992 resultados para Bacteroides fragilis


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1) Ingesamt 11 Profile aus sechs Mooren und Seen im Gebiet des Hannoverschen Wendlandes wurden pollenanalytisch untersucht. Die Ablagerungen umfassen den Zeitraum vom Beginn der Älteren Tundrenzeit bis zur Gegenwart. 2) Die Waldgeschichte des Hannoverschen Wendlandes weist teils Merkmale der atlantisch geprägten Gebiete Nordwestdeutschlands, teils solche des kontinental beeinflußten nordostdeutschen Raumes auf und nimmt damit eine Zwischenstellung ein. 3) Die Kiefer wandert zu Beginn der Allerödzeit ein, d.h. später als im mecklenburgisch-märkischen Gebiet und im mitteldeutschen Trockengebiet. Im Verlauf der Allerödzeit bildeten sich hier wie dort lichte Kiefern-Birken-Wälder aus. 4) In der Jüngeren Tundrenzeit fand zunächst nur eine geringe Auflichtung der Wälder statt, und die Kiefer überwog weiterhin. Erst im späteren Verlauf dieser stadialen Phase breitete sich die Birke aus und verdrängte die Kiefer. Der späte Rückgang der Kiefer stellt eine Parallele zu der Entwicklung in Südostmecklenburg und in der Altmark dar. Die Abgrenzung dieser Phasen in der Jüngeren Tundrenzeit ist durch eine 14C-Datierung gesichert. 5) Noch im Atlantikum ähneln die Diagramme aus dem Gartower Talsandgebiet im Osten des Wendlandes in ihren hohen Kiefernanteilen denen der Sandergebiete in Brandenburg. Die Diagramme aus dem Moränengebiet des westlichen Wendlandes schließen dagegen mehr an die der östlichen Lüneburger Heide und des Hamburger Gebietes an. Dieser Unterschied wird auf edaphische Unterschiede zurückgeführt. 6) Seit dem frühen Subboreal glich auch die Vegetation des Gartower Gebietes mehr den buchenarmen Waldgesellschaften auf sauren Sandböden, wie sie im atlantischen Westen vorkommen. Die Kiefern sind fast ganz aus dem Waldbild verschwunden, wobei der rasche Rückgang zu Beginn des Subboreals sicher zu einem wesentlichen Teil vom Menschen beeinflusst worden ist. Die anschließende kiefernarme Zeit dauerte im gesamten Wendland bis zum Beginn der Kieferaufforstungen in der Neuzeit. 7) In allen untersuchten Diagrammen ist etwa seit dem Subboreal eine Besiedlung nachzuweisen. Diese muß im Osten des Wendlandes intensiver gewesen sein als im Westen. Es lassen sich Phasen geringer und intensiver Besiedlung nachweisen. 8) Seit Beginn des Subboreals ist das Waldbild schon so stark vom Menschen beeinflusst, dass die Ausbreitungsgeschichte der Laubwaldarten nicht ohne Berücksichtigung der Siedlungsphasen diskutiert werden kann. Besonders im Westen bestand eine ausgedehnte Lindenphase, die durch eine Siedlungszeit (Bronzezeit) beendet wurde. Beim folgenden Rückgang der Siedlungsintensität breitet sich bevorzugt die Hainbuche aus, die dann bei der nächsten Besiedlungsphase (Eisenzeit) zurückging. Erst danach erfolgte die maximale Rotbuchenausbreitung, die nur im Westteil des Wendlandes bedeutende Ausmaße zeigte, während im Ostteil rot- und hainbuchenreiche Eichenwälder entstanden. 9) Seit Beginn der mittelalterlichen Besiedlung ist dann der Eingriff des Menschen so stark gewesen, dass die edaphisch bedingten Unterschiede zwischen Moränen- und Sandergebieten im Pollenspektrum verwischt wurden. Sowohl die buchenreichen Wälder des westlichen als auch die buchenarmen Wälder des mittleren und des östlichen Teilgebietes müssen zu fast reinen Eichenwäldern geworden sein. 10) Calluna-Heiden sind im östlichen Wendland schon in vorgeschichtlicher Zeit nachzuweisen. Im Mittelalter und in der Neuzeit treten sie im gesamten Wendland auf. Etwa im 18. und 19. Jahrhundert war die Ausdehnung der Heideflächen am größten. Erst danach wurden sie im Zuge der Kiefernaufforstungen bis auf geringe Reste verdrängt. 11) Während in der spätglazialen Vegetation Juniperus auftritt, ist der Wacholder sowohl in vorgeschichtlicher als auch in geschichtlicher Zeit - im Gegensatz zur Lüneburger Heide - wohl niemals ein Bestandteil der anthropogenen Calluna-Heiden gewesen.

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Palynological investigation of a 410 cm long core section from Tso Kar (33°10'N, 78°E, 4527 m a.s.l.), an alpine lake situated in the arid Ladakh area of NW India at the limit of the present-day Indian summer monsoon, was performed in order to reconstruct post-glacial regional vegetation and climate dynamics. The area was covered with alpine desert vegetation from ca. 15.2 to 14 kyr BP (1 kyr=1000 cal. years), reflecting dry and cold conditions. High influx values of long-distance transported Pinus sylvestris type pollen suggest prevailing air flow from the west and northwest. The spread of alpine meadow communities and local aquatic vegetation is a weak sign of climate amelioration after ca. 14 kyr BP. Pollen data (e.g. influx values of Pinus roxburghii type and Quercus) suggest that this was due to a strengthening of the summer monsoon and the reduced activity of westerly winds. The further spread of Artemisia and species-rich meadows occurred in response to improved moisture conditions between ca. 12.9 and 12.5 kyr BP. The subsequent change towards drier desert-steppe vegetation likely indicates more frequent westerly disturbances and associated snowfalls, which favoured the persistence of alpine meadows on edaphically moist sites. The spread of Chenopodiaceae-dominated vegetation associated with an extremely weak monsoon occurred at ca. 12.2-11.8 kyr BP during the Younger Dryas interstadial. A major increase in humidity is inferred from the development of Artemisia-dominated steppe and wet alpine meadows with Gentianaceae after the late glacial/early Holocene transition in response to the strengthening of the summer monsoon. Monsoonal influence reached maximum activity in the Tso Kar region between ca. 10.9 and 9.2 kyr BP. The subsequent development of the alpine meadow, steppe and desert-steppe vegetation points to a moderate reduction in the moisture supply, which can be linked to the weaker summer monsoon and the accompanying enhancement of the winter westerly flow from ca. 9.2 to 4.8 kyr BP. The highest water levels of Tso Kar around 8 kyr BP probably reflect combined effect of both monsoonal and westerly influence in the region. An abrupt shift towards aridity in the Tso Kar region occurred after ca. 4.8 kyr BP, as evidenced by an expansion of Chenopodiaceae-dominated desert-steppe. Low pollen influx values registered ca. 2.8-1.3 kyr BP suggest scarce vegetation cover and unfavourable growing conditions likely associated with a further weakening of the Indian Monsoon.

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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.

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While engaged in geoecological field work on Victoria Island, 277 new plants could be recorded for the vicinities of Holman, Cambridge Bay, Wellington Bay, Mt. Pelly, Richardson Islands, Hadley Bay, and Minto lnlet; 8 of them were new for Victoria Island, 6 for the western Canadian arctic archipelago.

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Lower Cretaceous and Jurassic sediments from Ocean Drilling Program Leg 129 (Sites 800, 801, and 802) and Deep Sea Drilling Project Sites 167, 195, 196, and 463 were analyzed for palynomorphs. In contrast to Atlantic occurrences, all Cretaceous pelagic sediments at these sites in the Pacific are barren of preserved palynomorphs. This absence of palynomorphs appears to be independent of facies, sedimentation rate, paleodepth, and paleolatitude. Except for one sample, the dinocyst-bearing sediments also contain spores and pollen grains. The only palynomorphs observed were in redeposited material having sources near former emergent seamounts. Among the dinoflagellate cysts at Site 802, Dingodinium cerviculum, Odontochitina operculata, Canninginopsis colliveri, and Oligosphaeridium complex are the most important species. Based on the presence of these species and their known biostratigraphic ranges, this basal interval of Site 802 is considered to be Aptian/earliest Albian in age. The lack of dinocysts within the Pacific pelagic sediments may be the result of ubiquitous oxygenated bottom waters throughout the Cretaceous or may indicate that open-marine dinoflagellate populations in this ocean did not produce cysts.

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A series of excellent upper Miocene through Quaternary diatomaceous sequences recovered at four sites during Leg 127 was examined for diatoms. The diagenetic transition from opal-A to opal-CT is a diachronic horizon from the uppermost part of the Denticulopsis katayamae Zone (8.5 Ma) at Hole 797B to the uppermost part of the Neodenticula kamtschatica Zone (5.73 Ma) at Hole 795A. The diatom zonation of Koizumi (1985) best divides the upper Miocene to Quaternary sequences above the opal-A/opal-CT boundary and also is useful to date carbonate concretions including diatoms below the boundary. Forty diatom datum levels were evaluated biostratigraphically based on the sediment accumulation rate curve, and several isochronous datum levels are newly proposed for the Japan Sea area. A warm-water current did not penetrated into the Japan Sea through the Tsushima strait during the late Miocene and Pliocene time, because subtropical warm-water diatoms are essentially not present in such sediment samples. The occurrences of diatom are cyclic throughout the Quaternary sediments and are affected by eustatic sea level changes.

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Diatoms occur sporadically in lower Miocene to Holocene sediments recovered at ODP Site 645 and in upper Pliocene to Holocene sediments at ODP Site 646. The diatom assemblage at Site 645 contains rare stratigraphic indicators. Fragmentation of frustules and the occurrence of species characteristic of high-latitude shelf, upper-slope environments suggest current transportation from the shelf. The diatom abundance and preservation at Site 646 probably reflect climatic changes and are also affected by dissolution, but it is not possible to detect the dominant factor. Therefore, the stratigraphic ranges of the primary and secondary biostratigraphic indicators are often unreliable.

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Pollen analysis of samples taken from the core of the water well Fersina 2 (Adige Valley, Prov. Trento, NE Italy) did not reveal any indication of an interglacial or Holocene age of the uppermost 190 m in the sediment sequence deposited in the over-deepened Adige River Valley. The sediment sequence dates entirely from late-glacial times. Four radiocarbon ages of pieces of wood indicate that about 165 m of the upper part of the profile are of Younger Dryas age. The lower part of the sequence dates from the Allerød or Bølling/Allerød and a preceding cold phase, probably the Oldest Dryas. Accordingly the deposition of the sequence took about 2500 or 3500 years and was completed long before the onset of the Neolithic. Our results are in excellent agreement with findings in other formerly glaciated alpine valleys (e.g. the Traun, Salzach and Enns valleys in the Northern Alps). The final depth of the Fersina 2 well is 190 m. It is very likely that the sediment sequence found below this level in the nearby 423 m deep Fersina 1 well was also deposited after the deglaciation of the Adige Valley at the end of the last glacial period.

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In a borehole in the southern outskirts of the town of Göttingen, limnic sediments of several Pleistocene warm periods occur intercalated with coarse solifluction debris and gravel of the river Leine. Pollen analysis of the limnic sediments in a borehole at Ottostrasse gave evidence of three warm periods of interglacial character, followed by three interstadial phases. The warm phases are separated one from another by stadial phases with, at least in one case, indications of periglacial solifluction. This sequence belongs to the Brunhes magnetic epoch. The pollen data allow to exclude an Eemian or Holsteinian age of the warm period sediments. Thus a Cromerian age is assumed, though the exact position of the newly described warm periods within the ''Cromerian'' remains uncertain. A section in a borehole at Akazienweg is of Holsteinian age.