246 resultados para Trichinella spiralis


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The results of an investigation of tintinnids from the western Arabian Sea are described. A total of 134 closing-net samples was obtained from 22 stations of the German "Meteor" expedition 1964/1965. Distribution charts of the dominant species of tintinnids from the study area are presented as well as a list of the world-wide distribution of these species as derived from the literature. Tintinnids were most abundant in the surface waters. The layer from 0 - 25 m yielded a maximum 94.3% and a minimum of 61.3% of the tintinnids present from 0 - 175 m; the mean was 80%. There was no significant difference in the vertical distribution between day and night stations nor was there any indication of the influence of the thermocline upon vertical distribution of tintinnids. TS-diagrams show different water types in the western Arabian Sea. Temperatur-salinity-tintinnid -diagrams indicate regional patterns in the distribution of various species of tintinnids. Some tintinnids can be used as indicator species: Climacocylis scalaria, Parundella lohmanni and Amphorella amphora were typical for the Somali Current whereas Rhabdonella apophysata and Branditella palliata indicated the presence of East African Coastal Current water. The concentration of tintinnids in the upper 25 m raged between 4,800 and 39,300 individuals/m**3 (mean 19,000/m**3). Plasma volume of tintinnids was calculated to permit comparison of different links in the food chain. There was a mean of 51 mm**3/m**2 in the upper layer, equivalent to a concentration of 2 mm**3/m**3. Carbon values were computed from the plasma volume of tintinnids, phytoplankton and larger zooplankton. The ratio of phytoplankton plus microzooplankton carbon to large zooplankton carbon was 1 : 0.8 in the Somali Current, 1 : 0.4 in the East African Coastal Current and 1 : 1.2 in the mixing zone of these current systems. Tintinnids are one of the first links in the food chain. It is very likely that a part of the organic detritus and of the nanoplankton is transfered to large herbivores or omnivores via tintinnids and other protozoans. This mechanism might be especially effective during seasons when large phytoplankters are not available in the ocean.

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The latest Campanian-earliest Maastrichtian interval is well known as a period of intense climate cooling. This cooling caused a distinctive bipolar biogeographic distribution of calcareous nannofossil assemblages: High latitude settings were dominated by newly evolving endemic taxa, former cosmopolitan species disappeared at the same time and equatorial communities experienced an invasion of cool water taxa. The impact of this cooling on northern mid-latitude assemblages is, however, less well known. In order to overcome this gap we studied the Kronsmoor section (northwest Germany). This section provides a continuous upper Campanian - lower Maastrichtian succession with moderately to well preserved nannofossils. Uppermost Campanian assemblages are dominated by Prediscosphaera cretacea; other common taxa include Prediscosphaera stoveri, Watznaueria barnesiae and Micula staurophora. The lower Maastrichtian is characterized by lower numbers of P. cretacea and frequent Kamptnerius magnificus, Arkhangelskiella cymbiformis and Cribrosphaerella ehrenbergii. These changes reflect, in part, the Campanian-Maastrichtian boundary cooling since some successful taxa (e.g. K. magnificus) are related to cool surface waters. Other shifts in the nannofossil communities were perhaps the result of a changing nutrient regime. Stronger latitudinal gradients may have increased wind velocities and thus the eolian input of ferruginous dust required by N-fixing bacteria. The enhanced high latitude deep-water formation probably changed the bottom-water environment in disfavor of denitrificating organisms. A decline of chemical weathering and fluviatile transport may have reduced the amount of bioavailable phosphate. These processes led to an increased nitrate and a decreased phosphate content shifting the nutrient regime from nitrate towards phosphate limitation.

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Late Cenozoic benthic foraminiferal faunas from the Caribbean Deep Sea Drilling Project (DSDP) Site 502 (3052 m) and East Pacific DSDP Site 503 (3572 m) were analyzed to interpret bottom-water masses and paleoceanographic changes occurring as the Isthmus of Panama emerged. Major changes during the past 7 Myr occur at 6.7-6.2, 3.4, 2.0, and 1.1 Ma in the Caribbean and 6.7-6.4, 4.0-3.2, 2.1, 1.4, and 0.7 Ma in the Pacific. Prior to 6.7 Ma, benthic foraminiferal faunas at both sites indicate the presence of Antarctic Bottom Water (AABW). After 6.7 Ma benthic foraminiferal faunas indicate a shift to warmer water masses: North Atlantic Deep Water (NADW) in the Caribbean and Pacific Deep Water (PDW) in the Pacific. Flow of NADW may have continued across the rising sill between the Caribbean and Pacific until 5.6 Ma when the Pacific benthic foraminiferal faunas suggest a decrease in bottom-water temperatures. After 5.6 Ma deep-water to intermediate-water flow across the sill appears to have stopped as the bottom-water masses on either side of the sill diverge. The second change recorded by benthic foraminiferal faunas occurs at 3.4 Ma in the Caribbean and 4.0-3.2 Ma in the Pacific. At this time the Caribbean is flooded with cold AABW, which is either gradually warmed or is replaced by Glacial Bottom Water (GBW) at 2.0 Ma and by NADW at 1.1 Ma. These changes are related to global climatic events and to the depth of the sill between the Caribbean and Atlantic rather than the rising Isthmus of Panama. Benthic foraminiferal faunas at East Pacific Site 503 indicate a gradual change from cold PDW to warmer PDW between 4.0 and 3.2 Ma. The PDW is replaced by the warmer, poorly oxygenated PIW at 2.1 Ma. Although the PDW affects the faunas during colder intervals between 1.4 and 0.7 Ma, the PIW remains the principal bottom-water mass in the Guatemala Basin of the East Pacific.

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Although they are fossils of uncertain origin, bolboforms are the best calcareous microfossil group for Neogene biostratigraphy in the North Atlantic. Fifty-two Bolboforma species were observed at the Hatton-Rockall Basin in Ocean Drilling Program Holes 982A (26 samples) and 982B (301 samples) and in Deep Sea Drilling Project Hole 116 (71 samples). The sequence investigated spans the interval from lower Miocene to upper Pliocene. Fourteen zones/subzones were identified and correlated with the calcareous nannoplankton zones, the planktonic foraminifer biostratigraphy, and the time (Ma). The last occurrence of the genus Bolboforma can be dated to 2.84 Ma. Different Bolboforma specimens of middle Miocene age, observed in upper Miocene and upper middle Miocene sediments at Site 982, document redeposition of sediment from the Rockall Bank into the Hatton-Rockall Basin during the latest middle Miocene and late Miocene.

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Rich radiolarian faunas were obtained continuously from Middle Jurassic to Lower Cretaceous radiolarite sequences at Sites 800 and 801, drilled during Ocean Drilling Program Leg 129 in the western Pacific. Occurrences of 90 taxa are presented in tables for these sites. Seven radiolarian zones, Dibolachras tytthopora, Cecrops septemporatus, Pseudodictyomitra carpatica, Pseudodictyomitra primitiva, Cinguloturris carpatica, Stylocapsa spiralis, and Tricolocapsa conexa in descending order, were recognized in this interval. The radiolarite sequences of Sites 800 and 801 encompass approximately the Berriasian to Hauterivian (or to Barremian) and the Bathonian/Callovian to Valanginian ages, respectively. At Site 801, a hiatus of early Oxfordian was identified.

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During Leg 198 of the Ocean Drilling Program (ODP), Paleogene sediments were recovered form 10 holes at four sites along a bathymetric transect from the Southern High of Shatsky Rise. In terms of age, the Paleogene successions span from the Cretaceous/Paleocene boundary to the early Oligocene. Sediments are mainly composed of tan nannofossil ooze with scattered darker layers richer in clay. This data report concerns planktonic foraminiferal biostratigraphy from three holes, specifically Hole 1209A (water depth = 2387 m), Hole 1210A (water depth = 2573 m), and Hole 1211A (water depth = 2907 m). The thickness of Paleogene sediments is 105.90 m in Hole 1209A, 95.05 m in Hole 1210A, and 56.11 m in the deepest Hole 1211A. Preliminary investigations conducted on board revealed that at Site 1209 the succession was mostly complete, whereas the succession was more condensed at Site 1211.