Paucituberculatashrew opossums

Today, this order of marsupials is represented by one small family of shrew-like animals, the Caenolestidae, with 5 species. All caenolestids live in western South America. In the past, the order included the amazingly rodent-like Argyrolagidae (Oligocene to Pliocene) and a few other families. The characteristics given here apply only to living forms.

Caenolestids are small, shrew-like animals with small eyes, and thick, gray or gray-brown pelage. The margin of each upper lip is interrupted by a distinctive flap of skin. Their tails are long but not prehensile, and their feet are not syndactylous. Females lack a pouch. Caenolestids have a rounded cranium, weak zygomatic arches, and a long and conical rostrum. Each lower jaw has a large incisor that extends forward from the lower jaw ( diprotodont), followed by six or seven small and simple incisors, canines, and premolars, each separated by a space. The upper canines are large stabbing teeth. The first three upper molars have a hypocone (small on the third). The dental formula is 4/3-4, 1/1, 3/3, 4/4 = 46 or 48.

Caenolestids have peculiarly paired sperm. They share this very unusual trait with didelphids, and it provides strong evidence for uniting these two groups in the Cohort Ameridelphia (see account of Metatheria). Paired sperm are not found in any Australian marsupials.

Caenolestids are believed to feed mostly on insects, but they have been seen to use their projecting lower incisors to repeatedly stab baby rodents (which they then ate). They forage in dense vegetation on the ground in dense, cold, and wet forests either at high elevations in the Andes or along the southern coast of Chile.

The earliest members of this group are found in Oligocene faunas of South America. They were diverse in the Oligocene and Miocene.

Technical characters

Literature and references cited

Aplin, K. P., and M. Archer. 1987. Recent advances in marsupial systematics with a new syncretic classification. Pp. xv-lxxii in Archer, M. (ed.), Possums and Opossums: Studies in Evolution, Vol. I. Surrey Beatty and Sons PTY Limited, Chipping Norton. lxxii+400 pp.

Carroll, R. L. 1988. Vertebrate Paleontology and Evolution. W. H. Freeman and Co., New York. xiv + 698 pp.

Feldhamer, G. A., L. C. Drickamer, S. H. Vessey, and J. F. Merritt. 1999. Mammalogy. Adaptation, Diversity, and Ecology. WCB McGraw-Hill, Boston. xii+563pp.

Marshall, L. G. 1984. Monotremes and marsupials. Pp 59-115 in Anderson, S. and J. Knox Jones, eds, Orders and Families of Recent Mammals of the World. John Wiley and Sons, NY. xii+686 pp.

Vaughan, T. A. 1986. Mammalogy. Third Edition. Saunders College Publishing, Fort Worth. vi+576 pp.

Vaughan, T. A., J. M. Ryan, N. J. Czaplewski. 2000. Mammalogy. Fourth Edition. Saunders College Publishing, Philadelphia. vii+565pp.

Wilson, D. E., and D. M. Reeder. 1993. Mammal Species of the World, A Taxonomic and Geographic Reference. 2nd edition. Smithsonian Institution Press, Washington. xviii+1206 pp.


bilateral symmetry

having body symmetry such that the animal can be divided in one plane into two mirror-image halves. Animals with bilateral symmetry have dorsal and ventral sides, as well as anterior and posterior ends. Synapomorphy of the Bilateria.


uses smells or other chemicals to communicate


animals that use metabolically generated heat to regulate body temperature independently of ambient temperature. Endothermy is a synapomorphy of the Mammalia, although it may have arisen in a (now extinct) synapsid ancestor; the fossil record does not distinguish these possibilities. Convergent in birds.


having the capacity to move from one place to another.


reproduction that includes combining the genetic contribution of two individuals, a male and a female


uses touch to communicate