Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
1
|
Charles Darwin
|
140,949
|
4,546
|
FA
|
Top
|
2
|
Neanderthal
|
133,525
|
4,307
|
GA
|
Mid
|
3
|
Eugenics
|
89,709
|
2,893
|
C
|
Mid
|
4
|
Parthenogenesis
|
83,191
|
2,683
|
B
|
High
|
5
|
Human evolution
|
83,068
|
2,679
|
C
|
High
|
6
|
List of common misconceptions
|
77,181
|
2,489
|
List
|
Low
|
7
|
Sexual dimorphism
|
74,386
|
2,399
|
B
|
High
|
8
|
Evolution
|
73,187
|
2,360
|
FA
|
Top
|
9
|
Racism
|
70,397
|
2,270
|
B
|
Mid
|
10
|
Epicanthic fold
|
69,477
|
2,241
|
C
|
Low
|
11
|
Richard Dawkins
|
69,173
|
2,231
|
GA
|
Mid
|
12
|
Cretaceous–Paleogene extinction event
|
68,243
|
2,201
|
FA
|
High
|
13
|
Species
|
66,988
|
2,160
|
GA
|
Top
|
14
|
List of X-Men members
|
58,989
|
1,902
|
List
|
Low
|
15
|
Extinction
|
54,601
|
1,761
|
C
|
High
|
16
|
Biodiversity
|
53,816
|
1,736
|
C
|
Mid
|
17
|
Abiogenesis
|
49,500
|
1,596
|
GA
|
Top
|
18
|
Fossil
|
47,892
|
1,544
|
B
|
Mid
|
19
|
Carcinisation
|
46,902
|
1,512
|
Start
|
Top
|
20
|
Cousin
|
42,534
|
1,372
|
Start
|
Low
|
21
|
Scopes trial
|
42,036
|
1,356
|
B
|
High
|
22
|
Ecology
|
41,767
|
1,347
|
GA
|
Top
|
23
|
Binomial nomenclature
|
41,159
|
1,327
|
C
|
Low
|
24
|
Scientific racism
|
39,263
|
1,266
|
C
|
Low
|
25
|
Inbreeding
|
38,264
|
1,234
|
C
|
High
|
26
|
William Jennings Bryan
|
37,624
|
1,213
|
B
|
High
|
27
|
Cro-Magnon
|
37,570
|
1,211
|
GA
|
Mid
|
28
|
Early modern human
|
36,884
|
1,189
|
B
|
Mid
|
29
|
Genetics
|
36,361
|
1,172
|
FA
|
Top
|
30
|
Paleontology
|
33,175
|
1,070
|
GA
|
Top
|
31
|
Natural selection
|
32,422
|
1,045
|
GA
|
Top
|
32
|
On the Origin of Species
|
32,334
|
1,043
|
FA
|
Top
|
33
|
Mutation
|
32,188
|
1,038
|
B
|
Top
|
34
|
Timeline of human evolution
|
32,054
|
1,034
|
C
|
Low
|
35
|
Hybrid (biology)
|
31,364
|
1,011
|
GA
|
High
|
36
|
Altruism
|
29,997
|
967
|
B
|
High
|
37
|
HeLa
|
29,477
|
950
|
C
|
Low
|
38
|
Archaic humans
|
29,179
|
941
|
Start
|
Low
|
39
|
Domestication of the dog
|
28,508
|
919
|
B
|
Low
|
40
|
Origin of language
|
27,315
|
881
|
C
|
Low
|
41
|
Patrilineality
|
26,462
|
853
|
Start
|
Low
|
42
|
Last universal common ancestor
|
26,322
|
849
|
GA
|
Top
|
43
|
Darwinism
|
26,022
|
839
|
Start
|
High
|
44
|
Homo floresiensis
|
25,878
|
834
|
B
|
Mid
|
45
|
Convergent evolution
|
25,352
|
817
|
GA
|
High
|
46
|
Clade
|
24,986
|
806
|
C
|
High
|
47
|
Neontology
|
24,735
|
797
|
Start
|
Mid
|
48
|
Population bottleneck
|
24,723
|
797
|
C
|
High
|
49
|
Cambrian explosion
|
24,627
|
794
|
B
|
High
|
50
|
Anus
|
24,241
|
781
|
Start
|
Mid
|
51
|
Fear
|
23,626
|
762
|
B
|
Low
|
52
|
Lamarckism
|
22,200
|
716
|
GA
|
High
|
53
|
Upper Paleolithic
|
21,917
|
707
|
C
|
Low
|
54
|
Great Oxidation Event
|
21,833
|
704
|
C
|
Mid
|
55
|
Human taxonomy
|
21,149
|
682
|
C
|
Low
|
56
|
Camouflage
|
20,476
|
660
|
GA
|
Mid
|
57
|
Karyotype
|
20,142
|
649
|
C
|
Low
|
58
|
Eusociality
|
19,597
|
632
|
GA
|
Mid
|
59
|
Timeline of the evolutionary history of life
|
19,123
|
616
|
B
|
Top
|
60
|
Institutional racism
|
18,799
|
606
|
B
|
Mid
|
61
|
Haplogroup
|
18,624
|
600
|
C
|
Mid
|
62
|
Selective breeding
|
18,343
|
591
|
C
|
Low
|
63
|
Extant taxon
|
18,279
|
589
|
NA
|
NA
|
64
|
Homology (biology)
|
18,213
|
587
|
GA
|
Top
|
65
|
Matrilineality
|
18,157
|
585
|
C
|
Low
|
66
|
Major histocompatibility complex
|
18,108
|
584
|
B
|
Low
|
67
|
History of life
|
17,842
|
575
|
GA
|
Top
|
68
|
Alfred Russel Wallace
|
17,768
|
573
|
FA
|
Top
|
69
|
Sex differences in intelligence
|
17,713
|
571
|
B
|
Low
|
70
|
Stromatolite
|
17,625
|
568
|
B
|
Mid
|
71
|
Aposematism
|
17,494
|
564
|
GA
|
Mid
|
72
|
Living fossil
|
17,438
|
562
|
C
|
Mid
|
73
|
Stephen Jay Gould
|
16,813
|
542
|
GA
|
Mid
|
74
|
Wallace Line
|
16,453
|
530
|
Start
|
Mid
|
75
|
Nordicism
|
16,425
|
529
|
B
|
Low
|
76
|
Earliest known life forms
|
16,417
|
529
|
C
|
Top
|
77
|
Origin of COVID-19
|
16,086
|
518
|
Start
|
Mid
|
78
|
Sociality
|
16,020
|
516
|
C
|
Mid
|
79
|
Jean-Baptiste Lamarck
|
15,759
|
508
|
B
|
Top
|
80
|
Hardy–Weinberg principle
|
15,623
|
503
|
C
|
High
|
81
|
Survival of the fittest
|
15,601
|
503
|
B
|
Low
|
82
|
Phylogenetics
|
15,544
|
501
|
C
|
High
|
83
|
Ronald Fisher
|
15,213
|
490
|
B
|
High
|
84
|
Eugenics in the United States
|
15,001
|
483
|
Start
|
Low
|
85
|
Antimicrobial resistance
|
14,876
|
479
|
B
|
Unknown
|
86
|
Instinct
|
14,788
|
477
|
C
|
Low
|
87
|
Bipedalism
|
14,785
|
476
|
B
|
Mid
|
88
|
The Selfish Gene
|
14,761
|
476
|
B
|
High
|
89
|
Chicken or the egg
|
14,603
|
471
|
Start
|
Low
|
90
|
Australopithecine
|
14,556
|
469
|
C
|
High
|
91
|
Genetic drift
|
14,383
|
463
|
GA
|
Top
|
92
|
Sexual selection
|
14,378
|
463
|
GA
|
High
|
93
|
Pan (genus)
|
14,338
|
462
|
B
|
High
|
94
|
Domestication of the cat
|
14,240
|
459
|
C
|
Mid
|
95
|
Three-domain system
|
14,192
|
457
|
C
|
Mid
|
96
|
Ediacaran biota
|
14,163
|
456
|
FA
|
Low
|
97
|
Darwin's finches
|
13,899
|
448
|
C
|
High
|
98
|
Tiktaalik
|
13,851
|
446
|
GA
|
High
|
99
|
Mimicry
|
13,801
|
445
|
GA
|
High
|
100
|
Founder effect
|
13,763
|
443
|
C
|
Mid
|
101
|
Vestigiality
|
13,588
|
438
|
C
|
High
|
102
|
Human Y-chromosome DNA haplogroup
|
13,563
|
437
|
C
|
Mid
|
103
|
Thomas Henry Huxley
|
13,326
|
429
|
B
|
Mid
|
104
|
Nazi eugenics
|
12,956
|
417
|
C
|
Low
|
105
|
Triune brain
|
12,909
|
416
|
Start
|
Low
|
106
|
E. O. Wilson
|
12,866
|
415
|
B
|
Mid
|
107
|
Human vestigiality
|
12,814
|
413
|
C
|
Mid
|
108
|
Ernst Haeckel
|
12,528
|
404
|
B
|
High
|
109
|
Evolutionary psychology
|
12,389
|
399
|
C
|
High
|
110
|
Panthera hybrid
|
12,371
|
399
|
C
|
Low
|
111
|
Anthropometry
|
12,257
|
395
|
C
|
Low
|
112
|
Peking Man
|
12,103
|
390
|
GA
|
Mid
|
113
|
Adaptation
|
12,029
|
388
|
GA
|
Top
|
114
|
Great American Interchange
|
11,717
|
377
|
C
|
Mid
|
115
|
Evolution of the horse
|
11,668
|
376
|
B
|
Mid
|
116
|
Fertility
|
11,566
|
373
|
C
|
High
|
117
|
Human mating strategies
|
11,485
|
370
|
B
|
Low
|
118
|
Evolution of mammals
|
11,454
|
369
|
B
|
High
|
119
|
R/K selection theory
|
11,376
|
366
|
C
|
High
|
120
|
Polymorphism (biology)
|
11,339
|
365
|
B
|
High
|
121
|
Behavioral modernity
|
11,325
|
365
|
C
|
Low
|
122
|
Objections to evolution
|
11,277
|
363
|
GA
|
Mid
|
123
|
Evolutionary biology
|
11,274
|
363
|
C
|
Top
|
124
|
Rare Earth hypothesis
|
11,217
|
361
|
B
|
Low
|
125
|
Stoned ape theory
|
11,193
|
361
|
C
|
Low
|
126
|
RNA world
|
11,037
|
356
|
C
|
High
|
127
|
Speciation
|
10,789
|
348
|
C
|
High
|
128
|
Horizontal gene transfer
|
10,685
|
344
|
C
|
High
|
129
|
Origin of birds
|
10,442
|
336
|
B
|
Mid
|
130
|
Red Queen hypothesis
|
10,317
|
332
|
Start
|
Mid
|
131
|
Symbiogenesis
|
10,238
|
330
|
GA
|
High
|
132
|
Most recent common ancestor
|
10,220
|
329
|
B
|
High
|
133
|
List of human evolution fossils
|
10,187
|
328
|
List
|
High
|
134
|
Evolution of sexual reproduction
|
10,168
|
328
|
B
|
High
|
135
|
Primordial soup
|
9,982
|
322
|
Start
|
Mid
|
136
|
Adaptive radiation
|
9,959
|
321
|
Start
|
High
|
137
|
J. B. S. Haldane
|
9,794
|
315
|
C
|
Mid
|
138
|
Lek mating
|
9,709
|
313
|
GA
|
Mid
|
139
|
Recent human evolution
|
9,459
|
305
|
B
|
Mid
|
140
|
Cladistics
|
9,456
|
305
|
C
|
Mid
|
141
|
Symmetry in biology
|
9,310
|
300
|
C
|
High
|
142
|
CpG site
|
9,276
|
299
|
C
|
Mid
|
143
|
Punctuated equilibrium
|
9,252
|
298
|
GA
|
High
|
144
|
Monophyly
|
9,197
|
296
|
C
|
Mid
|
145
|
Common descent
|
8,976
|
289
|
C
|
Top
|
146
|
Basal (phylogenetics)
|
8,946
|
288
|
C
|
Mid
|
147
|
Linnaean taxonomy
|
8,890
|
286
|
C
|
Mid
|
148
|
Julian Huxley
|
8,873
|
286
|
B
|
Mid
|
149
|
Evolutionary history of plants
|
8,865
|
285
|
B
|
High
|
150
|
Lower Paleolithic
|
8,805
|
284
|
C
|
High
|
151
|
Female promiscuity
|
8,733
|
281
|
C
|
Low
|
152
|
Allopatric speciation
|
8,709
|
280
|
C
|
High
|
153
|
Signalling theory
|
8,700
|
280
|
GA
|
Mid
|
154
|
Offspring
|
8,692
|
280
|
Start
|
Mid
|
155
|
Genetic diversity
|
8,688
|
280
|
C
|
Mid
|
156
|
Homo longi
|
8,651
|
279
|
GA
|
Low
|
157
|
Feathered dinosaur
|
8,627
|
278
|
C
|
High
|
158
|
Sexual cannibalism
|
8,556
|
276
|
B
|
Low
|
159
|
Felid hybrids
|
8,539
|
275
|
Start
|
Low
|
160
|
Autosome
|
8,440
|
272
|
Start
|
High
|
161
|
Biogeography
|
8,434
|
272
|
Start
|
Mid
|
162
|
Human mitochondrial DNA haplogroup
|
8,399
|
270
|
Start
|
Mid
|
163
|
History of evolutionary thought
|
8,248
|
266
|
FA
|
Top
|
164
|
Evolutionary algorithm
|
8,110
|
261
|
C
|
Low
|
165
|
Island gigantism
|
8,100
|
261
|
Start
|
Low
|
166
|
Sex differences in human physiology
|
8,092
|
261
|
C
|
High
|
167
|
Fitness (biology)
|
7,923
|
255
|
B
|
High
|
168
|
Species complex
|
7,708
|
248
|
B
|
Mid
|
169
|
Bergmann's rule
|
7,707
|
248
|
C
|
Low
|
170
|
Evolutionary origin of religion
|
7,666
|
247
|
C
|
Low
|
171
|
Evolution of human intelligence
|
7,513
|
242
|
Start
|
High
|
172
|
Insular dwarfism
|
7,429
|
239
|
C
|
Low
|
173
|
Middle Paleolithic
|
7,316
|
236
|
C
|
High
|
174
|
Evolution of fish
|
7,299
|
235
|
C
|
High
|
175
|
Population genetics
|
7,247
|
233
|
C
|
High
|
176
|
Missing link (human evolution)
|
7,147
|
230
|
Start
|
Mid
|
177
|
Jebel Irhoud
|
7,103
|
229
|
C
|
Low
|
178
|
Evolution of cetaceans
|
7,094
|
228
|
GA
|
Mid
|
179
|
Gene flow
|
7,091
|
228
|
Start
|
High
|
180
|
Recapitulation theory
|
7,011
|
226
|
C
|
Mid
|
181
|
Variability hypothesis
|
6,912
|
222
|
C
|
Low
|
182
|
Inbreeding depression
|
6,879
|
221
|
Start
|
Mid
|
183
|
Sex differences in psychology
|
6,817
|
219
|
C
|
High
|
184
|
Aquatic ape hypothesis
|
6,802
|
219
|
C
|
Low
|
185
|
Cladogram
|
6,710
|
216
|
C
|
Mid
|
186
|
List of related male and female reproductive organs
|
6,648
|
214
|
List
|
Mid
|
187
|
Frameshift mutation
|
6,617
|
213
|
B
|
High
|
188
|
Batesian mimicry
|
6,586
|
212
|
GA
|
Mid
|
189
|
Evolution of primates
|
6,506
|
209
|
Start
|
Low
|
190
|
Religious views of Charles Darwin
|
6,457
|
208
|
B
|
Low
|
191
|
Spiral Dynamics
|
6,398
|
206
|
C
|
Low
|
192
|
Genetic variation
|
6,315
|
203
|
Start
|
High
|
193
|
Transitional fossil
|
6,302
|
203
|
GA
|
Top
|
194
|
The Descent of Man, and Selection in Relation to Sex
|
6,235
|
201
|
Start
|
High
|
195
|
Anisogamy
|
6,202
|
200
|
C
|
High
|
196
|
Ontogeny
|
6,178
|
199
|
B
|
High
|
197
|
Introduction to evolution
|
6,161
|
198
|
B
|
Mid
|
198
|
Islamic views on evolution
|
6,053
|
195
|
C
|
Low
|
199
|
Thomas Hunt Morgan
|
6,015
|
194
|
B
|
High
|
200
|
Heather Heying
|
6,005
|
193
|
Start
|
Low
|
201
|
Anatomically modern human
|
5,986
|
193
|
NA
|
NA
|
202
|
Peppered moth evolution
|
5,967
|
192
|
GA
|
High
|
203
|
Sexual selection in humans
|
5,944
|
191
|
C
|
Low
|
204
|
Evolution of birds
|
5,927
|
191
|
C
|
High
|
205
|
Modern synthesis (20th century)
|
5,908
|
190
|
GA
|
High
|
206
|
Evolution of the wolf
|
5,846
|
188
|
B
|
Low
|
207
|
Sympatric speciation
|
5,750
|
185
|
Start
|
Mid
|
208
|
Assortative mating
|
5,700
|
183
|
C
|
Mid
|
209
|
Sexy son hypothesis
|
5,689
|
183
|
C
|
Mid
|
210
|
Sequence homology
|
5,636
|
181
|
C
|
High
|
211
|
Apomorphy and synapomorphy
|
5,628
|
181
|
C
|
Low
|
212
|
Divergent evolution
|
5,538
|
178
|
Start
|
Mid
|
213
|
Aggressive mimicry
|
5,530
|
178
|
GA
|
Mid
|
214
|
Complex adaptive system
|
5,516
|
177
|
C
|
Mid
|
215
|
Kin selection
|
5,411
|
174
|
GA
|
High
|
216
|
Evolution as fact and theory
|
5,410
|
174
|
C
|
Low
|
217
|
Reproductive isolation
|
5,206
|
167
|
C
|
High
|
218
|
Climate change adaptation
|
5,167
|
166
|
B
|
Mid
|
219
|
Evolution of the brain
|
5,164
|
166
|
Start
|
High
|
220
|
History of eugenics
|
5,158
|
166
|
B
|
Low
|
221
|
Müllerian mimicry
|
5,045
|
162
|
GA
|
Mid
|
222
|
Incertae sedis
|
5,036
|
162
|
C
|
Low
|
223
|
Rejection of evolution by religious groups
|
4,989
|
160
|
B
|
High
|
224
|
Speculative evolution
|
4,958
|
159
|
B
|
Low
|
225
|
Human sperm competition
|
4,907
|
158
|
C
|
Low
|
226
|
History of biology
|
4,836
|
156
|
FA
|
High
|
227
|
Maladaptation
|
4,811
|
155
|
Start
|
Mid
|
228
|
Neo-Darwinism
|
4,802
|
154
|
Start
|
Mid
|
229
|
The Naked Woman
|
4,779
|
154
|
Stub
|
Low
|
230
|
Relict (biology)
|
4,727
|
152
|
C
|
Mid
|
231
|
Handicap principle
|
4,667
|
150
|
GA
|
High
|
232
|
First universal common ancestor
|
4,645
|
149
|
Start
|
Unknown
|
233
|
Crown group
|
4,553
|
146
|
C
|
Mid
|
234
|
Directional selection
|
4,497
|
145
|
Start
|
Mid
|
235
|
Allele frequency
|
4,458
|
143
|
Start
|
Mid
|
236
|
Hunter versus farmer hypothesis
|
4,399
|
141
|
C
|
Low
|
237
|
Fisher's principle
|
4,398
|
141
|
Start
|
Mid
|
238
|
Evolution of the eye
|
4,392
|
141
|
C
|
High
|
239
|
Coevolution
|
4,391
|
141
|
GA
|
High
|
240
|
Peppered moth
|
4,382
|
141
|
B
|
Low
|
241
|
Level of support for evolution
|
4,359
|
140
|
C
|
Mid
|
242
|
Protocell
|
4,314
|
139
|
C
|
Mid
|
243
|
Systematics
|
4,302
|
138
|
C
|
High
|
244
|
Neanderthal genetics
|
4,295
|
138
|
C
|
High
|
245
|
Lagerstätte
|
4,257
|
137
|
B
|
Mid
|
246
|
Japanese Paleolithic
|
4,242
|
136
|
Start
|
High
|
247
|
List of examples of convergent evolution
|
4,241
|
136
|
List
|
High
|
248
|
Multiregional origin of modern humans
|
4,224
|
136
|
C
|
Mid
|
249
|
Spandrel (biology)
|
4,206
|
135
|
B
|
Mid
|
250
|
Gene duplication
|
4,191
|
135
|
C
|
Mid
|
251
|
Australopithecus sediba
|
4,183
|
134
|
GA
|
Low
|
252
|
Altruism (biology)
|
4,170
|
134
|
C
|
Mid
|
253
|
Self-preservation
|
4,169
|
134
|
C
|
High
|
254
|
Purple Earth hypothesis
|
4,137
|
133
|
Stub
|
Mid
|
255
|
Evolutionary developmental biology
|
4,062
|
131
|
GA
|
High
|
256
|
Evolutionary game theory
|
4,029
|
129
|
C
|
High
|
257
|
Devolution (biology)
|
4,014
|
129
|
C
|
Low
|
258
|
Herto Man
|
4,010
|
129
|
GA
|
Low
|
259
|
Haplodiploidy
|
3,984
|
128
|
C
|
Mid
|
260
|
Sperm competition
|
3,951
|
127
|
Start
|
Mid
|
261
|
Phenotypic plasticity
|
3,922
|
126
|
C
|
Mid
|
262
|
Sister group
|
3,911
|
126
|
Start
|
Low
|
263
|
Four Fs (evolution)
|
3,894
|
125
|
C
|
Low
|
264
|
Parental investment
|
3,893
|
125
|
Start
|
High
|
265
|
March of Progress
|
3,853
|
124
|
C
|
Low
|
266
|
Fisherian runaway
|
3,804
|
122
|
Start
|
Low
|
267
|
Evidence of common descent
|
3,778
|
121
|
B
|
Mid
|
268
|
Killer ape theory
|
3,775
|
121
|
Start
|
Low
|
269
|
Ernst Mayr
|
3,752
|
121
|
C
|
High
|
270
|
Stabilizing selection
|
3,739
|
120
|
Start
|
Mid
|
271
|
Gene polymorphism
|
3,720
|
120
|
Start
|
Mid
|
272
|
Allometry
|
3,649
|
117
|
C
|
Mid
|
273
|
Orthogenesis
|
3,595
|
115
|
GA
|
Mid
|
274
|
Parental care
|
3,587
|
115
|
B
|
Mid
|
275
|
Evolution of reptiles
|
3,573
|
115
|
C
|
High
|
276
|
Future generations
|
3,565
|
115
|
Start
|
Low
|
277
|
Kenyanthropus
|
3,550
|
114
|
GA
|
Low
|
278
|
Disruptive selection
|
3,536
|
114
|
C
|
Mid
|
279
|
List of fossil sites
|
3,527
|
113
|
List
|
Top
|
280
|
Geological history of oxygen
|
3,493
|
112
|
C
|
Low
|
281
|
Evolutionism
|
3,444
|
111
|
C
|
Mid
|
282
|
Solo Man
|
3,437
|
110
|
FA
|
Low
|
283
|
Acceptance of evolution by religious groups
|
3,398
|
109
|
C
|
Low
|
284
|
Life history theory
|
3,394
|
109
|
C
|
High
|
285
|
Island syndrome
|
3,390
|
109
|
Start
|
Unknown
|
286
|
E. coli long-term evolution experiment
|
3,365
|
108
|
B
|
Mid
|
287
|
Reciprocal altruism
|
3,311
|
106
|
B
|
Mid
|
288
|
The Expression of the Emotions in Man and Animals
|
3,295
|
106
|
Start
|
Mid
|
289
|
Expelled: No Intelligence Allowed
|
3,292
|
106
|
B
|
Low
|
290
|
Evolutionary computation
|
3,282
|
105
|
C
|
High
|
291
|
Exaptation
|
3,281
|
105
|
C
|
High
|
292
|
Body plan
|
3,252
|
104
|
C
|
Mid
|
293
|
Evolutionarily stable strategy
|
3,241
|
104
|
B
|
Mid
|
294
|
Ring species
|
3,229
|
104
|
C
|
High
|
295
|
Sexual conflict
|
3,176
|
102
|
Start
|
High
|
296
|
History of ecology
|
3,167
|
102
|
C
|
Mid
|
297
|
Macroevolution
|
3,155
|
101
|
B
|
Top
|
298
|
Theodosius Dobzhansky
|
3,142
|
101
|
C
|
Mid
|
299
|
Germline mutation
|
3,096
|
99
|
B
|
High
|
300
|
Why Is Sex Fun?
|
3,090
|
99
|
C
|
Low
|
301
|
Sociobiological theories of rape
|
3,088
|
99
|
C
|
Mid
|
302
|
Stotting
|
3,077
|
99
|
GA
|
Low
|
303
|
Cline (biology)
|
3,052
|
98
|
C
|
Low
|
304
|
Gene pool
|
3,041
|
98
|
Start
|
High
|
305
|
Hominina
|
3,022
|
97
|
NA
|
NA
|
306
|
Endurance running hypothesis
|
3,021
|
97
|
Start
|
Low
|
307
|
Domestication syndrome
|
2,991
|
96
|
C
|
Low
|
308
|
Eukaryogenesis
|
2,978
|
96
|
C
|
High
|
309
|
Group selection
|
2,967
|
95
|
GA
|
High
|
310
|
Evolution of photosynthesis
|
2,966
|
95
|
Start
|
High
|
311
|
The Blind Watchmaker
|
2,964
|
95
|
C
|
Mid
|
312
|
Parallel evolution
|
2,945
|
95
|
Start
|
High
|
313
|
Gene-centered view of evolution
|
2,936
|
94
|
B
|
High
|
314
|
Fish intelligence
|
2,880
|
92
|
B
|
Low
|
315
|
Alternatives to Darwinian evolution
|
2,868
|
92
|
B
|
Mid
|
316
|
Evolutionary pressure
|
2,796
|
90
|
C
|
Mid
|
317
|
Mach bands
|
2,790
|
90
|
Start
|
Mid
|
318
|
Ursid hybrid
|
2,700
|
87
|
C
|
Low
|
319
|
W. D. Hamilton
|
2,695
|
86
|
C
|
Low
|
320
|
Alloparenting
|
2,692
|
86
|
C
|
Low
|
321
|
Clonally transmissible cancer
|
2,671
|
86
|
C
|
Low
|
322
|
Grandmother hypothesis
|
2,656
|
85
|
C
|
Mid
|
323
|
Inclusive fitness
|
2,642
|
85
|
C
|
High
|
324
|
Somatic mutation
|
2,641
|
85
|
C
|
Low
|
325
|
Muller's ratchet
|
2,628
|
84
|
Start
|
Mid
|
326
|
Beta diversity
|
2,620
|
84
|
C
|
Mid
|
327
|
Struggle for existence
|
2,582
|
83
|
C
|
Mid
|
328
|
Microevolution
|
2,575
|
83
|
C
|
High
|
329
|
The Spandrels of San Marco and the Panglossian Paradigm
|
2,573
|
83
|
Start
|
Mid
|
330
|
Cro-Magnon rock shelter
|
2,571
|
82
|
Start
|
Mid
|
331
|
Evolution of tetrapods
|
2,564
|
82
|
C
|
High
|
332
|
John Maynard Smith
|
2,554
|
82
|
C
|
High
|
333
|
Neutral theory of molecular evolution
|
2,542
|
82
|
Start
|
High
|
334
|
Coalescent theory
|
2,533
|
81
|
C
|
Low
|
335
|
Parapatric speciation
|
2,498
|
80
|
C
|
Mid
|
336
|
Molecular evolution
|
2,479
|
79
|
C
|
Top
|
337
|
Creation and evolution in public education
|
2,461
|
79
|
B
|
Mid
|
338
|
Rotating locomotion in living systems
|
2,440
|
78
|
FA
|
High
|
339
|
Human skeletal changes due to bipedalism
|
2,422
|
78
|
B
|
Mid
|
340
|
Shadow biosphere
|
2,387
|
77
|
Start
|
Mid
|
341
|
Evolutionary radiation
|
2,348
|
75
|
Start
|
Mid
|
342
|
Pangenesis
|
2,346
|
75
|
C
|
Low
|
343
|
Homo sapiens sapiens
|
2,338
|
75
|
NA
|
NA
|
344
|
Evolution of morality
|
2,329
|
75
|
C
|
High
|
345
|
Duane Gish
|
2,294
|
74
|
C
|
Low
|
346
|
Two-domain system
|
2,278
|
73
|
C
|
Low
|
347
|
Panmixia
|
2,269
|
73
|
Start
|
Mid
|
348
|
Haldane's rule
|
2,268
|
73
|
C
|
Low
|
349
|
Origin of speech
|
2,267
|
73
|
C
|
Mid
|
350
|
Radiation hormesis
|
2,242
|
72
|
B
|
Mid
|
351
|
August Weismann
|
2,242
|
72
|
Start
|
High
|
352
|
Evolutionary taxonomy
|
2,231
|
71
|
C
|
Mid
|
353
|
Evolution of cells
|
2,132
|
68
|
Start
|
High
|
354
|
Heterochrony
|
2,129
|
68
|
GA
|
Mid
|
355
|
Evolutionary arms race
|
2,078
|
67
|
Start
|
High
|
356
|
Genotype–phenotype distinction
|
2,064
|
66
|
Start
|
High
|
357
|
Meganthropus
|
2,053
|
66
|
Start
|
Low
|
358
|
Disappearing blonde gene
|
2,008
|
64
|
Start
|
Low
|
359
|
Evolutionary mismatch
|
2,004
|
64
|
C
|
Low
|
360
|
Peripatric speciation
|
2,003
|
64
|
B
|
Mid
|
361
|
Asa Gray
|
1,998
|
64
|
GA
|
Low
|
362
|
Codon usage bias
|
1,990
|
64
|
B
|
Low
|
363
|
Evolutionary anachronism
|
1,982
|
63
|
List
|
Mid
|
364
|
Darwin's Dangerous Idea
|
1,976
|
63
|
C
|
Mid
|
365
|
Outgroup (cladistics)
|
1,960
|
63
|
Start
|
Mid
|
366
|
Bateman's principle
|
1,953
|
63
|
B
|
Mid
|
367
|
Computational phylogenetics
|
1,938
|
62
|
C
|
Mid
|
368
|
Models of DNA evolution
|
1,905
|
61
|
B
|
Low
|
369
|
Heterozygote advantage
|
1,902
|
61
|
Start
|
Mid
|
370
|
Negative selection (natural selection)
|
1,900
|
61
|
Stub
|
Mid
|
371
|
Gene family
|
1,894
|
61
|
C
|
High
|
372
|
Racist
|
1,886
|
60
|
NA
|
NA
|
373
|
Price equation
|
1,881
|
60
|
C
|
Low
|
374
|
Late Stone Age
|
1,881
|
60
|
Start
|
Low
|
375
|
Jerry Coyne
|
1,878
|
60
|
Start
|
Low
|
376
|
Evolution of flagella
|
1,875
|
60
|
Start
|
Mid
|
377
|
Mutationism
|
1,857
|
59
|
GA
|
Low
|
378
|
Fitness landscape
|
1,853
|
59
|
B
|
High
|
379
|
The Third Chimpanzee
|
1,830
|
59
|
C
|
Low
|
380
|
Background extinction rate
|
1,827
|
58
|
Start
|
Mid
|
381
|
Primitive (phylogenetics)
|
1,811
|
58
|
Start
|
Mid
|
382
|
Baldwin effect
|
1,803
|
58
|
GA
|
Low
|
383
|
Oceanic dispersal
|
1,802
|
58
|
Start
|
Low
|
384
|
Homoplasy
|
1,797
|
57
|
Start
|
Low
|
385
|
Peptide nucleic acid
|
1,777
|
57
|
Start
|
Low
|
386
|
Bird hybrid
|
1,754
|
56
|
Start
|
Low
|
387
|
Evolution of cephalopods
|
1,751
|
56
|
C
|
Low
|
388
|
Reproductive success
|
1,747
|
56
|
Start
|
High
|
389
|
Red Deer Cave people
|
1,735
|
55
|
Start
|
Low
|
390
|
Down House
|
1,728
|
55
|
C
|
Low
|
391
|
Siblicide
|
1,716
|
55
|
Start
|
Low
|
392
|
Robert Trivers
|
1,712
|
55
|
Start
|
Low
|
393
|
Tend and befriend
|
1,711
|
55
|
C
|
Low
|
394
|
Biology and political orientation
|
1,697
|
54
|
C
|
Low
|
395
|
Metapopulation
|
1,696
|
54
|
B
|
Mid
|
396
|
Indel
|
1,694
|
54
|
Start
|
Mid
|
397
|
Evolution of mammalian auditory ossicles
|
1,682
|
54
|
B
|
Mid
|
398
|
Nuptial gift
|
1,660
|
53
|
Start
|
Mid
|
399
|
Satoshi Kanazawa
|
1,656
|
53
|
C
|
Unknown
|
400
|
Extended evolutionary synthesis
|
1,642
|
52
|
B
|
High
|
401
|
Modern humans
|
1,640
|
52
|
NA
|
NA
|
402
|
Evolution of snake venom
|
1,618
|
52
|
GA
|
Mid
|
403
|
Red dress effect
|
1,617
|
52
|
Start
|
Low
|
404
|
Embryological origins of the mouth and anus
|
1,580
|
50
|
Start
|
Low
|
405
|
Ka/Ks ratio
|
1,578
|
50
|
C
|
Mid
|
406
|
Snow camouflage
|
1,576
|
50
|
GA
|
Low
|
407
|
Evolution of biological complexity
|
1,568
|
50
|
C
|
Mid
|
408
|
Aerobic fermentation
|
1,535
|
49
|
B
|
Low
|
409
|
Racism in the LGBT community
|
1,526
|
49
|
C
|
Low
|
410
|
Grimaldi man
|
1,506
|
48
|
C
|
Low
|
411
|
Angraecum sesquipedale
|
1,502
|
48
|
B
|
Mid
|
412
|
Evolution of emotion
|
1,500
|
48
|
Start
|
Unknown
|
413
|
Evolutionary psychology of religion
|
1,473
|
47
|
Start
|
Low
|
414
|
Sexual selection in birds
|
1,465
|
47
|
C
|
Low
|
415
|
Population structure (genetics)
|
1,464
|
47
|
Start
|
Low
|
416
|
Experimental evolution
|
1,459
|
47
|
Start
|
High
|
417
|
1860 Oxford evolution debate
|
1,454
|
46
|
B
|
Mid
|
418
|
Junkyard tornado
|
1,450
|
46
|
C
|
Low
|
419
|
Character displacement
|
1,450
|
46
|
B
|
Mid
|
420
|
Numerical taxonomy
|
1,442
|
46
|
Start
|
Mid
|
421
|
Isua Greenstone Belt
|
1,435
|
46
|
C
|
Mid
|
422
|
Teleology in biology
|
1,432
|
46
|
GA
|
High
|
423
|
Genetic divergence
|
1,427
|
46
|
Start
|
High
|
424
|
History of anthropometry
|
1,426
|
46
|
C
|
Low
|
425
|
Taforalt
|
1,421
|
45
|
C
|
Low
|
426
|
Saltation (biology)
|
1,396
|
45
|
C
|
Mid
|
427
|
Initial Upper Paleolithic
|
1,383
|
44
|
B
|
Unknown
|
428
|
Anagenesis
|
1,382
|
44
|
C
|
Mid
|
429
|
Genetic pollution
|
1,374
|
44
|
C
|
Low
|
430
|
Jewish views on evolution
|
1,370
|
44
|
B
|
Low
|
431
|
Acritarch
|
1,365
|
44
|
C
|
Low
|
432
|
Nothing in Biology Makes Sense Except in the Light of Evolution
|
1,365
|
44
|
C
|
Mid
|
433
|
Endosymbiotic theory
|
1,362
|
43
|
NA
|
NA
|
434
|
Population biology
|
1,360
|
43
|
Stub
|
Low
|
435
|
Major histocompatibility complex and sexual selection
|
1,356
|
43
|
C
|
Mid
|
436
|
Balancing selection
|
1,356
|
43
|
Start
|
Mid
|
437
|
Evolutionary anthropology
|
1,353
|
43
|
Start
|
Low
|
438
|
Embryonic diapause
|
1,337
|
43
|
Start
|
Low
|
439
|
George R. Price
|
1,326
|
42
|
C
|
Low
|
440
|
Evolution of bacteria
|
1,325
|
42
|
C
|
Mid
|
441
|
Frequency-dependent selection
|
1,323
|
42
|
Start
|
High
|
442
|
Parasite-stress theory
|
1,322
|
42
|
C
|
Mid
|
443
|
Ovulatory shift hypothesis
|
1,314
|
42
|
GA
|
Low
|
444
|
Iron–sulfur world hypothesis
|
1,313
|
42
|
C
|
Low
|
445
|
Niche construction
|
1,311
|
42
|
B
|
Low
|
446
|
Snake detection theory
|
1,303
|
42
|
Start
|
Mid
|
447
|
Neural Darwinism
|
1,300
|
41
|
C
|
Unknown
|
448
|
Blending inheritance
|
1,298
|
41
|
GA
|
Low
|
449
|
Entrainment (biomusicology)
|
1,296
|
41
|
Start
|
Low
|
450
|
List of prehistoric cartilaginous fish genera
|
1,294
|
41
|
List
|
Mid
|
451
|
Budgerigar colour genetics
|
1,290
|
41
|
Start
|
Low
|
452
|
Mating call
|
1,281
|
41
|
C
|
Low
|
453
|
Green-beard effect
|
1,280
|
41
|
Start
|
Low
|
454
|
Origin of avian flight
|
1,270
|
40
|
Start
|
Mid
|
455
|
Diana Fleischman
|
1,250
|
40
|
Start
|
Low
|
456
|
Hybrid fruit
|
1,241
|
40
|
Stub
|
Low
|
457
|
Evolutionary approaches to depression
|
1,238
|
39
|
Start
|
Low
|
458
|
Cooperation (evolution)
|
1,235
|
39
|
B
|
Mid
|
459
|
Evolution of nervous systems
|
1,229
|
39
|
B
|
Mid
|
460
|
Synonymous substitution
|
1,216
|
39
|
Start
|
Mid
|
461
|
Reinforcement (speciation)
|
1,211
|
39
|
GA
|
Mid
|
462
|
Incomplete lineage sorting
|
1,209
|
39
|
Start
|
Mid
|
463
|
Paternal care
|
1,205
|
38
|
C
|
Low
|
464
|
Elizabeth, Lady Hope
|
1,198
|
38
|
C
|
Low
|
465
|
Systemic racism
|
1,195
|
38
|
NA
|
NA
|
466
|
David Krakauer (scientist)
|
1,185
|
38
|
Start
|
Low
|
467
|
Cognitive tradeoff hypothesis
|
1,176
|
37
|
C
|
Low
|
468
|
Dmanisi
|
1,170
|
37
|
Start
|
Mid
|
469
|
David Sloan Wilson
|
1,168
|
37
|
Start
|
Unknown
|
470
|
Adaptationism
|
1,166
|
37
|
Start
|
Mid
|
471
|
Mate value
|
1,165
|
37
|
C
|
Low
|
472
|
Evolution of lemurs
|
1,154
|
37
|
FA
|
Low
|
473
|
Phenetics
|
1,151
|
37
|
Start
|
Mid
|
474
|
Joan Roughgarden
|
1,145
|
36
|
C
|
Unknown
|
475
|
Bayesian inference in phylogeny
|
1,142
|
36
|
C
|
Low
|
476
|
Timeline of fish evolution
|
1,137
|
36
|
List
|
Low
|
477
|
Project Steve
|
1,134
|
36
|
C
|
Low
|
478
|
Single-access key
|
1,132
|
36
|
C
|
Low
|
479
|
Female sperm storage
|
1,130
|
36
|
C
|
Low
|
480
|
Of Pandas and People
|
1,111
|
35
|
C
|
Low
|
481
|
Josiah C. Nott
|
1,107
|
35
|
C
|
Low
|
482
|
Bruniquel Cave
|
1,101
|
35
|
Start
|
Mid
|
483
|
Snaiad
|
1,100
|
35
|
B
|
Low
|
484
|
Endemism in the Hawaiian Islands
|
1,094
|
35
|
Start
|
Low
|
485
|
Artificial selection
|
1,088
|
35
|
NA
|
NA
|
486
|
Extinction vortex
|
1,081
|
34
|
Start
|
Low
|
487
|
Caveasphaera
|
1,078
|
34
|
Start
|
Low
|
488
|
Wonderful Life (book)
|
1,074
|
34
|
Stub
|
Low
|
489
|
Plant evolution
|
1,070
|
34
|
Start
|
High
|
490
|
Motion camouflage
|
1,070
|
34
|
GA
|
Low
|
491
|
Universal Darwinism
|
1,070
|
34
|
C
|
Low
|
492
|
History of creationism
|
1,059
|
34
|
B
|
Mid
|
493
|
Genotype frequency
|
1,058
|
34
|
Start
|
Mid
|
494
|
Extended female sexuality
|
1,047
|
33
|
B
|
Mid
|
495
|
Strategic pluralism
|
1,035
|
33
|
Stub
|
Low
|
496
|
Protein superfamily
|
1,035
|
33
|
B
|
Mid
|
497
|
Jonathan Wells (intelligent design advocate)
|
1,028
|
33
|
Start
|
Low
|
498
|
Androgenesis
|
1,018
|
32
|
C
|
Low
|
499
|
Dollo's law of irreversibility
|
1,017
|
32
|
Start
|
High
|
500
|
Evolution of color vision in primates
|
1,007
|
32
|
C
|
Low
|
501
|
Evolution of ageing
|
1,003
|
32
|
B
|
High
|
502
|
Chemical defense
|
992
|
32
|
C
|
Low
|
503
|
Operational sex ratio
|
991
|
31
|
Start
|
Low
|
504
|
The Greatest Show on Earth: The Evidence for Evolution
|
989
|
31
|
Start
|
Low
|
505
|
Savannah hypothesis
|
981
|
31
|
Start
|
Low
|
506
|
Canalisation (genetics)
|
977
|
31
|
Start
|
Mid
|
507
|
Trivers–Willard hypothesis
|
975
|
31
|
Start
|
Low
|
508
|
Crocoduck
|
966
|
31
|
C
|
Low
|
509
|
Sociobiology: The New Synthesis
|
960
|
30
|
GA
|
Mid
|
510
|
Conservative replacement
|
959
|
30
|
Start
|
Low
|
511
|
Troglomorphism
|
953
|
30
|
Stub
|
Low
|
512
|
Lagar Velho 1
|
951
|
30
|
Stub
|
Low
|
513
|
Parent–offspring conflict
|
949
|
30
|
Start
|
Mid
|
514
|
Davis's law
|
942
|
30
|
Start
|
Low
|
515
|
Motoo Kimura
|
939
|
30
|
B
|
High
|
516
|
Seminal fluid protein
|
932
|
30
|
Start
|
Low
|
517
|
Lantian Man
|
928
|
29
|
GA
|
Low
|
518
|
Henry Walter Bates
|
919
|
29
|
C
|
High
|
519
|
Domestication of the goat
|
918
|
29
|
B
|
Mid
|
520
|
Race suicide
|
910
|
29
|
Start
|
Mid
|
521
|
Polyphenism
|
909
|
29
|
Start
|
Mid
|
522
|
Telescoping generations
|
907
|
29
|
Stub
|
Unknown
|
523
|
Autapomorphy
|
905
|
29
|
C
|
Low
|
524
|
Sexual selection in mammals
|
900
|
29
|
C
|
Low
|
525
|
Cladogenesis
|
892
|
28
|
Start
|
Mid
|
526
|
Mormon views on evolution
|
891
|
28
|
C
|
Low
|
527
|
Evolution of color vision
|
882
|
28
|
Start
|
Low
|
528
|
Sperm Wars
|
881
|
28
|
Start
|
Mid
|
529
|
Evolutionary ecology
|
879
|
28
|
C
|
Mid
|
530
|
Natural Theology or Evidences of the Existence and Attributes of the Deity
|
876
|
28
|
GA
|
Low
|
531
|
Cryptic female choice
|
872
|
28
|
B
|
Low
|
532
|
List of non-avian dinosaur species preserved with evidence of feathers
|
869
|
28
|
List
|
Low
|
533
|
Allogamy
|
867
|
27
|
Start
|
Mid
|
534
|
Polytomy
|
866
|
27
|
Start
|
Mid
|
535
|
Disposable soma theory of aging
|
866
|
27
|
C
|
Mid
|
536
|
Last eukaryotic common ancestor
|
863
|
27
|
NA
|
High
|
537
|
Outline of evolution
|
848
|
27
|
List
|
Top
|
538
|
Yuanmou Man
|
836
|
26
|
GA
|
Low
|
539
|
Ornithophily
|
827
|
26
|
B
|
Low
|
540
|
List of transitional fossils
|
822
|
26
|
NA
|
NA
|
541
|
Social selection
|
820
|
26
|
C
|
Low
|
542
|
Gut (anatomy)
|
812
|
26
|
NA
|
Low
|
543
|
Phyletic gradualism
|
798
|
25
|
Start
|
Mid
|
544
|
Evolutionary suicide
|
780
|
25
|
Start
|
Low
|
545
|
Koobi Fora
|
774
|
24
|
C
|
Mid
|
546
|
Cytotaxonomy
|
771
|
24
|
Stub
|
Mid
|
547
|
List of Neanderthal fossils
|
761
|
24
|
List
|
Low
|
548
|
The Red Queen: Sex and the Evolution of Human Nature
|
759
|
24
|
Start
|
Low
|
549
|
The Genetical Theory of Natural Selection
|
756
|
24
|
Start
|
Mid
|
550
|
Evolutionary psychiatry
|
755
|
24
|
Stub
|
Low
|
551
|
Fisher's fundamental theorem of natural selection
|
742
|
23
|
Start
|
Mid
|
552
|
Mosaic evolution
|
740
|
23
|
Start
|
Low
|
553
|
Vertebrate land invasion
|
740
|
23
|
C
|
Mid
|
554
|
Phylogenetic comparative methods
|
737
|
23
|
C
|
Low
|
555
|
Costly signaling theory in evolutionary psychology
|
733
|
23
|
C
|
Mid
|
556
|
Elaine Morgan
|
732
|
23
|
C
|
Low
|
557
|
Selection coefficient
|
726
|
23
|
Stub
|
Mid
|
558
|
George Christopher Williams
|
726
|
23
|
Start
|
Mid
|
559
|
Island hopping
|
723
|
23
|
NA
|
Low
|
560
|
Emsleyan mimicry
|
719
|
23
|
C
|
Low
|
561
|
Hologenome theory of evolution
|
714
|
23
|
Start
|
Mid
|
562
|
Muscular evolution in humans
|
714
|
23
|
Start
|
Low
|
563
|
Genetic isolate
|
707
|
22
|
Stub
|
Low
|
564
|
Evolvability
|
705
|
22
|
C
|
High
|
565
|
Bet hedging (biology)
|
703
|
22
|
B
|
Mid
|
566
|
Host–parasite coevolution
|
699
|
22
|
GA
|
Mid
|
567
|
Ecological speciation
|
699
|
22
|
B
|
High
|
568
|
Cooperative eye hypothesis
|
697
|
22
|
Start
|
Low
|
569
|
The Vital Question
|
697
|
22
|
GA
|
Low
|
570
|
Robert Edmond Grant
|
696
|
22
|
Start
|
Low
|
571
|
Bias in the introduction of variation
|
688
|
22
|
B
|
Low
|
572
|
Cope's rule
|
682
|
22
|
Start
|
Mid
|
573
|
Konstantin Mereschkowski
|
681
|
21
|
GA
|
Unknown
|
574
|
Group living
|
681
|
21
|
Start
|
Low
|
575
|
Rate of evolution
|
678
|
21
|
Start
|
Low
|
576
|
Genetic erosion
|
671
|
21
|
C
|
Low
|
577
|
Schizocoely
|
655
|
21
|
Start
|
Mid
|
578
|
Darwinian demon
|
648
|
20
|
Stub
|
Low
|
579
|
Haplogroup C-V20
|
648
|
20
|
Unknown
|
Unknown
|
580
|
Kettlewell's experiment
|
646
|
20
|
Start
|
Mid
|
581
|
Alternative abiogenesis scenarios
|
643
|
20
|
C
|
Low
|
582
|
Edward Blyth
|
643
|
20
|
B
|
High
|
583
|
The 10,000 Year Explosion
|
642
|
20
|
B
|
Mid
|
584
|
Weasel program
|
642
|
20
|
B
|
Low
|
585
|
Hybrid zone
|
639
|
20
|
C
|
Mid
|
586
|
Disassortative mating
|
636
|
20
|
C
|
Mid
|
587
|
Caminalcules
|
634
|
20
|
Start
|
Mid
|
588
|
Man's Genesis
|
627
|
20
|
Start
|
Low
|
589
|
Ecomorphology
|
627
|
20
|
B
|
Low
|
590
|
Black Queen hypothesis
|
619
|
19
|
Start
|
Low
|
591
|
Man's Place in Nature
|
606
|
19
|
Start
|
Mid
|
592
|
Philosophie zoologique
|
605
|
19
|
GA
|
Low
|
593
|
Precambrian body plans
|
605
|
19
|
B
|
Low
|
594
|
Cryptic species complex
|
602
|
19
|
NA
|
NA
|
595
|
Sex differences in memory
|
601
|
19
|
Start
|
Low
|
596
|
Wushan Man
|
599
|
19
|
Start
|
Low
|
597
|
Australopithecus deyiremeda
|
598
|
19
|
GA
|
Low
|
598
|
Genome evolution
|
597
|
19
|
C
|
Top
|
599
|
Vestigial response
|
595
|
19
|
Stub
|
Low
|
600
|
Development of Darwin's theory
|
585
|
18
|
B
|
Mid
|
601
|
Evolutionary grade
|
582
|
18
|
Start
|
High
|
602
|
Willi Hennig
|
580
|
18
|
Start
|
Mid
|
603
|
Viral phylodynamics
|
580
|
18
|
B
|
Low
|
604
|
The Major Transitions in Evolution
|
579
|
18
|
Stub
|
Low
|
605
|
PAH world hypothesis
|
579
|
18
|
Start
|
Low
|
606
|
Racism on the Internet
|
575
|
18
|
Start
|
Low
|
607
|
Origin and function of meiosis
|
575
|
18
|
Start
|
Low
|
608
|
Automimicry
|
573
|
18
|
GA
|
Mid
|
609
|
Franz Weidenreich
|
572
|
18
|
Stub
|
Mid
|
610
|
Buya, Eritrea
|
563
|
18
|
C
|
Unknown
|
611
|
Long branch attraction
|
559
|
18
|
Start
|
Low
|
612
|
Darwin and women
|
559
|
18
|
Stub
|
Low
|
613
|
Evolution: The Game of Intelligent Life
|
558
|
18
|
Start
|
Low
|
614
|
Polyandry in fish
|
556
|
17
|
C
|
Low
|
615
|
Francis Maitland Balfour
|
555
|
17
|
Start
|
Low
|
616
|
James Cowles Prichard
|
554
|
17
|
C
|
High
|
617
|
Bat wing development
|
554
|
17
|
Start
|
Low
|
618
|
Precambrian rabbit
|
554
|
17
|
C
|
Low
|
619
|
Unit of selection
|
550
|
17
|
C
|
High
|
620
|
McLean v. Arkansas
|
550
|
17
|
Start
|
Low
|
621
|
Reticulate evolution
|
545
|
17
|
C
|
Mid
|
622
|
Evolution of eusociality
|
538
|
17
|
C
|
Low
|
623
|
St. George Jackson Mivart
|
537
|
17
|
Start
|
Low
|
624
|
Glossary of genetics and evolutionary biology
|
536
|
17
|
List
|
Top
|
625
|
Vocal learning
|
536
|
17
|
B
|
Low
|
626
|
Ray Lankester
|
535
|
17
|
B
|
Low
|
627
|
Loren Cordain
|
531
|
17
|
Stub
|
Low
|
628
|
Allochronic speciation
|
527
|
17
|
B
|
Mid
|
629
|
Court jester hypothesis
|
526
|
16
|
C
|
Low
|
630
|
Zlatý kůň woman
|
526
|
16
|
Start
|
Low
|
631
|
Genetic assimilation
|
526
|
16
|
GA
|
Low
|
632
|
Allan Wilson (biologist)
|
522
|
16
|
C
|
Low
|
633
|
Laboratory experiments of speciation
|
517
|
16
|
List
|
Low
|
634
|
Nina Jablonski
|
512
|
16
|
B
|
Low
|
635
|
Endless Forms Most Beautiful (book)
|
511
|
16
|
GA
|
Low
|
636
|
Biogenesis
|
508
|
16
|
NA
|
High
|
637
|
Spiegelman's Monster
|
508
|
16
|
Start
|
Low
|
638
|
The Evolution of Desire
|
505
|
16
|
Start
|
Unknown
|
639
|
Lilliput effect
|
501
|
16
|
Start
|
Low
|
640
|
Evolution of cognition
|
498
|
16
|
C
|
Low
|
641
|
Herman Bernhard Lundborg
|
497
|
16
|
Start
|
Low
|
642
|
The Goodness Paradox
|
489
|
15
|
Start
|
Low
|
643
|
Bateson–Dobzhansky–Muller model
|
475
|
15
|
Unknown
|
Unknown
|
644
|
Winner and loser effects
|
475
|
15
|
C
|
Low
|
645
|
The Structure of Evolutionary Theory
|
474
|
15
|
Start
|
Low
|
646
|
Evolution (TV series)
|
473
|
15
|
Start
|
Low
|
647
|
Power, Sex, Suicide
|
472
|
15
|
Stub
|
Low
|
648
|
Coloration evidence for natural selection
|
470
|
15
|
GA
|
Mid
|
649
|
Helitron (biology)
|
468
|
15
|
B
|
Low
|
650
|
Error threshold (evolution)
|
466
|
15
|
C
|
Mid
|
651
|
Demonic Males
|
464
|
14
|
C
|
Unknown
|
652
|
Evolutionary aesthetics
|
463
|
14
|
C
|
High
|
653
|
Intragenomic conflict
|
462
|
14
|
C
|
Mid
|
654
|
Great Hippocampus Question
|
462
|
14
|
B
|
Low
|
655
|
Bitter taste evolution
|
460
|
14
|
Start
|
Low
|
656
|
Enterocoely
|
459
|
14
|
Stub
|
Mid
|
657
|
Proavis
|
458
|
14
|
Start
|
Low
|
658
|
Inferring horizontal gene transfer
|
453
|
14
|
B
|
Low
|
659
|
Timeline of zoology
|
453
|
14
|
List
|
Mid
|
660
|
Eukaryote hybrid genome
|
452
|
14
|
B
|
Low
|
661
|
Natural Selection (manuscript)
|
452
|
14
|
Stub
|
Low
|
662
|
Saldanha man
|
447
|
14
|
Stub
|
Low
|
663
|
Darwinian literary studies
|
446
|
14
|
C
|
Low
|
664
|
Lek paradox
|
444
|
14
|
C
|
Low
|
665
|
Selection shadow
|
444
|
14
|
Start
|
Low
|
666
|
Evolutionary developmental psychology
|
444
|
14
|
C
|
Low
|
667
|
Douglas J. Futuyma
|
442
|
14
|
C
|
Low
|
668
|
Klepton
|
442
|
14
|
Start
|
Low
|
669
|
Annual vs. perennial plant evolution
|
441
|
14
|
C
|
Low
|
670
|
Chemoton
|
439
|
14
|
Start
|
Low
|
671
|
Alloplastic adaptation
|
439
|
14
|
Stub
|
Low
|
672
|
Quasispecies model
|
439
|
14
|
C
|
Mid
|
673
|
Ancestral sequence reconstruction
|
439
|
14
|
C
|
Low
|
674
|
Glacial refugium
|
438
|
14
|
Stub
|
Low
|
675
|
History of speciation
|
430
|
13
|
C
|
Low
|
676
|
Patrick Matthew
|
430
|
13
|
B
|
Mid
|
677
|
Evolutionary physiology
|
428
|
13
|
B
|
High
|
678
|
List of Neanderthal sites
|
426
|
13
|
List
|
Low
|
679
|
Emergent evolution
|
419
|
13
|
C
|
Low
|
680
|
Reciprocal altruism in humans
|
418
|
13
|
Start
|
Low
|
681
|
Undeniable: Evolution and the Science of Creation
|
418
|
13
|
Unknown
|
Unknown
|
682
|
Neofunctionalization
|
416
|
13
|
Start
|
Low
|
683
|
Mate guarding
|
414
|
13
|
Unknown
|
Mid
|
684
|
Sex Power Money
|
412
|
13
|
C
|
Low
|
685
|
Evolutionary dynamics
|
412
|
13
|
Stub
|
Mid
|
686
|
Co-adaptation
|
408
|
13
|
C
|
Low
|
687
|
History of zoology through 1859
|
404
|
13
|
C
|
High
|
688
|
Dawkins vs. Gould
|
402
|
12
|
Start
|
Low
|
689
|
Sibling species
|
400
|
12
|
NA
|
NA
|
690
|
The Evolution of Beauty
|
400
|
12
|
Start
|
Low
|
691
|
Fritz Müller
|
400
|
12
|
B
|
Mid
|
692
|
Adaptation and Natural Selection
|
397
|
12
|
Start
|
Low
|
693
|
Quantum evolution
|
397
|
12
|
C
|
Mid
|
694
|
Evolutionary models of human drug use
|
395
|
12
|
C
|
Low
|
695
|
Inheritance of acquired characteristics
|
395
|
12
|
NA
|
NA
|
696
|
The Variation of Animals and Plants Under Domestication
|
393
|
12
|
C
|
Low
|
697
|
Polydactyly in stem-tetrapods
|
392
|
12
|
Start
|
Low
|
698
|
Proteinoid
|
390
|
12
|
Start
|
Low
|
699
|
Red King hypothesis
|
390
|
12
|
Start
|
Low
|
700
|
Nanjing Man
|
385
|
12
|
C
|
Low
|
701
|
Deep homology
|
383
|
12
|
Start
|
Mid
|
702
|
Applications of evolution
|
380
|
12
|
B
|
Low
|
703
|
Secondarily aquatic tetrapods
|
379
|
12
|
Stub
|
Mid
|
704
|
Evolutionary fauna
|
379
|
12
|
Start
|
Low
|
705
|
Megaevolution
|
379
|
12
|
Start
|
Mid
|
706
|
Biogeographic regions of Europe
|
378
|
12
|
Start
|
Mid
|
707
|
Expensive tissue hypothesis
|
378
|
12
|
C
|
Low
|
708
|
Katie Hinde
|
377
|
12
|
C
|
Low
|
709
|
W. Tecumseh Fitch
|
373
|
12
|
Stub
|
Low
|
710
|
Religion Explained
|
372
|
12
|
Start
|
Low
|
711
|
Nearly neutral theory of molecular evolution
|
372
|
12
|
Start
|
Low
|
712
|
Sexual selection in scaled reptiles
|
372
|
12
|
Start
|
Low
|
713
|
On Being the Right Size
|
370
|
11
|
C
|
Mid
|
714
|
Inclusive fitness in humans
|
369
|
11
|
C
|
Low
|
715
|
Evo-devo gene toolkit
|
367
|
11
|
Start
|
Mid
|
716
|
Niche adaptation
|
365
|
11
|
NA
|
Low
|
717
|
Isolation by distance
|
365
|
11
|
Start
|
Low
|
718
|
Epic of evolution
|
364
|
11
|
C
|
Low
|
719
|
Self-decoration camouflage
|
359
|
11
|
GA
|
Low
|
720
|
Nylon-eating bacteria and creationism
|
357
|
11
|
B
|
Low
|
721
|
Horizontal gene transfer in evolution
|
356
|
11
|
Start
|
High
|
722
|
Museum of Human Evolution
|
353
|
11
|
Start
|
Unknown
|
723
|
Evolutionary neuroscience
|
346
|
11
|
Start
|
High
|
724
|
Zinnia Kumar
|
345
|
11
|
Start
|
Low
|
725
|
Randy Thornhill
|
345
|
11
|
Start
|
Mid
|
726
|
Digital organism
|
344
|
11
|
Stub
|
Low
|
727
|
Shane Campbell-Staton
|
344
|
11
|
Start
|
Low
|
728
|
Paul W. Ewald
|
344
|
11
|
Start
|
Low
|
729
|
Viral eukaryogenesis
|
338
|
10
|
Start
|
Mid
|
730
|
David Lack
|
335
|
10
|
C
|
Low
|
731
|
Directed evolution (transhumanism)
|
334
|
10
|
Stub
|
Low
|
732
|
Tradeoffs for locomotion in air and water
|
332
|
10
|
C
|
Mid
|
733
|
Rensch's rule
|
331
|
10
|
Start
|
Low
|
734
|
Weapon (biology)
|
331
|
10
|
Stub
|
Low
|
735
|
Stenogale
|
329
|
10
|
Stub
|
Low
|
736
|
Intergradation
|
326
|
10
|
Start
|
Low
|
737
|
The Seven Pillars of Life
|
325
|
10
|
Start
|
Low
|
738
|
Postcanine megadontia
|
322
|
10
|
C
|
Low
|
739
|
Edward Bagnall Poulton
|
319
|
10
|
Start
|
Mid
|
740
|
Icons of Evolution
|
318
|
10
|
C
|
Low
|
741
|
Natural morality
|
318
|
10
|
Stub
|
Low
|
742
|
Evolution of metal ions in biological systems
|
318
|
10
|
C
|
Low
|
743
|
Qikiqtania
|
318
|
10
|
Stub
|
Unknown
|
744
|
Constructive neutral evolution
|
315
|
10
|
C
|
Low
|
745
|
What Darwin Got Wrong
|
314
|
10
|
Start
|
Low
|
746
|
Davidson Black
|
314
|
10
|
C
|
Mid
|
747
|
Sir William Lawrence, 1st Baronet
|
313
|
10
|
B
|
High
|
748
|
Behavioral plasticity
|
313
|
10
|
Start
|
Low
|
749
|
Marcus Feldman
|
312
|
10
|
Start
|
Low
|
750
|
Index of evolutionary biology articles
|
310
|
10
|
List
|
High
|
751
|
Push of the past
|
307
|
9
|
C
|
Low
|
752
|
Insectivorous Plants (book)
|
307
|
9
|
Start
|
Low
|
753
|
Alfred Newton
|
306
|
9
|
C
|
Low
|
754
|
Biodiversity of Kosovo
|
304
|
9
|
C
|
Low
|
755
|
Fuyan Cave
|
303
|
9
|
C
|
Low
|
756
|
Ecological fitting
|
301
|
9
|
B
|
Low
|
757
|
Scott F. Gilbert
|
301
|
9
|
C
|
Low
|
758
|
Evolutionary theodicy
|
298
|
9
|
C
|
Low
|
759
|
Evidence for speciation by reinforcement
|
297
|
9
|
List
|
Low
|
760
|
E. B. Ford
|
297
|
9
|
C
|
Low
|
761
|
Psammosere
|
297
|
9
|
Stub
|
Mid
|
762
|
Evolutionary invasion analysis
|
293
|
9
|
Start
|
Low
|
763
|
Automixis
|
291
|
9
|
Start
|
Unknown
|
764
|
Shifting balance theory
|
287
|
9
|
Stub
|
Low
|
765
|
Urban evolution
|
287
|
9
|
C
|
Unknown
|
766
|
William Henry Flower
|
286
|
9
|
B
|
Low
|
767
|
Hybrid swarm
|
284
|
9
|
Start
|
Mid
|
768
|
Paragroup
|
283
|
9
|
Stub
|
Low
|
769
|
Evolutionary trap
|
282
|
9
|
Start
|
Low
|
770
|
Homo consumericus
|
281
|
9
|
Start
|
Low
|
771
|
The Neutral Theory of Molecular Evolution
|
280
|
9
|
Stub
|
Low
|
772
|
Idealised population
|
280
|
9
|
C
|
Mid
|
773
|
Evolutionary landscape
|
279
|
9
|
C
|
High
|
774
|
Richard Prum
|
276
|
8
|
Start
|
Low
|
775
|
Multispecies coalescent process
|
275
|
8
|
Start
|
Low
|
776
|
Evolution of olfaction
|
274
|
8
|
C
|
Low
|
777
|
Modern human
|
274
|
8
|
NA
|
NA
|
778
|
Sexual selection in insects
|
271
|
8
|
B
|
Low
|
779
|
G-value paradox
|
270
|
8
|
C
|
Low
|
780
|
Cellularization
|
270
|
8
|
Stub
|
Low
|
781
|
The Theory of Evolution
|
269
|
8
|
Stub
|
Low
|
782
|
Concerted evolution
|
269
|
8
|
Stub
|
Low
|
783
|
Molecular Phylogenetics and Evolution
|
267
|
8
|
Stub
|
Low
|
784
|
Michael Majerus
|
262
|
8
|
Start
|
Mid
|
785
|
Segregating site
|
260
|
8
|
Start
|
Low
|
786
|
Gavin de Beer
|
257
|
8
|
C
|
Low
|
787
|
Adaptive behavior (ecology)
|
256
|
8
|
C
|
Mid
|
788
|
Phylotypic stage
|
256
|
8
|
C
|
Low
|
789
|
Subfunctionalization
|
256
|
8
|
Start
|
Low
|
790
|
Evolution of brachiopods
|
256
|
8
|
Start
|
Low
|
791
|
Evolutionary psychology of language
|
255
|
8
|
Start
|
Low
|
792
|
Fisher's geometric model
|
254
|
8
|
Start
|
Low
|
793
|
Mutation accumulation theory
|
254
|
8
|
C
|
Low
|
794
|
Law of Life
|
250
|
8
|
Stub
|
Low
|
795
|
Background selection
|
250
|
8
|
Start
|
Low
|
796
|
Biodiversity of Wales
|
250
|
8
|
C
|
Low
|
797
|
Herbivore adaptations to plant defense
|
249
|
8
|
B
|
Low
|
798
|
Cultural selection theory
|
244
|
7
|
C
|
Low
|
799
|
Mutation bias
|
244
|
7
|
C
|
Mid
|
800
|
Clonal interference
|
241
|
7
|
Stub
|
Mid
|
801
|
Ecology and evolutionary biology
|
241
|
7
|
Start
|
Low
|
802
|
Darwinian threshold
|
240
|
7
|
Start
|
Mid
|
803
|
Pseudoextinction
|
240
|
7
|
Start
|
Low
|
804
|
Biological constraints
|
236
|
7
|
Start
|
Mid
|
805
|
Jeremiah Kianga
|
235
|
7
|
Start
|
Low
|
806
|
Proto-mitochondrion
|
234
|
7
|
Start
|
Mid
|
807
|
Stephen Blair Hedges
|
234
|
7
|
Start
|
Low
|
808
|
V. C. Wynne-Edwards
|
232
|
7
|
Start
|
Low
|
809
|
Hydrogen hypothesis
|
231
|
7
|
Start
|
Low
|
810
|
GADV-protein world hypothesis
|
230
|
7
|
Start
|
Low
|
811
|
Ileret
|
230
|
7
|
Stub
|
Low
|
812
|
Dynamic mutation
|
228
|
7
|
Stub
|
Low
|
813
|
TalkOrigins Archive
|
228
|
7
|
Start
|
Low
|
814
|
Nancy A. Moran
|
227
|
7
|
C
|
Low
|
815
|
Alexander von Humboldt Biological Resources Research Institute
|
225
|
7
|
Stub
|
Low
|
816
|
Species-typical behavior
|
224
|
7
|
Start
|
Low
|
817
|
Key innovation
|
224
|
7
|
Start
|
Mid
|
818
|
Hyrax Hill
|
223
|
7
|
B
|
Low
|
819
|
Paraspecies
|
222
|
7
|
Stub
|
Low
|
820
|
Distractive markings
|
221
|
7
|
C
|
Low
|
821
|
Inversion (evolutionary biology)
|
220
|
7
|
Start
|
Mid
|
822
|
Human somatic variation
|
220
|
7
|
C
|
Mid
|
823
|
Evolutionary models of food sharing
|
220
|
7
|
C
|
Low
|
824
|
Infinite sites model
|
218
|
7
|
Start
|
Low
|
825
|
John Tyler Bonner
|
216
|
6
|
C
|
Mid
|
826
|
Mesozoic–Cenozoic radiation
|
214
|
6
|
Stub
|
Low
|
827
|
Cospeciation
|
212
|
6
|
Start
|
Mid
|
828
|
Tree rearrangement
|
210
|
6
|
Start
|
Low
|
829
|
Phylogenetic signal
|
210
|
6
|
C
|
Mid
|
830
|
Wing-assisted incline running
|
207
|
6
|
Start
|
Low
|
831
|
Hologenomics
|
206
|
6
|
Stub
|
Low
|
832
|
Conservation-induced extinction
|
203
|
6
|
Start
|
Mid
|
833
|
Peter J. Bowler
|
203
|
6
|
Start
|
Low
|
834
|
Prejudice from an evolutionary perspective
|
201
|
6
|
Start
|
Low
|
835
|
John Endler
|
201
|
6
|
Start
|
Low
|
836
|
Archaic Homo sapiens
|
201
|
6
|
NA
|
NA
|
837
|
Polymorphism in Lepidoptera
|
201
|
6
|
C
|
High
|
838
|
Modularity (biology)
|
200
|
6
|
Start
|
Low
|
839
|
The Origin of Birds
|
200
|
6
|
GA
|
High
|
840
|
Maternal behavior in vertebrates
|
199
|
6
|
C
|
Low
|
841
|
Felsenstein's tree-pruning algorithm
|
198
|
6
|
Stub
|
Low
|
842
|
Evolution by gene duplication
|
198
|
6
|
Start
|
High
|
843
|
David Hillis
|
193
|
6
|
Start
|
Low
|
844
|
Reproductive suppression
|
193
|
6
|
C
|
Mid
|
845
|
Heterotopy
|
190
|
6
|
Stub
|
Low
|
846
|
Turnover-pulse hypothesis
|
188
|
6
|
Start
|
Low
|
847
|
Mimicry in vertebrates
|
188
|
6
|
Start
|
Low
|
848
|
Storage effect
|
187
|
6
|
B
|
Mid
|
849
|
History of molecular evolution
|
186
|
6
|
C
|
Mid
|
850
|
Autoplastic adaptation
|
186
|
6
|
Stub
|
Low
|
851
|
Social immunity
|
185
|
5
|
B
|
High
|
852
|
Strong reciprocity
|
183
|
5
|
B
|
Low
|
853
|
Human reproductive ecology
|
182
|
5
|
Start
|
Low
|
854
|
History of zoology (1859–present)
|
181
|
5
|
C
|
High
|
855
|
Hybrid incompatibility
|
180
|
5
|
C
|
Low
|
856
|
Maternal effect dominant embryonic arrest
|
180
|
5
|
Start
|
Low
|
857
|
Formamide-based prebiotic chemistry
|
176
|
5
|
Start
|
Low
|
858
|
Alpheus Hyatt
|
176
|
5
|
Start
|
Low
|
859
|
Eugenics in Mexico
|
175
|
5
|
Start
|
Low
|
860
|
Evolutionary capacitance
|
175
|
5
|
C
|
Mid
|
861
|
Evolutionary psychology and culture
|
175
|
5
|
Start
|
Low
|
862
|
Endogenosymbiosis
|
174
|
5
|
Start
|
Low
|
863
|
Skeletal changes of vertebrates transitioning from water to land
|
172
|
5
|
C
|
Low
|
864
|
List of Nepenthes natural hybrids
|
172
|
5
|
List
|
Low
|
865
|
International Year of Biodiversity
|
168
|
5
|
Start
|
High
|
866
|
Mutation accumulation experiments
|
167
|
5
|
C
|
Low
|
867
|
Contest competition
|
167
|
5
|
Stub
|
Low
|
868
|
Reciprocal causation
|
167
|
5
|
C
|
Low
|
869
|
Resource holding potential
|
167
|
5
|
Stub
|
Low
|
870
|
Runcaria
|
166
|
5
|
Start
|
Low
|
871
|
Evolutionary approaches to postpartum depression
|
166
|
5
|
C
|
Low
|
872
|
The Apportionment of Human Diversity
|
163
|
5
|
C
|
Low
|
873
|
WLH-50
|
163
|
5
|
Start
|
Unknown
|
874
|
The Correlation between Relatives on the Supposition of Mendelian Inheritance
|
162
|
5
|
Start
|
Mid
|
875
|
Orgel's rules
|
162
|
5
|
Stub
|
Low
|
876
|
Evolution Day
|
161
|
5
|
Unknown
|
Unknown
|
877
|
Francisc Rainer
|
160
|
5
|
B
|
Low
|
878
|
How the Snake Lost Its Legs
|
160
|
5
|
GA
|
Low
|
879
|
Genomic evolution of birds
|
160
|
5
|
C
|
Low
|
880
|
Preadaptation
|
160
|
5
|
NA
|
Mid
|
881
|
Parasite load
|
159
|
5
|
C
|
Low
|
882
|
Evolutionary Psychology (journal)
|
159
|
5
|
Stub
|
Unknown
|
883
|
Gard model
|
157
|
5
|
Start
|
Low
|
884
|
Moritz Wagner (naturalist)
|
156
|
5
|
Start
|
Low
|
885
|
Phylogenetic inertia
|
155
|
5
|
Start
|
Mid
|
886
|
Mark Ridley (zoologist)
|
154
|
4
|
Stub
|
Low
|
887
|
Carboniferous-Earliest Permian Biodiversification Event
|
154
|
4
|
NA
|
Low
|
888
|
Russell Lande
|
153
|
4
|
Start
|
Low
|
889
|
William Charles Wells
|
152
|
4
|
B
|
High
|
890
|
Interlocus sexual conflict
|
152
|
4
|
B
|
Mid
|
891
|
Interactor
|
151
|
4
|
Stub
|
Low
|
892
|
Egg taphonomy
|
151
|
4
|
C
|
Low
|
893
|
Laura Landweber
|
149
|
4
|
Start
|
Low
|
894
|
Landscape genomics
|
148
|
4
|
Stub
|
Low
|
895
|
Resource defense polygyny
|
148
|
4
|
Stub
|
Unknown
|
896
|
Commemoration of Charles Darwin
|
147
|
4
|
C
|
Mid
|
897
|
Wonderful life theory
|
146
|
4
|
Stub
|
Low
|
898
|
Evolutionary rescue
|
144
|
4
|
Start
|
Low
|
899
|
Host switch
|
143
|
4
|
C
|
Low
|
900
|
Kapthurin Formation
|
142
|
4
|
C
|
Low
|
901
|
Fluctuating selection
|
142
|
4
|
Start
|
Low
|
902
|
Interpolation theory
|
141
|
4
|
Start
|
Low
|
903
|
Melissa A. Wilson
|
139
|
4
|
C
|
Low
|
904
|
Phagomimicry
|
138
|
4
|
Stub
|
Low
|
905
|
Scott V. Edwards
|
137
|
4
|
C
|
Low
|
906
|
Cousin couple
|
135
|
4
|
NA
|
Low
|
907
|
Talk.origins
|
133
|
4
|
Start
|
Low
|
908
|
Unique-event polymorphism
|
132
|
4
|
Start
|
Low
|
909
|
James A. Lake
|
132
|
4
|
Start
|
Low
|
910
|
Epididymis evolution from reptiles to mammals
|
131
|
4
|
B
|
Low
|
911
|
Eraclie Sterian
|
131
|
4
|
C
|
Low
|
912
|
Darwin (unit)
|
131
|
4
|
Stub
|
Low
|
913
|
Intralocus sexual conflict
|
130
|
4
|
Start
|
Mid
|
914
|
Ecological evolutionary developmental biology
|
130
|
4
|
Start
|
Low
|
915
|
Founder takes all
|
129
|
4
|
Stub
|
Low
|
916
|
Marcello Barbieri
|
129
|
4
|
Start
|
Low
|
917
|
Zoology of the Voyage of H.M.S. Beagle
|
128
|
4
|
Stub
|
Low
|
918
|
List of ecoregions with high endemism
|
127
|
4
|
List
|
Low
|
919
|
Hyposphene-hypantrum articulation
|
126
|
4
|
Start
|
Low
|
920
|
Thorson's rule
|
126
|
4
|
Start
|
Low
|
921
|
Mark Siddall
|
125
|
4
|
Start
|
Unknown
|
922
|
Phylogenetic reconciliation
|
125
|
4
|
Unknown
|
Unknown
|
923
|
Axel Meyer
|
125
|
4
|
Start
|
Unknown
|
924
|
Ecological selection
|
124
|
4
|
Start
|
Mid
|
925
|
Ruth Mace
|
124
|
4
|
Start
|
Low
|
926
|
Reductive evolution
|
123
|
3
|
Start
|
Low
|
927
|
Despeciation
|
123
|
3
|
Start
|
Low
|
928
|
Escape and radiate coevolution
|
122
|
3
|
C
|
Unknown
|
929
|
OneZoom
|
121
|
3
|
Start
|
Unknown
|
930
|
Facilitated variation
|
119
|
3
|
Stub
|
Low
|
931
|
ASUDAS
|
119
|
3
|
Start
|
Unknown
|
932
|
Molecular drive
|
118
|
3
|
Stub
|
Low
|
933
|
Dan Willard
|
118
|
3
|
C
|
Low
|
934
|
Tip dating
|
117
|
3
|
Stub
|
Low
|
935
|
European Society for Evolutionary Biology
|
116
|
3
|
Stub
|
Low
|
936
|
Eric Charnov
|
116
|
3
|
Start
|
Low
|
937
|
Ecological inheritance
|
115
|
3
|
Stub
|
Low
|
938
|
Diversitas
|
114
|
3
|
C
|
Low
|
939
|
The Great Monkey Trial
|
113
|
3
|
Start
|
Low
|
940
|
Evolution of Macropodidae
|
113
|
3
|
Start
|
Low
|
941
|
Rupert Riedl
|
112
|
3
|
Start
|
Low
|
942
|
SK 847
|
112
|
3
|
Start
|
Low
|
943
|
Countergradient variation
|
112
|
3
|
Start
|
Low
|
944
|
Evolution of Infectious Disease
|
111
|
3
|
Stub
|
Low
|
945
|
Andrew Berry (biologist)
|
110
|
3
|
Stub
|
Low
|
946
|
Corrie Moreau
|
110
|
3
|
C
|
Low
|
947
|
Karl Kessler
|
110
|
3
|
Stub
|
Low
|
948
|
Graham Bell (biologist)
|
109
|
3
|
Stub
|
Low
|
949
|
Jennifer E. Smith (biologist)
|
109
|
3
|
Start
|
Unknown
|
950
|
Hox genes in amphibians and reptiles
|
108
|
3
|
C
|
Low
|
951
|
Institute of Human Origins
|
108
|
3
|
Start
|
Low
|
952
|
Phylo (video game)
|
108
|
3
|
Start
|
Low
|
953
|
Arthur Cain
|
107
|
3
|
C
|
Low
|
954
|
Ecotron
|
106
|
3
|
Stub
|
Low
|
955
|
Transformed cladistics
|
105
|
3
|
C
|
Low
|
956
|
Nonecological speciation
|
105
|
3
|
Start
|
Low
|
957
|
Kindred: Neanderthal Life, Love, Death and Art
|
104
|
3
|
Stub
|
Low
|
958
|
J. T. Gulick
|
104
|
3
|
Start
|
Low
|
959
|
Stan Wood (fossil hunter)
|
103
|
3
|
Stub
|
Unknown
|
960
|
Stepwise mutation model
|
100
|
3
|
Stub
|
Low
|
961
|
Punctuated gradualism
|
100
|
3
|
Start
|
Low
|
962
|
Wallace effect
|
99
|
3
|
NA
|
NA
|
963
|
Sex differences in sensory systems
|
99
|
3
|
Start
|
Mid
|
964
|
Patty Brennan
|
99
|
3
|
Start
|
Unknown
|
965
|
Identity in social insects
|
99
|
3
|
Start
|
Low
|
966
|
Largest-scale trends in evolution
|
98
|
3
|
Start
|
High
|
967
|
Anti-black racism in the United States
|
97
|
3
|
NA
|
NA
|
968
|
Grit, not grass hypothesis
|
97
|
3
|
C
|
Low
|
969
|
Locomotor mimicry
|
96
|
3
|
Start
|
Low
|
970
|
Swamping argument
|
95
|
3
|
Stub
|
Low
|
971
|
Germ-Soma Differentiation
|
94
|
3
|
C
|
Low
|
972
|
Stephen W. Pacala
|
94
|
3
|
Start
|
Low
|
973
|
Differential fitness
|
92
|
2
|
C
|
Low
|
974
|
Darwinian anthropology
|
92
|
2
|
B
|
Unknown
|
975
|
George Rolleston
|
92
|
2
|
Start
|
Low
|
976
|
Non-Darwinian Evolution (paper)
|
91
|
2
|
Stub
|
Low
|
977
|
Victoria Arbour
|
91
|
2
|
Start
|
Low
|
978
|
Kira Makarova
|
91
|
2
|
Start
|
Low
|
979
|
Panina (subtribe)
|
91
|
2
|
NA
|
NA
|
980
|
Benjamin Chan
|
90
|
2
|
Start
|
Low
|
981
|
Adriana Briscoe
|
89
|
2
|
B
|
Low
|
982
|
Human evolutionary developmental biology
|
88
|
2
|
C
|
Mid
|
983
|
Tim Lewens
|
88
|
2
|
Start
|
Unknown
|
984
|
Nonadaptive radiation
|
88
|
2
|
Start
|
Low
|
985
|
Society for the Study of Evolution
|
88
|
2
|
Stub
|
Low
|
986
|
Jena Phyletisches Museum
|
87
|
2
|
Start
|
Low
|
987
|
Joan E. Strassmann
|
87
|
2
|
Start
|
Low
|
988
|
Cooperative coevolution
|
87
|
2
|
Start
|
Unknown
|
989
|
Species group
|
86
|
2
|
NA
|
NA
|
990
|
Romanticism in evolution theory
|
85
|
2
|
Start
|
Low
|
991
|
Assisted evolution
|
85
|
2
|
C
|
Low
|
992
|
Parallel speciation
|
84
|
2
|
Unknown
|
Low
|
993
|
The Myth of the One Percent
|
84
|
2
|
Start
|
Low
|
994
|
Evolution Without Selection
|
82
|
2
|
Start
|
Low
|
995
|
Darwinian puzzle
|
81
|
2
|
Start
|
Low
|
996
|
Jeremy Yoder
|
81
|
2
|
Start
|
Low
|
997
|
Cost of reproduction hypothesis
|
81
|
2
|
Start
|
Mid
|
998
|
Theology of creationism and evolution
|
81
|
2
|
Start
|
Low
|
999
|
The Neanderthals Rediscovered
|
81
|
2
|
GA
|
Low
|
1000
|
Kinetotroph
|
80
|
2
|
Start
|
Low
|