Discussion and Conclusions-The Eocene-Oligocene Transition: The Gateway Opens | Table of Contents
DISCUSSION AND CONCLUSIONS (continued)
Paleocene-Eocene Paleoenvironments: Before the Gateway OpenedHighly restricted nearshore conditions in the middle to early late Eocene at all sites are
indicated by a wide range of criteria including pervasive pollen and spore assemblages, abundant
continuous low-diversity assemblages of organic dinocysts indicative of eutrophic and brackish
surface waters, and limited representation of open-ocean planktonic microfossils. Diverse pollen
and spore assemblages are particularly abundant in the Paleocene sequence at Site 1171, indicating
particularly strong continental influence with abundant, diverse plant communities. In situ
assemblages of planktonic foraminifers and radiolarians are largely absent, diatoms are rare, and
calcareous nannofossils are uncommon. Good preservation of calcareous nannofossils suggests
that they are uncommon, not because of dissolution, but because of the restricted coastal setting in
conjunction with high sedimentation rates. However, the presence of foraminiferal linings suggests
dissolution of foraminifers at some levels.
Ventilation on the shelves over much of the region was poor to limited throughout the middle
to early late Eocene judging from high TOC, limited bioturbation, and benthic foraminiferal
assemblages dominated by agglutinated forms and nodosariids. The sediments at Sites 1168 and
1170 suggest that the eastern, remote end of the narrow, restricted Australo-Antarctic Gulf was
poorly ventilated. Low oxygen levels in waters of the eastern Gulf would have developed because
of the restricted circulation (2000 km from the open Indian Ocean) and the proximity of inferred
abundant terrestrial organic sources from the surrounding land masses, including Antarctica, warm
climatic conditions, and possible high marine biotic productivity in eutrophic conditions.
Ventilation was especially poor at Site 1168, off western Tasmania, as indicated by laminated
sediments. Deeper water sediments at nearby Site 282 were also poorly oxygenated. Anoxic to
dysoxic depositional environments would be expected within an expanded oxygen minimum zone
that extended up onto the continental shelf at Site 1168. Eocene sediments at Site 1170, in the
extreme southeastern corner of the Gulf, were also deposited in poorly oxygenated conditions on a
tranquil shelf. Here, the absence of laminations and a slight increase in bioturbation in some
intervals suggest greater shelf ventilation than at Site 1168, but circulation was almost certainly
sluggish.
The poor ventilation in such shallow-water depths at Site 1170 suggests that the Tasmanian
Gateway generally was closed to even shallow waters (~100 m) during the middle and early late
Eocene, at least in the developing rift basin between Antarctica and the STR. This is supported by
the contrasting Eocene record at Site 1171, near the developing seaway on the Pacific side of the
Tasmanian Land Bridge, where the shelf sediments are well bioturbated, suggesting with other
evidence more strongly ventilated conditions than in the Gulf and no oxygen minimum zone. If the
Tasmanian Gateway had been open widely at shallow depths, there would have been little basin to
basin fractionation and, hence, little contrast in sedimentary environments. Middle Eocene
sedimentation at Site 1172 bears considerable resemblance to that at Site 1171, but it was in a more
oceanic, better ventilated environment within the open Pacific Ocean. The proximity of Site 1172
to the large and newly formed subaerial Cascade Seamount may have increased the speed of
bottom currents nearby, thus enhancing ventilation.
The middle through upper Eocene sediment sequence at Sites 1170 and 1171 reveals distinct
cycles in physical properties, sediments, and microfossil assemblages. Alternations between dark,
poorly bioturbated, nannofossil-poor sediments lacking glauconite and lighter, more nannofossil
abundant, bioturbated sediments containing glauconite probably result from changes in water-mass
ventilation. Quantitative changes in dinocyst assemblages are cyclic. The darker sedimentary
intervals are associated with higher abundances of dinocysts (including massive monotaxic
blooms) characteristic of eutrophic conditions and suggesting high nutrient supply to surface
waters. In contrast, dinocysts characteristic of more oligotrophic surface waters dominate the
lighter intervals in association with more abundant calcareous nannofossils. Clear cyclicity with
probable Milankovitch periodicity is also evident in Th abundance in the logging data.
These middle to late Eocene shelfal cycles almost certainly will be shown to correlate with
changes in sediment and biotic characteristics. The cause of the cycles is yet to be determined, but
they probably resulted from minor climatic oscillations at high southern latitudes, perhaps
associated with small sea-level changes, which caused changes in siliciclastic sediment supply,
upwelling, and nutrient supply, and associated changes in bottom-water ventilation. The relative
importance of marine vs. terrestrial sources of organic carbon varied at the different margin
locations during the Eocene. At Site 1168, terrestrial carbon sources dominate, but marine organic
carbon dominates at Sites 1170 and 1171, where marine productivity was high in a restricted
nearshore setting. In contrast, Paleocene sediments, sampled only at Site 1171 on the southern
STR, clearly exhibit a much stronger terrestrial influence with abundant terrestrial plant materials
(e.g., pollen and spores). Throughout the Paleocene to middle Eocene, sedimentation kept up with
subsidence and compaction.
Evidence for glaciation is completely lacking during the Paleocene and Eocene. Both marine
and terrestrial microfossils indicate cool, temperate conditions throughout the middle and late
Eocene. Calcareous nannofossil assemblages are of relatively high diversity and appear to be
slightly warmer in this sector of the Antarctic than at comparable latitudes elsewhere (although
almost completely lacking warmth-loving discoasters). Their diversity suggests an absence of
seasonal sea ice over the shelf and marine conditions during much of the time. Middle Eocene clay
assemblages at Site 1170 are completely dominated by smectite, suggesting warm temperatures,
seasonal rainfall, and a predominance of chemical over physical weathering.
Relatively warm, cosmopolitan dinocyst assemblages of the middle Eocene were in part
replaced during the late Eocene by cooler, endemic Antarctic forms. This inferred cooling is
consistent with stable isotopic records that indicate progressive cooling of the Southern Ocean
during the middle and late Eocene (Shackleton and Kennett, 1975; Stott et al., 1990; Kennett and
Stott, 1990). Cooler continental conditions during the late Eocene are indicated by conspicuous
increases in illite relative to smectite clays at Sites 1170 and 1171, suggesting a reduction in
continental chemical weathering, perhaps in combination with increased tectonism near the
expanding rift. Nevertheless, the character and abundance of the organic dinocyst and diatom
assemblages throughout the entire middle to upper Eocene suggest that at no time was cooling
sufficient to form important seasonal sea ice in this Antarctic region. Pollen and spore records
suggest that the middle and late Eocene plant communities on the hinterlands were diverse and
cool temperate. Floras were dominated by Nothofagus, podocarps, and other forms with an
understory of ferns, similar to a floral assemblage of similar age previously documented in the
Weddell Sea sector of Antarctica (Mohr, 1990). Although upper Eocene pollen assemblages
appear cooler, they still indicate relative warmth along the Antarctic margin compared with the
distinctly cooler Oligocene that followed. Oligocene floras, if they existed, left no record because
palynomorphs were not preserved in the pervasive carbonate sediments, probably because of
oxidation. Therefore, a nonglaciated, cool, temperate climate prevailed on this sector of the
Antarctic margin during the middle to late Eocene. This contrasts with the Prydz Bay margin,
where clear evidence exists for late Eocene glaciation (Barron et al., 1991a) and early Oligocene
development of a major ice sheet (Zachos et al., 1992, 1993, 1996).
In summary, the contrast between the poorly oxygenated, shallow-marine waters of the shelf of the Australo-Antarctic Gulf and the better oxygenated waters in the Pacific Ocean suggests a general lack of interchange between southern Indian and Pacific Ocean waters. The evidence discussed above suggests that the Tasmanian Gateway remained more or less closed, even to shallow-surface waters, until the late Eocene at ~36 Ma. Sites 1168 and 1170 in the Gulf are much more poorly ventilated than Sites 1171 and 1172 in the Pacific Ocean.
Discussion and Conclusions-The Eocene-Oligocene Transition: The Gateway Opens | Table of Contents