Origin and evolution of Cycladophora davisiana (Radiolaria) in DSDP Hole 19-192, Northwest Pacific

This paper documents the evolutionary history of Cycladophora davisiana Ehrenberg from an uppermost Miocene to Pleistocene sedimentary record in the high-latitude Northwest Pacific. It apparently evolved from C. sakaii Motoyama through a series of intermediates. C. sakaii has a relatively large shell with an external spongy layer. The evolutionary transition is characterized by a relatively rapid decrease in thorax size with a reduction of the spongy appendage. This change occurred during about 0.4 m.y. from 2.8 to 2.4 Ma without cladogenesis. Following this interval, a decrease in thorax size continued gradually up to the Recent, resulting in a very small morphology. Although the population of C. davisiana first appeared at about 2.5 Ma, some morphotypic specimens may occur in earlier periods as indistinguishable very small endmembers in the C. sakaii populations. Timing of the first appearance events both of morphotypic specimens and of a population of C. davisiana in Site 192 and previously reported cores does not disprove the idea that C. davisiana evolved first in the Northwest Pacific region, and later migrated into other regions of the world ocean. Biometrics clearly indicate no direct phylogenetic relationships between C. davisiana and C. cornutoides Kling in the studied core. Thus, the latter species, which was originally described as a variation and later elevated to a subspecies of the former species, is separated from the former species and raised to the species rank.

Middle Eocene to Miocene calcareous nannofossil of ODP Leg 125

During Ocean Drilling Program Leg 125, a thick sequence of middle Eocene to Pleistocene pelagic sediments, volcanogenic sediments, and predominantly extrusive volcanic rocks was recovered. Calcareous nannofossils were examined from 15 holes at nine sites, but Eocene to Miocene calcareous nannofossils were found only from Holes 782A, 784A, 786A, and 786B. In portions of Holes 786A and 786B, datable nannofossil oozes were found intercalated among volcanic flows. The nannofossil biostratigraphy of these holes indicates the presence of three well-defined hiatuses: within the lower Oligocene, between the upper Oligocene and middle Miocene, and between the middle and upper Miocene. An attempt was made to correlate the magnetochronological data with the first or last occurrences of the following species: Sphenolithus distentus, Reticulofenestra bisecta, Reticulofenestra reticulata, and Cyclicargolithus floridanus abisectus n. comb. The results indicate that the FO of Sphenolithus distentus can extend down to Zone CP16 (34.7 Ma), the LO of Reticulofenestra bisecta best defines the boundary between CP19a and CP19b (23.5 Ma), and the LO of Cyclicargolithus f. abisectus n. comb, can extend up to Subzone CN5a (12.5 Ma). No latest Oligocene Cyclicargolithus f. abisectus n. comb, acme was observed. Cyclicargolithus abisectus is considered a subspecies or variant of Cyclicargolithus floridanus because their LOs coincide. As a consequence of these observations, we have modified the definitions of Bukry's Subzones CP14a, CP14b, and CNla. Analyses of sediment-accumulation rates indicate that the rates increased gradually from the Eocene to Miocene. This is especially evident since the late Miocene in Hole 782A. In different parts of the Izu-Bonin forearc basin, however, the rate is not everywhere the same and appears to vary according to the import of volcanogenic materials.

Cretaceous calcareous nannofossils of ODP Leg 103 holes

Ocean Drilling Program Leg 103 recovered Lower Cretaceous sediments from the Galicia margin off the coast of Iberia. The high diversity and abundance of assemblages makes this excellent material for the study of Early Cretaceous calcareous nannofossils. With the exception of a hiatus between the upper Hauterivian and lower Barremian, nannofossil distributions form a continuous composite section from the lower Valanginian to lower Cenomanian sediments recovered at the four sites. The sedimentation history of this rifted continental margin is complex, and careful examination of the nannofossil content and lithology is necessary in order to obtain optimum biostratigraphic resolution. The Lower Cretaceous sequence consists of a lower Valanginian calpionellid marlstone overlain by terrigenous sandstone turbidites deposited in the Valanginian and Hauterivian during initial rifting of this part of the margin. Interbedded calcareous marl and claystone microturbidites overlie the sandstone turbidites. Rifting processes culminated in the late Aptian-early Albian, resulting in the deposition of a calcareous, clastic turbidite sequence. The subsequent deposition of dark carbonaceous claystones (black shales) represents the beginning of seafloor spreading, as the margin continued to subside to depths near or below the CCD. The diversity, abundance, and preservation of nannofossils within these varied lithologies differ, and an attempt to distinguish between near shore and open-marine assemblages is made. Genera used for this purpose include Nannoconus, Micrantholithus, Pickelhaube, and Lithraphidites. In this study, six new species and one new subspecies are described and documented. Ranges of other species are extended, and an attempt is made to clarify existing, yet poorly understood, taxonomic concepts. A technique in which a single specimen is viewed with both light and scanning electron microscopes was used extensively to aid in this task. In addition, further subdivisions of the Sissingh (1977) zonation are suggested in order to increase biostratigraphic resolution.

Neogene planktonic foraminifera of DSDP Leg 41 holes

During Leg 41 Neogene sediments were recovered from five sites off northwest Africa. On the Sierra Leone Rise (Site 366), Neogene sediments consist of nanno oozes, nanno chalk, and calcareous clays 230 meters thick, resting conformably on the late Oligocene sediments. The common succession of zones occurs with two hiatuses. The lower gap corresponds to an interval around the lower/middle Miocene boundary (the Praeorbulina glomerosa and Orbulina suturalis-Globorotalia peri-pheroronda zones are absent) and the upper gap coincides with an interval around the middle/upper Miocene boundary (the Sphaeroidinellopsis sub-dehiscens-GIobigerina druryi, Globigerina nepenthes-Globorotalia siakensis and Globorotalia conlinuosa zones are missing). In the Cape Verde Basin (Site 367) deep-water Neogene turbidites (about 200-250 m thick) contain poor fauna of redeposited and sorted Cretaceous, Eocene, Oligocene, and Neogene species. On the Cape Verde Rise (Site 368) the Neogene section starts with slightly calcareous and non-calcareous clays with poor planktonic foraminifers of the lower Miocene. Later on this area was uplifted and clayey sediments have been replaced upsection in order by more shallow-water clayey nanno and nanno-foraminifer oozes and marls and pure calcareous oozes. In the middle Miocene, planktonic foraminifers are still not diverse, but since the level of the Globigerina nepenthes-Globorotalia siakensis Zone, almost all Neogene zones have been traced. The minimum thickness of the Neogene sediments is about 230 meters. On the continental slope off Spanish Sahara (Site 369) monotonous calcareous pelagic sediments of Neogene age (164 m thick) overlie the late Oligocene comformably, or with a small time gap. A set of zones beginning from the Globigerinoides primordis-Globorotaiia kugleri Zone up to the Globorotalia fohsi fohsi Zone has been revealed with a gap corresponding to the Globigerinita stainforthi and the Globigerinatella insueta-Globigerinoides irilobus zones. Above that follow sediments with heterogeneous microfauna which result from redeposition or mixing of sediments during drilling. The section ends with sediments of the late Miocene and lower Pliocene with abundant planktonic foraminifers. The latter are unconformably overlain by the Quaternary ooze. In the Morocco basin (Site 370) deep-water marls and calcareous clays of the lower Miocene contain poor assemblages of planktonic foraminifers. The middle and upper Miocene are represented by turbidites (alternation of nanno oozes, clays, siltstones, and sands) with heterogeneous microfauna. Total thickness of Neogene is up to 200 meters. In general the Neogene foraminifer microfauna of the area studied includes the majority of species which developed within the tropical-subtropical belt. The entire succession of the Miocene and Pliocene foraminifer zones occurs. The only exclusion is the Sphaeroidinellopsis subdehiscens-Globigerina druryi Zone of the middle Miocene. The distribution of species is shown on three tables. Comments are given for 47 species and subspecies of foraminifers (stratigraphic ranges, peculiarities of morphology, and ultrastructure of the shell wall).

Macrobenthic abundance, biomass, productivity and production in the deep Arctic ocean

The few existing studies on macrobenthic communities of the deep Arctic Ocean report low standing stocks, and confirm a gradient with declining biomass from the slopes down to the basins as commonly reported for deep-sea benthos. In this study we have further investigated the relationship of faunal abundance (N), biomass (B) as well as community production (P) with water depth, geographical latitude and sea ice concentration. The underlying dataset combines legacy data from the past 20 years, as well as recent field studies selected according to standardized quality control procedures. Community P/B and production were estimated using the multi-parameter ANN model developed by Brey (2012). We could confirm the previously described negative relationship of water depth and macrofauna standing stock in the Arctic deep-sea. Furthermore, the sea-ice cover increasing with high latitudes, correlated with decreasing abundances of down to < 200 individuals/m**2, biomasses of < 65 mg C/m**2 and P of < 75 mg C/m**2/y. Stations under influence of the seasonal ice zone (SIZ) showed much higher standing stock and P means between 400 - 1400 mg C/m**2/y; even at depths up to 3700 m. We conclude that particle flux is the key factor structuring benthic communities in the deep Arctic ocean, explaining both the low values in the ice-covered Arctic basins and the high values along the SIZ.

(Table 2) Details of laminated intervals of ODP Leg 158 holes

Scanning electron microscope (SEM)-based analyses of the laminated diatom oozes encountered during Leg 138 reveal three major laminae types. The first lamina type is composed of multiple layers of ~20-?m-thick diatom mats, which form laminae dominated by assemblages of the pennate diatom, Thalassiothrix longissima. More than one variety/subspecies of T. longissima occurs within these laminae (referred to as the T. longissima Group). The second lamina type is composed of a mixed-assemblage of several species of diatoms (centric and pennate varieties), calcareous nannofossils, and subordinate quantities of radiolarians, silicoflagellates and foraminifers. The third lamina type is dominated by an assemblage of nannofossils and minor amounts of those fossil components mentioned above. This last form of lamination is compositionally similar to the background sediment type, foraminifernannofossil ooze (F-NO). Two lamina associations occur within the laminated intervals; the first comprises alternations of T. longissima Group and mixed-assemblage laminae (average thickness is ~6 mm) and the second is composed of T. longissima and nannofossil-rich laminae (average thickness is ~3.5 mm). The arrangement of laminae probably originates from the deposition of multiple layers of 20-?m-thick mats from one mat-flux episode. The much thinner nannofossil-rich laminae are interpreted to represent periods of more ônormalö deposition between mat-flux episodes. The occurrence of several varieties/subspecies of T. longissima within individual mat layers is consistent with observations of Rhizosolenia diatom mats in the modern world ocean.

Dioxin-like and non-dioxin like contaminants in the herring Clupea harengus in the Norwegian and North Sea

The Norwegian spring spawning (NSS) herring is an ecologically important fish stock in the Norwegian Sea, and with a catch volume exceeding one million tons a year it is also economically important and a valuable food source. In order to provide a baseline of the levels of contaminants in this fish stock, the levels of organohalogen compounds were determined in 800 individual herring sampled at 29 positions in the Norwegian Sea and off the coast of Norway. Due to seasonal migration, the herring were sampled where they were located during the different seasons. Concentrations of dioxins and dioxin-like PCBs, non-dioxin-like PCBs (PCB7) and PBDEs were determined in fillet samples of individual herring, and found to be relatively low, with means (min-max) of 0.77 (0.24-3.5) ngTEQ/kg wet weight (ww), 5.0 (1.4-24) µg/kg ww and 0.47 (0.091-3.1) µg/kg ww, respectively. The concentrations varied throughout the year due to the feeding- and spawning cycle: Starved, pre-spawning herring caught off the Norwegian coast in January-February had the highest levels and those caught in the Norwegian Sea in April-June, after further starvation and spawning, had the lowest levels. These results show that the concentrations of organohalogen compounds in NSS herring are relatively low and closely tied to their physiological condition, and that in the future regular monitoring of NSS herring should be made in the spawning areas off the Norwegian coast in late winter.

Age determination and foraminiferal faunas in sediment core MD99-2275

A high-resolution study of palaeoceanographic changes off North Iceland during the time period 8600-5200 cal year BP is based on benthic and planktonic foraminiferal assemblages. The core material (MD99-2275) was obtained from about 440 m water depth on the eastern part of the North Icelandic shelf. Changes in the faunal composition are interpreted to be mainly caused by variations in the strength of the relatively warm, high-salinity Irminger Current and the cold East Icelandic Current, which have been shown to be linked to the climatic changes in the North Atlantic region. Environmental proxies at that site are particularly sensitive to palaeoceanographic changes due to its position close to the marine Polar Front. Benthic assemblages show that relatively cold conditions prevailed at the base of the record. An increase in the influence of Atlantic water masses at the sea floor is seen at around 8400 cal year BP, whereas the surface waters were relatively warm already at 8600 cal year BP. The warming was interrupted by a cold event at around 8100-8000 cal year BP, registered both in the bottom and surface waters and correlated with the so-called 8.2 kyr cooling event. Both the benthic and the planktonic faunal compositions indicate that the Irminger Current had maximum influence in the area between 8000 and about 7300 cal year BP, followed by a gradually decreasing influence through the remaining part of the studied time interval. It is suggested that the contribution of Atlantic water masses from the east and north-east to the Arctic Surface waters off North Iceland increased after around 7000 cal year BP, and that this was further intensified after 6200 cal year BP. At present, the Arctic Surface Water north of Iceland consists of Polar waters, intermittently with direct influence from the East Greenland Current, mixed with Atlantic waters derived from the eastern part of the Nordic Seas. A comparison of the mean values of selected environmental proxies in the interval 8600-5200 cal year BP with the upper part of the same core shows that the water masses north of Iceland were considerably warmer during the Holocene thermal maximum than during the last 2000 cal year. In general, results from core MD99-2275 are in accordance with other marine records from the North Icelandic shelf and the northern North Atlantic region, although a detailed comparison on a centennial time scale is hampered by problems with spatial as well as temporal changes in the marine reservoir ages in the region.

Silicoflagellates of DSDP Leg 90 sites

Silicoflagellates are described from Sites 588 (middle Eocene), 591 (middle Miocene to lower Pliocene), and 594 (middle Miocene to Quaternary) in the southwest Pacific. At Sites 591 and 594 a detailed silicoflagellate zonation is possible, although there are some obvious differences arising from the latitudinal position of the sites in the silicoflagellate assemblages. Comparison between the sequences recovered at Sites 591 and 206 (Leg 21) revealed two hiatuses in the latter, but helped to establish a zonation for this area from the lower Miocene to the Pleistocene and a correlation to standard nannoplankton zones. The stratigraphic implications of the taxonomy used by various authors and the species concept presented here are discussed in detail. Special reference is made to types described by Ehrenberg and to later synonyma, because the Ehrenberg collection is the base for all subsequent descriptions and evaluations of silicoflagellate taxa. Two new genera (Neonaviculopsis, Paramesocena), two new subspecies (Dictyocha fibula subsp. asymmetrica, Neonaviculopsis neonautica subsp. praenautica), and three new forms (Dictyocha perlaevis f. pentaradiata, Distephanus speculum subsp. speculum f. nonarius, and Mesocena ? hexalitha f. heptalitha) are described from the southwest Pacific Neogene and Pleistocene. Associated sponge spicules were noted and will be described in detail in a later paper, but some are documented on Plate 13.

Diversity and Genetic structure of the Spanish collection of durum wheat (Triticum turgidum L) landraces

The objectives of this study were to assess diversity and genetic structure of a collection of Spanish durum wheat (Triticum turgidum L) landraces, using SSRs, DArTs and gliadin-markers, and to correlate the distribution of diversity with geographic and climatic features, as well as agro-morphological traits. A high level of diversity was detected in the genotypes analyzed, which were separated into nine populations with a moderate to great genetic divergence among them. The three subspecies taxa, dicoccon, turgidum and durum, present in the collection, largely determined the clustering of the populations. Genotype variation was lower in dicoccon (one major population) and turgidum (two major populations) than in durum (five major populations). Genetic differentiation by the agro-ecological zone of origin was greater in dicoccon and turgidum than in durum. DArT markers revealed two geographic substructures, east-west for dicoccon and northeast-southwest for turgidum. The ssp. durum had a more complex structure, consisting of seven populations with high intra-population variation. DArT markers allowed the detection of subgroups within some populations, with agro-morphological and gliadin differences, and distinct agro-ecological zones of origin. Two different phylogenetic groups were detected; revealing that some durum populations were more related to ssp. turgidum from northern Spain, while others seem to be more related to durum wheats from North Africa

Creation and Validation of the Spanish Durum Wheat Core Collection.

Spanish wheat (Triticum spp.) landraces have a considerable polymorphism, containing many unique alleles, relative to other collections. The existence of a core collection is a favored approach for breeders to efficiently explore novel variation and enhance the use of germplasm. In this study, the Spanish durum wheat (Triticum turgidum L.) core collection (CC) was created using a population structure–based method, grouping accessions by subspecies and allocating the number of genotypes among populations according to the diversity of simple sequence repeat (SSR) markers. The CC of 94 genotypes was established, which accounted for 17% of the accessions in the entire collection. An alternative core collection (CH), with the same number of genotypes per subspecies and maximizing the coverage of SSR alleles, was assembled with the Core Hunter software. The quality of both core collections was compared with a random core collection and evaluated using geographic, agromorphological, and molecular marker data not previously used in the selection of genotypes. Both core collections had a high genetic representativeness, which validated their sampling strategies. Geographic and agromorphological variation, phenotypic correlations, and gliadin alleles of the original collection were more accurately depicted by the CC. Diversity arrays technology (DArT) markers revealed that the CC included genotypes less similar than the CH. Although more SSR alleles were retained by the CH (94%) than by the CC (91%), the results showed that the CC was better than CH for breeding purposes.