of Neanderthal sites
|
361
|
11
|
List
|
Low
|
686
|
Evolutionary developmental psychology
|
358
|
11
|
C
|
Low
|
687
|
Nanjing Man
|
358
|
11
|
C
|
Low
|
688
|
History of zoology (1859–present)
|
358
|
11
|
C
|
High
|
689
|
Randy Thornhill
|
358
|
11
|
Start
|
Mid
|
690
|
The Structure of Evolutionary Theory
|
355
|
11
|
Start
|
Low
|
691
|
Evolutionary psychology of language
|
353
|
11
|
Start
|
Low
|
692
|
Douglas J. Futuyma
|
350
|
11
|
C
|
Low
|
693
|
Epic of evolution
|
347
|
11
|
C
|
Low
|
694
|
Allan Wilson (biologist)
|
346
|
11
|
C
|
Low
|
695
|
Evo-devo gene toolkit
|
343
|
11
|
Start
|
Mid
|
696
|
Quantum evolution
|
341
|
11
|
C
|
Mid
|
697
|
Power, Sex, Suicide
|
341
|
11
|
Stub
|
Low
|
698
|
Vocal learning
|
338
|
10
|
B
|
Low
|
699
|
Group living
|
337
|
10
|
Start
|
Low
|
700
|
Evolution of descended testes in mammals
|
336
|
10
|
Unknown
|
Unknown
|
701
|
Lilliput effect
|
335
|
10
|
Start
|
Low
|
702
|
Quasispecies model
|
334
|
10
|
C
|
Mid
|
703
|
Enterocoely
|
334
|
10
|
Stub
|
Mid
|
704
|
Miguelón
|
334
|
10
|
Unknown
|
Unknown
|
705
|
Tradeoffs for locomotion in air and water
|
334
|
10
|
C
|
Mid
|
706
|
Queen mandibular pheromone
|
333
|
10
|
Start
|
Low
|
707
|
W. Tecumseh Fitch
|
331
|
10
|
Stub
|
Low
|
708
|
Tristram Wyatt
|
331
|
10
|
Start
|
Low
|
709
|
Lek paradox
|
329
|
10
|
C
|
Low
|
710
|
Evolutionary dynamics
|
329
|
10
|
Stub
|
Mid
|
711
|
David Lack
|
324
|
10
|
C
|
Low
|
712
|
Insectivorous Plants (book)
|
324
|
10
|
Start
|
Low
|
713
|
Secondarily aquatic tetrapods
|
321
|
10
|
Stub
|
Mid
|
714
|
Evolution (TV series)
|
317
|
10
|
Start
|
Low
|
715
|
Bitter taste evolution
|
315
|
10
|
Start
|
Low
|
716
|
Hybrid zone
|
307
|
9
|
C
|
Mid
|
717
|
Museum of Human Evolution
|
306
|
9
|
Start
|
Unknown
|
718
|
Scott F. Gilbert
|
306
|
9
|
C
|
Low
|
719
|
Sexual selection in scaled reptiles
|
305
|
9
|
Start
|
Low
|
720
|
Emergent evolution
|
304
|
9
|
C
|
Low
|
721
|
Darwinian threshold
|
304
|
9
|
Start
|
Mid
|
722
|
Contingency (evolutionary biology)
|
301
|
9
|
Start
|
Low
|
723
|
Rensch's rule
|
295
|
9
|
Start
|
Low
|
724
|
Inclusive fitness in humans
|
294
|
9
|
C
|
Low
|
725
|
Evolutionary tradeoff
|
294
|
9
|
Unknown
|
Unknown
|
726
|
Digital organism
|
293
|
9
|
Stub
|
Low
|
727
|
Ancestral sequence reconstruction
|
292
|
9
|
C
|
Low
|
728
|
Marcus Feldman
|
290
|
9
|
Start
|
Low
|
729
|
Icons of Evolution
|
287
|
9
|
C
|
Low
|
730
|
Nylon-eating bacteria and creationism
|
285
|
9
|
B
|
Low
|
731
|
Automixis
|
284
|
9
|
Start
|
Unknown
|
732
|
Germ-Soma Differentiation
|
284
|
9
|
C
|
Low
|
733
|
On Being the Right Size
|
282
|
9
|
C
|
Mid
|
734
|
Proto-mitochondrion
|
281
|
9
|
Start
|
Mid
|
735
|
Evolutionary invasion analysis
|
280
|
9
|
Start
|
Low
|
736
|
Francis Maitland Balfour
|
279
|
9
|
Start
|
Low
|
737
|
Viral phylodynamics
|
274
|
8
|
B
|
Low
|
738
|
Evolutionary trap
|
272
|
8
|
Start
|
Low
|
739
|
Cultural selection theory
|
270
|
8
|
C
|
Low
|
740
|
Adaptation and Natural Selection
|
268
|
8
|
Start
|
Low
|
741
|
Alloplastic adaptation
|
268
|
8
|
Stub
|
Low
|
742
|
Deep homology
|
267
|
8
|
Start
|
Mid
|
743
|
Reciprocity (evolution)
|
266
|
8
|
Unknown
|
Unknown
|
744
|
Helitron (biology)
|
265
|
8
|
B
|
Low
|
745
|
What Darwin Got Wrong
|
258
|
8
|
Start
|
Low
|
746
|
Index of evolutionary biology articles
|
254
|
8
|
List
|
High
|
747
|
Reciprocal altruism in humans
|
254
|
8
|
Start
|
Low
|
748
|
Inversion (evolutionary biology)
|
252
|
8
|
Start
|
Mid
|
749
|
William Henry Flower
|
250
|
8
|
B
|
Low
|
750
|
Cellularization
|
249
|
8
|
Stub
|
Low
|
751
|
Idealised population
|
249
|
8
|
C
|
Mid
|
752
|
Gavin de Beer
|
248
|
8
|
C
|
Low
|
753
|
Russell Lande
|
247
|
7
|
Start
|
Low
|
754
|
Davidson Black
|
246
|
7
|
C
|
Mid
|
755
|
Evolutionary fauna
|
244
|
7
|
Start
|
Low
|
756
|
Paul W. Ewald
|
242
|
7
|
Start
|
Low
|
757
|
Postcanine megadontia
|
242
|
7
|
C
|
Low
|
758
|
Intergradation
|
242
|
7
|
Start
|
Low
|
759
|
Human somatic variation
|
240
|
7
|
C
|
Mid
|
760
|
Eugenics in Mexico
|
239
|
7
|
Start
|
Low
|
761
|
Phylotypic stage
|
238
|
7
|
C
|
Low
|
762
|
Constructive neutral evolution
|
238
|
7
|
C
|
Low
|
763
|
Alfred Newton
|
235
|
7
|
C
|
Low
|
764
|
Sexual antagonistic coevolution
|
233
|
7
|
Unknown
|
Unknown
|
765
|
Stenogale
|
232
|
7
|
Stub
|
Low
|
766
|
Isolation by distance
|
231
|
7
|
Start
|
Low
|
767
|
Push of the past
|
231
|
7
|
C
|
Low
|
768
|
Paragroup
|
228
|
7
|
Stub
|
Low
|
769
|
Homo consumericus
|
228
|
7
|
Start
|
Low
|
770
|
Urban evolution
|
224
|
7
|
C
|
Unknown
|
771
|
Kettlewell's experiment
|
223
|
7
|
Start
|
Mid
|
772
|
The Seven Pillars of Life
|
223
|
7
|
Start
|
Low
|
773
|
Evolutionary models of food sharing
|
223
|
7
|
C
|
Low
|
774
|
Parasite load
|
222
|
7
|
C
|
Low
|
775
|
Sir William Lawrence, 1st Baronet
|
222
|
7
|
B
|
High
|
776
|
Joan E. Strassmann
|
220
|
7
|
Start
|
Low
|
777
|
Orgel's rules
|
219
|
7
|
Stub
|
Low
|
778
|
Undeniable: Evolution and the Science of Creation
|
218
|
7
|
Start
|
Low
|
779
|
Behavioral plasticity
|
218
|
7
|
Start
|
Low
|
780
|
Fuyan Cave
|
217
|
7
|
C
|
Low
|
781
|
Expensive tissue hypothesis
|
216
|
6
|
C
|
Low
|
782
|
Edward Bagnall Poulton
|
215
|
6
|
Start
|
Mid
|
783
|
Psammosere
|
213
|
6
|
Stub
|
Mid
|
784
|
Evolution of brachiopods
|
212
|
6
|
Start
|
Low
|
785
|
Biodiversity of Kosovo
|
212
|
6
|
C
|
Low
|
786
|
Law of Life
|
211
|
6
|
Stub
|
Low
|
787
|
Reproductive suppression
|
211
|
6
|
C
|
Mid
|
788
|
Neofunctionalization
|
211
|
6
|
Start
|
Low
|
789
|
Ecology and evolutionary biology
|
210
|
6
|
Start
|
Low
|
790
|
GADV-protein world hypothesis
|
210
|
6
|
Start
|
Low
|
791
|
The Theory of Evolution
|
209
|
6
|
Stub
|
Low
|
792
|
Adaptive behavior (ecology)
|
208
|
6
|
C
|
Mid
|
793
|
Mimicry in vertebrates
|
208
|
6
|
Start
|
Low
|
794
|
Megaevolution
|
205
|
6
|
Start
|
Mid
|
795
|
Red King hypothesis
|
205
|
6
|
Start
|
Low
|
796
|
Alpheus Hyatt
|
204
|
6
|
Start
|
Low
|
797
|
Maternal effect dominant embryonic arrest
|
204
|
6
|
Start
|
Low
|
798
|
Ileret
|
204
|
6
|
Stub
|
Low
|
799
|
Proteinoid
|
203
|
6
|
Start
|
Low
|
800
|
Background selection
|
203
|
6
|
Start
|
Low
|
801
|
Paul Sniegowski
|
199
|
6
|
Start
|
Low
|
802
|
Modern human
|
198
|
6
|
NA
|
NA
|
803
|
Applications of evolution
|
198
|
6
|
B
|
Low
|
804
|
Recurrent evolution
|
198
|
6
|
Unknown
|
Unknown
|
805
|
Rapid modes of evolution
|
197
|
6
|
Unknown
|
Unknown
|
806
|
Molecular Phylogenetics and Evolution
|
197
|
6
|
Stub
|
Low
|
807
|
Biogeographic regions of Europe
|
197
|
6
|
Start
|
Mid
|
808
|
Qikiqtania
|
197
|
6
|
C
|
Unknown
|
809
|
Nearly neutral theory of molecular evolution
|
196
|
6
|
Start
|
Low
|
810
|
Evolutionary psychology and culture
|
196
|
6
|
Start
|
Low
|
811
|
Tree rearrangement
|
195
|
6
|
Start
|
Low
|
812
|
Maternal behavior in vertebrates
|
195
|
6
|
C
|
Low
|
813
|
History of molecular evolution
|
194
|
6
|
C
|
Mid
|
814
|
The Origin of Birds
|
194
|
6
|
GA
|
High
|
815
|
Wing-assisted incline running
|
192
|
6
|
Start
|
Low
|
816
|
Peter J. Bowler
|
191
|
6
|
Start
|
Low
|
817
|
Prejudice from an evolutionary perspective
|
189
|
6
|
Start
|
Low
|
818
|
Eukaryote hybrid genome
|
189
|
6
|
B
|
Low
|
819
|
Ecological evolutionary developmental biology
|
188
|
6
|
Start
|
Low
|
820
|
Sexual selection in insects
|
187
|
6
|
B
|
Low
|
821
|
Hybrid swarm
|
186
|
6
|
Start
|
Mid
|
822
|
Evolutionary Psychology (journal)
|
186
|
6
|
Stub
|
Unknown
|
823
|
Heterotopy
|
186
|
6
|
Stub
|
Low
|
824
|
Jeremiah Kianga
|
186
|
6
|
Start
|
Low
|
825
|
Selection shadow
|
185
|
5
|
Start
|
Low
|
826
|
Philosophy of evolution
|
184
|
5
|
C
|
Mid
|
827
|
Pseudoextinction
|
183
|
5
|
Start
|
Low
|
828
|
Biological constraints
|
183
|
5
|
Start
|
Mid
|
829
|
Shifting balance theory
|
183
|
5
|
Stub
|
Low
|
830
|
Ecological fitting
|
183
|
5
|
B
|
Low
|
831
|
Social immunity
|
183
|
5
|
B
|
High
|
832
|
History of speciation
|
182
|
5
|
C
|
Low
|
833
|
Modularity (biology)
|
180
|
5
|
Start
|
Low
|
834
|
Herbivore adaptations to plant defense
|
179
|
5
|
B
|
Low
|
835
|
Developmental bias
|
178
|
5
|
Unknown
|
Unknown
|
836
|
Bias in the introduction of variation
|
176
|
5
|
B
|
Low
|
837
|
Evolution of olfaction
|
175
|
5
|
C
|
Low
|
838
|
John Tyler Bonner
|
174
|
5
|
C
|
Mid
|
839
|
William Charles Wells
|
173
|
5
|
B
|
High
|
840
|
The Genealogical Adam and Eve
|
173
|
5
|
Start
|
Low
|
841
|
Carboniferous-Earliest Permian Biodiversification Event
|
172
|
5
|
NA
|
Low
|
842
|
John Endler
|
170
|
5
|
Start
|
Low
|
843
|
Runcaria
|
170
|
5
|
Start
|
Low
|
844
|
Multispecies coalescent process
|
169
|
5
|
Start
|
Low
|
845
|
Phylogenetic signal
|
168
|
5
|
C
|
Mid
|
846
|
TalkOrigins Archive
|
167
|
5
|
Start
|
Low
|
847
|
Species-typical behavior
|
165
|
5
|
Start
|
Low
|
848
|
Commemoration of Charles Darwin
|
165
|
5
|
C
|
Mid
|
849
|
Turnover-pulse hypothesis
|
164
|
5
|
Start
|
Low
|
850
|
Evolutionary landscape
|
163
|
5
|
C
|
High
|
851
|
Felsenstein's tree-pruning algorithm
|
163
|
5
|
Stub
|
Low
|
852
|
Concerted evolution
|
163
|
5
|
Stub
|
Low
|
853
|
The Neutral Theory of Molecular Evolution
|
162
|
5
|
Stub
|
Low
|
854
|
Biodiversity of Wales
|
162
|
5
|
C
|
Low
|
855
|
V. C. Wynne-Edwards
|
161
|
5
|
Start
|
Low
|
856
|
Natural morality
|
161
|
5
|
Start
|
Low
|
857
|
Mutation accumulation theory
|
161
|
5
|
C
|
Low
|
858
|
Local adaptation
|
160
|
5
|
Unknown
|
Unknown
|
859
|
Distractive markings
|
159
|
5
|
C
|
Low
|
860
|
The Correlation between Relatives on the Supposition of Mendelian Inheritance
|
158
|
5
|
Start
|
Mid
|
861
|
Hydrogen hypothesis
|
157
|
5
|
Start
|
Low
|
862
|
Largest-scale trends in evolution
|
157
|
5
|
Start
|
High
|
863
|
Arthur Cain
|
155
|
5
|
C
|
Low
|
864
|
International Year of Biodiversity
|
155
|
5
|
Start
|
High
|
865
|
Hyrax Hill
|
154
|
4
|
B
|
Low
|
866
|
Cospeciation
|
154
|
4
|
Start
|
Mid
|
867
|
How the Snake Lost Its Legs
|
153
|
4
|
GA
|
Low
|
868
|
G-value paradox
|
153
|
4
|
C
|
Low
|
869
|
Alexander von Humboldt Biological Resources Research Institute
|
150
|
4
|
Stub
|
Low
|
870
|
Karl Kessler
|
149
|
4
|
Stub
|
Low
|
871
|
Horizontal gene transfer in evolution
|
148
|
4
|
Start
|
High
|
872
|
Fisher's geometric model
|
148
|
4
|
Start
|
Low
|
873
|
Nama assemblage
|
147
|
4
|
Start
|
Low
|
874
|
Hologenomics
|
146
|
4
|
Stub
|
Low
|
875
|
Interactor
|
145
|
4
|
Stub
|
Low
|
876
|
Zoology of the Voyage of H.M.S. Beagle
|
145
|
4
|
Stub
|
Low
|
877
|
Interlocus sexual conflict
|
143
|
4
|
B
|
Mid
|
878
|
Talk.origins
|
142
|
4
|
Start
|
Low
|
879
|
Nancy A. Moran
|
142
|
4
|
C
|
Low
|
880
|
Coloration evidence for natural selection
|
141
|
4
|
GA
|
Mid
|
881
|
Axel Meyer
|
140
|
4
|
Start
|
Unknown
|
882
|
Ruth Mace
|
139
|
4
|
Start
|
Low
|
883
|
List of ecoregions with high endemism
|
138
|
4
|
List
|
Low
|
884
|
The Great Monkey Trial
|
137
|
4
|
Start
|
Low
|
885
|
Mutation bias
|
137
|
4
|
C
|
Mid
|
886
|
Allochronic speciation
|
137
|
4
|
B
|
Mid
|
887
|
Formamide-based prebiotic chemistry
|
136
|
4
|
Start
|
Low
|
888
|
The Apportionment of Human Diversity
|
136
|
4
|
C
|
Low
|
889
|
List of Nepenthes natural hybrids
|
135
|
4
|
List
|
Low
|
890
|
Moritz Wagner (naturalist)
|
135
|
4
|
Start
|
Low
|
891
|
Gard model
|
135
|
4
|
Start
|
Low
|
892
|
Institute of Human Origins
|
135
|
4
|
Start
|
Low
|
893
|
Preadaptation
|
134
|
4
|
NA
|
Mid
|
894
|
Mark Ridley (zoologist)
|
133
|
4
|
Stub
|
Low
|
895
|
Francisc Rainer
|
133
|
4
|
B
|
Low
|
896
|
Character evolution
|
133
|
4
|
Unknown
|
Unknown
|
897
|
Evolutionary capacitance
|
132
|
4
|
C
|
Mid
|
898
|
Hox genes in amphibians and reptiles
|
131
|
4
|
C
|
Low
|
899
|
Segregating site
|
130
|
4
|
Start
|
Low
|
900
|
White Sea assemblage
|
130
|
4
|
Stub
|
Low
|
901
|
Michael Majerus
|
129
|
4
|
Start
|
Mid
|
902
|
David Hillis
|
129
|
4
|
Start
|
Low
|
903
|
Evolution of Macropodidae
|
129
|
4
|
Start
|
Low
|
904
|
Dan Willard
|
128
|
4
|
C
|
Low
|
905
|
Jeremy Yoder
|
127
|
4
|
Start
|
Low
|
906
|
Stan Wood (fossil hunter)
|
127
|
4
|
Stub
|
Unknown
|
907
|
Storage effect
|
126
|
4
|
B
|
Mid
|
908
|
Evolutionary approaches to postpartum depression
|
126
|
4
|
C
|
Low
|
909
|
Unique-event polymorphism
|
125
|
4
|
Start
|
Low
|
910
|
Molecular drive
|
125
|
4
|
Stub
|
Low
|
911
|
Key innovation
|
125
|
4
|
Start
|
Mid
|
912
|
Founder takes all
|
125
|
4
|
Stub
|
Low
|
913
|
Man's Genesis
|
125
|
4
|
Start
|
Low
|
914
|
Corrie Moreau
|
124
|
4
|
C
|
Low
|
915
|
Laura Landweber
|
124
|
4
|
Start
|
Low
|
916
|
Autoplastic adaptation
|
123
|
3
|
Stub
|
Low
|
917
|
Romanticism in evolution theory
|
123
|
3
|
Start
|
Low
|
918
|
Mesozoic–Cenozoic radiation
|
121
|
3
|
Stub
|
Low
|
919
|
Alison P. Galvani
|
121
|
3
|
Start
|
Mid
|
920
|
Sibling species
|
120
|
3
|
NA
|
NA
|
921
|
Discredited hypotheses for the Cambrian explosion
|
120
|
3
|
Stub
|
Mid
|
922
|
Evolutionary theodicy
|
120
|
3
|
C
|
Low
|
923
|
Phylogenetic reconciliation
|
118
|
3
|
Unknown
|
Unknown
|
924
|
Evolution Day
|
117
|
3
|
Start
|
Low
|
925
|
European Society for Evolutionary Biology
|
116
|
3
|
Stub
|
Low
|
926
|
Scott V. Edwards
|
116
|
3
|
C
|
Low
|
927
|
Society for the Study of Evolution
|
115
|
3
|
Stub
|
Low
|
928
|
Darwin (unit)
|
115
|
3
|
Stub
|
Low
|
929
|
Genomic evolution of birds
|
113
|
3
|
C
|
Low
|
930
|
Graham Bell (biologist)
|
112
|
3
|
Stub
|
Low
|
931
|
Human reproductive ecology
|
112
|
3
|
Start
|
Low
|
932
|
Facilitated variation
|
111
|
3
|
Stub
|
Low
|
933
|
Stephen Blair Hedges
|
111
|
3
|
Start
|
Low
|
934
|
Archaic Homo sapiens
|
110
|
3
|
NA
|
NA
|
935
|
Hybrid incompatibility
|
110
|
3
|
C
|
Low
|
936
|
Dynamic mutation
|
109
|
3
|
Stub
|
Low
|
937
|
Wallace effect
|
109
|
3
|
NA
|
NA
|
938
|
Skeletal changes of vertebrates transitioning from water to land
|
109
|
3
|
C
|
Low
|
939
|
Evidence for speciation by reinforcement
|
109
|
3
|
List
|
Low
|
940
|
Reductive evolution
|
108
|
3
|
Start
|
Low
|
941
|
Obligate mutualism
|
108
|
3
|
C
|
Low
|
942
|
Contest competition
|
106
|
3
|
Stub
|
Low
|
943
|
Resource holding potential
|
105
|
3
|
Stub
|
Low
|
944
|
Kindred: Neanderthal Life, Love, Death and Art
|
103
|
3
|
Stub
|
Low
|
945
|
Clonal interference
|
102
|
3
|
Stub
|
Mid
|
946
|
Subfunctionalization
|
102
|
3
|
Start
|
Low
|
947
|
Infinite sites model
|
102
|
3
|
Start
|
Low
|
948
|
Locomotor mimicry
|
102
|
3
|
Start
|
Low
|
949
|
Nonecological speciation
|
102
|
3
|
Start
|
Low
|
950
|
James A. Lake
|
100
|
3
|
Start
|
Low
|
951
|
Ecological inheritance
|
98
|
3
|
Stub
|
Low
|
952
|
Egg taphonomy
|
98
|
3
|
C
|
Low
|
953
|
Elizabeth Arnold (scientist)
|
98
|
3
|
Start
|
Unknown
|
954
|
The Different Forms of Flowers on Plants of the Same Species
|
97
|
3
|
Start
|
Low
|
955
|
Fluctuating selection
|
97
|
3
|
Start
|
Low
|
956
|
Inferring horizontal gene transfer
|
97
|
3
|
B
|
Low
|
957
|
Landscape genomics
|
97
|
3
|
Stub
|
Low
|
958
|
Human Behavior and Evolution Society
|
96
|
3
|
Start
|
Low
|
959
|
Evolution by gene duplication
|
96
|
3
|
Start
|
High
|
960
|
Grit, not grass hypothesis
|
96
|
3
|
C
|
Low
|
961
|
Hyposphene-hypantrum articulation
|
95
|
3
|
Start
|
Low
|
962
|
OneZoom
|
95
|
3
|
Start
|
Unknown
|
963
|
Nonadaptive radiation
|
94
|
3
|
Start
|
Low
|
964
|
Non-Darwinian Evolution (paper)
|
93
|
3
|
Stub
|
Low
|
965
|
Benjamin Chan
|
93
|
3
|
Start
|
Low
|
966
|
The Panda's Thumb (blog)
|
92
|
2
|
Start
|
Low
|
967
|
Sex differences in sensory systems
|
92
|
2
|
Start
|
Mid
|
968
|
Intralocus sexual conflict
|
92
|
2
|
Start
|
Mid
|
969
|
Epididymis evolution from reptiles to mammals
|
92
|
2
|
B
|
Low
|
970
|
Species group
|
91
|
2
|
NA
|
NA
|
971
|
Tim Lewens
|
91
|
2
|
Start
|
Unknown
|
972
|
Phylo (video game)
|
91
|
2
|
Start
|
Low
|
973
|
Darwinian anthropology
|
91
|
2
|
B
|
Unknown
|
974
|
Host switch
|
91
|
2
|
C
|
Low
|
975
|
WLH-50
|
90
|
2
|
Start
|
Unknown
|
976
|
Liran Carmel
|
89
|
2
|
C
|
Low
|
977
|
Andrew Berry (biologist)
|
88
|
2
|
Stub
|
Low
|
978
|
Kinetotroph
|
88
|
2
|
Start
|
Low
|
979
|
Fear of the unknown
|
87
|
2
|
NA
|
NA
|
980
|
Henric Sanielevici
|
87
|
2
|
B
|
Low
|
981
|
Human evolutionary developmental biology
|
86
|
2
|
C
|
Mid
|
982
|
J. T. Gulick
|
84
|
2
|
Start
|
Low
|
983
|
International Code of Area Nomenclature
|
84
|
2
|
Stub
|
Low
|
984
|
George Rolleston
|
84
|
2
|
Start
|
Low
|
985
|
Despeciation
|
84
|
2
|
Start
|
Low
|
986
|
Calcichordate hypothesis
|
83
|
2
|
Start
|
Mid
|
987
|
Rupert Riedl
|
82
|
2
|
Start
|
Low
|
988
|
Paraspecies
|
82
|
2
|
Stub
|
Low
|
989
|
Raissa Berg
|
82
|
2
|
C
|
Low
|
990
|
Victoria Arbour
|
82
|
2
|
Start
|
Low
|
991
|
Fisheries-induced evolution
|
82
|
2
|
C
|
Low
|
992
|
Sulphobes
|
81
|
2
|
Stub
|
Low
|
993
|
Jena Phyletisches Museum
|
80
|
2
|
Start
|
Low
|
994
|
Thorson's rule
|
79
|
2
|
Start
|
Low
|
995
|
Jeffrey Barrick
|
79
|
2
|
B
|
Low
|
996
|
Adriana Briscoe
|
78
|
2
|
B
|
Low
|
997
|
Ecological selection
|
76
|
2
|
NA
|
Mid
|
998
|
Interpolation theory
|
76
|
2
|
Start
|
Low
|
999
|
Evolution of hair
|
76
|
2
|
NA
|
NA
|
1000
|
Resource defense polygyny
|
76
|
2
|
Stub
|
Unknown
|