Rank
|
Page title
|
Views
|
Daily average
|
Assessment
|
Importance
|
1
|
Neanderthal
|
109,425
|
3,647
|
GA
|
Mid
|
2
|
Charles Darwin
|
102,107
|
3,403
|
FA
|
Top
|
3
|
Parthenogenesis
|
82,327
|
2,744
|
B
|
High
|
4
|
Eugenics
|
82,173
|
2,739
|
B
|
Mid
|
5
|
Sexual dimorphism
|
76,580
|
2,552
|
B
|
High
|
6
|
List of common misconceptions
|
73,140
|
2,438
|
List
|
Low
|
7
|
Richard Dawkins
|
67,786
|
2,259
|
GA
|
Mid
|
8
|
Human evolution
|
67,590
|
2,253
|
C
|
High
|
9
|
Species
|
59,550
|
1,985
|
GA
|
Top
|
10
|
Cretaceous–Paleogene extinction event
|
53,149
|
1,771
|
FA
|
High
|
11
|
Racism
|
52,185
|
1,739
|
B
|
Mid
|
12
|
Extinction
|
50,903
|
1,696
|
C
|
High
|
13
|
Carcinisation
|
45,423
|
1,514
|
Start
|
Top
|
14
|
Evolution
|
41,219
|
1,373
|
FA
|
Top
|
15
|
Abiogenesis
|
40,415
|
1,347
|
GA
|
Top
|
16
|
Biodiversity
|
39,380
|
1,312
|
C
|
Mid
|
17
|
Cousin
|
38,560
|
1,285
|
Start
|
Low
|
18
|
Scientific racism
|
33,155
|
1,105
|
C
|
Low
|
19
|
Binomial nomenclature
|
33,153
|
1,105
|
C
|
Low
|
20
|
Cro-Magnon
|
32,561
|
1,085
|
GA
|
Mid
|
21
|
Early modern human
|
32,419
|
1,080
|
B
|
Mid
|
22
|
List of X-Men members
|
32,067
|
1,068
|
List
|
Low
|
23
|
Scopes trial
|
31,620
|
1,054
|
B
|
High
|
24
|
William Jennings Bryan
|
30,575
|
1,019
|
B
|
High
|
25
|
Inbreeding
|
30,519
|
1,017
|
C
|
High
|
26
|
Archaic humans
|
29,748
|
991
|
Start
|
Low
|
27
|
Epicanthic fold
|
29,546
|
984
|
C
|
Low
|
28
|
Fossil
|
28,938
|
964
|
B
|
Mid
|
29
|
Clade
|
27,821
|
927
|
C
|
High
|
30
|
Timeline of human evolution
|
27,721
|
924
|
C
|
Low
|
31
|
Genetics
|
26,318
|
877
|
FA
|
Top
|
32
|
Ecology
|
25,996
|
866
|
GA
|
Top
|
33
|
Natural selection
|
25,433
|
847
|
GA
|
Top
|
34
|
Hybrid (biology)
|
25,090
|
836
|
GA
|
High
|
35
|
Patrilineality
|
24,068
|
802
|
Start
|
Low
|
36
|
Neontology
|
23,990
|
799
|
Start
|
Mid
|
37
|
Altruism
|
23,945
|
798
|
B
|
High
|
38
|
Paleontology
|
23,899
|
796
|
GA
|
Top
|
39
|
Domestication of the dog
|
23,839
|
794
|
B
|
Low
|
40
|
Origin of language
|
22,785
|
759
|
C
|
Low
|
41
|
On the Origin of Species
|
22,025
|
734
|
FA
|
Top
|
42
|
Last universal common ancestor
|
21,386
|
712
|
GA
|
Top
|
43
|
Origin of COVID-19
|
20,644
|
688
|
Start
|
Mid
|
44
|
Mutation
|
20,530
|
684
|
B
|
Top
|
45
|
Homo floresiensis
|
20,510
|
683
|
B
|
Mid
|
46
|
Darwinism
|
19,875
|
662
|
Start
|
High
|
47
|
Wallace Line
|
19,548
|
651
|
Start
|
Mid
|
48
|
Cambrian explosion
|
19,183
|
639
|
B
|
High
|
49
|
Upper Paleolithic
|
19,098
|
636
|
C
|
Low
|
50
|
Eusociality
|
19,029
|
634
|
GA
|
Mid
|
51
|
HeLa
|
18,693
|
623
|
C
|
Low
|
52
|
Convergent evolution
|
18,506
|
616
|
GA
|
High
|
53
|
Anus
|
17,938
|
597
|
Start
|
Mid
|
54
|
Sociality
|
17,781
|
592
|
C
|
Mid
|
55
|
Extant taxon
|
17,767
|
592
|
NA
|
NA
|
56
|
Great Oxidation Event
|
17,448
|
581
|
C
|
Mid
|
57
|
Fear
|
17,242
|
574
|
B
|
Low
|
58
|
Nordicism
|
16,889
|
562
|
B
|
Low
|
59
|
Lamarckism
|
16,239
|
541
|
GA
|
High
|
60
|
Phylogenetics
|
15,787
|
526
|
C
|
High
|
61
|
Aposematism
|
15,713
|
523
|
GA
|
Mid
|
62
|
Rare Earth hypothesis
|
15,607
|
520
|
B
|
Low
|
63
|
Australopithecine
|
15,548
|
518
|
C
|
High
|
64
|
Human taxonomy
|
15,420
|
514
|
C
|
Low
|
65
|
Population bottleneck
|
15,309
|
510
|
C
|
High
|
66
|
Haplogroup
|
15,170
|
505
|
C
|
Mid
|
67
|
The Selfish Gene
|
14,559
|
485
|
B
|
High
|
68
|
Domestication of the cat
|
14,366
|
478
|
C
|
Mid
|
69
|
Pan (genus)
|
14,275
|
475
|
B
|
High
|
70
|
Stromatolite
|
14,191
|
473
|
B
|
Mid
|
71
|
Institutional racism
|
14,112
|
470
|
B
|
Mid
|
72
|
Living fossil
|
14,094
|
469
|
C
|
Mid
|
73
|
Selective breeding
|
14,045
|
468
|
C
|
Low
|
74
|
Stephen Jay Gould
|
13,605
|
453
|
GA
|
Mid
|
75
|
Matrilineality
|
13,511
|
450
|
C
|
Low
|
76
|
History of life
|
13,466
|
448
|
GA
|
Top
|
77
|
Major histocompatibility complex
|
13,424
|
447
|
B
|
Low
|
78
|
Bipedalism
|
13,353
|
445
|
B
|
Mid
|
79
|
Karyotype
|
13,070
|
435
|
C
|
Low
|
80
|
Camouflage
|
12,906
|
430
|
GA
|
Mid
|
81
|
Timeline of the evolutionary history of life
|
12,857
|
428
|
B
|
Top
|
82
|
Human Y-chromosome DNA haplogroup
|
12,724
|
424
|
C
|
Mid
|
83
|
Alfred Russel Wallace
|
12,685
|
422
|
FA
|
Top
|
84
|
Sex differences in intelligence
|
12,580
|
419
|
B
|
Low
|
85
|
Homology (biology)
|
12,567
|
418
|
GA
|
Top
|
86
|
Sexual selection
|
12,330
|
411
|
GA
|
High
|
87
|
Antimicrobial resistance
|
12,121
|
404
|
B
|
Unknown
|
88
|
Eugenics in the United States
|
12,044
|
401
|
Start
|
Low
|
89
|
Stoned ape theory
|
11,984
|
399
|
C
|
Low
|
90
|
Earliest known life forms
|
11,900
|
396
|
C
|
Top
|
91
|
Red Queen hypothesis
|
11,358
|
378
|
Start
|
Mid
|
92
|
Ronald Fisher
|
11,177
|
372
|
B
|
High
|
93
|
Nazi eugenics
|
11,023
|
367
|
C
|
Low
|
94
|
Human mating strategies
|
10,818
|
360
|
B
|
Low
|
95
|
Tiktaalik
|
10,779
|
359
|
GA
|
High
|
96
|
Evolutionary psychology
|
10,757
|
358
|
C
|
High
|
97
|
Genetic drift
|
10,687
|
356
|
GA
|
Top
|
98
|
Hardy–Weinberg principle
|
10,612
|
353
|
C
|
High
|
99
|
E. O. Wilson
|
10,515
|
350
|
B
|
Mid
|
100
|
Panthera hybrid
|
10,512
|
350
|
C
|
Low
|
101
|
Peking Man
|
10,414
|
347
|
GA
|
Mid
|
102
|
Chicken or the egg
|
10,367
|
345
|
Start
|
Low
|
103
|
Thomas Henry Huxley
|
10,320
|
344
|
B
|
Mid
|
104
|
Vestigiality
|
10,287
|
342
|
C
|
High
|
105
|
Evolution of mammals
|
10,131
|
337
|
B
|
High
|
106
|
Anthropometry
|
9,955
|
331
|
C
|
Low
|
107
|
Survival of the fittest
|
9,825
|
327
|
B
|
Low
|
108
|
Three-domain system
|
9,814
|
327
|
C
|
Mid
|
109
|
Origin of birds
|
9,693
|
323
|
B
|
Mid
|
110
|
Triune brain
|
9,690
|
323
|
Start
|
Low
|
111
|
Behavioral modernity
|
9,689
|
322
|
C
|
Low
|
112
|
Founder effect
|
9,589
|
319
|
C
|
Mid
|
113
|
Jean-Baptiste Lamarck
|
9,503
|
316
|
B
|
Top
|
114
|
R/K selection theory
|
9,476
|
315
|
C
|
High
|
115
|
Ernst Haeckel
|
9,438
|
314
|
B
|
High
|
116
|
Most recent common ancestor
|
9,433
|
314
|
B
|
High
|
117
|
Lower Paleolithic
|
9,325
|
310
|
C
|
High
|
118
|
Mimicry
|
9,111
|
303
|
GA
|
High
|
119
|
List of human evolution fossils
|
8,926
|
297
|
List
|
High
|
120
|
Polymorphism (biology)
|
8,807
|
293
|
B
|
High
|
121
|
RNA world
|
8,767
|
292
|
C
|
High
|
122
|
Sexual cannibalism
|
8,658
|
288
|
B
|
Low
|
123
|
Human vestigiality
|
8,588
|
286
|
C
|
Mid
|
124
|
Adaptation
|
8,500
|
283
|
GA
|
Top
|
125
|
Evolutionary biology
|
8,248
|
274
|
C
|
Top
|
126
|
Ediacaran biota
|
8,194
|
273
|
FA
|
Low
|
127
|
Fertility
|
8,191
|
273
|
C
|
High
|
128
|
Evolution of the horse
|
8,178
|
272
|
B
|
Mid
|
129
|
Cladistics
|
8,116
|
270
|
C
|
Mid
|
130
|
Symbiogenesis
|
8,100
|
270
|
GA
|
High
|
131
|
Sex differences in human physiology
|
8,096
|
269
|
C
|
High
|
132
|
Recent human evolution
|
8,069
|
268
|
B
|
Mid
|
133
|
Instinct
|
8,039
|
267
|
C
|
Low
|
134
|
Monophyly
|
7,893
|
263
|
C
|
Mid
|
135
|
Phenotypic disparity
|
7,836
|
261
|
C
|
Mid
|
136
|
Basal (phylogenetics)
|
7,825
|
260
|
C
|
Mid
|
137
|
Horizontal gene transfer
|
7,790
|
259
|
C
|
High
|
138
|
Sexy son hypothesis
|
7,766
|
258
|
C
|
Mid
|
139
|
Darwin's finches
|
7,708
|
256
|
C
|
High
|
140
|
Feathered dinosaur
|
7,677
|
255
|
C
|
High
|
141
|
Offspring
|
7,670
|
255
|
Start
|
Mid
|
142
|
Objections to evolution
|
7,511
|
250
|
GA
|
Mid
|
143
|
Primordial soup
|
7,489
|
249
|
Start
|
Mid
|
144
|
Julian Huxley
|
7,453
|
248
|
B
|
Mid
|
145
|
Female promiscuity
|
7,396
|
246
|
C
|
Low
|
146
|
Speciation
|
7,370
|
245
|
C
|
High
|
147
|
Linnaean taxonomy
|
7,364
|
245
|
C
|
Mid
|
148
|
Jebel Irhoud
|
7,342
|
244
|
C
|
Low
|
149
|
Felid hybrids
|
7,289
|
242
|
Start
|
Low
|
150
|
Evolutionary algorithm
|
7,258
|
241
|
C
|
Low
|
151
|
Bergmann's rule
|
7,234
|
241
|
C
|
Low
|
152
|
Signalling theory
|
7,157
|
238
|
GA
|
Mid
|
153
|
Species complex
|
7,154
|
238
|
B
|
Mid
|
154
|
Middle Paleolithic
|
7,112
|
237
|
C
|
High
|
155
|
Evolution of human intelligence
|
7,095
|
236
|
Start
|
High
|
156
|
Evolution of sexual reproduction
|
7,059
|
235
|
B
|
High
|
157
|
Island gigantism
|
7,023
|
234
|
Start
|
Low
|
158
|
Common descent
|
7,013
|
233
|
C
|
Top
|
159
|
Evolutionary history of plants
|
6,856
|
228
|
B
|
High
|
160
|
Evolutionary origin of religion
|
6,845
|
228
|
C
|
Low
|
161
|
Great American Interchange
|
6,840
|
228
|
C
|
Mid
|
162
|
Human mitochondrial DNA haplogroup
|
6,838
|
227
|
Start
|
Mid
|
163
|
Insular dwarfism
|
6,773
|
225
|
C
|
Low
|
164
|
Batesian mimicry
|
6,685
|
222
|
GA
|
Mid
|
165
|
Symmetry in biology
|
6,680
|
222
|
C
|
High
|
166
|
CpG site
|
6,579
|
219
|
C
|
Mid
|
167
|
Missing link (human evolution)
|
6,576
|
219
|
Start
|
Mid
|
168
|
Punctuated equilibrium
|
6,562
|
218
|
GA
|
High
|
169
|
J. B. S. Haldane
|
6,562
|
218
|
C
|
Mid
|
170
|
Anisogamy
|
6,533
|
217
|
C
|
High
|
171
|
Homo longi
|
6,520
|
217
|
GA
|
Low
|
172
|
Sex differences in psychology
|
6,315
|
210
|
C
|
High
|
173
|
Neanderthal genetics
|
6,286
|
209
|
C
|
High
|
174
|
Evolution of primates
|
6,215
|
207
|
Start
|
Low
|
175
|
Autosome
|
6,175
|
205
|
Start
|
High
|
176
|
Sexual selection in humans
|
6,122
|
204
|
C
|
Low
|
177
|
Adaptive radiation
|
6,105
|
203
|
Start
|
High
|
178
|
Inbreeding depression
|
6,062
|
202
|
Start
|
Mid
|
179
|
Duane Gish
|
6,026
|
200
|
C
|
Low
|
180
|
Fitness (biology)
|
5,911
|
197
|
B
|
High
|
181
|
Aquatic ape hypothesis
|
5,902
|
196
|
C
|
Low
|
182
|
Lek mating
|
5,896
|
196
|
GA
|
Mid
|
183
|
Spiral Dynamics
|
5,823
|
194
|
C
|
Low
|
184
|
Genetic diversity
|
5,738
|
191
|
C
|
Mid
|
185
|
Anatomically modern human
|
5,653
|
188
|
NA
|
NA
|
186
|
Biogeography
|
5,614
|
187
|
Start
|
Mid
|
187
|
History of evolutionary thought
|
5,573
|
185
|
FA
|
Top
|
188
|
List of related male and female reproductive organs
|
5,569
|
185
|
List
|
Mid
|
189
|
Modern synthesis (20th century)
|
5,475
|
182
|
GA
|
High
|
190
|
Allopatric speciation
|
5,460
|
182
|
C
|
High
|
191
|
Evolution of fish
|
5,429
|
180
|
C
|
High
|
192
|
Recapitulation theory
|
5,417
|
180
|
C
|
Mid
|
193
|
Müllerian mimicry
|
5,398
|
179
|
GA
|
Mid
|
194
|
Human sperm competition
|
5,345
|
178
|
C
|
Low
|
195
|
Evolution as fact and theory
|
5,239
|
174
|
C
|
Low
|
196
|
Evolution of birds
|
5,117
|
170
|
C
|
High
|
197
|
Variability hypothesis
|
5,087
|
169
|
C
|
Low
|
198
|
Climate change adaptation
|
5,044
|
168
|
B
|
Mid
|
199
|
The Descent of Man, and Selection in Relation to Sex
|
4,983
|
166
|
Start
|
High
|
200
|
Expelled: No Intelligence Allowed
|
4,884
|
162
|
B
|
Low
|
201
|
Population genetics
|
4,874
|
162
|
C
|
High
|
202
|
Evolution of the wolf
|
4,870
|
162
|
B
|
Low
|
203
|
Religious views of Charles Darwin
|
4,866
|
162
|
B
|
Low
|
204
|
Genetic variation
|
4,845
|
161
|
Start
|
High
|
205
|
Incertae sedis
|
4,823
|
160
|
C
|
Low
|
206
|
Relict (biology)
|
4,817
|
160
|
C
|
Mid
|
207
|
Evolution of cetaceans
|
4,695
|
156
|
GA
|
Mid
|
208
|
Hominina
|
4,690
|
156
|
NA
|
NA
|
209
|
Ontogeny
|
4,619
|
153
|
B
|
High
|
210
|
Kin selection
|
4,567
|
152
|
GA
|
High
|
211
|
Maladaptation
|
4,516
|
150
|
Start
|
Mid
|
212
|
Complex adaptive system
|
4,508
|
150
|
C
|
Mid
|
213
|
The Naked Woman
|
4,453
|
148
|
Stub
|
Low
|
214
|
Devolution (biology)
|
4,449
|
148
|
C
|
Low
|
215
|
Aggressive mimicry
|
4,423
|
147
|
GA
|
Mid
|
216
|
Frameshift mutation
|
4,413
|
147
|
B
|
High
|
217
|
Sperm competition
|
4,412
|
147
|
Start
|
Mid
|
218
|
Neo-Darwinism
|
4,392
|
146
|
Start
|
Mid
|
219
|
Speculative evolution
|
4,367
|
145
|
B
|
Low
|
220
|
Introduction to evolution
|
4,303
|
143
|
B
|
Mid
|
221
|
Islamic views on evolution
|
4,120
|
137
|
C
|
Low
|
222
|
Transitional fossil
|
4,092
|
136
|
GA
|
Top
|
223
|
Apomorphy and synapomorphy
|
4,039
|
134
|
C
|
Low
|
224
|
Crown group
|
4,033
|
134
|
C
|
Mid
|
225
|
Australopithecus sediba
|
3,960
|
132
|
GA
|
Low
|
226
|
Peppered moth evolution
|
3,952
|
131
|
GA
|
High
|
227
|
First universal common ancestor
|
3,939
|
131
|
Start
|
Unknown
|
228
|
Purple Earth hypothesis
|
3,926
|
130
|
Start
|
Mid
|
229
|
Spandrel (biology)
|
3,913
|
130
|
B
|
Mid
|
230
|
Rejection of evolution by religious groups
|
3,866
|
128
|
B
|
High
|
231
|
Evolution of the brain
|
3,800
|
126
|
Start
|
High
|
232
|
Gene flow
|
3,779
|
125
|
Start
|
High
|
233
|
Fisher's principle
|
3,747
|
124
|
Start
|
Mid
|
234
|
Lagerstätte
|
3,723
|
124
|
B
|
Mid
|
235
|
Evolution of the eye
|
3,723
|
124
|
C
|
High
|
236
|
Sequence homology
|
3,633
|
121
|
C
|
High
|
237
|
Gene polymorphism
|
3,632
|
121
|
Start
|
Mid
|
238
|
Systematics
|
3,616
|
120
|
C
|
High
|
239
|
Multiregional origin of modern humans
|
3,596
|
119
|
C
|
Mid
|
240
|
Self-preservation
|
3,566
|
118
|
C
|
High
|
241
|
History of biology
|
3,551
|
118
|
FA
|
High
|
242
|
Assortative mating
|
3,540
|
118
|
C
|
Mid
|
243
|
Sympatric speciation
|
3,539
|
117
|
Start
|
Mid
|
244
|
Allele frequency
|
3,537
|
117
|
Start
|
Mid
|
245
|
Herto Man
|
3,507
|
116
|
GA
|
Low
|
246
|
Ursid hybrid
|
3,503
|
116
|
C
|
Low
|
247
|
History of eugenics
|
3,484
|
116
|
B
|
Low
|
248
|
Thomas Hunt Morgan
|
3,477
|
115
|
B
|
High
|
249
|
The Expression of the Emotions in Man and Animals
|
3,411
|
113
|
Start
|
Mid
|
250
|
Altruism (biology)
|
3,394
|
113
|
C
|
Mid
|
251
|
Sister group
|
3,385
|
112
|
Start
|
Low
|
252
|
Evolutionary developmental biology
|
3,382
|
112
|
GA
|
High
|
253
|
Peppered moth
|
3,358
|
111
|
B
|
Low
|
254
|
Future generations
|
3,355
|
111
|
Start
|
Low
|
255
|
Kenyanthropus
|
3,308
|
110
|
GA
|
Low
|
256
|
Parental investment
|
3,297
|
109
|
Start
|
High
|
257
|
Cladogram
|
3,267
|
108
|
C
|
Mid
|
258
|
Evolutionary game theory
|
3,242
|
108
|
C
|
High
|
259
|
The Blind Watchmaker
|
3,237
|
107
|
C
|
Mid
|
260
|
List of examples of convergent evolution
|
3,233
|
107
|
List
|
High
|
261
|
Reproductive isolation
|
3,186
|
106
|
C
|
High
|
262
|
Haplodiploidy
|
3,175
|
105
|
C
|
Mid
|
263
|
Four Fs (evolution)
|
3,173
|
105
|
C
|
Low
|
264
|
Fisherian runaway
|
3,150
|
105
|
Start
|
Low
|
265
|
Gene duplication
|
3,144
|
104
|
C
|
Mid
|
266
|
Hunter versus farmer hypothesis
|
3,118
|
103
|
C
|
Low
|
267
|
Sexual conflict
|
3,113
|
103
|
Start
|
High
|
268
|
Geological history of oxygen
|
3,041
|
101
|
C
|
Low
|
269
|
Ernst Mayr
|
3,033
|
101
|
C
|
High
|
270
|
List of fossil sites
|
3,029
|
100
|
List
|
Top
|
271
|
Japanese Paleolithic
|
3,022
|
100
|
Start
|
High
|
272
|
Evolutionary computation
|
3,014
|
100
|
C
|
High
|
273
|
Acceptance of evolution by religious groups
|
3,012
|
100
|
C
|
Low
|
274
|
Endurance running hypothesis
|
3,004
|
100
|
Start
|
Low
|
275
|
Domestication syndrome
|
2,993
|
99
|
C
|
Low
|
276
|
Level of support for evolution
|
2,966
|
98
|
C
|
Mid
|
277
|
Evolution of photosynthesis
|
2,938
|
97
|
Start
|
High
|
278
|
Divergent evolution
|
2,935
|
97
|
Start
|
Mid
|
279
|
Phenotypic plasticity
|
2,924
|
97
|
C
|
Mid
|
280
|
Life history theory
|
2,883
|
96
|
C
|
High
|
281
|
Handicap principle
|
2,869
|
95
|
GA
|
High
|
282
|
Parental care
|
2,863
|
95
|
B
|
Mid
|
283
|
Gene-centered view of evolution
|
2,826
|
94
|
B
|
High
|
284
|
Orthogenesis
|
2,818
|
93
|
GA
|
Mid
|
285
|
Body plan
|
2,816
|
93
|
C
|
Mid
|
286
|
Allometry
|
2,808
|
93
|
C
|
Mid
|
287
|
Shadow biosphere
|
2,780
|
92
|
Start
|
Mid
|
288
|
Sociobiological theories of rape
|
2,772
|
92
|
C
|
Mid
|
289
|
Why Is Sex Fun?
|
2,754
|
91
|
C
|
Low
|
290
|
Evolutionarily stable strategy
|
2,748
|
91
|
B
|
Mid
|
291
|
Eukaryogenesis
|
2,727
|
90
|
C
|
High
|
292
|
Protocell
|
2,691
|
89
|
C
|
Mid
|
293
|
Solo Man
|
2,651
|
88
|
FA
|
Low
|
294
|
Heather Heying
|
2,615
|
87
|
Start
|
Low
|
295
|
Alloparenting
|
2,572
|
85
|
C
|
Low
|
296
|
Coevolution
|
2,570
|
85
|
GA
|
High
|
297
|
Reciprocal altruism
|
2,566
|
85
|
B
|
Mid
|
298
|
Stotting
|
2,558
|
85
|
GA
|
Low
|
299
|
March of Progress
|
2,551
|
85
|
C
|
Low
|
300
|
Fish intelligence
|
2,540
|
84
|
B
|
Low
|
301
|
Heterochrony
|
2,508
|
83
|
GA
|
Mid
|
302
|
Macroevolution
|
2,507
|
83
|
B
|
Top
|
303
|
E. coli long-term evolution experiment
|
2,506
|
83
|
B
|
Mid
|
304
|
Exaptation
|
2,497
|
83
|
C
|
High
|
305
|
Somatic mutation
|
2,473
|
82
|
C
|
Low
|
306
|
Evidence of common descent
|
2,450
|
81
|
B
|
Mid
|
307
|
Parallel evolution
|
2,423
|
80
|
Start
|
High
|
308
|
Bateman's principle
|
2,418
|
80
|
B
|
Mid
|
309
|
Evolution of reptiles
|
2,409
|
80
|
C
|
High
|
310
|
Haldane's rule
|
2,394
|
79
|
C
|
Low
|
311
|
Cro-Magnon rock shelter
|
2,375
|
79
|
Start
|
Mid
|
312
|
Group selection
|
2,352
|
78
|
GA
|
High
|
313
|
Killer ape theory
|
2,350
|
78
|
Start
|
Low
|
314
|
Biology and political orientation
|
2,346
|
78
|
C
|
Low
|
315
|
Beta diversity
|
2,339
|
77
|
C
|
Mid
|
316
|
Cline (biology)
|
2,334
|
77
|
C
|
Low
|
317
|
Gene pool
|
2,313
|
77
|
Start
|
High
|
318
|
Theodosius Dobzhansky
|
2,308
|
76
|
C
|
Mid
|
319
|
Evolution of morality
|
2,298
|
76
|
C
|
High
|
320
|
Ring species
|
2,296
|
76
|
C
|
High
|
321
|
Braarudosphaera bigelowii
|
2,291
|
76
|
Start
|
Low
|
322
|
Inclusive fitness
|
2,277
|
75
|
C
|
High
|
323
|
Germline mutation
|
2,244
|
74
|
B
|
High
|
324
|
History of ecology
|
2,244
|
74
|
C
|
Mid
|
325
|
Rotating locomotion in living systems
|
2,238
|
74
|
FA
|
High
|
326
|
Origin of speech
|
2,164
|
72
|
C
|
Mid
|
327
|
Radiation hormesis
|
2,156
|
71
|
B
|
Mid
|
328
|
Human skeletal changes due to bipedalism
|
2,141
|
71
|
B
|
Mid
|
329
|
Evolutionary radiation
|
2,140
|
71
|
Start
|
Mid
|
330
|
John Maynard Smith
|
2,134
|
71
|
C
|
High
|
331
|
Alternatives to Darwinian evolution
|
2,108
|
70
|
B
|
Mid
|
332
|
Microevolution
|
2,107
|
70
|
C
|
High
|
333
|
Disappearing blonde gene
|
2,096
|
69
|
Start
|
Low
|
334
|
Mach bands
|
2,095
|
69
|
Start
|
Mid
|
335
|
Clonally transmissible cancer
|
2,095
|
69
|
C
|
Low
|
336
|
Evolutionary taxonomy
|
2,092
|
69
|
C
|
Mid
|
337
|
Evolutionary pressure
|
2,070
|
69
|
C
|
Mid
|
338
|
Extended evolutionary synthesis
|
2,059
|
68
|
B
|
High
|
339
|
Homo sapiens sapiens
|
2,042
|
68
|
NA
|
NA
|
340
|
Directional selection
|
2,033
|
67
|
Start
|
Mid
|
341
|
Evolution of emotion
|
2,011
|
67
|
Start
|
Unknown
|
342
|
Neutral theory of molecular evolution
|
1,990
|
66
|
Start
|
High
|
343
|
Two-domain system
|
1,983
|
66
|
C
|
Low
|
344
|
Bruniquel Cave
|
1,948
|
64
|
Start
|
Mid
|
345
|
Ovulatory shift hypothesis
|
1,946
|
64
|
GA
|
Low
|
346
|
Late Stone Age
|
1,936
|
64
|
Start
|
Low
|
347
|
Asa Gray
|
1,933
|
64
|
GA
|
Low
|
348
|
Pangenesis
|
1,932
|
64
|
C
|
Low
|
349
|
Evolutionism
|
1,915
|
63
|
C
|
Mid
|
350
|
Coalescent theory
|
1,905
|
63
|
C
|
Low
|
351
|
Evolutionary arms race
|
1,893
|
63
|
Start
|
High
|
352
|
Island syndrome
|
1,890
|
63
|
Start
|
Unknown
|
353
|
Racism in the LGBT community
|
1,887
|
62
|
C
|
Low
|
354
|
1860 Oxford evolution debate
|
1,874
|
62
|
B
|
Mid
|
355
|
Evolutionary anachronism
|
1,862
|
62
|
List
|
Mid
|
356
|
W. D. Hamilton
|
1,857
|
61
|
C
|
Low
|
357
|
Primitive (phylogenetics)
|
1,857
|
61
|
Start
|
Mid
|
358
|
Meganthropus
|
1,855
|
61
|
Start
|
Low
|
359
|
Darwin's Dangerous Idea
|
1,851
|
61
|
C
|
Mid
|
360
|
Strategic pluralism
|
1,784
|
59
|
Stub
|
Low
|
361
|
Negative selection (natural selection)
|
1,779
|
59
|
Stub
|
Mid
|
362
|
Bird hybrid
|
1,765
|
58
|
Start
|
Low
|
363
|
Motion camouflage
|
1,715
|
57
|
GA
|
Low
|
364
|
Price equation
|
1,704
|
56
|
C
|
Low
|
365
|
Computational phylogenetics
|
1,666
|
55
|
C
|
Mid
|
366
|
Snake detection theory
|
1,663
|
55
|
Start
|
Mid
|
367
|
Genotype–phenotype distinction
|
1,657
|
55
|
Start
|
High
|
368
|
Jerry Coyne
|
1,657
|
55
|
Start
|
Low
|
369
|
Struggle for existence
|
1,633
|
54
|
C
|
Mid
|
370
|
Creation and evolution in public education
|
1,623
|
54
|
B
|
Mid
|
371
|
Red Deer Cave people
|
1,615
|
53
|
Start
|
Low
|
372
|
Muller's ratchet
|
1,606
|
53
|
Start
|
Mid
|
373
|
The Third Chimpanzee
|
1,604
|
53
|
C
|
Low
|
374
|
Grandmother hypothesis
|
1,600
|
53
|
C
|
Mid
|
375
|
Evolution of cells
|
1,599
|
53
|
Start
|
High
|
376
|
August Weismann
|
1,595
|
53
|
Start
|
High
|
377
|
Baldwin effect
|
1,594
|
53
|
GA
|
Low
|
378
|
Evolutionary mismatch
|
1,592
|
53
|
C
|
Low
|
379
|
Molecular evolution
|
1,591
|
53
|
C
|
Top
|
380
|
Oceanic dispersal
|
1,591
|
53
|
Start
|
Low
|
381
|
Modern humans
|
1,563
|
52
|
NA
|
NA
|
382
|
Panmixia
|
1,556
|
51
|
Start
|
Mid
|
383
|
Evolution of tetrapods
|
1,543
|
51
|
C
|
High
|
384
|
Siblicide
|
1,540
|
51
|
Start
|
Low
|
385
|
Numerical taxonomy
|
1,523
|
50
|
Start
|
Mid
|
386
|
Stabilizing selection
|
1,520
|
50
|
Start
|
Mid
|
387
|
Down House
|
1,519
|
50
|
C
|
Low
|
388
|
Evolution of nervous systems
|
1,513
|
50
|
B
|
Mid
|
389
|
Mate choice in humans
|
1,492
|
49
|
B
|
Unknown
|
390
|
Evolution of biological complexity
|
1,479
|
49
|
C
|
Mid
|
391
|
Indel
|
1,468
|
48
|
Start
|
Mid
|
392
|
Embryological origins of the mouth and anus
|
1,468
|
48
|
Start
|
Low
|
393
|
Codon usage bias
|
1,456
|
48
|
B
|
Low
|
394
|
Nuptial gift
|
1,454
|
48
|
Start
|
Mid
|
395
|
Cognitive tradeoff hypothesis
|
1,423
|
47
|
C
|
Low
|
396
|
Initial Upper Paleolithic
|
1,421
|
47
|
B
|
Unknown
|
397
|
Disruptive selection
|
1,420
|
47
|
C
|
Mid
|
398
|
Nicholas Miklouho-Maclay
|
1,413
|
47
|
C
|
Low
|
399
|
Red dress effect
|
1,409
|
46
|
Start
|
Low
|
400
|
Fitness landscape
|
1,400
|
46
|
B
|
High
|
401
|
Tend and befriend
|
1,399
|
46
|
C
|
Low
|
402
|
Evolutionary psychology of religion
|
1,397
|
46
|
Start
|
Low
|
403
|
Grimaldi man
|
1,397
|
46
|
C
|
Low
|
404
|
Evolution of mammalian auditory ossicles
|
1,394
|
46
|
B
|
Mid
|
405
|
Snaiad
|
1,392
|
46
|
B
|
Low
|
406
|
Androgenesis
|
1,364
|
45
|
C
|
Low
|
407
|
Evolution of snake venom
|
1,362
|
45
|
GA
|
Mid
|
408
|
Neural Darwinism
|
1,334
|
44
|
C
|
Unknown
|
409
|
Reproductive success
|
1,330
|
44
|
Start
|
High
|
410
|
Background extinction rate
|
1,329
|
44
|
Start
|
Mid
|
411
|
Evolution of cephalopods
|
1,318
|
43
|
C
|
Low
|
412
|
Models of DNA evolution
|
1,313
|
43
|
B
|
Low
|
413
|
Robert Trivers
|
1,312
|
43
|
Start
|
Low
|
414
|
Parapatric speciation
|
1,312
|
43
|
C
|
Mid
|
415
|
Heterozygote advantage
|
1,308
|
43
|
Start
|
Mid
|
416
|
Junkyard tornado
|
1,305
|
43
|
C
|
Low
|
417
|
Evolutionary approaches to depression
|
1,285
|
42
|
Start
|
Low
|
418
|
Taforalt
|
1,263
|
42
|
C
|
Low
|
419
|
Embryonic diapause
|
1,253
|
41
|
Start
|
Low
|
420
|
Metapopulation
|
1,252
|
41
|
B
|
Mid
|
421
|
Green-beard effect
|
1,245
|
41
|
Start
|
Low
|
422
|
Acritarch
|
1,241
|
41
|
C
|
Low
|
423
|
History of anthropometry
|
1,224
|
40
|
C
|
Low
|
424
|
Evolution of ageing
|
1,214
|
40
|
B
|
High
|
425
|
Extinction vortex
|
1,199
|
39
|
Start
|
Low
|
426
|
George R. Price
|
1,183
|
39
|
C
|
Low
|
427
|
Satoshi Kanazawa
|
1,179
|
39
|
C
|
Unknown
|
428
|
Gene family
|
1,177
|
39
|
C
|
High
|
429
|
Universal Darwinism
|
1,175
|
39
|
C
|
Low
|
430
|
Snow camouflage
|
1,175
|
39
|
GA
|
Low
|
431
|
Entrainment (biomusicology)
|
1,168
|
38
|
Start
|
Low
|
432
|
Evolution of bacteria
|
1,168
|
38
|
C
|
Mid
|
433
|
Anagenesis
|
1,164
|
38
|
C
|
Mid
|
434
|
Aerobic fermentation
|
1,155
|
38
|
B
|
Low
|
435
|
Homoplasy
|
1,148
|
38
|
Start
|
Low
|
436
|
Nothing in Biology Makes Sense Except in the Light of Evolution
|
1,138
|
37
|
C
|
Mid
|
437
|
Trivers–Willard hypothesis
|
1,135
|
37
|
Start
|
Low
|
438
|
Ka/Ks ratio
|
1,134
|
37
|
C
|
Mid
|
439
|
Genetic divergence
|
1,131
|
37
|
Start
|
High
|
440
|
List of Neanderthal fossils
|
1,129
|
37
|
List
|
Low
|
441
|
Peripatric speciation
|
1,119
|
37
|
B
|
Mid
|
442
|
Jonathan Wells (intelligent design advocate)
|
1,115
|
37
|
Start
|
Low
|
443
|
Cryptic species complex
|
1,108
|
36
|
NA
|
NA
|
444
|
Diana Fleischman
|
1,104
|
36
|
Start
|
Low
|
445
|
Mating call
|
1,102
|
36
|
C
|
Low
|
446
|
Population structure (genetics)
|
1,097
|
36
|
Start
|
Low
|
447
|
Peptide nucleic acid
|
1,096
|
36
|
Start
|
Low
|
448
|
Population biology
|
1,096
|
36
|
Stub
|
Low
|
449
|
Wonderful Life (book)
|
1,094
|
36
|
Stub
|
Low
|
450
|
Evolution of lemurs
|
1,094
|
36
|
FA
|
Low
|
451
|
Racist
|
1,090
|
36
|
NA
|
NA
|
452
|
List of prehistoric cartilaginous fish genera
|
1,085
|
36
|
List
|
Mid
|
453
|
Budgerigar colour genetics
|
1,084
|
36
|
Start
|
Low
|
454
|
Dmanisi
|
1,077
|
35
|
Start
|
Mid
|
455
|
Mate value
|
1,067
|
35
|
C
|
Low
|
456
|
Isua Greenstone Belt
|
1,050
|
35
|
C
|
Mid
|
457
|
Niche construction
|
1,046
|
34
|
B
|
Low
|
458
|
Balancing selection
|
1,045
|
34
|
Start
|
Mid
|
459
|
David Krakauer (scientist)
|
1,043
|
34
|
Start
|
Low
|
460
|
Paternal care
|
1,041
|
34
|
C
|
Low
|
461
|
Operational sex ratio
|
1,038
|
34
|
Start
|
Low
|
462
|
Evolutionary anthropology
|
1,024
|
34
|
Start
|
Low
|
463
|
Hybrid fruit
|
1,023
|
34
|
Stub
|
Low
|
464
|
Origin of avian flight
|
1,020
|
34
|
Start
|
Mid
|
465
|
Major histocompatibility complex and sexual selection
|
1,020
|
34
|
C
|
Mid
|
466
|
Genetic pollution
|
1,006
|
33
|
C
|
Low
|
467
|
Teleology in biology
|
1,004
|
33
|
GA
|
High
|
468
|
Balanced lethal systems
|
1,000
|
33
|
C
|
Low
|
469
|
Iron–sulfur world hypothesis
|
999
|
33
|
C
|
Low
|
470
|
Systemic racism
|
979
|
32
|
NA
|
NA
|
471
|
Josiah C. Nott
|
977
|
32
|
C
|
Low
|
472
|
The Genetical Theory of Natural Selection
|
968
|
32
|
Start
|
Mid
|
473
|
Last eukaryotic common ancestor
|
961
|
32
|
NA
|
High
|
474
|
Costly signaling theory in evolutionary psychology
|
954
|
31
|
C
|
Mid
|
475
|
Joan Roughgarden
|
953
|
31
|
C
|
Unknown
|
476
|
Synonymous substitution
|
952
|
31
|
Start
|
Mid
|
477
|
Sexual selection in birds
|
951
|
31
|
C
|
Low
|
478
|
David Sloan Wilson
|
946
|
31
|
Start
|
Unknown
|
479
|
Evolution of color vision in primates
|
944
|
31
|
C
|
Low
|
480
|
Outgroup (cladistics)
|
928
|
30
|
Start
|
Mid
|
481
|
The Greatest Show on Earth: The Evidence for Evolution
|
925
|
30
|
Start
|
Low
|
482
|
Frequency-dependent selection
|
908
|
30
|
Start
|
High
|
483
|
Autapomorphy
|
905
|
30
|
C
|
Low
|
484
|
Seminal fluid protein
|
898
|
29
|
Start
|
Low
|
485
|
Blending inheritance
|
897
|
29
|
GA
|
Low
|
486
|
Parasite-stress theory
|
896
|
29
|
C
|
Mid
|
487
|
Extended female sexuality
|
894
|
29
|
B
|
Mid
|
488
|
Saltation (biology)
|
893
|
29
|
C
|
Mid
|
489
|
Of Pandas and People
|
888
|
29
|
C
|
Low
|
490
|
Endemism in the Hawaiian Islands
|
881
|
29
|
Start
|
Low
|
491
|
Telescoping generations
|
868
|
28
|
Stub
|
Unknown
|
492
|
Jewish views on evolution
|
856
|
28
|
B
|
Low
|
493
|
Mutationism
|
854
|
28
|
GA
|
Low
|
494
|
Phenetics
|
849
|
28
|
Start
|
Mid
|
495
|
Endosymbiotic theory
|
849
|
28
|
NA
|
NA
|
496
|
Caveasphaera
|
846
|
28
|
Start
|
Low
|
497
|
Crocoduck
|
839
|
27
|
C
|
Low
|
498
|
Experimental evolution
|
836
|
27
|
Start
|
High
|
499
|
Bayesian inference in phylogeny
|
835
|
27
|
C
|
Low
|
500
|
Cladogenesis
|
833
|
27
|
Start
|
Mid
|
501
|
Human jaw shrinkage
|
820
|
27
|
Unknown
|
Unknown
|
502
|
Female sperm storage
|
811
|
27
|
C
|
Low
|
503
|
Savannah hypothesis
|
810
|
27
|
Start
|
Low
|
504
|
Character displacement
|
809
|
26
|
B
|
Mid
|
505
|
Cooperation (evolution)
|
808
|
26
|
B
|
Mid
|
506
|
Davis's law
|
806
|
26
|
Start
|
Low
|
507
|
Evolution of color vision
|
801
|
26
|
Start
|
Low
|
508
|
Evolutionary psychiatry
|
797
|
26
|
Stub
|
Low
|
509
|
Timeline of fish evolution
|
796
|
26
|
List
|
Low
|
510
|
Sociobiology: The New Synthesis
|
789
|
26
|
GA
|
Mid
|
511
|
Polyphenism
|
785
|
26
|
Start
|
Mid
|
512
|
Artificial selection
|
781
|
26
|
NA
|
NA
|
513
|
Mormon views on evolution
|
780
|
26
|
C
|
Low
|
514
|
Lagar Velho 1
|
779
|
25
|
Stub
|
Low
|
515
|
Protein superfamily
|
776
|
25
|
B
|
Mid
|
516
|
Adaptationism
|
771
|
25
|
Start
|
Mid
|
517
|
Polytomy
|
770
|
25
|
Start
|
Mid
|
518
|
Elizabeth, Lady Hope
|
767
|
25
|
C
|
Low
|
519
|
Gut (anatomy)
|
764
|
25
|
NA
|
Low
|
520
|
Lantian Man
|
762
|
25
|
GA
|
Low
|
521
|
Social selection
|
759
|
25
|
C
|
Low
|
522
|
Incomplete lineage sorting
|
749
|
24
|
Start
|
Mid
|
523
|
The Spandrels of San Marco and the Panglossian Paradigm
|
745
|
24
|
Start
|
Mid
|
524
|
Sperm Wars
|
744
|
24
|
Start
|
Mid
|
525
|
Parent–offspring conflict
|
740
|
24
|
Start
|
Mid
|
526
|
The Red Queen: Sex and the Evolution of Human Nature
|
734
|
24
|
Start
|
Low
|
527
|
Single-access key
|
733
|
24
|
C
|
Low
|
528
|
Domestication of the goat
|
730
|
24
|
B
|
Mid
|
529
|
Dollo's law of irreversibility
|
717
|
23
|
Start
|
High
|
530
|
Henry Walter Bates
|
714
|
23
|
C
|
High
|
531
|
Sexual selection in mammals
|
707
|
23
|
C
|
Low
|
532
|
Cope's rule
|
705
|
23
|
Start
|
Mid
|
533
|
List of non-avian dinosaur species preserved with evidence of feathers
|
704
|
23
|
List
|
Low
|
534
|
Annual vs. perennial plant evolution
|
699
|
23
|
C
|
Low
|
535
|
Project Steve
|
695
|
23
|
C
|
Low
|
536
|
Canalisation (genetics)
|
692
|
23
|
Start
|
Mid
|
537
|
Cryptic female choice
|
684
|
22
|
B
|
Low
|
538
|
Outline of evolution
|
678
|
22
|
List
|
Top
|
539
|
History of creationism
|
676
|
22
|
B
|
Mid
|
540
|
The 10,000 Year Explosion
|
672
|
22
|
B
|
Mid
|
541
|
Motoo Kimura
|
662
|
22
|
B
|
High
|
542
|
Allogamy
|
660
|
22
|
Start
|
Mid
|
543
|
Mosaic evolution
|
660
|
22
|
Start
|
Low
|
544
|
Emsleyan mimicry
|
659
|
21
|
C
|
Low
|
545
|
Chemical defense
|
658
|
21
|
C
|
Low
|
546
|
Evolutionary models of human drug use
|
657
|
21
|
C
|
Low
|
547
|
Race suicide
|
652
|
21
|
Start
|
Mid
|
548
|
Angraecum sesquipedale
|
646
|
21
|
B
|
Mid
|
549
|
Conservative replacement
|
639
|
21
|
Start
|
Low
|
550
|
Disposable soma theory of aging
|
637
|
21
|
C
|
Mid
|
551
|
Yuanmou Man
|
635
|
21
|
GA
|
Low
|
552
|
Host–parasite coevolution
|
633
|
21
|
GA
|
Mid
|
553
|
Hologenome theory of evolution
|
631
|
21
|
Start
|
Mid
|
554
|
Weasel program
|
629
|
20
|
B
|
Low
|
555
|
Genotype frequency
|
625
|
20
|
Start
|
Mid
|
556
|
Evolutionary ecology
|
618
|
20
|
C
|
Mid
|
557
|
Island hopping
|
609
|
20
|
NA
|
Low
|
558
|
Genetic erosion
|
609
|
20
|
C
|
Low
|
559
|
Phyletic gradualism
|
607
|
20
|
Start
|
Mid
|
560
|
PAH world hypothesis
|
606
|
20
|
Start
|
Low
|
561
|
Natural Theology or Evidences of the Existence and Attributes of the Deity
|
606
|
20
|
GA
|
Low
|
562
|
Endless Forms Most Beautiful (book)
|
605
|
20
|
GA
|
Low
|
563
|
Koobi Fora
|
604
|
20
|
C
|
Mid
|
564
|
Plant evolution
|
604
|
20
|
Start
|
High
|
565
|
Ecomorphology
|
604
|
20
|
B
|
Low
|
566
|
Haplogroup C-V20
|
604
|
20
|
Unknown
|
Unknown
|
567
|
Court jester hypothesis
|
598
|
19
|
C
|
Low
|
568
|
The Vital Question
|
596
|
19
|
GA
|
Low
|
569
|
Evolvability
|
591
|
19
|
C
|
High
|
570
|
Atelocyanobacterium thalassa
|
591
|
19
|
C
|
Low
|
571
|
Winner and loser effects
|
590
|
19
|
C
|
Low
|
572
|
Evolution of eusociality
|
588
|
19
|
C
|
Low
|
573
|
Disassortative mating
|
579
|
19
|
C
|
Mid
|
574
|
Robert Edmond Grant
|
575
|
19
|
Start
|
Low
|
575
|
List of Neanderthal sites
|
571
|
19
|
List
|
Low
|
576
|
Directed evolution (transhumanism)
|
570
|
19
|
Stub
|
Low
|
577
|
Polyandry in fish
|
569
|
18
|
C
|
Low
|
578
|
Genetic isolate
|
567
|
18
|
Stub
|
Low
|
579
|
Ecological speciation
|
565
|
18
|
B
|
High
|
580
|
Dawkins vs. Gould
|
564
|
18
|
Start
|
Low
|
581
|
Cooperative eye hypothesis
|
560
|
18
|
Start
|
Low
|
582
|
Evolution of flagella
|
553
|
18
|
Start
|
Mid
|
583
|
Fisher's fundamental theorem of natural selection
|
547
|
18
|
Start
|
Mid
|
584
|
Schizocoely
|
546
|
18
|
Start
|
Mid
|
585
|
Australopithecus deyiremeda
|
545
|
18
|
GA
|
Low
|
586
|
George Christopher Williams
|
544
|
18
|
Start
|
Mid
|
587
|
Development of Darwin's theory
|
544
|
18
|
B
|
Mid
|
588
|
Cytotaxonomy
|
544
|
18
|
Stub
|
Mid
|
589
|
Darwinian demon
|
543
|
18
|
Stub
|
Low
|
590
|
Phylogenetic comparative methods
|
528
|
17
|
C
|
Low
|
591
|
Reinforcement (speciation)
|
525
|
17
|
GA
|
Mid
|
592
|
The Major Transitions in Evolution
|
524
|
17
|
Stub
|
Low
|
593
|
Proavis
|
524
|
17
|
Start
|
Low
|
594
|
Elaine Morgan
|
522
|
17
|
C
|
Low
|
595
|
Evolution: The Game of Intelligent Life
|
522
|
17
|
Start
|
Low
|
596
|
Vertebrate land invasion
|
521
|
17
|
C
|
Mid
|
597
|
Automimicry
|
520
|
17
|
GA
|
Mid
|
598
|
Vestigial response
|
516
|
17
|
Stub
|
Low
|
599
|
Loren Cordain
|
514
|
17
|
Stub
|
Low
|
600
|
Precambrian rabbit
|
512
|
17
|
C
|
Low
|
601
|
Patrick Matthew
|
510
|
17
|
B
|
Mid
|
602
|
Insectivorous Plants (book)
|
510
|
17
|
Start
|
Low
|
603
|
Biogenesis
|
507
|
16
|
NA
|
High
|
604
|
Bitter taste evolution
|
507
|
16
|
Start
|
Low
|
605
|
Reticulate evolution
|
502
|
16
|
C
|
Mid
|
606
|
Horizontal gene transfer in evolution
|
499
|
16
|
Start
|
High
|
607
|
Black Queen hypothesis
|
498
|
16
|
Start
|
Low
|
608
|
Habitable zone for complex life
|
497
|
16
|
C
|
Unknown
|
609
|
Demonic Males
|
496
|
16
|
C
|
Unknown
|
610
|
Muscular evolution in humans
|
491
|
16
|
Start
|
Low
|
611
|
Ornithophily
|
486
|
16
|
B
|
Low
|
612
|
Evolutionary grade
|
481
|
16
|
Start
|
High
|
613
|
Evolution of cognition
|
477
|
15
|
C
|
Low
|
614
|
Franz Weidenreich
|
474
|
15
|
Stub
|
Mid
|
615
|
Bet hedging (biology)
|
473
|
15
|
B
|
Mid
|
616
|
Adaptation and Natural Selection
|
468
|
15
|
Start
|
Low
|
617
|
Saldanha man
|
468
|
15
|
Stub
|
Low
|
618
|
Alternative abiogenesis scenarios
|
468
|
15
|
C
|
Low
|
619
|
Evolutionary suicide
|
466
|
15
|
Start
|
Low
|
620
|
Long branch attraction
|
463
|
15
|
Start
|
Low
|
621
|
Mate guarding
|
462
|
15
|
Unknown
|
Mid
|
622
|
Power, Sex, Suicide
|
461
|
15
|
Stub
|
Low
|
623
|
Philosophie zoologique
|
460
|
15
|
GA
|
Low
|
624
|
Inheritance of acquired characteristics
|
457
|
15
|
NA
|
NA
|
625
|
Ray Lankester
|
455
|
15
|
B
|
Low
|
626
|
The Genealogical Adam and Eve
|
452
|
15
|
Start
|
Low
|
627
|
Selection coefficient
|
450
|
15
|
Stub
|
Mid
|
628
|
Inferring horizontal gene transfer
|
449
|
14
|
B
|
Low
|
629
|
Darwin and women
|
449
|
14
|
Stub
|
Low
|
630
|
Buya, Eritrea
|
444
|
14
|
C
|
Unknown
|
631
|
Genome evolution
|
443
|
14
|
C
|
Top
|
632
|
Unit of selection
|
436
|
14
|
C
|
High
|
633
|
Chemoton
|
436
|
14
|
Start
|
Low
|
634
|
Rate of evolution
|
436
|
14
|
Start
|
Low
|
635
|
Natural Selection (manuscript)
|
434
|
14
|
Stub
|
Low
|
636
|
Racism on the Internet
|
431
|
14
|
Start
|
Low
|
637
|
Sex Power Money
|
431
|
14
|
C
|
Low
|
638
|
Evolutionary tradeoff
|
431
|
14
|
Unknown
|
Unknown
|
639
|
Vocal learning
|
426
|
14
|
B
|
Low
|
640
|
Man's Place in Nature
|
425
|
14
|
Start
|
Mid
|
641
|
Epic of evolution
|
424
|
14
|
C
|
Low
|
642
|
Timeline of zoology
|
423
|
14
|
List
|
Mid
|
643
|
Nina Jablonski
|
420
|
14
|
B
|
Low
|
644
|
Evolutionary developmental psychology
|
418
|
13
|
C
|
Low
|
645
|
Great Hippocampus Question
|
418
|
13
|
B
|
Low
|
646
|
Nanjing Man
|
415
|
13
|
C
|
Low
|
647
|
Lilliput effect
|
414
|
13
|
Start
|
Low
|
648
|
Glossary of genetics and evolutionary biology
|
414
|
13
|
List
|
Top
|
649
|
Zlatý kůň woman
|
413
|
13
|
Start
|
Low
|
650
|
Darwinian literary studies
|
411
|
13
|
C
|
Low
|
651
|
James Cowles Prichard
|
405
|
13
|
C
|
High
|
652
|
Troglomorphism
|
405
|
13
|
Stub
|
Low
|
653
|
The Variation of Animals and Plants Under Domestication
|
404
|
13
|
C
|
Low
|
654
|
Error threshold (evolution)
|
403
|
13
|
C
|
Mid
|
655
|
Cytonuclear discordance
|
403
|
13
|
Start
|
Unknown
|
656
|
Weapon (biology)
|
402
|
13
|
Stub
|
Low
|
657
|
Sexual selection in scaled reptiles
|
400
|
13
|
Start
|
Low
|
658
|
Zinnia Kumar
|
400
|
13
|
C
|
Low
|
659
|
Edward Blyth
|
399
|
13
|
B
|
High
|
660
|
What Darwin Got Wrong
|
399
|
13
|
Start
|
Low
|
661
|
Klepton
|
399
|
13
|
Start
|
Low
|
662
|
Genetic purging
|
399
|
13
|
Unknown
|
Unknown
|
663
|
Female line
|
399
|
13
|
NA
|
NA
|
664
|
The Evolution of Desire
|
397
|
13
|
Start
|
Unknown
|
665
|
St. George Jackson Mivart
|
396
|
13
|
Start
|
Low
|
666
|
McLean v. Arkansas
|
396
|
13
|
Start
|
Low
|
667
|
The Goodness Paradox
|
393
|
13
|
Start
|
Low
|
668
|
Laboratory experiments of speciation
|
390
|
13
|
List
|
Low
|
669
|
Willi Hennig
|
389
|
12
|
Start
|
Mid
|
670
|
Shane Campbell-Staton
|
389
|
12
|
Start
|
Low
|
671
|
Glacial refugium
|
388
|
12
|
Stub
|
Low
|
672
|
Sex differences in memory
|
384
|
12
|
Start
|
Low
|
673
|
Lek paradox
|
383
|
12
|
C
|
Low
|
674
|
Conservation-induced extinction
|
383
|
12
|
Start
|
Mid
|
675
|
Genetic assimilation
|
381
|
12
|
GA
|
Low
|
676
|
Caminalcules
|
381
|
12
|
Start
|
Mid
|
677
|
Wushan Man
|
380
|
12
|
Start
|
Low
|
678
|
Evolution of descended testes in mammals
|
380
|
12
|
Unknown
|
Unknown
|
679
|
Spiegelman's Monster
|
379
|
12
|
Start
|
Low
|
680
|
The Evolution of Beauty
|
378
|
12
|
Start
|
Low
|
681
|
Herman Bernhard Lundborg
|
377
|
12
|
Start
|
Low
|
682
|
Origin and function of meiosis
|
377
|
12
|
Start
|
Low
|
683
|
Inclusive fitness in humans
|
377
|
12
|
C
|
Low
|
684
|
Konstantin Mereschkowski
|
376
|
12
|
GA
|
Unknown
|
685
|
Eugenics in Mexico
|
376
|
12
|
Start
|
Low
|
686
|
Hybrid zone
|
373
|
12
|
C
|
Mid
|
687
|
Enterocoely
|
366
|
12
|
Stub
|
Mid
|
688
|
Evolutionary trap
|
366
|
12
|
Start
|
Low
|
689
|
List of transitional fossils
|
365
|
12
|
NA
|
NA
|
690
|
Bat wing development
|
365
|
12
|
Start
|
Low
|
691
|
Evolution of metal ions in biological systems
|
365
|
12
|
C
|
Low
|
692
|
Randy Thornhill
|
363
|
12
|
Start
|
Mid
|
693
|
Bateson–Dobzhansky–Muller model
|
359
|
11
|
Unknown
|
Unknown
|
694
|
Quasispecies model
|
356
|
11
|
C
|
Mid
|
695
|
Precambrian body plans
|
356
|
11
|
B
|
Low
|
696
|
Emergent evolution
|
354
|
11
|
C
|
Low
|
697
|
Expensive tissue hypothesis
|
354
|
11
|
C
|
Low
|
698
|
Germ-Soma Differentiation
|
353
|
11
|
C
|
Low
|
699
|
Intragenomic conflict
|
349
|
11
|
C
|
Mid
|
700
|
Religion Explained
|
343
|
11
|
Start
|
Low
|
701
|
Fritz Müller
|
340
|
11
|
B
|
Mid
|
702
|
Evolutionary neuroscience
|
338
|
11
|
Start
|
High
|
703
|
Evolution (TV series)
|
338
|
11
|
Start
|
Low
|
704
|
Reciprocal altruism in humans
|
338
|
11
|
Start
|
Low
|
705
|
Allan Wilson (biologist)
|
335
|
11
|
C
|
Low
|
706
|
Museum of Human Evolution
|
335
|
11
|
Start
|
Unknown
|
707
|
History of zoology through 1859
|
334
|
11
|
C
|
High
|
708
|
Deep homology
|
333
|
11
|
Start
|
Mid
|
709
|
Intergradation
|
330
|
11
|
Start
|
Low
|
710
|
Helitron (biology)
|
324
|
10
|
B
|
Low
|
711
|
Douglas J. Futuyma
|
323
|
10
|
C
|
Low
|
712
|
Red King hypothesis
|
323
|
10
|
Start
|
Low
|
713
|
Evolutionary physiology
|
321
|
10
|
B
|
High
|
714
|
Group living
|
319
|
10
|
Start
|
Low
|
715
|
Isolation by distance
|
315
|
10
|
Start
|
Low
|
716
|
Scott F. Gilbert
|
313
|
10
|
C
|
Low
|
717
|
The Structure of Evolutionary Theory
|
312
|
10
|
Start
|
Low
|
718
|
Marcus Feldman
|
312
|
10
|
Start
|
Low
|
719
|
Megaevolution
|
312
|
10
|
Start
|
Mid
|
720
|
David Lack
|
311
|
10
|
C
|
Low
|
721
|
Quantum evolution
|
309
|
10
|
C
|
Mid
|
722
|
Evo-devo gene toolkit
|
308
|
10
|
Start
|
Mid
|
723
|
Digital organism
|
306
|
10
|
Stub
|
Low
|
724
|
Polydactyly in stem-tetrapods
|
305
|
10
|
Start
|
Low
|
725
|
Alfred Newton
|
304
|
10
|
C
|
Low
|
726
|
Self-decoration camouflage
|
303
|
10
|
GA
|
Low
|
727
|
Psammosere
|
298
|
9
|
Stub
|
Mid
|
728
|
Cultural selection theory
|
294
|
9
|
C
|
Low
|
729
|
Viral eukaryogenesis
|
292
|
9
|
Start
|
Mid
|
730
|
Postcanine megadontia
|
292
|
9
|
C
|
Low
|
731
|
Evolutionary aesthetics
|
292
|
9
|
C
|
High
|
732
|
Alloplastic adaptation
|
291
|
9
|
Stub
|
Low
|
733
|
Law of Life
|
290
|
9
|
Stub
|
Low
|
734
|
Kettlewell's experiment
|
289
|
9
|
Start
|
Mid
|
735
|
Jeremiah Kianga
|
289
|
9
|
Start
|
Low
|
736
|
Co-adaptation
|
288
|
9
|
C
|
Low
|
737
|
W. Tecumseh Fitch
|
288
|
9
|
Stub
|
Low
|
738
|
Homo consumericus
|
288
|
9
|
Start
|
Low
|
739
|
Evolutionary psychology of language
|
288
|
9
|
Start
|
Low
|
740
|
Push of the past
|
287
|
9
|
C
|
Low
|
741
|
Evolutionary dynamics
|
285
|
9
|
Stub
|
Mid
|
742
|
Biogeographic regions of Europe
|
285
|
9
|
Start
|
Mid
|
743
|
On Being the Right Size
|
282
|
9
|
C
|
Mid
|
744
|
Background selection
|
279
|
9
|
Start
|
Low
|
745
|
Neofunctionalization
|
279
|
9
|
Start
|
Low
|
746
|
Tradeoffs for locomotion in air and water
|
278
|
9
|
C
|
Mid
|
747
|
Evolutionary fauna
|
274
|
9
|
Start
|
Low
|
748
|
Rensch's rule
|
273
|
9
|
Start
|
Low
|
749
|
Reciprocity (evolution)
|
270
|
9
|
Unknown
|
Unknown
|
750
|
The Neutral Theory of Molecular Evolution
|
267
|
8
|
Stub
|
Low
|
751
|
Behavioral plasticity
|
265
|
8
|
Start
|
Low
|
752
|
Secondarily aquatic tetrapods
|
264
|
8
|
Stub
|
Mid
|
753
|
Sexual antagonistic coevolution
|
259
|
8
|
Unknown
|
Unknown
|
754
|
Automixis
|
256
|
8
|
Start
|
Unknown
|
755
|
Ancestral sequence reconstruction
|
256
|
8
|
C
|
Low
|
756
|
Evolutionary theodicy
|
255
|
8
|
C
|
Low
|
757
|
Shifting balance theory
|
254
|
8
|
Stub
|
Low
|
758
|
Coloration evidence for natural selection
|
253
|
8
|
GA
|
Mid
|
759
|
Paragroup
|
252
|
8
|
Stub
|
Low
|
760
|
Undeniable: Evolution and the Science of Creation
|
249
|
8
|
Start
|
Low
|
761
|
Davidson Black
|
248
|
8
|
C
|
Mid
|
762
|
Evolution of olfaction
|
248
|
8
|
C
|
Low
|
763
|
Constructive neutral evolution
|
248
|
8
|
C
|
Low
|
764
|
Paul W. Ewald
|
246
|
8
|
Start
|
Low
|
765
|
The Seven Pillars of Life
|
245
|
8
|
Start
|
Low
|
766
|
Evidence for speciation by reinforcement
|
244
|
8
|
List
|
Low
|
767
|
Darwinian threshold
|
244
|
8
|
Start
|
Mid
|
768
|
Natural morality
|
242
|
8
|
Start
|
Low
|
769
|
Icons of Evolution
|
241
|
8
|
C
|
Low
|
770
|
Evolutionary invasion analysis
|
241
|
8
|
Start
|
Low
|
771
|
Qikiqtania
|
241
|
8
|
Stub
|
Unknown
|
772
|
Molecular Phylogenetics and Evolution
|
240
|
8
|
Stub
|
Low
|
773
|
William Henry Flower
|
239
|
7
|
B
|
Low
|
774
|
Nylon-eating bacteria and creationism
|
239
|
7
|
B
|
Low
|
775
|
Local adaptation
|
238
|
7
|
Unknown
|
Unknown
|
776
|
Mutation accumulation theory
|
235
|
7
|
C
|
Low
|
777
|
Stenogale
|
235
|
7
|
Stub
|
Low
|
778
|
Concerted evolution
|
232
|
7
|
Stub
|
Low
|
779
|
Cellularization
|
231
|
7
|
Stub
|
Low
|
780
|
The Theory of Evolution
|
231
|
7
|
Stub
|
Low
|
781
|
Fisher's geometric model
|
231
|
7
|
Start
|
Low
|
782
|
Reproductive suppression
|
230
|
7
|
C
|
Mid
|
783
|
Dynamic mutation
|
230
|
7
|
Stub
|
Low
|
784
|
Nearly neutral theory of molecular evolution
|
230
|
7
|
Start
|
Low
|
785
|
Francis Maitland Balfour
|
229
|
7
|
Start
|
Low
|
786
|
Multispecies coalescent process
|
228
|
7
|
Start
|
Low
|
787
|
Phylogenetic signal
|
228
|
7
|
C
|
Mid
|
788
|
Richard Prum
|
227
|
7
|
Start
|
Low
|
789
|
Fuyan Cave
|
226
|
7
|
C
|
Low
|
790
|
Joan E. Strassmann
|
225
|
7
|
Start
|
Low
|
791
|
Parasite load
|
224
|
7
|
C
|
Low
|
792
|
Alexander von Humboldt Biological Resources Research Institute
|
224
|
7
|
Stub
|
Low
|
793
|
Applications of evolution
|
223
|
7
|
B
|
Low
|
794
|
Peter J. Bowler
|
221
|
7
|
Start
|
Low
|
795
|
Gavin de Beer
|
219
|
7
|
C
|
Low
|
796
|
History of speciation
|
219
|
7
|
C
|
Low
|
797
|
Idealised population
|
218
|
7
|
C
|
Mid
|
798
|
Ileret
|
217
|
7
|
Stub
|
Low
|
799
|
Edward Bagnall Poulton
|
216
|
7
|
Start
|
Mid
|
800
|
Index of evolutionary biology articles
|
214
|
7
|
List
|
High
|
801
|
Modern human
|
213
|
7
|
NA
|
NA
|
802
|
Evolutionary psychology and culture
|
213
|
7
|
Start
|
Low
|
803
|
Philosophy of evolution
|
212
|
7
|
C
|
Mid
|
804
|
Proto-mitochondrion
|
211
|
7
|
Start
|
Mid
|
805
|
Inversion (evolutionary biology)
|
211
|
7
|
Start
|
Mid
|
806
|
Contingency (evolutionary biology)
|
210
|
7
|
Start
|
Low
|
807
|
Selection shadow
|
210
|
7
|
Start
|
Low
|
808
|
Herbivore adaptations to plant defense
|
209
|
6
|
B
|
Low
|
809
|
G-value paradox
|
206
|
6
|
C
|
Low
|
810
|
Orgel's rules
|
205
|
6
|
Stub
|
Low
|
811
|
Sexual selection in insects
|
205
|
6
|
B
|
Low
|
812
|
Alpheus Hyatt
|
203
|
6
|
Start
|
Low
|
813
|
Biodiversity of Kosovo
|
202
|
6
|
C
|
Low
|
814
|
Evolution of brachiopods
|
200
|
6
|
Start
|
Low
|
815
|
Biological constraints
|
198
|
6
|
Start
|
Mid
|
816
|
Sir William Lawrence, 1st Baronet
|
197
|
6
|
B
|
High
|
817
|
Subfunctionalization
|
196
|
6
|
Start
|
Low
|
818
|
Maternal behavior in vertebrates
|
194
|
6
|
C
|
Low
|
819
|
Viral phylodynamics
|
193
|
6
|
B
|
Low
|
820
|
Pseudoextinction
|
192
|
6
|
Start
|
Low
|
821
|
Phylotypic stage
|
191
|
6
|
C
|
Low
|
822
|
Evolutionary models of food sharing
|
191
|
6
|
C
|
Low
|
823
|
Distractive markings
|
191
|
6
|
C
|
Low
|
824
|
Urban evolution
|
191
|
6
|
C
|
Unknown
|
825
|
Allochronic speciation
|
191
|
6
|
B
|
Mid
|
826
|
Bias in the introduction of variation
|
191
|
6
|
B
|
Low
|
827
|
Hybrid incompatibility
|
190
|
6
|
C
|
Low
|
828
|
Heterotopy
|
189
|
6
|
Stub
|
Low
|
829
|
Phagomimicry
|
188
|
6
|
Stub
|
Low
|
830
|
Maternal effect dominant embryonic arrest
|
185
|
6
|
Start
|
Low
|
831
|
Interlocus sexual conflict
|
185
|
6
|
B
|
Mid
|
832
|
Rapid modes of evolution
|
183
|
6
|
Unknown
|
Unknown
|
833
|
Human somatic variation
|
183
|
6
|
C
|
Mid
|
834
|
Evolutionary landscape
|
181
|
6
|
C
|
High
|
835
|
Species-typical behavior
|
179
|
5
|
Start
|
Low
|
836
|
Developmental bias
|
178
|
5
|
Unknown
|
Unknown
|
837
|
Tree rearrangement
|
175
|
5
|
Start
|
Low
|
838
|
Mutation bias
|
175
|
5
|
C
|
Mid
|
839
|
Ecological inheritance
|
173
|
5
|
Stub
|
Low
|
840
|
List of Nepenthes natural hybrids
|
172
|
5
|
List
|
Low
|
841
|
Paraspecies
|
171
|
5
|
Stub
|
Low
|
842
|
Recurrent evolution
|
171
|
5
|
Unknown
|
Unknown
|
843
|
Segregating site
|
170
|
5
|
Start
|
Low
|
844
|
E. B. Ford
|
169
|
5
|
C
|
Low
|
845
|
Evolutionary Psychology (journal)
|
169
|
5
|
Stub
|
Unknown
|
846
|
Proteinoid
|
168
|
5
|
Start
|
Low
|
847
|
The Correlation between Relatives on the Supposition of Mendelian Inheritance
|
168
|
5
|
Start
|
Mid
|
848
|
Evolutionary approaches to postpartum depression
|
168
|
5
|
C
|
Low
|
849
|
Hydrogen hypothesis
|
167
|
5
|
Start
|
Low
|
850
|
Biodiversity of Wales
|
166
|
5
|
C
|
Low
|
851
|
Wing-assisted incline running
|
166
|
5
|
Start
|
Low
|
852
|
V. C. Wynne-Edwards
|
164
|
5
|
Start
|
Low
|
853
|
History of zoology (1859–present)
|
164
|
5
|
C
|
High
|
854
|
Ecology and evolutionary biology
|
161
|
5
|
Start
|
Low
|
855
|
Adaptive behavior (ecology)
|
161
|
5
|
C
|
Mid
|
856
|
The Origin of Birds
|
161
|
5
|
GA
|
High
|
857
|
Hybrid swarm
|
158
|
5
|
Start
|
Mid
|
858
|
Modularity (biology)
|
156
|
5
|
Start
|
Low
|
859
|
Clonal interference
|
156
|
5
|
Stub
|
Mid
|
860
|
TalkOrigins Archive
|
154
|
5
|
Start
|
Low
|
861
|
Storage effect
|
154
|
5
|
B
|
Mid
|
862
|
Molecular drive
|
153
|
5
|
Stub
|
Low
|
863
|
Ecological fitting
|
153
|
5
|
B
|
Low
|
864
|
GADV-protein world hypothesis
|
153
|
5
|
Start
|
Low
|
865
|
Formamide-based prebiotic chemistry
|
152
|
5
|
Start
|
Low
|
866
|
International Year of Biodiversity
|
150
|
5
|
Start
|
High
|
867
|
Hyrax Hill
|
149
|
4
|
B
|
Low
|
868
|
Prejudice from an evolutionary perspective
|
146
|
4
|
Start
|
Low
|
869
|
Preadaptation
|
145
|
4
|
NA
|
Mid
|
870
|
Zoology of the Voyage of H.M.S. Beagle
|
145
|
4
|
Stub
|
Low
|
871
|
Eukaryote hybrid genome
|
145
|
4
|
B
|
Low
|
872
|
Evolution by gene duplication
|
144
|
4
|
Start
|
High
|
873
|
John Tyler Bonner
|
142
|
4
|
C
|
Mid
|
874
|
Runcaria
|
142
|
4
|
Start
|
Low
|
875
|
Carboniferous-Earliest Permian Biodiversification Event
|
142
|
4
|
NA
|
Low
|
876
|
Intralocus sexual conflict
|
141
|
4
|
Start
|
Mid
|
877
|
History of molecular evolution
|
140
|
4
|
C
|
Mid
|
878
|
Key innovation
|
140
|
4
|
Start
|
Mid
|
879
|
List of ecoregions with high endemism
|
140
|
4
|
List
|
Low
|
880
|
Landscape genomics
|
139
|
4
|
Stub
|
Low
|
881
|
Mark Ridley (zoologist)
|
138
|
4
|
Stub
|
Low
|
882
|
Sibling species
|
137
|
4
|
NA
|
NA
|
883
|
Dan Willard
|
137
|
4
|
C
|
Low
|
884
|
David Hillis
|
136
|
4
|
Start
|
Low
|
885
|
White Sea assemblage
|
136
|
4
|
Stub
|
Low
|
886
|
Felsenstein's tree-pruning algorithm
|
135
|
4
|
Stub
|
Low
|
887
|
Arthur Cain
|
134
|
4
|
C
|
Low
|
888
|
Commemoration of Charles Darwin
|
134
|
4
|
C
|
Mid
|
889
|
Cospeciation
|
134
|
4
|
Start
|
Mid
|
890
|
Phylosymbiosis
|
134
|
4
|
Start
|
Low
|
891
|
How the Snake Lost Its Legs
|
130
|
4
|
GA
|
Low
|
892
|
Nama assemblage
|
130
|
4
|
Start
|
Low
|
893
|
Talk.origins
|
129
|
4
|
Start
|
Low
|
894
|
Host switch
|
129
|
4
|
C
|
Low
|
895
|
Founder takes all
|
128
|
4
|
Stub
|
Low
|
896
|
William Charles Wells
|
127
|
4
|
B
|
High
|
897
|
Autoplastic adaptation
|
125
|
4
|
Stub
|
Low
|
898
|
Moritz Wagner (naturalist)
|
124
|
4
|
Start
|
Low
|
899
|
Social immunity
|
124
|
4
|
B
|
High
|
900
|
Evolutionary capacitance
|
121
|
4
|
C
|
Mid
|
901
|
Laura Landweber
|
121
|
4
|
Start
|
Low
|
902
|
Russell Lande
|
120
|
4
|
Start
|
Low
|
903
|
Hologenomics
|
119
|
3
|
Stub
|
Low
|
904
|
Ecological evolutionary developmental biology
|
119
|
3
|
Start
|
Low
|
905
|
Darwin (unit)
|
117
|
3
|
Stub
|
Low
|
906
|
Character evolution
|
116
|
3
|
Unknown
|
Unknown
|
907
|
Man's Genesis
|
116
|
3
|
Start
|
Low
|
908
|
Nancy A. Moran
|
115
|
3
|
C
|
Low
|
909
|
Infinite sites model
|
114
|
3
|
Start
|
Low
|
910
|
Phylogenetic reconciliation
|
114
|
3
|
Unknown
|
Unknown
|
911
|
Polymorphism in Lepidoptera
|
113
|
3
|
C
|
High
|
912
|
Genomic evolution of birds
|
113
|
3
|
C
|
Low
|
913
|
Evolutionary rescue
|
113
|
3
|
Start
|
Low
|
914
|
Resource holding potential
|
112
|
3
|
Stub
|
Low
|
915
|
Mesozoic–Cenozoic radiation
|
112
|
3
|
Stub
|
Low
|
916
|
Paleohistology
|
112
|
3
|
C
|
Unknown
|
917
|
The Great Monkey Trial
|
111
|
3
|
Start
|
Low
|
918
|
Archaic Homo sapiens
|
111
|
3
|
NA
|
NA
|
919
|
Interactor
|
109
|
3
|
Stub
|
Low
|
920
|
Nonadaptive radiation
|
109
|
3
|
Start
|
Low
|
921
|
Graham Bell (biologist)
|
108
|
3
|
Stub
|
Low
|
922
|
Unique-event polymorphism
|
108
|
3
|
Start
|
Low
|
923
|
Gard model
|
108
|
3
|
Start
|
Low
|
924
|
Jeremy Yoder
|
108
|
3
|
Start
|
Low
|
925
|
ASUDAS
|
108
|
3
|
Start
|
Unknown
|
926
|
Contest competition
|
107
|
3
|
Stub
|
Low
|
927
|
Phylo (video game)
|
106
|
3
|
Start
|
Low
|
928
|
Kindred: Neanderthal Life, Love, Death and Art
|
106
|
3
|
Stub
|
Low
|
929
|
Ecological selection
|
104
|
3
|
Start
|
Mid
|
930
|
Michael Majerus
|
104
|
3
|
Start
|
Mid
|
931
|
Edwin Stephen Goodrich
|
104
|
3
|
C
|
Low
|
932
|
Wallace effect
|
103
|
3
|
NA
|
NA
|
933
|
Grit, not grass hypothesis
|
103
|
3
|
C
|
Low
|
934
|
Skeletal changes of vertebrates transitioning from water to land
|
103
|
3
|
C
|
Low
|
935
|
Phylogenetic inertia
|
103
|
3
|
Start
|
Mid
|
936
|
Hyposphene-hypantrum articulation
|
102
|
3
|
Start
|
Low
|
937
|
John Endler
|
101
|
3
|
Start
|
Low
|
938
|
Axel Meyer
|
100
|
3
|
Start
|
Unknown
|
939
|
WLH-50
|
100
|
3
|
Start
|
Unknown
|
940
|
Reciprocal causation
|
100
|
3
|
C
|
Low
|
941
|
Katie Hinde
|
100
|
3
|
C
|
Low
|
942
|
Resource defense polygyny
|
100
|
3
|
Stub
|
Unknown
|
943
|
Facilitated variation
|
98
|
3
|
Stub
|
Low
|
944
|
Turnover-pulse hypothesis
|
98
|
3
|
Start
|
Low
|
945
|
The Apportionment of Human Diversity
|
98
|
3
|
C
|
Low
|
946
|
Species group
|
97
|
3
|
NA
|
NA
|
947
|
James A. Lake
|
97
|
3
|
Start
|
Low
|
948
|
European Society for Evolutionary Biology
|
96
|
3
|
Stub
|
Low
|
949
|
Stephen Blair Hedges
|
96
|
3
|
Start
|
Low
|
950
|
Molly Jahn
|
96
|
3
|
C
|
Unknown
|
951
|
Interpolation theory
|
95
|
3
|
Start
|
Low
|
952
|
Ruth Mace
|
95
|
3
|
Start
|
Low
|
953
|
Mimicry in vertebrates
|
95
|
3
|
Start
|
Low
|
954
|
Assisted evolution
|
95
|
3
|
C
|
Low
|
955
|
Darwinian anthropology
|
94
|
3
|
B
|
Unknown
|
956
|
Fluctuating selection
|
94
|
3
|
Start
|
Low
|
957
|
Despeciation
|
93
|
3
|
Start
|
Low
|
958
|
Epididymis evolution from reptiles to mammals
|
92
|
3
|
B
|
Low
|
959
|
Lomagundi-Jatuli Carbon Isotope Excursion
|
91
|
3
|
B
|
Unknown
|
960
|
Evolution of Infectious Disease
|
90
|
3
|
Stub
|
Low
|
961
|
Egg taphonomy
|
90
|
3
|
C
|
Low
|
962
|
Thorson's rule
|
89
|
2
|
Start
|
Low
|
963
|
Largest-scale trends in evolution
|
89
|
2
|
Start
|
High
|
964
|
Non-Darwinian Evolution (paper)
|
89
|
2
|
Stub
|
Low
|
965
|
Karl Kessler
|
89
|
2
|
Stub
|
Low
|
966
|
Francisc Rainer
|
89
|
2
|
B
|
Low
|
967
|
Scott V. Edwards
|
89
|
2
|
C
|
Low
|
968
|
Romanticism in evolution theory
|
88
|
2
|
Start
|
Low
|
969
|
OneZoom
|
88
|
2
|
Start
|
Unknown
|
970
|
Evolution Day
|
87
|
2
|
Unknown
|
Unknown
|
971
|
Bitter Springs anomaly
|
87
|
2
|
C
|
Unknown
|
972
|
Locomotor mimicry
|
86
|
2
|
Start
|
Low
|
973
|
Harrison's rule
|
86
|
2
|
Unknown
|
Unknown
|
974
|
Eric Charnov
|
85
|
2
|
Start
|
Low
|
975
|
Rupert Riedl
|
84
|
2
|
Start
|
Low
|
976
|
Evolution of Macropodidae
|
84
|
2
|
Start
|
Low
|
977
|
Henric Sanielevici
|
84
|
2
|
B
|
Low
|
978
|
Tip dating
|
84
|
2
|
Stub
|
Low
|
979
|
Sex differences in sensory systems
|
83
|
2
|
Start
|
Mid
|
980
|
The Different Forms of Flowers on Plants of the Same Species
|
83
|
2
|
Start
|
Low
|
981
|
Institute of Human Origins
|
83
|
2
|
Start
|
Low
|
982
|
Victoria Arbour
|
82
|
2
|
Start
|
Low
|
983
|
Nonecological speciation
|
82
|
2
|
Start
|
Low
|
984
|
Fisheries-induced evolution
|
81
|
2
|
C
|
Low
|
985
|
Reductive evolution
|
80
|
2
|
Start
|
Low
|
986
|
The Panda's Thumb (blog)
|
79
|
2
|
Start
|
Low
|
987
|
Swamping argument
|
79
|
2
|
Stub
|
Low
|
988
|
Human evolutionary developmental biology
|
78
|
2
|
C
|
Mid
|
989
|
Escape and radiate coevolution
|
77
|
2
|
C
|
Unknown
|
990
|
Dieter Ebert
|
76
|
2
|
C
|
Low
|
991
|
Ecotron
|
76
|
2
|
Stub
|
Low
|
992
|
Andrew Berry (biologist)
|
75
|
2
|
Stub
|
Low
|
993
|
Tim Lewens
|
75
|
2
|
Start
|
Unknown
|
994
|
Marcello Barbieri
|
75
|
2
|
Start
|
Low
|
995
|
Human reproductive ecology
|
74
|
2
|
Start
|
Low
|
996
|
Compilospecies
|
73
|
2
|
Stub
|
Low
|
997
|
J. T. Gulick
|
72
|
2
|
Start
|
Low
|
998
|
Identity in social insects
|
72
|
2
|
Start
|
Low
|
999
|
Hox genes in amphibians and reptiles
|
72
|
2
|
C
|
Low
|
1000
|
International Code of Area Nomenclature
|
71
|
2
|
Stub
|
Low
|