Birdsong learning, like human speech, depends on the early memorization of auditory models, yet how initial auditory experiences are formed and consolidated is unclear. In songbirds, a putative cortical locus is the caudomedial nidopallium (NCM), and one mechanism to facilitate auditory consolidation is 17β-estradiol (E2), which is associated with human speech-language development, and is abundant in both NCM and human temporal cortex. Circulating and NCM E2 levels are dynamic during learning, suggesting E2's involvement in encoding recent auditory experiences. Therefore, we tested this hypothesis in juvenile male songbirds using a comprehensive assessment of neuroanatomy, behavior, and neurophysiology. First, we found that brain aromatase expression, and thus the capacity to synthesize neuroestrogens, remains high in the auditory cortex throughout development. Further, while systemic estrogen synthesis blockade suppressed juvenile song production, neither systemic nor unilateral E2 synthesis inhibition in NCM disrupted eventual song imitation. Surprisingly, early life neuroestrogen synthesis blockade in NCM enhanced the neural representations of both the birds' own song and the tutor song in NCM and a downstream sensorimotor region, HVC, respectively. Taken together, these findings indicate that E2 plays a multifaceted role during development, and that, contrary to prediction, tutor song memorization is unimpaired by unilateral estrogen synthesis blockade in the auditory cortex. While many animals use sounds to communicate with one another (vocal communication), the ability to learn to vocally communicate is relatively rare 1. In vocal learning animals, such as humans and songbirds, vocal learning occurs across two main phases: an auditory memorization ('sensory') phase, followed by a sensorimotor phase ('babbling' , error correction/feedback) 2,3. While much is known about sensorimotor learning, the mechanisms that guide the formation and consolidation of auditory memories early in life are less clear. One brain region likely involved in storing auditory memories in songbirds is the caudomedial nidopallium (NCM) 4. NCM, comparable to mammalian secondary auditory cortex, is required for accurate song learning. Blocking ERK-signaling or mTOR bilaterally in NCM during tutoring leads to poor song imitation 5,6. Tutoring naïve juvenile songbirds leads to an increased proportion of tutor-song-selective neurons in NCM 7. Further, bilateral NCM lesions abolish innate preference for tutor song in adults 8 , but see 9,10. Thus, NCM contains a putative tutor 'engram'; however, the neuromodulatory mechanisms that shape this auditory memory formation and consolidation remain unknown. Consolidating recent experience in other contexts and systems require presynaptic signaling molecules ('neuromodulators'), such as brain-derived estrogens 11. The predominant estrogen 17β-estradiol (E2) is a candidate neuromodulator required for auditory memory consolidation, as is evident in a similar role in adult hippocampal-dependent cognit...