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The venous system of the head and neck of the opossum, Didelphis virginiana, was studied by injecting the veins with a tinctorial mass. Gross dissection specimens injected with a colored gelatin solution and corrosion specimens prepared by Batson's technique (Batson, ' 5 5 ) were utilized to describe the venous pattern in greater detail than is presently available in the literature. The venous drainage of the superficial structures of the head is principally by way of the V. jugularis externa and its tributaries. Although small emissary veins connect the Sinus cavernosus with the Plexus pterygoideus and the V. maxillaris, the dural venous sinuses drain primarily into the Plexus vertebralis internus and into the V. maxillaris by way of the V. emissaria foraminis retroarticularis. The small V. jugularis interna receives minor connections from the PZexus pterygoideus, the Sinus cavernosus and the Sinus petrosus ventralis as well as anastomotic tributaries from the Plexus vertebralis and the plexus of veins around the hyoid bone. However, the V. jugularis interna serves mainly as a pathway for venous drainage from the deeper structures of the neck and only minimally for draining the brain.

Projections from the spinal cord and dorsal column nuclei to more rostral levels of the neuraxis were investigated in seventeen adult opossums by the Nauta-Gygax and Fink-Heimer techniques. In all cases with spinal cord lesions a greater number of degenerating fibers distributed to the medulla and pons than to the midbrain and diencephalon. Numerous degenerating fibers ended within the medial reticular formation of the medulla and caudal pons, and within the lateral reticular formation of the rostral pons and midbrain. Degenerating fibers were numerous in the reticular formation following cervical and thoracic lesions, but sparse in specimens with damage restricted to either the lumbar or sacral spinal cord. The dorsal column nuclei received afferent connections from the well known dorsal funicular pathway and, although to a much lesser extent, from the main ventrolateral spinal bundle. Although most of the latter fibers ended in the subnucleus dorsalis and spinal vestibular nucleus, some penetrated into the gracile and cuneate nuclei. Conspicuous terminal degeneration was present within the inferior olivary nucleus following cervical and thoracic lesions, but was lacking in cases of either caudal lumbar or sacral cord lesions. The location of terminal degeneration within the lateral reticular nucleus is dependent upon the level of the lesion in the spinal cord. Degenerating fibers ended within the lateral vestibular nucleus in all cases of spinal cord hemisection, and within the medial portion of the facial nucleus in cases with a lesion rostral to C-4. After cervical and thoracic hemisections terminal fiber degeneration was present within the midbrain tegmentum, the periaqueductal gray, the intercollicular nucleus (Mehler, '69), the posterior thalamic nucleus, the ventrobasal nucleus, the parafascicular nuclei and the caudal nucleus ventralis lateralis. All thalamic nomenclature was taken from Oswaldo-Cruz and RochaMiranda, '68. In animals with more caudal lesions, no fiber degeneration was evident within the nucleus ventralis lateralis and so little within the ventrobasal nucleus that it was impossible to ascertain a somatotopic pattern of spinothalamic projections.Lesions of the dorsal column nuclei caused terminal degeneration within the inferior olivary nucleus, the pars lateralis of the nucleus of the inferior colliculus, the zona incerta, the posterior thalamic nucleus, the caudal part of the ventral lateral thalamic nucleus and the ventrobasal nucleus of the thalamus. Diffuse connections with the reticular formation, periaqueductal gray, midbrain tegmentum and the parafascicular complex were also observed. The results from small lesions indicate that the input to the ventrobasal nucleus in the opossum is organized in the typical mammalian fashion.Studies of spino-bulbar and spinothalamic connections have been reported previously for the opossum (Mehler, '69), the rat (Lund and Webster, '67b; Mehler, '69), the cat (Brodal, '49; Brodal et al., '50; Getz, '52; Brodal and Gogstad, '57; Rossi and ...

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The origin, course and distribution of cerebellopontine fibers was studied in the opossum by employing the Nauta-Gygax and Fink-Heimer techniques. Our results substantiate and extend those of Brodal, Destombes, Lacerda and Angaut ('72) concerning the existence of cerebellopontine projections and provide evidence for a hitherto unreported fastigial projection to the basilar pons. Destruction of the caudal, medial division of the fastigial nucleus elicits bilateral degeneration in a restricted area of the medial pontine nucleus. This small terminal field is located in the angle between the medial lemniscus and the pyramidal tract and is found throughout the caudal three-fifths of the pons. The degenerating fibers do not course within the descending brachium conjunctivum, but reach the pons by filtering through the reticular formation from the uncinate fasciculus. Lesions that involve either the interpositus anterior or the dentate nucleus produce degeneration within the contralateral descending brachium conjunctivum and basilar pons. Terminal fields are located within the median, medial (paramedian nucleus of cat), peduncular, ventral and lateral nuclei. The heaviest degeneration is in the medial nucleus.Although cerebellar and cortical projections have different targets in the basilar pons, there is some overlap. Fastigial and preorbital fibers have partial overlap in the dorsal part of the medial nucleus, whereas the peduncular and lateral nuclei are the areas of overlap between the interpositus anterior and dentate projections with those from forelimb (and probably face) cortical areas. This overlap is particularly obvious in the caudal part of the lateral nucleus and occurs between fibers from limb motor-sensory cortex and those arising mainly within the anterior interpositus nucleus. There is no pontine overlap between cerebellar and visual or auditory cortical projections.In a recent study in our laboratory, fibers from the opossum interpositus and dentate nuclei were traced to their termination within the basilar pons (Martin, '73; Martin, King and Dom, '73). Although most accounts of efferent cerebellar pathways do not mention these projections (see review by Larsell and Jansen, '72), they have been observed in the rat (Mehler, personal communication) and monkey ( Strominger, personal communication), and described in considerable detail for the cat (Brodnl et al., '72). Preliminary examination of our material, however, suggested J. COMP. NEKIR., 154: 257-286. that these connections are particularly extensive in the opossum and furthermore, that an additional projection to the basilar pons arises within the fastigial nuclei. In the light of these findings and because of the potential significance of such connections as part of cerebellar feedback circuits, we have undertaken further study of their origin, course and termination in the opossum.Although Brodal et al. ('72) provided some information regarding possible overlap of cerebellar and cortical projections to the basilar pontine gray, the ob...