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Permian coprolites from Graphite Peak, Antarctica

GREGORY J. RETALLACK and EVELYN S. KRULL, Department of Geological Sciences, University of Oregon, Eugene, Oregon 97403

We report here the first known evidence for Permian vertebrates in Antarctica in the form of coprolites. Numerous coprolites were collected (Condon Collection, University of Oregon specimens F35111-35123) from a sandstone of the lower Buckley Formation [270 meters (m) below contact with Fremouw Formation in measured section of Barrett, Elliot, and Lindsay (1986)] of mid-Permian age (Farabee, Taylor, and Taylor 1991) in the slopes just above the moraine wall of the Falkenhof Glacier below Graphite Peak, central Transantarctic Mountains (85°2.9'S 172°21.3'E, elevation 2,600 m; figure 1). The sandstone matrix has large trough crossbeds similar to those found in paleochannels. It also contains large blocks of paleosol claystone and numerous permineralized logs in its basal 3 m. The coprolites are most common within a 2-m interval, 6 m above the base of the paleochannel. Our measurements of the long axis of 56 specimens showed a surprising uniformity of orientation (figure 2), aligned with paleocurrents for the Buckley Formation at Graphite Peak (Isbell 1991).

The coprolites are helical, pupiform, and discoidal in shape (figure 3). The helical coprolites have internal seams of carbonaceous sandstone marking the internally juxtaposed coils (figure 3 D ). They lack internal lumen or mucosal folds. They also are variable in degree of unravelling and in size, so were probably not fossilized intestinal contents [enterospirae or cololites of McAllister (1985)]. Pupiform coprolites show a terminal segment helically wrapped and probably were also pinched off from a helically valvate anus before full extrusion. Some of the discoidal masses with radiating cracks and ridges are preserved in the same manner as the associated helical and pupiform coprolites, and appear to be unravelled helices (figure 3 E and F ).

The coprolites consist of sandstone. Their matrix is 22.8 volume percent calcite and 9.0 percent clay by point counting 500 points in petrographic thin section. Most of the grains are sand-size and consist of quartz (23 percent), feldspar (12.4 percent), and metamorphic rock fragments (22.4 percent), with traces of hornblende (3.0 percent), mica (2.4 percent), coal fragments (0.2 percent), and other dark brown grains (3.8 percent). Many of the dark brown grains had an internal structure like that of ganoin (figure 3 G ) and are probably scales of paleoniscid fish. The scales are 0.5-1 millimeters (mm) long and 0.2-0.4 mm thick. From observations of complete Permian paleoniscid fish fossils from Germany and Texas, these scales would have come from animals 10-30 centimeters (cm) long. The elongate helical coprolites average 173 mm long (n=10, sn=41 mm, r=99-240 mm), 75 mm wide (n=10, sn=14 mm, r=50-100) but only 44 mm thick (n=10, sn=8 mm, r=34-64) due to postdepositional compaction. They are comparable in size and shape to a specimen of Triassic age from Graphite Peak (misidentified as a large snail by Barrett et al. 1986). They are much larger than Jurassic helical coprolites previously recorded from Antarctica (Tasch 1976; Doyle and Witham 1991).

Helical coprolites are formed by the helical intestine of many kinds of fish, including cyclostomes, placoderms, acanthodians, bowfin (Amia) , garpike ( Lepisosteus ), chimaeras, sharks, and lungfish (Jain 1983; Coy 1995). Freshwater sharks and lungfish have a fossil record in the Middle Devonian of Antarctica and Australia (Long 1991; Young 1993) and sharks in the Permian of Australia (Long 1991). A loose helix and unravelling after sitting on the bottom for a few hours are characteristics of lungfish feces (Jain 1983), which are very similar to the fossils. A dipnoan bottom-feeding behavior would also be compatible with the sediment-rich nature of the coprolites, as argued for comparable scroll coprolites (Gilmore 1992). Coprolites of this size would be produced by living lungfish ( Neoceratodus forsteri ) some 2-6 m long (Jain 1983).

We thank David Elliot and Kevin Kililea of the 1995-1996 Shackleton Glacier Camp. Work was funded by National Science Foundation grant OPP 93-15228.

References

Barrett, P.J., D.H. Elliot, and J.F. Lindsay. 1986. The Beacon Supergroup (Devonian-Triassic) and Ferrar Group (Jurassic) in the Beardmore Glacier area, Antarctica. In M.D. Turner and J.F. Splettstoesser (Eds.), Geology of the central Transantarctic Mountains (Antarctic Research Series, Vol. 36). Washington, D.C: American Geophysical Union.

Coy, C.E. 1995. The first record of spiral coprolites from the Dinosaur Park Formation (Judith River Group, Upper Cretaceous), southern Alberta, Canada. Journal of Paleontology, 69(6), 1191-1194.

Doyle, P., and A.G. Witham. 1991. Palaeoenvironments of the Nordenskjöld Formation: An antarctic Late Jurassic-Early Cretaceous black shale-tuff sequence. In R.V. Tyson and T.H. Pearson (Eds.), Modern and ancient shelf anoxia (Special Paper of the Geological Society of London, No. 58). London: Geological Society of London.

Farabee, M.J., E.L. Taylor, and T.N. Taylor. 1991. Late Permian palynomorphs from the Buckley Formation, central Transantarctic Mountains, Antarctica. Review of Palaeobotany and Palynology , 69(4), 353-368.

Gilmore, B.G. 1992. Scroll coprolites from the Silurian of Ireland and the feeding of early vertebrates. Palaeontology 35(2), 319-333.

Isbell, J.L. 1991. Evidence for a low-gradient alluvial fan from the paleo-Pacific margin in the upper Permian Buckley Formation, Beardmore Glacier area, Antarctica. In M.R.A. Thomson, J.A. Crame, and J.W. Thomson (Eds.), Geological evolution of Antarctica. Cambridge: Cambridge University Press.

Jain, S.L. 1983. Spirally-coiled coprolites from the Upper Triassic Maleri Formation, India. Palaeontology , 26(4), 813-829.

Long, J. 1991. The long history of Australian fossil fishes. In P. Vickers-Rich, J.M. Monaghan, R.F. Baird, and T.H. Rich (Eds.), Vertebrate palaeontology of Australasia . Melbourne: Monash University Press.

McAllister, J.A. 1985. Reevaluation of the formation of spiral coprolites (University of Kansas Paleontological Contributions Paper, No. 114). Lawrence: University of Kansas.

Tasch, P. 1976. Jurassic non-marine trace fossils (Transantarctic Mountains) and the food web. Journal of Paleontology , 50(4), 754-758.

Young, G.C. 1993. Middle Paleozoic macrovertebrate biostratigraphy of eastern Gondwana. In J.A. Long (Ed.), Palaeozoic vertebrate biostratigraphy and biogeography . Baltimore: Johns Hopkins University Press.