Distribution and abundance of calcareous-nannoplankton species in the Cretaceous sediments of DSDP Leg 62 Holes

Cretaceous sediments were recovered at all four sites (Sites 463-466) of the central North Pacific drilled during Leg 62 of the Deep Sea Drilling Project. One of the objectives was to get more information about the development of ocean plankton communities and early evolution of planktonic groups of the Mesozoic. In this article, the Cretaceous calcareous nannofossils from two areas of the central North Pacific (Mid-Pacific Mountains and Hess Rise) are listed and discussed. (The Cenozoic calcareous nannofossils are discussed by R. Schmidt 1981). Coring was continuous at all sites. Mesozoic calcareous nannoplankton assemblages range on the Mid-pacific Mountains from Barremian to Early Maastrichtian, and on Hess Rise from Albian to Late Maastrichtian. (No calcareous nannofossils older than Barremian or Albian respectively were found).

Stable isotope ratios and foraminiferal abundance of sediment cores from the Western Iberian Margin

Rapid climate changes at the onset of the last deglaciation and during Heinrich Event H4 were studied in detail at IMAGES cores MD95-2039 and MD95-2040 from the Western Iberian margin. A major reorganisation of surface water hydrography, benthic foraminiferal community structure, and deepwater isotopic composition commenced already 540 years before the Last Isotopic Maximum (LIM) at 17.43 cal. ka and within 670 years affected all environments. Changes were initiated by meltwater spill in the Nordic Seas and northern North Atlantic that commenced 100 years before concomitant changes were felt off western Iberia. Benthic foraminiferal associations record the drawdown of deepwater oxygenation during meltwater and subsequent Heinrich Events H1 and H4 with a bloom of dysoxic species. At a water depth of 3380 m, benthic oxygen isotopes depict the influence of brines from sea ice formation during ice-rafting pulses and meltwater spill. The brines conceivably were a source of ventilation and provided oxygen to the deeper water masses. Some if not most of the lower deep water came from the South Atlantic. Benthic foraminiferal assemblages display a multi-centennial, approximately 300-year periodicity of oxygen supply at 2470-m water depth. This pattern suggests a probable influence of atmospheric oscillations on the thermohaline convection with frequencies similar to Holocene climate variations. For Heinrich Events H1 and H4, response times of surface water properties off western Iberia to meltwater injection to the Nordic Seas were extremely short, in the range of a few decades only. The ensuing reduction of deepwater ventilation commenced within 500-600 years after the first onset of meltwater spill. These fast temporal responses lend credence to numerical simulations that indicate ocean-climate responses on similar and even faster time scales.

Macroinvertebrate abundance and proportion of trait categories in river biotopes across England and Wales

There is a long tradition of river monitoring using macroinvertebrate communities to assess environmental quality in Europe. A promising alternative is the use of species life-history traits. Both methods, however, have relied on the time-consuming identification of taxa. River biotopes, 1-100 m**2 'habitats' with associated species assemblages, have long been seen as a useful and meaningful way of linking the ecology of macroinvertebrates and river hydro-morphology and can be used to assess hydro-morphological degradation in rivers. Taxonomic differences, however, between different rivers had prevented a general test of this concept until now. The species trait approach may overcome this obstacle across broad geographical areas, using biotopes as the hydro-morphological units which have characteristic species trait assemblages. We collected macroinvertebrate data from 512 discrete patches, comprising 13 river biotopes, from seven rivers in England and Wales. The aim was to test whether river biotopes were better predictors of macroinvertebrate trait profiles than taxonomic composition (genera, families, orders) in rivers, independently of the phylogenetic effects and catchment scale characteristics (i.e. hydrology, geography and land cover). We also tested whether species richness and diversity were better related to biotopes than to rivers. River biotopes explained 40% of the variance in macroinvertebrate trait profiles across the rivers, largely independently of catchment characteristics. There was a strong phylogenetic signature, however. River biotopes were about 50% better at predicting macroinvertebrate trait profiles than taxonomic composition across rivers, no matter which taxonomic resolution was used. River biotopes were better than river identity at explaining the variability in taxonomic richness and diversity (40% and <=10%, respectively). Detailed trait-biotope associations agreed with independent a priori predictions relating trait categories to near river bed flows. Hence, species traits provided a much needed mechanistic understanding and predictive ability across a broad geographical area. We show that integration of the multiple biological trait approach with river biotopes at the interface between ecology and hydro-morphology provides a wealth of new information and potential applications for river science and management.

Planktonic foraminifera abundance in sediments of ODP Leg 170 sites

From October to December in 1996, Sites 1039 through 1043 were drilled on the lower continental slope and the bottom of the Middle American Trench. Planktonic foraminifers were obtained from 377 samples of the total 487 examined. The Pliocene- to Pleistocene-age sediments of Sites 1039 and 1043 are continuous from Zones N19 through N23. At Sites 1039 and 1040, middle Miocene sediments are also continuous, encompassing Zones N8 through N12. The sequences of the upper part of Sites 1040, 1041, 1042, and 1043 are décollements, tentatively assignable to Zone N19 for Sites 1040, 1041, and 1042 and to Zone N22 for Site 1043. The oldest sediments of these sites are assigned to Zone N7 (latest early Miocene), ~17 Ma in age.