We examined the internal organization and connections of the primary visual area, V1, in the South American marsupial Monodelphis domestica. Multiunit electrophysiological recording techniques were used to record from neurons at multiple sites. Receptive field location, size, progressions, and reversals were systematically examined to determine the visuotopic organization of V1 and its boundaries with adjacent visual areas. As in other mammals, a virtually complete representation of the visual hemifield was observed in V1, which was coextensive with a region of dense myelination. The vertical meridian was represented at the rostrolateral boundary of the field, the upper visual quadrant was represented caudolaterally, whereas the lower visual quadrant was represented rostromedially. Injections of fluorescent tracers into V1 revealed dense connections with cortex immediately adjacent to the rostrolateral boundary, in peristriate cortex (PS or V2). Connections were also consistently observed with a caudotemporal area (CT), entorhinal cortex (EC), and multimodal cortex (auditory/visual, A/V). These results demonstrate that M. domestica possess a highly differentiated neocortex with clear functional and architectonic cortical field boundaries, as well as discrete patterns of cortical connections. Some connections of V1 are similar to those observed in eutherian mammals, such as connections with V2 and extrastriate areas (e.g., CT), which suggests that there are general features of visual system organization that all mammals possess due to retention from a common ancestor. On the other hand, connections of V1 with EC and multimodal cortex may be a primitive feature of visual cortex that was lost in some lineages, may be a derived feature of marsupial neocortex, or may be a feature particular to mammals with small brains.