Radiolarian biostratigraphy and chronology of radiolarian events of ODP Leg 199 sites and EW9709 sediment cores

A generally rich radiolarian fauna ranging in age from Quaternary to early Eocene (Zone RP7) was found at five of the eight sites drilled during Ocean Drilling Program (ODP) Leg 199. Of particular interest are the stratigraphically complete assemblages that range in age from middle Miocene (Zone RN5) to early Eocene (Zone RP7), composites of Sites 1218, 1219, and 1220. At the same sites, multisensor track (MST) data show consistent cycles in gamma ray attenuation density, color, and carbonate content that can be correlated on a submeter scale from the early Miocene to early Eocene. In addition, the magnetic reversal records from these three sites allow construction of an absolute timescale. A series of 305 radiolarian morphologic first and last occurrences and evolutionary transitions for radiolarians were determined and correlated directly with the accompanying MST and paleomagnetic data, resulting in a detailed and accurate dating of events. Since many of the bioevents are found at more than one site, it was also possible to test their reliability within the study area. Twelve new species are described: Calocycletta (Calocycletta) anekathen, Dorcadospyris anastasis, Dorcadospyris copelata, Dorcadospyris cyclacantha, Dorcadospyris ombros, Dorcadospyris scambos, Eucyrtidium mitodes, Theocyrtis careotuberosa, Theocyrtis perpumila, Theocyrtis perysinos, Theocyrtis setanios, and Thyrsocyrtis (Pentalacorys) orthotenes.

Eocene and Oligocene radiolarian biostratigraphy from the Southern Ocean

Eocene-Oligocene radiolarians from Ocean Drilling Program Sites 699, 702, and 703, Leg 114 of the Subantarctic Atlantic were examined in order to extend the tripartite zonation for the recovered cores based on results of similar analysis of Leg 120 submarine sediments from the Indian Ocean. Correlation of the two oceans is made by examining 23 biohorizons and the three zones, Eucyrtidium spinosum, Axoprunum irregularis, and Lychnocanoma conica, in ascending stratigraphic order. One new species, Eucyrtidium nishimurae, is described.

Abundance and biomass of the benthic infauna of the North Sea

In 1986 participants of the Benthos Ecology Working Group of ICES conducted a synoptic mapping of the infauna of the southern and central North Sea. Together with a mapping of the infauna of the northern North Sea by Eleftheriou and Basford (1989, doi:10.1017/S0025315400049158) this provides the database for the description of the benthic infauna of the whole North Sea in this paper. Division of the infauna into assemblages by TWINSPAN analysis separated northern assemblages from southern assemblages along the 70 m depth contour. Assemblages were further separated by the 30, 50 m and 100 m depth contour as well as by the sediment type. In addition to widely distributed species, cold water species do not occur further south than the northern edge of the Dogger Bank, which corresponds to the 50 m depth contour. Warm water species were not found north of the 100 m depth contour. Some species occur on all types of sediment but most are restricted to a special sediment and therefore these species are limited in their distribution. The factors structuring species distributions and assemblages seem to be temperature, the influence of different water masses, e.g. Atlantic water, the type of sediment and the food supply to the benthos.

Radiolarians from the Southwest Pacific

Radiolarians are very rare in all Leg 90 sites. They are relatively more frequent only in Neogene sediments from Sites 586 and 594, and in Eocene sediments at Site 592. In this chapter radiolarian abundances are recorded as comparative percentages for 92 Neogene morphotypes at Site 586B. Relative abundances only are estimated at Sites 592 and 594, where preservation is poor to moderate. A tentative correlation of radiolarian events at Hole 586B and Site 594 shows that only a few species can be found in both tropical and subantarctic areas. New evolutionary lineages are proposed. 1. Middle Miocene eucyrtids like Eucyrtidium teuscheri group evolved into a widespread species (E. teuscheri teuscheri) ranging from middle Miocene to Holocene and a temperate species (E. teuscheri orthoporus) ranging from middle Miocene to early Pleistocene. 2. Phormostichoartus pitomorphus appears to be a temperate descendant of the cosmopolitan P. fistula and disappears in early Pleistocene time. 3. The discovery of Lamprocyrtis daniellae n.sp. calls into question the lineage L. heteroporos -> L. nigriniae. 4. The evolution of Lamprocyclas maritalis from an ancestor group (L. aff. maritalis) is located in the early part of the Pterocanium prismatium Zone.

Late middle Eocene to late Oligocene radiolarian biostratigraphy of ODP Hole 113-689B of Maud Rise, Southern Ocean

We propose a new biostratigraphic scheme comprising the Eucyrtidium spinosum, Eucyrtidium antiquum (new), Lychnocanoma conica (emended), Clinorhabdus robusta (emended) and Stylosphaera radiosa (emended) Zones, in ascending order, in Eocene to Oligocene sediments drilled on Maud Rise in Southern Atlantic Ocean (Site 689, Ocean Drilling Program Leg 113). The bases of these zones are defined by the lowermost occurrences of E. spinosum, E. antiquum, L. conica, C. robusta and the uppermost occurrence of Axoprunum irregularis (?), respectively. From correlation to the magnetostratigraphic data, the E. spinosum, E. antiquum, L. conica, C. robusta and S. radiosa Zones are assigned to the late middle Eocene through late Eocene (Subchrons C17n2 to C13r), earliest Oligocene (C13n to C11n), late early Oligocene (C11n to C10n2), early late Oligocene (C10n1 to C8r) and latest Oligocene (C8r to C7An), respectively. The four boundary datum levels and supplementary datum levels such as the lowermost occurrences of A. irregularis (?), Dicolocapsa microcephala and Lithomelissa challengerae may be recognized in other ODP sites in the Southern Ocean. The first occurrence of E. antiquum approximates the Eocene-Oligocene boundary in Southern Ocean but the last occurrences of many species such as Periphaena decora, D. microcephala and the Lithomelissa sphaerocephalis group are commonly diachronous between high latitude sites. Two new species, Theocyrtis (?) triapenna and Spirocyrtis parvaturris, are described.

Radiolarian Paleogene biostratigraphy in the southern Indian Ocean, ODP Leg 120

During Ocean Drilling Program Leg 120, an almost complete Paleogene sediment section on the Kerguelen Plateau in the southern Indian Ocean was recovered. The biostratigraphy of radiolarians from these sediments at Sites 748 and 749 is studied. A biostratigraphic framework established in low and middle latitudes is not applicable because of the absence of most zonal marker species. Biogenic opal is present only in middle Eocene to Oligocene sediments, and three new zones-Lychnocanoma conica, Axoprunum (?) irregularis, and Eucyrtidium spinosum zones-are proposed. The Paleogene antarctic radiolarian fauna is different from that in low and middle latitudes. Three new species, Axoprunum (?) irregularis, Eucyrtidium cheni, and Eucyrtidium spinosum, are described.

Occurrence of radiolarians in DSDP Hole 11-98 (Table 1)

Site 634, drilled during ODP Leg 101, was essentially a reoccupation of Site 98, drilled during DSDP Leg 11 (Hollister, Ewing, et al., 1972, doi:10.2973/dsdp.proc.11.1972; Table 1, Fig. 1). At Site 634, the upper 144 m of sediment was washed in an attempt to reach the Upper Cretaceous target horizon in the time remaining for the cruise (Austin, Schlager, et al., 1986, doi:10.2973/odp.proc.ir.101.1986). Figure 2 illustrates the spatial relationship of Site 98 (2750 m water depth) and Site 634 (2835 m water depth), 0.2 nmi to the northwest. Radiolarians were observed in Site 98 samples from 100 to 240 meters below seafloor (mbsf) during Leg 11, but no detailed biostratigraphic analyses were conducted. Thus, Site 98 presented us an opportunity to sample material correlating with the washed section at Site 634. Samples were taken from Cores 101-634A-2R through 101-634A-4R to study radiolarians, but all proved barren, nor were radiolarians observed in shipboard smear slides. A correlation between Sites 98 and 634 (Fig. 2) suggests that these cores represent the same interval as that recovered in Cores 11-98-10 and 11-98-11, which were also barren. These results are presented separately from other Leg 101 radiolarian studies (Palmer, 1988, datasets: doi:10.1594/PANGAEA.743055) because the Site 98 fauna was predominantly Eocene, while other radiolarian assemblages studied were Oligocene and Miocene.

Late Eocene-early Oligocene radiolarian events and abundances in ODP Leg 199 sediments

During Ocean Drilling Program Leg 199, eight sites (Sites 1215-1222) were cored in the Central Pacific. Late Eocene-early Oligocene thick radiolarian-rich biogenic sediments were collected from Holes 1218A, 1219A, and 1220A. This is the first attempt to calibrate the ages of Paleogene radiolarian events using magnetostratigraphy in this region. A total of 107 species and species groups, which are valuable for stratigraphic correlation, are listed with numeric data and figures. Among these three holes, a total of 77 radiolarian events were recognized and their ages were calibrated by correlation with paleomagnetic events recorded in Hole 1220A.

Range charts of stratigraphically important radiolarian species in sediments of ODP Leg 165 sites

The Paleogene sequences from three sites in the Caribbean were examined for radiolarians. In general, samples are highly lithified, requiring lengthy and repetitive cleaning procedures, and the assemblages are usually fragmented and/or partially dissolved. Both abundances and preservation of the assemblages vary considerably from site to site and within a single site; even within a single sample more than one degree of preservation was observed. It was possible, however, to construct at least partial stratigraphies for each of the three sites. Because the abundance of radiolarians is high even in extremely poorly preserved assemblages, we conclude that the differences in biogenic silica preservation are the result of postdepositional processes and not productivity. In both Sites 999 and 1001, near the Paleocene/Eocene boundary (Bekoma bidartensis Zone [RP7]), there is a short interval in which the abundance and preservation state of the radiolarians improves relative to overlying and underlying assemblages. In each case the intervals corresponds to the level, identified by calcareous microfossils, as representing changes in paleoceanographic conditions associated with the late Paleocene thermal maximum.

Macrofauna abundance and sediment characteristics during R/V Senckenberg cruise west of Sylt in september 2010

The continuously influence of human impacts on the seafloor and benthic habitats demands the knowledge of clearly defined habitats to assess recent conditions and to monitor future changes. In this study, a benthic habitat dominated by sorted bedforms was mapped in 2010 using biological, sedimentological and acoustic data. This approach reveals the first interdisciplinary analysis of macrofauna communities in sorted bedforms in the German Bight. The study area covered 4 km², and was located ca. 3.5 km west of island of Sylt. Sorted bedforms formed as sinuous depressions with an east west orientation. Inside these depressions coarse sand covers the seafloor, while outside predominantly fine to medium sand was found. Based on the hydroacoustic data, two seafloor classes were identified. Acoustic class 1 was linked to coarse sand (type A) found inside these sorted bedforms, whereas acoustic class 2 was related to mainly fine to medium sands (type B). The two acoustic classes and sediment types corresponded with the macrofauna communities 1 and 2. The Aoinides paucibranchiata-Goniadella bobretzkii community on coarse sand and the Spiophanes bombyx - Magelona johnstonii community on fine sand. A transitional community 3 (Scoloplos armiger - Ophelia community), with species found in communities 1 and 2, could not be detected by hydroacoustic methods. This study showed the limits of the used acoustic methods, which were unable to detect insignificant differences in the fauna composition of sandy areas.