Organic-walled dinoflagellate cysts analysis and statistical analysis of 116 surface sediment samples from the eastern Indian Ocean

Assemblages of organic-walled dinoflagellate cysts (dinocysts) from 116 marine surface samples have been analysed to assess the relationship between the spatial distribution of dinocysts and modern local environmental conditions [e.g. sea surface temperature (SST), sea surface salinity (SSS), productivity] in the eastern Indian Ocean. Results from the percentage analysis and statistical methods such as multivariate ordination analysis and end-member modelling, indicate the existence of three distinct environmental and oceanographic regions in the study area. Region 1 is located in western and eastern Indonesia and controlled by high SSTs and a low nutrient content of the surface waters. The Indonesian Throughflow (ITF) region (Region 2) is dominated by heterotrophic dinocyst species reflecting the region's high productivity. Region 3 is encompassing the area offshore north-west and west Australia which is characterised by the water masses of the Leeuwin Current, a saline and nutrient depleted southward current featuring energetic eddies.

Sporomorphs and dinoflagellate cysts of ODP Leg 113 holes

Palynological studies were carried out on Paleogene sections from Sites 693 and 696 of Ocean Drilling Project Leg 113 in the Weddell Sea region. Dinoflagellate cysts and sporomorphs were recovered at Site 696 (61°S, 42°W) indicating a middle Eocene to late Eocene/earliest Oligocene age for a glauconitic silt/sandstone. At Site 693 (70°S, 14°W) early Oligocene siliciclastic mud contains a low diversity palynoflora. In an upper Oligocene section (Site 693) only rare, reworked Mesozoic palynomorphs were encountered. Palynological data from Kerogen analyses, dinocysts, and sporomorphs are used to reconstruct the climatic change on the South Orkney microcontinent from the middle Eocene to the late Eocene/earliest Oligocene at Site 696 and the late early Oligocene/early late Oligocene time interval at Site 693 near the continental margin. The middle Eocene was a warm period in the Orkney region with good growing conditions for a warm temperate Nothofagus/conifer forest with an admixture of Proteaceae. Temperate surface water masses, which allowed the growth of a reasonably diverse dinocyst assemblage (ca. 15-20 species), persisted until the end of the Eocene at Site 696. Late early Oligocene sediments of Site 693 (Antarctic continental margin) contain only a low diversity dinocyst flora (two species). The major Cenozoic cooling event in the Weddell Sea region probably occurred at the Eocene/Oligocene boundary. A second dramatic climatic deterioration seems to have taken place during the late early/early late Oligocene, when dinocysts disappeared at the Dronning Maud Land margin area.

Late Cretaceous dinoflagellate cysts of ODP Hole 120-748C

At Ocean Drilling Program Hole 748C in the Southern Indian Ocean, a total of 171 Late Cretaceous dinoflagellate taxa were encountered in 38 productive samples from Cores 120-748C-27R through 120-748C-62R (407-740 mbsf). Four provisional dinoflagellate assemblage zones and five subzones were recognized based on the character of the dinoflagellate flora and the first/last occurrences of some key species. Isabelidinium korojonense and Nelsoniella aceras occur in Zone A together with Oligosphaeridium pulcherrimum and Trithyrodinium suspect urn. Zone B was delineated by the total range of Odontochitina cribropoda. Zone C was separated from Zone B by the presence of Satyrodinium haumuriense, and Zone D is dominated by new taxa. The dinocyst assemblages bear a strong affinity to Australian assemblages. Paleoenvironmental interpretations based mainly on dinocysts suggest that during the ?Santonian-Campanian to the Maestrichtian this portion of the Kerguelen Plateau was a shallow submerged plateau, similar to nearshore to offshore to upper slope environments with water depths of tens to hundreds of meters, but isolated from the major continents of the Southern Hemisphere. Starting perhaps in the late Cenomanian (Mohr and Gee, 1992, doi:10.2973/odp.proc.sr.120.196.1992), the Late Cretaceous transgression over the plateau reached its maximum during the late Campanian. The plateau may have been exposed above sea level and subjected to weathering during the latest Maestrichtian. The studied dinocyst assemblages characterized by species of Amphidiadema, Nelsoniella, Satyrodinium, and Xenikoon together with abundant Chatangiella (the large-size species) and Isabelidinium suggest that a South Indian Province (tentatively named the Helby suite) may have existed during the Campanian-Maestrichtian in comparison with the other four provinces of Lentin and Williams. One new genus, three new species, and two new subspecies of dinocysts are described.

Figures of dinoflagellate cysts (relative abundance, temperature, salinity and nutrients)

This Atlas summarises the global distribution of extant organic-walled dinoflagellate cysts in the form of 61 maps illustrated by the relative abundance of individual cyst taxa in recent marine sediments from the Atlantic Ocean and adjacent basins, the Antarctic region (South Atlantic, southwestern Pacific and southern Indian Ocean sections), the Arabian Sea and the northwestern Pacific. This synthesis is based on the integration of literature sources together with data from 835 marine surface sediments prepared on a comparable methodology and taxonomy. The relationships between distribution patterns of cyst species and the surface-water parameters (temperature, salinity, phosphate and nitrate concentrations) are documented with graphs depicting the relative abundance of species in relation to seasonal and annual values of the above mentioned parameters at the sample sites. Two ordination techniques (detrended correspondence analysis and canonical correspondence analysis) have been carried out to statistically illustrate the relationships between species distribution and sea-surface conditions. Results have been compared with previously published records and an overview of the ecological significance of each individual species is presented. Characterisations of selected environments as well as a discussion about how additional processes such as preservation and transport could have affected the present dataset are included.

Lower Cretaceous dinoflagellate cysts of Exmouth Plateau, Nortwest Australia

Cores from Leg 122, Sites 762 and 763, were sampled at intervals of one sample per 1.5-m section in the Lower Cretaceous sequences. More than 400 samples were studied, most of which contained dinoflagellate cysts, spores, pollen, and various types of palynoclasts. From the entire palynomorph assemblage mainly dinoflagellate cysts were studied to give a stratigraphic outline for the Lower Cretaceous. Stratigraphic units were interpreted in terms of zones in use for the Jurassic and Cretaceous of Australia. At both sites a condensed Valanginian to Aptian sequence and an expanded middle to late Berriasian sequence containing a rich microplankton assemblage were recovered. Sites 762 and 763 can be correlated with each other and with the wells Eendracht-1 and Vinck-1.

X-ray fluorescence data (calcium and iron), bulk organic d13C, and dinoflagellate cysts of ODP Hole 189-1172D

The 'Paleocene/Eocene Thermal Maximum' or PETM (~55 Ma) was associated with dramatic warming of the oceans and atmosphere, pronounced changes in ocean circulation and chemistry, and upheaval of the global carbon cycle. Many relatively complete PETM sequences have by now been reported from around the world, but most are from ancient low- to midlatitude sites. ODP Leg 189 in the Tasman Sea recovered sediments from this critical phase in Earth history at Sites 1171 and 1172, potentially representing the southernmost PETM successions ever encountered (at ~70° to 65° S paleolatitude). Downhole and core logging data, in combination with dinoflagellate cyst biostratigraphy, magneto-stratigraphy, and stable isotope geochemistry indicate that the sequences at both sites were deposited in a high accumulation-rate, organic rich, marginal marine setting. Furthermore, Site 1172 indeed contains a fairly complete P-E transition, whereas at Site 1171, only the lowermost Eocene is recovered. However, at Site 1172, the typical PETM-indicative acme of the dinocyst Apectodinium was not recorded. We conclude that unfortunately, the critical latest Paleocene and PETM intervals are missing at Site 1172. We relate the missing section to a sea level driven hiatus and/or condensed section and recovery problems. Nevertheless, our integrated records provide a first-ever portrait of the trend toward, and aftermath of, the PETM in a marginal marine, southern high-latitude setting.