230 resultados para Proboscidea
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An exceptionally favourable stratigraphic and chronologic context concerning the Miocene series in Lisbon allows us to stress that there are two successive data as far as the Proboscideans' immigration into western Europe is concerned: firstly, that of Gomphotheres, and later that of Deinotheres. The study of a Langhian (in age) tusk has shown that Deinotherinm havaricum was still present then. The time span of this species could be accurately recognized. A discussion on the genus Deinotherium is presented, as well as its occurrence in Portugal and on its ecologic meaning.
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This study attempts to understand the significance of Uvigerina proboscidea in paleoceanographic reconstructions at the northern (tropical) Indian Ocean DSDP Site 214 from the Late Miocene through the Pleistocene. In this interval at this site, U. proboscidea is the most abundant species of the benthic assemblage and shows abrupt frequency changes (about 1-74%). Based on relative percentages of U. proboscidea calibrated with oxygen and carbon isotope record and the sediment accumulation rates, the modern distribution of the species in the Indian Ocean, and other evidence, the peaks of abundance of U. proboscidea are inferred to represent times of high-surface productivity, This productivity is related to intensified trade winds during strong southwest (SW) Indian monsoons, causing widespread upwelling along equatorial divergemce in the Indian Ocean. The sudden increase of U. proboscidea abundance at approximately 8.5-7.5 Ma reflects significant upwelling at the equatorial divergence. This event corresponds to the permanent build-up of West Antarctic ice sheets, and a major increase in SW Indian monsoons related upwelling in the northwestern Indian Ocean. The Chron-6 carbon shift at approximately 6.2 Ma is marked by another peak of abundance, reflecting widespread ocean fertility. The highest abundances of U. proboscidea and highest sediment accumulation rates occur between 5.8 and 5.1 Ma, which coincidies with the greatest development of Antarctic ice sheets and strong southwest monsoons. The higher percentages at 3.2-3.1 Ma, approximately 2.4 Ma, and 1.6 Ma all represent phases of high productivity at the equatorial divergence.
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The paleontological richness of Morocco has been scientifically known since at least the early 20th century. The region of the Middle Atlas, more specifically the Boulemane area, has been however only sparsely studied since the 60’s when it supplied various vertebrate fossils from the Middle Jurassic.In the beginning of the 2000’s some fossil bones were discovered in a new fossil-site near the village of Taghrout, in the Boulemane area and in September 2013 a Moroccan-Portuguese expedition made excavations in the site with the help locals from the village of Taghrout. The site is Pleistocene in age and is located on a rare bone bearing small high-altitude sedimentary basin, non-charted in previous geological maps. The excavations yielded new bone material from large mammals. The most common findings are elephants ascribed to the genus Elephas, but artiodactyls, turtles, and in-situ hominid Acheulean tools were also collected. During the excavation campaign the Jurassic sites were revisited and new dinosaur trails and possible crocodilomorph bones were discovered. Surface collection of in a cave near Taghrout with Holocene mammal material, including the genera Canis, Capra, Bos, Panthera and Hystrix was also conducted and its fossils elements identified.
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Leptospirosis is considered a worldwide distributed zoonosis, caused by the bacteria Leptospira spp. Since several species of wildlife animals are reportedly reservoirs, the aim of the present study was to know the epidemiology of leptospirosis at the Sorocaba Zoo, Southern Brazil. Serum samples of wild mammals from Artiodactyla, Carnivora, Didelphimorphia, Diprotodontia, Perissodactyla, Pilosa, Primates, Proboscidea and Rodentia orders, kept in captivity as well as from zoological staff were assayed by microscopic agglutination test (MAT). Whole blood, urine and tissue samples from wild mammals and synanthropic animals were assayed by polymerase chain reaction (PCR). An epidemiological survey was applied to evaluate the risk factors for animal infection and staff level of knowledge on leptospirosis. A total of 13/229 (5.68%; CI95% 3.37-9.47%) serum samples from wild mammals were reagent on MAT. Serology from synanthropic animals, zoo staff and molecular analysis of animal samples were all negative. Leptospirosis knowledge of zoo park staff was considered medium. In conclusion, leptospiral infection occurs at the studied zoo but due to the low occurrence found, the lowest reported in literature, wild captive mammals do not act as source of infection of leptospirosis to other animals and human beings.
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Fácies marinhas e costeiras associadas a eventos transgressivos-regressivos quaternários ocorrem na Planície Costeira do Rio Grande do Sul e na plataforma continental adjacente. Enquanto as fácies expostas na planície costeira apresentam uma composição essencialmente siliciclástica, as fácies submersas, hoje aflorantes na antepraia e plataforma interna, apresentam, muitas vezes, uma composição carbonática. Formada por coquinas e arenitos de praia fortemente cimentados, estas fácies destacam-se do fundo oceânico como altos topográficos submersos. Os altos topográficos da antepraia têm atuado como fonte de boa parte dos sedimentos e bioclastos de origem marinha encontrados nas praias da área de estudo. Os bioclastos carbonáticos que ocorrem nestes locais caracterizam uma Associação Heterozoa, ou seja, são formados por carbonatos de águas frias, característicos de médias latitudes, e são representados principalmente por moluscos, equinodermos irregulares, anelídeos, crustáceos decápodos, restos esqueletais de peixes ósseos e cartilaginosos, cetáceos, tartarugas e aves semelhantes à fauna atual. Além destes bioclastos de origem marinha, as praias estudadas apresentam a ocorrência de fragmentos orgânicos provenientes de afloramentos continentais fossilíferos, contendo abundantes restos esqueletais de mamíferos terrestres gigantes extintos, das ordens Edentada, Notoungulada, Litopterna, Proboscidea, Artiodactila, Perissodactila, Carnívora e Rodentia. A concentração dos bioclastos na praia resultada da ação direta dos processos hidrodinâmicos que atuam na região de estudo (ondas de tempestade, deriva litorânea, correntes, etc). A variação no tamanho médio dos bioclastos encontrados ao longo da linha de costa está relacionada ao limite da ação das ondas de tempestades sobre o fundo oceânico, o qual é controlado principalmente pela profundidade. Os afloramentos-fonte submersos podem ser divididos em holocênicos e pleistocênicos. A tafonomia dos bioclastos pleistocênicos permite argumentar que após o penúltimo máximo transgressivo que resultou na formação do sistema deposicional Laguna-Barreira III (aproximadamente 120 ka) parte dos depósitos lagunares permaneceram emersos e não estiveram sob a ação marinha (barrancas do arroio Chuí, com a megafauna preservada in situ), enquanto que parte dos depósitos lagunares esteve sob ação direta do ambiente praial. Em diversas feições submersas observam-se coquinas contendo fósseis de mamíferos terrestres, indicando o retrabalhamento dos sedimentos lagunares em ambiente praial. As coquinas que apresentam moluscos pouco arredondados e de maior granulometria são aqui definidas, informalmente, como Coquinas do Tipo 1. Como conseqüência da última regressão pleistocênica (iniciada após o máximo transgressivo de 120 ka) estas coquinas ficaram submetidas a uma exposição subaérea. Este fato possibilitou a dissolução diferenciada dos componentes carbonáticos existentes nos depósitos (coquinas e arenitos) e sua recristalização (calcita espática) em ambientes saturados em água doce. A Transgressão Pós-Glacial (iniciada em torno de 18 ka) foi responsável pelo retrabalhamento dos arenitos e coquinas, recristalizando mais uma vez os elementos carbonáticos. Devido ao seu grau de consolidação estes depósitos resistiram à erosão associada à elaboração da superfície de ravinamento e encontram-se atualmente expostos na antepraia e, mesmo, na linha de praia atual. Pelo menos há 8 ka houve novamente um período favorável à precipitação de carbonato de cálcio, ocorrendo a litificação de rochas sedimentares em uma linha de praia numa cota batimétrica inferior a atual. Neste intervalo de tempo formaram-se as coquinas e arenitos não recristalizados, apresentando fragmentos de moluscos muito fragmentados e arredondados e de menor granulometria, aqui definidas, informalmente, como Coquinas do Tipo 2. A interpretação da tafonomia dos bioclastos de idade holocênica sugere pelo menos duas fácies deposicionais: (a) Fósseis articulados numa matriz areno-síltica, preenchidos por silte e argila, interpretados como originalmente depositados em regime transgressivo no ambiente Mesolitoral (foreshore) para Infralitoral superior (upper shoreface), com baixa ação de ondas. (b) Fragmentos de carapaças e quelas isoladas encontradas numa coquina fortemente cimentada por calcita espática, por vezes recristalizada, interpretados como concentrados na Zona de Arrebentação por ondas de tempestades. A dinâmica costeira atual retrabalha novamente os sedimentos inconsolidados enquanto as rochas sedimentares consolidadas (formadas pelas Coquinas Tipo 1 e 2) resistem parcialmente à erosão e constituem os altos topográficos submersos (parcéis) descritos neste trabalho.
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Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
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Composition and distribution of megabenthic communities around Svalbard were investigated in June/July 1991 with 20 Agassiz trawl and 5 bottom trawl hauls in depths between 100 and 2100 m. About 370 species, ranging from sponges to fish, were identified in the catches. Species numbers per station ranged from 21 to 86. Brittle stars, such as Ophiacantha bidentata, Ophiura sarsi and Ophiocten sericeum, were most important in terms of constancy and relative abundance in the catches. Other prominent faunal elements were eunephthyid alcyonarians, bivalves, shrimps, sea stars and fish (Gadidae, Zoarcidae, Cottidae). Multivariate analyses of the species and environmental data sets showed that the spatial distribution of the megabenthos was characterized by a pronounced depth zonation: abyssal, bathyal, off-shore shelf and fjordic communities were discriminated. However, a gradient in sediment properties, especially the organic carbon content, seemed to superimpose on the bathymetric pattern. Both main factors are interpreted as proxies of the average food availability, which is, hence, suggested to have the strongest influence in structuring megabenthic communities off Svalbard.
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Sediments from the western and southern part of the Arabian Sea were collected periodically in the spring intermonsoon between March and May 1997 and additionally at the end of the Northeast Monsoon in February 1998. Assemblages of Rose Bengal stained, living deep-sea benthic foraminifera, their densities, vertical distribution pattern, and diversity were analysed after the Northeast Monsoon and short-time changes were recorded. In the western Arabian Sea, foraminiferal numbers increased steadily between March and the beginning of May, especially in the smaller size classes (30-63 µm, 63-125 µm). At the same time, the deepening of the foraminiferal living horizon, variable diversity and rapid variations between dominant foraminiferal communities were observed. We interpret these observations as the time-dependent response of benthic foraminifera to enhanced organic carbon fluxes during and after the Northeast Monsoon. In the southern Arabian Sea, constant low foraminiferal abundances during time, no distinctive change in the vertical distribution, reduced diversity, and more stable foraminiferal communities were noticed, which indicates no or little influence of the Northeast Monsoon to benthic foraminifera in this region.
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The relative abundances of benthic foraminifers from the Oman margin have been analyzed from ODP Sites 725 and 726 near the upper boundary of the oxygen-minimum zone (OMZ) and 728 near the lower boundary. The relative abundance pattern of the benthic foraminiferal species in the two shallow sites show synchronous changes, which, together with variations in the faunal composition, may be attributed to changes in the location of the upper boundary of the OMZ during the last 7 million years. At the deeper site, the relative abundance pattern shows considerable variation in the faunal composition during the last 8 million years. The strong dominance of the shallow-water species Ammonia beccarii during the early Pliocene at Site 728 suggests a water depth less than 400 m during the early Pliocene and subsequent subsidence during the middle and late Pliocene to the present > 1400 m water depth.
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Live (Rose Bengal stained) and dead benthic foraminiferal communities (hard-shelled species only) from the Pakistan continental margin oxygen minimum zone (OMZ) have been studied in order to determine the relation between faunal composition and the oxygenation of bottom waters. During R.R.S. Charles Darwin Cruises 145 and 146 (12 March to May 28 2003), 11 multicores were taken on the continental margin off Karachi, Pakistan. Two transects were sampled, constituting a composite bathymetric profile from 136 m (above the OMZ in spring 2003) down to 1870 m water depth. Cores (surface area 25.5 cm2) were processed as follows: for stations situated above, and in the upper part of the OMZ, sediment slices were taken for the 0-0.5 and 0.5-1 cm intervals, and then in 1 cm intervals down to 10 cm. For the lower part of the OMZ, the second centimetre was also sliced in half-centimetre intervals. Each sample was stored in 10 % borax-buffered formalin for further processing. Onshore, the samples were wet sieved over 63 µm, 150 µm and 300 µm sieves and the residues were stained for one week in ethanol with Rose Bengal. After staining, the residue was washed again. The stained faunas were picked wet in three granulometric fractions (63-150 µm, 150-300 µm and >300 µm), down to 10 cm depth. To gain more insight into the population dynamics we investigated the dead (unstained) foraminifera in the 2-3 cm level for the fractions 150-300 µm and >300 µm. The fractions >300 µm and 150-300 µm show nearly the same faunal distribution and therefore the results are presented here for both fractions combined (i.e. the >150 µm fraction). Live foraminiferal densities show a clear maximum in the first half centimetre of the sediment; only few specimens are found down to 4 cm depth. The faunas exhibit a clear zonation across the Pakistan margin OMZ. Down to 500 m water depth, Uvigerina ex gr. U. semiornata and Bolivina aff. B. dilatata dominate the assemblages. These taxa are largely restricted to the upper cm of the sediment. They are adapted to the very low bottom-water oxygen values (ab. 0.1 ml/l in the OMZ core) and the extremely high input of organic carbon on the upper continental slope. The lower part of the OMZ is characterized by cosmopolitan faunas, containing also some taxa that in other areas have been described in deep infaunal microhabitats.
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Assemblages of living deep-sea benthic foraminifera, their densities, vertical distribution pattern, and diversity, were investigated in the intermonsoon period after the northeast monsoon in the Arabian Sea in spring 1997. Foraminiferal numbers show a distinct gradient from north to south, with a maximum of 623 foraminifera in 50 cm**3 at the northern site. High percentages of small foraminifera were found in the western and northern part of the Arabian Sea. Most stations show a typical vertical distribution with a maximum in the first centimeter and decreasing numbers with increasing sediment depths. But at the central station, high densities can be found even in deeper sediment layers. Diversity is very high at the northern and western sites, but reduced at the central and southern stations. Data and faunal assemblages were compared with studies carried out in 1995. A principal component analysis of intermonsoon assemblages shows that the living benthic foraminifera can be characterized by five principal component communities. Dominant communities influencing each site differ strongly between the two years. In spring 1997, stations in the north, west and central Arabian Sea were dominated by opportunistic species, indicating the influence of fresh sedimentation pulses or enhanced organic carbon fluxes after the northeast monsoon.
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Biostratigraphy and paleoenvironmental history of deep and surficial waters of the Japan Sea are addressed using sequences recovered from the floor of the backarc basin. The study is divided into two parts: (1) foraminifer biostratigraphy and paleoenvironmental assessment of sedimentary sequences recovered from above igneous basement at the four sites and (2) detailed planktonic foraminifer paleoenvironmental analysis of Quaternary and Pliocene sequences from Sites 794 and 797 in the Yamato Basin. A total of 253 samples were examined for the foraminifer biostratigraphy and 325 samples for the detailed paleoenvironmental study of Quaternary and Pliocene sequences. Low abundance and sporadic occurrence of foraminifers limited interpretation of results. Foraminifer-bearing intervals were correlated where possible to diatom and calcareous nannofossil zonations, and the sequences were successfully assigned to the foraminifer zonation of Matsunaga. Unfortunately, extensive barren intervals and sporadic occurrences of planktonic foraminifers prevented zonation of Quaternary and Pliocene intervals, although some interesting conclusions about paleoenvironment were possible and are listed below. A sequence of Neogene (sensu lato) paleoenvironmental events were identified: (1) deepening of the Yamato basins to middle bathyal depths by the early to middle Miocene, an event contemporaneous with the age of some deep basins known from uplifted sections adjacent to the Japan Basin; (2) cooling of the Japan Sea in the early middle Miocene; (3) oxygenation of deep waters in the late Miocene; (4) further cooling of surficial water masses between the Olduvai Subchron and the Brunhes/Matuyama Boundary; and (5) extermination of lower middle bathyal faunas and replacement by upper middle bathyal faunas near the base of the Quaternary.