327 resultados para Malpighia glabra


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Water depth zonation of fifty nine benthonic foraminiferal species in marine sediment surfaces has been described. Some species are combined to groups which mark particular depth zones: an upper and lower shelf-fauna, an upper and lower slope fauna, and a shelf-slope fauna. Dependence on latitude could be ascertained for Textularia panamensis, and submergence effects for Hyalinea balthica.

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Four long sediment cores from locations in the Framstrait, the Norwegian-Greenland Seas and the northern North Atlantic were analysed in a high resolution sampling mode (1 - 2 cm density) for their benthic foraminiferal content. In particular the impact of the intense climatic changes at glacial/interglacial transitions (terminations I and II) on the benthic community have been of special interest. The faunal data were investigated by means of multivariate analysis and represented in their chronological occurence. The most prominent species of benthic foraminifera in the Norwegian-Greenland Seas are Oridorsalis umbonatus, Cibicidoides wuellerstorfi, the group of Cassidulina, Pyrgo rotalaria, Globocassidulina subglobosa and fragmented tubes of arenaceous species. The climatic signal of termination I as well as termination II is recorded in the fossil foraminiferal tests as divided transition from glacial to interglacial. The elder INDAR maximum (individuals accumulation rate = individuals/sq cm * 1.000 y; Norwegian-Greenland Seas: average 3.000 - 6.000 individuals/sq cm * 1.000 y; northern North Atlantic: average 150 individuals/sq cm * 1.000 y) is followed by a period of decreased values. The second, younger maximum reaches comparable values as the elder maximum. The interglacial INDAR are in average 700 individuals/sq cm * 1.000 y in the Norwegian-Greenland Seas and 200 individuals/sq cm * 1.000 y in average in the northern North Atlantic. The occurence of the elder INDAR maximum shows a distinct chronological transgressivity between the northern North Atlantic (12.400 ybp.) and the Framstrait (8.900 ybp.). The time shift from south to north amounts 3.500 yrs., the average expanding velocity 0,78 km per year. Within the Norwegian-Greenland Seas the average expanding velocity amounts 0,48 km per year. This chronological transgressivity is interpreted as impact of the progressive expanding of the North Atlantic and the Norwegian Current during the deglaciation. The dynamic of the faunal development is defined as increasing INDAR per time. The elder INDAR maximum shows in both glacial/interglacial transitions an exponential increase from south to north. Termination II is characterized by a general higher dynamic as termination I. By means of the high resolution sampling density the impact of regional isotopic recognized melt-water events is recognized by an increase of endobenthic and t-ubiquitous species in the Norwegian-Greenland Seas sediments. During termination I the relative minimum between both INDAR maxima occur chronological with an decrease of calculated sea surface temperatures. This is interpreted as indication of the close pelagic - benthic coupling. The climatic signal in the northern North Atlantic recorded in the fossil benthic foraminiferal community shows a lower amplitude as in the Norwegian-Greenland Seas. The occurence of the epibenthic Cibicidoides wuellersforfi allows to evaluate the variability of the bottom water mass. In general at all core locations increasing lateral bottom currents are recognized with the occurence of the second younger INDAR maximum. In comparison with various paleo-climatological data sets fossil benthic foraminifers show a distinct koherence with changes of the atmospheric temperatures, the SSTs and the postglacial sea level increase. The benthic foraminiferal fauna is bound indirectly on and indicative for regional climatic changes, but principal dependent upon global climatic changes.

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Presented are physical and biological data for the region extending from the Barents Sea to the Kara Sea during 158 scientific cruises for the period 1913-1999. Maps with the temporal distribution of physical and biological variables of the Barents and Kara Seas are presented, with proposed quality control criteria for phytoplankton and zooplankton data. Changes in the plankton community structure between the 1930s, 1950s, and 1990s are discussed. Multiple tables of Arctic Seas phytoplankton and zooplankton species are presented, containing ecological and geographic characteristics for each species, and images of live cells for the dominant phytoplankton species.

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During "Meteor"cruise 1965 the author collected 134 samples of surface sediments from the Iranian part of the Persian Gulf. Benthic Foraminifera populations have been analysed for determining their depth zonation. These data are supposed to allow detailed depth interpretation of Pleistocene sediments found in cores. In addition, the ecological information might be usefull to reconstruct the depositional environment of fossil sediments in similar shallow epicontinental seas. The investigation is published in two parts: the present part 1 contains the catalogue of species with short discussions of taxonomic problems, notes on the distribution within the Persian Gulf and 11 plates, partly with scanning electron micrographs. The results of the statistical analysis are given in data tables which include number of species, percentages of 2 (and 5) ranked species, standing crop and foraminiferal numbers. The author used "species groups" to avoid ambiguities with species requiring additional taxonomic studies. However, species numbers within these units are estimated to yield applicable diversity information. - A total of 52 species and 7 "species groups" were separated, 2 new species were described.

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Deep-sea benthic foraminiferal faunas were studied from Sites 608 (depth 3534 m, 42°50'N, 23°05'W) and 610 (depth 2427 m, 53°13'N, 18°53'W). The sampling interval corresponded to 0.1 to 0.5 m.y. at Site 608 and in the sections of Site 610 from which core recovery was continuous. First and last appearances of benthic foraminiferal taxa are generally not coeval at the two sites, although the faunal patterns are similar and many species occur at both sites. Major periods of changes in the benthic faunas, as indicated by the numbers of first and last appearances and changes in relative abundances, occurred in the early Miocene (19.2-17 Ma), the middle Miocene (15.5-13.5 Ma), the late Miocene (7-5.5 Ma), and the Pliocene-Pleistocene (3.5-0.7 Ma). A period of minor changes in the middle to late Miocene (10-9 Ma) was recognized at Site 608 only. These periods of faunal changes can be correlated with periods of paleoceanographic changes: there was a period of sluggish circulation in the northeastern North Atlantic from 19.2 to 17 Ma, and the deep waters of the oceans probably cooled between 15.5 and 13.5 Ma, as indicated by an increase in delta18O values in benthic foraminiferal tests. The period between 10 and 9 Ma was probably characterized by relatively vigorous bottom-water circulation in the northeastern Atlantic, as indicated by the presence of a widespread reflector. The faunal change at 7 to 5.5 Ma corresponds in time with a worldwide change in delta13C values, and with the Messinian closing of the Mediterranean. The last and largest faunal changes correspond in time with the onset and intensification of Northern Hemisphere glaciation.

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Detailed study of four Holocene sediment intervals from Ocean Drilling Program Site 1098 (Palmer Deep, Antarctic Peninsula) reveals that in situ dissolution of calcareous foraminifers in the core repository has significantly altered and in some cases eliminated calcareous foraminifers. Despite dissolution, the foraminifer and supporting diatom data show that the most open-ocean and reduced sea-ice conditions occurred in the early Holocene. The influence of Circumpolar Deep Water was greatest during the early Holocene but continued to be important throughout the Holocene. An increase in sea-ice proximal diatoms at 3500 cal. BP documents an expansion in the amount of persistent sea ice. The inferred increase in sea ice corresponds with an overall increase in magnetic susceptibility values. Benthic foraminifers are present in all samples from the Palmer Deep, including the middle Holocene pervasively laminated sediments with low magnetic susceptibility values. The consistent presence of mobile epifaunal benthic foraminifers in the laminated sediments demonstrates that the laminations do not represent anoxic conditions. The uniform composition of the agglutinated foraminifer fauna throughout the late Holocene suggests that the Palmer Deep did not experience bottom-water-mass changes associated with the alternating deposition of bioturbated or laminated sediments.

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Asterina ilicis Ellis

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The stratigraphic and biogeographic distribution of more than 170 species of deep-water agglutinated benthic foraminifers (DWAF) from the North Atlantic and adjacent marginal seas has been compared with paleoenvironmental data (e.g. paleobathymetry, oxygenation of the bottom waters, amount of terrigenous input and substrate disturbance). Six general types of assemblages, in which deep water agglutinated taxa occur, are defined from the Turonian to Maastrichtian times: 1. High latitude slope assemblages 2. Low to mid latitude slope assemblages 3. Flysch-type assemblages 4. Deep water limestone assemblages (,,Scaglia,,-type) 5. Abyssal mixed calcareous-agglutinated assemblages 6. Abyssal purely agglutinated assemblages Latitudinal differences in faunal composition are observed, the most important of which is the lack or extreme paucity of calcareous forms in high latitude assemblages. East-to-west differences appear to be of comparatively minor importance. Most DWAF species occur in all studied regions and are thus considered as cosmopolitan. Biostratigraphic turnovers in the taxonomic content of assemblages are observed in the lowermost Turonian, mid-Campanian and in the upper Maastrichtian to lowermost Paleocene. These datum levels correspond to inter-regional and time-constant paleooceanographic events, which probably also affected the deep-water benthic biota. This allows us to use deep-water agglutinated foraminifers for biostratigraphy in the North Atlantic sequences deposited below CCD and to geographically extend the currently used zonal schemes which have been established in the Carpathian and Alpine areas.