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. 2017 Mar 29;37(13):3555–3567. doi: 10.1523/JNEUROSCI.3213-16.2017

Table 1.

Task sequence in each cohort

Lighting condition Cohort Recognition task sequence
Condition 1: LD 1A (n = 8) H × 6 → (1) object × 4 → (2) object displacement × 2 → (3) object-in-place × 2
1B (n = 8) H × 6 → (1) object × 4 → (2) object displacement × 2 → (3) object-in-place × 2 → (4) odor × 4
1Ca (n = 8) H × 6 → (1) object × 4 → (2) object displacement × 2 → (3) object-in-place × 2
Condition 2: rLL 2Ab (n = 8) H × 6 → (1) object displacement × 2 → (2) object-in-place × 2 → (3) odor × 4
2Bc (n = 8) H × 6 → (1) odor × 4 → (2) object displacement × 2 → (3) object-in-place × 2 → (4) object × 4
2Cb (n = 8) H × 6 → (1) object displacement × 2 → (2) odor × 2
Control LL 3A (n = 16) H × 6 → (1) object × 2
3B (n = 8) H × 6 → (1) object-in-place × 2
3C (n = 16) H × 6 → (1) object × 2 (LD) → (2) odor × 2 (LL)

All mice received 6 habituation trials (H) in the empty arena (3 trials at ZT 6 and 3 trials at ZT 18 under LD) before recognition testing. In each cohort, half of the recognition trials were given at ZT/CT 6 and the remaining trials were given at ZT/CT 18.

aSample–test delay was 24 h for cohort 1C; for all other cohorts, the sample–test delay was 5 min.

bCohorts 2A and 2C experienced one cycle of LD–LL alternation before recognition testing.

cCohort 2B experienced four cycles of LD–LL alternation before recognition testing.