We present a biologically detailed extension of the classical Hopfield/Marr auto-associative memory model for CA3, implementing ten populations (two asymmetric pyramidal subtypes, eight GABAergic interneuron classes), forty-seven compartments, multi-rule plasticity (recurrent Hebb, BCM anti-saturation, mossy-fiber short-term, endocannabinoid iLTD, burst-gated Hebb), and a bimodal cholinergic encoding/consolidation cycle. Evaluated on pattern completion across auto-associative, associative, and temporal regimes, and on a controlled inhibitory-proportion manipulation at
N=256, the full architecture exhibits \emph{three qualitative signatures absent from a minimal Hopfield baseline}: (i)~multi-attractor cross-seed behaviour at
K=5 with biologically realistic inhibitory proportions, where two of five seeds converge to positive attractors with margin
+0.10−0.22 (Cohen's
d=0.71, one-sided
p=0.08); (ii)~target-selective associative recall in paired
(A,B) memory at
K≥5, where the full model retrieves
B from a partial cue of
A while the minimal model echoes
A (Pearson margin
Δ=+0.163 at
K=5); (iii)~reduced cross-seed variance of the full model below the minimal baseline under clean upstream, with ratios
1.0−3.0. These three signatures are architecture-specific: they appear consistently across independent regimes and are absent from the minimal control.