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50thKaikoura05 -1- Kaikoura 2005 CHARACTERISATION OF NEW ...

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VEGETATION AND CLIMATE CHANGE AT<br />

THE PALEOCENE-EOCENE TRANSITION<br />

E.M. Crouch, J.I. Raine & E.M. Kennedy<br />

GNS Science, PO Box 30368 Lower Hutt.<br />

(e.crouch*gns.cri.nz)<br />

Plant microfossil (spore/pollen) assemblages from<br />

New Zealand Paleocene–Eocene (P–E) sedimentary<br />

sections show a general change from predominantly<br />

gymnosperm-rich Paleocene floras (zone PM3) to<br />

Casuarina-dominated angiosperm-rich floras in the<br />

Early Eocene (zone MH1). Modern relatives of the<br />

fossil plant taxa and vegetation analogues indicate<br />

this change is related to significant climatic<br />

warming, although the precise timing and extent of<br />

more subtle vegetation change during the P–E<br />

transition remains poorly documented. Previous<br />

studies (e.g., Tawanui section, Hawkes Bay, and<br />

Moeraki-Hampden section, Otago) suggest that the<br />

main vegetation change in the Paleocene–Eocene<br />

occurred in the upper Waipawan Stage (earliest<br />

Eocene) and post-dated the significant climatic and<br />

carbon cycle perturbation at the P–E boundary (~55<br />

Ma). Plant microfossil records are currently being<br />

studied from a silica-sand quarry at Mt Somers,<br />

South Canterbury, and in the Kumara-2 core,<br />

central Westland, to elucidate the timing and scale<br />

of vegetation change during the P–E transition.<br />

Gymnosperm pollen and Proteaceae and small<br />

triporate angiosperm pollen are abundant in the<br />

lower part of the Kumara-2 core (1739-50 m), and a<br />

Late Paleocene age is suggested. Coastal marine<br />

sediments are present from ~1733-38 m, with<br />

abundant cysts of the marine dinoflagellate genus<br />

Apectodinium recorded in the middle of this unit.<br />

Coincident with the base of the marine horizon,<br />

pollen indicative of warm climates (e.g.,<br />

Cupanieidites orthoteichus, Spinizonocolpites<br />

prominatus) are first recognised and become a<br />

recognisable component of the spore/pollen<br />

assemblage. Spores/pollen are absent from a<br />

channel fill sand at 1722-33 m, but above this unit<br />

the assemblage is diverse, angiosperm pollen are<br />

abundant and Casuarina pollen (zone MH1)<br />

markedly increase in the upper part of the studied<br />

core. Abundant Apectodinium dinocysts in the<br />

coastal marine unit suggests this interval lies very<br />

close to the P–E boundary, and it appears this<br />

marine incursion may be related to a thermal<br />

expansion of ocean waters and slight sea-level rise<br />

at the time of extreme warming at the P–E<br />

boundary. Compound-specific organic carbon<br />

isotope analyses are currently being completed to<br />

confirm the presence and position of the P–E<br />

boundary.<br />

Within the sand dominated Broken River<br />

Formation-Homebush Sandstone section at Mt<br />

Somers, fine-grained mudstone layers were<br />

sampled where possible and palynomorph<br />

assemblages examined. A Late Paleocene sample<br />

contains common gymnosperms and appears to be<br />

terrestrial, although marine dinocysts have<br />

previously been recorded from a similar horizon.<br />

Above this, a prominent ~3 m grey mudstone<br />

contains abundant cysts of the marine dinoflagellate<br />

genus Apectodinium, indicating an early Waipawan<br />

age. Marine conditions persist in the overlying<br />

mudstone layers examined, with an uppermost<br />

glauconitic sandstone unit containing dinocysts<br />

indicative of the Mangaorapan Stage. Pollen<br />

indicative of warm climates are present by the early<br />

Waipawan (prominent mudstone unit), and<br />

Casuarina pollen (zone MH1) is abundant in the<br />

upper glauconitic sandstone unit.<br />

POSTER<br />

“100 KM PER MILLION YEARS” A<br />

HIGHLY-DYNAMIC DEPOSITIONAL<br />

MODEL FOR LATE MIOCENE ROCKS IN<br />

TARANAKI BASIN<br />

Martin Crundwell &MalcolmArnot<br />

Geological and Nuclear Science Limited, PO Box<br />

30-368, Lower Hutt, NZ<br />

(m.crundwell*gns.cri.nz)<br />

New biostratigraphic dating techniques challenge<br />

traditional exploration paradigms and suggest a<br />

highly dynamic depositional model is more<br />

appropriate for late Miocene rocks in Taranaki<br />

Basin, with multiple deep-water sedimentary<br />

systems of considerable thickness, developed on<br />

local geographic scales, over timescales of orbital<br />

proportions (40-100 kyr). Although the general<br />

pattern and tempo of late Miocene sedimentation<br />

are clearly dictated by climate forcing, suborbitalscale<br />

variations in sedimentary patterns and rates of<br />

deposition reflect a complex history of shelf<br />

progradation, tempered by sediment supply and<br />

accommodation, and tectonic controls within and<br />

adjacent to the basin. The observed dynamism in<br />

sedimentation is consistent with the tectonic<br />

development of the eastern Taranaki Basin margin<br />

(e.g. King and Thrasher, 1996), and with detailed<br />

outcrop based stratigraphic studies undertaken by<br />

GNS (e.g. King et al., 1993; Browne and Slatt,<br />

2002), and also with many of the problems<br />

associated with hydrocarbon reservoir sequences<br />

(e.g. poor correlation and dating, rapid facies<br />

variations, and variable reservoir characteristics).<br />

In this presentation, we outline some of the new<br />

biostratigraphic tools that have been developed<br />

specifically to address correlation problems<br />

associated with late Miocene rocks in Taranaki<br />

Basin. Examples from Pukearuhe-1 and outcrop<br />

studies are given, of extremely high estimated rates<br />

of sedimentation, based on weight standardized<br />

counts of planktic and benthic foraminifers,<br />

50 th <strong>Kaikoura</strong>05 -23- <strong>Kaikoura</strong> <strong>2005</strong>

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