fossil plants from the beardmore another focus of …...fossil plants from the beardmore glacier...

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Fossil plants from the Beardmore Glacier area T. N. TAYLOR Department of Botany and Institute of Polar Studies Ohio State University Columbus, Ohio 43210 E. L. SMOOT Department of Biology, Hope College Holland, Michigan 49423 With the exception of isolated pieces of silicified wood, by far most of the fossil plants from Antarctica are preserved as im- pressions in which cellular details are lacking. The discovery of silicified plant remains of Permian and Triassic age from the Beardmore Glacier area has provided a unique opportunity to examine the detailed cellular structure of these floral compo- nents. The silicified plants from these sites are especially impor- tant because they represent one of the very few deposits of this age in the world where it is possible to investigate detailed anatomical features of plants. Moreover, the Beardmore plants provide an important stratigraphic link with the late Car- boniferous floras which are also preserved as cellular per- mineralizations. A multifaceted research program directed at the antarctic floras is currently in progress and involves inves- tigations of several different types. Three of these are discussed briefly below. Paleobotanists have long speculated on the origin of modern cycads, with the medullosan pteridosperms suggested as the probable ancestors. One component of this research is con- cerned with cycadophyte stems (Taylor, Smoot, and Delevoryas 1983) of Triassic age that are anatomically similar to the stems of modern members of the Cycadales (e.g., Zamia, Bowenia). The stems measure approximately 5.0 centimeters in diameter and include well preserved petioles. The vascular system consists of endarch primary bundles that are associated with radial files of secondary tracheids possessing scalariform pits. A well pre- served vascular cambium and some secondary phloem is also present. Although paleobotanists have long speculated that modern cycads are related to the late Paleozoic medullosan pteridosperms, this assumption has been generally based on vegetative remains, and some common anatomical features of medullosan stems (Worsdell 1901). The discovery of cycad stems in the Triassic of Antarctica provides detailed histological information to indicate that the anatomical features of the stems are nearly identical with those of extant representatives of the order. Another focus of this paleobotanical program concerns the Permian foliage types Glossopteris and Gangamopteris. The spatu- late leaves of these two genera have been the subject of numer- ous contributions that have emphasized taxonomic details. To date, paleobotanists have had little success in distinguishing these two taxa using characters that have been consistently reliable over wide geographic regions. In addition, there have been few attempts to distinguish ontogenetic features from those that are phylogenetic. The discovery of anatomically preserved leaves of these two genera on rock surfaces provides an opportunity to correlate the morphology and histology of the leaves. This will enable re- searchers to relate the structurally preserved specimens with the more abundant, and widely occurring, impression-com- pression specimens. Preliminary investigations of these leaves indicate that the so-called midrib in Glossopteris is constructed of up to five closely spaced, parallel veins, each surrounded by a bundle sheath. This feature has been widely used to distinguish the two taxa, but may be of little taxonomic importance. A third component of the research is directed at structurally preserved fungi that are common in certain plant tissue sys- tems. In living plants it is estimated that more than 90 percent of all vascular plants are associated with certain mycorrhizal fungi. Endomycorrhizal fungi that are morphologically identical to the extant taxon Glomus have been described in the underground organs of a variety of Carboniferous plants (Wagner and Taylor 1982). The presence of similar structurally preserved fungi in the antarctic material not only extends the stratigraphic range of these fungi from the Devonian into the Triassic but also provides the opportunity to correlate the host-fungus rela- tionship through an extended segment of geologic time. The Beardmore specimens allow for an investigation of the anatomy of several groups of major plants that are currently very poorly understood and for which there is almost no infor- mation about cellular detail. The diversity of the flora from these sites is exceptional, and information about the fossils will contribute not only to details about the biology of the organisms but will also provide a much needed framework with which important evolutionary questions can now be considered. This research was supported by National Science Foundation grant DPP 82-13749. References Taylor, IN., E.L. Smoot, and T. Delevoryas. 1983. Structurally pre- served plants from Antarctica: A Triassic cycad stem. American Journal of Botany, 70, 80. Wagner, C.A., and TN. Taylor. 1982. Fungal chlamydospores from the Pennsylvanian of North America. Review of Palaeobotany and Pal- ynology, 37, 317-328. Worsdell, W.C. 1901. Contributions to the comparative anatomy of the Cycadaceae. Transactions of the Linnean Society, 2nd Series, Botany, 6, 109-121. 12 ANTARCTIC JOURNAL

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Page 1: Fossil plants from the Beardmore Another focus of …...Fossil plants from the Beardmore Glacier area T. N. TAYLORDepartment of Botany and Institute of Polar StudiesOhio State University

Fossil plants from the BeardmoreGlacier area

T. N. TAYLOR

Department of Botany and Institute of Polar StudiesOhio State University

Columbus, Ohio 43210

E. L. SMOOT

Department of Biology,Hope College

Holland, Michigan 49423

With the exception of isolated pieces of silicified wood, by farmost of the fossil plants from Antarctica are preserved as im-pressions in which cellular details are lacking. The discovery ofsilicified plant remains of Permian and Triassic age from theBeardmore Glacier area has provided a unique opportunity toexamine the detailed cellular structure of these floral compo-nents. The silicified plants from these sites are especially impor-tant because they represent one of the very few deposits of thisage in the world where it is possible to investigate detailedanatomical features of plants. Moreover, the Beardmore plantsprovide an important stratigraphic link with the late Car-boniferous floras which are also preserved as cellular per-mineralizations. A multifaceted research program directed atthe antarctic floras is currently in progress and involves inves-tigations of several different types. Three of these are discussedbriefly below.

Paleobotanists have long speculated on the origin of moderncycads, with the medullosan pteridosperms suggested as theprobable ancestors. One component of this research is con-cerned with cycadophyte stems (Taylor, Smoot, and Delevoryas1983) of Triassic age that are anatomically similar to the stems ofmodern members of the Cycadales (e.g., Zamia, Bowenia). Thestems measure approximately 5.0 centimeters in diameter andinclude well preserved petioles. The vascular system consists ofendarch primary bundles that are associated with radial files ofsecondary tracheids possessing scalariform pits. A well pre-served vascular cambium and some secondary phloem is alsopresent. Although paleobotanists have long speculated thatmodern cycads are related to the late Paleozoic medullosanpteridosperms, this assumption has been generally based onvegetative remains, and some common anatomical features ofmedullosan stems (Worsdell 1901). The discovery of cycadstems in the Triassic of Antarctica provides detailed histologicalinformation to indicate that the anatomical features of the stemsare nearly identical with those of extant representatives of theorder.

Another focus of this paleobotanical program concerns thePermian foliage types Glossopteris and Gangamopteris. The spatu-late leaves of these two genera have been the subject of numer-ous contributions that have emphasized taxonomic details. Todate, paleobotanists have had little success in distinguishingthese two taxa using characters that have been consistentlyreliable over wide geographic regions. In addition, there havebeen few attempts to distinguish ontogenetic features fromthose that are phylogenetic.

The discovery of anatomically preserved leaves of these twogenera on rock surfaces provides an opportunity to correlate themorphology and histology of the leaves. This will enable re-searchers to relate the structurally preserved specimens withthe more abundant, and widely occurring, impression-com-pression specimens. Preliminary investigations of these leavesindicate that the so-called midrib in Glossopteris is constructed ofup to five closely spaced, parallel veins, each surrounded by abundle sheath. This feature has been widely used to distinguishthe two taxa, but may be of little taxonomic importance.

A third component of the research is directed at structurallypreserved fungi that are common in certain plant tissue sys-tems. In living plants it is estimated that more than 90 percent ofall vascular plants are associated with certain mycorrhizal fungi.Endomycorrhizal fungi that are morphologically identical to theextant taxon Glomus have been described in the undergroundorgans of a variety of Carboniferous plants (Wagner and Taylor1982). The presence of similar structurally preserved fungi inthe antarctic material not only extends the stratigraphic range ofthese fungi from the Devonian into the Triassic but alsoprovides the opportunity to correlate the host-fungus rela-tionship through an extended segment of geologic time.

The Beardmore specimens allow for an investigation of theanatomy of several groups of major plants that are currentlyvery poorly understood and for which there is almost no infor-mation about cellular detail. The diversity of the flora fromthese sites is exceptional, and information about the fossils willcontribute not only to details about the biology of the organismsbut will also provide a much needed framework with whichimportant evolutionary questions can now be considered.

This research was supported by National Science Foundationgrant DPP 82-13749.

References

Taylor, IN., E.L. Smoot, and T. Delevoryas. 1983. Structurally pre-served plants from Antarctica: A Triassic cycad stem. American Journalof Botany, 70, 80.

Wagner, C.A., and TN. Taylor. 1982. Fungal chlamydospores from thePennsylvanian of North America. Review of Palaeobotany and Pal-ynology, 37, 317-328.

Worsdell, W.C. 1901. Contributions to the comparative anatomy of theCycadaceae. Transactions of the Linnean Society, 2nd Series, Botany, 6,109-121.

12 ANTARCTIC JOURNAL