Successive replacements in trios exposed to alarming objects |
chimpanzees |
Menzel et al. (1972) |
3 B |
habituation effect stable (17) |
Transmission chains, seeded with alarm calls to arbitrary object |
blackbirds |
Curio et al. (1978a,b)
|
3 C |
alarm calling stable (6) |
Whole groups exposed to novel cues to buried food; spread of discovery in groups documented |
baboons, vervets |
Cambefort (1981) |
1 A |
? |
Three nut-cracking chimpanzees mixed with nine naive ones |
chimpanzees |
Sumita et al. (1985) |
2A |
? |
Models pecked through paper covers, in wild and captive flocks |
pigeons |
Lefebvre (1986) |
4 A |
piercing stable over 55 days |
Spread of spontaneously initiated nut-cracking recorded in group |
chimpanzees |
Hannah & McGrew (1987) |
2 A |
? |
Transmission chains seeded with models digging up carrot pieces |
rats |
Laland & Plotkin (1990) |
4 C |
digging stable (8) |
Replication of 1990 study but incorporating a 24 hour delay |
rats |
Laland & Plotkin (1992) |
4 C |
stability less, with delay |
Opportunity provided for group to use tools to probe for honey |
chimpanzees |
Paquette (1992) |
1 A |
? |
Rearing conciliatory stump-tailed macaques with rhesus, among whom reconciliation is relatively rare |
rhesus macaques |
de Waal & Johanowicz (1993) |
5 A |
effect stable over six-week post-model phase |
Transmission chains seeded with rats preferring different flavours |
rats |
Laland & Plotkin (1993) |
7 C |
transmission shown (8) but fidelity variable |
Nuts cracked elsewhere introduced; spread in group recorded over several years |
chimpanzees |
Matsuzawa (1994) and Biro et al. (2003)
|
1 A |
? |
Successive replacements in groups with initial flavour preferences |
rats |
Galef & Allen (1995) |
5 B |
transmission shown, with slight waning (over 14) |
Wild groups seeded with individuals trained to open specific small doors to feed |
magpie jays (wild) |
Langan (1996) |
7 A |
door opening stable over 3 days, but not door chosen |
Spread of dipping for honey with specific natural tool documented |
chimpanzees |
Tonooka et al. (1997) |
1 A |
? |
Founder shoals were seeded with preference for one of two routes |
guppies |
Laland & Williams (1997) |
5 B |
differences transmitted (7) but waned by half |
Similar to 1997 paper but more efficient alternative available |
guppies |
Laland & Williams (1998) |
5 B |
differences transmitted (7) but waned |
Groups with mixed naive and experienced fishes created |
guppies |
Reader & Laland (2000) |
2 A |
? |
Young cowbirds housed with adults singing either of two different songs; repeated once first cohort became adults (models) |
cowbirds |
Freeberg (1998) and Freeberg et al. (2001)
|
5 A |
? |
Spread of route preference: models in familiarity and experience |
guppies |
Swaney et al. (2001) |
2 A |
? |
Spread logged off using either of two routes to escape a threat |
guppies |
Brown & Laland (2002) |
7 A |
social transmission not found |
Flocks exposed to models feeding on blood from mock hen |
chickens |
Cloutier et al. (2002) |
4 A |
rapid waning over three transitions |
Wild, banded birds exposed to model using novel foraging method |
keas (wild) |
Gajdon et al. (2004) |
3 A |
no significant evidence of social transmission |
Captive chimpanzees given rough leaves used medicinally in wild |
chimpanzees |
Huffman & Hirata (2004) |
1 A |
? |
Juveniles exposed to adults using either of two methods to get juice |
brown capuchins |
Fragaszy et al. (2004) |
6 A |
techniques spread but social learning unclear |
Two groups each seeded with model using tool in different way |
chimpanzees |
Whiten et al. (2005) |
7 A |
moderate fidelity but stable over two months |
Two transmission chains; opening artificial ‘fruit’ using alternative methods, plus control condition lacking model |
chimpanzees children |
Horner et al. (2006) |
7 C |
stable (8) |
Two groups, each seeded with arbitrary convention to obtain food |
chimpanzees |
Bonnie et al. (2006) |
7 A |
spread to half group: stable, one corruption |
As for 2005, but transfer between groups in foraging techniques |
chimpanzees |
Whiten et al. (2007) |
6 A |
stable, spread across three groups |
Replication of Whiten et al. (2005), with one untrained model |
chimpanzees |
Hopper et al. (2007) |
7 A |
minimal evidence of social transmission |
Two groups each seeded with a different foraging technique (via video) of related species model |
colobus monkeys |
Price & Caldwell (2007) |
6 A |
stable after 5 days with no model, one corruption |
Replication of Horner et al. (2006) with appropriately modified task |
brown capuchins |
Dindo et al. (2008) |
7 C |
stable (4) |
Successive replacements of fishes focused on novel food task |
guppies, playfish |
Stanley et al. (2008) |
4 B |
stable (13) |